Animal models of fibromyalgia
© BioMed Central Ltd. 2013
Published: 5 December 2013
Animal models of disease states are valuable tools for developing new treatments and investigating underlying mechanisms. They should mimic the symptoms and pathology of the disease and importantly be predictive of effective treatments. Fibromyalgia is characterized by chronic widespread pain with associated co-morbid symptoms that include fatigue, depression, anxiety and sleep dysfunction. In this review, we present different animal models that mimic the signs and symptoms of fibromyalgia. These models are induced by a wide variety of methods that include repeated muscle insults, depletion of biogenic amines, and stress. All potential models produce widespread and long-lasting hyperalgesia without overt peripheral tissue damage and thus mimic the clinical presentation of fibromyalgia. We describe the methods for induction of the model, pathophysiological mechanisms for each model, and treatment profiles.
Chronic pain is an abnormal and non-protective response that represents a significant health problem affecting over 100 million Americans - more than diabetes, cancer, and heart disease combined . It has been defined as pain that outlasts normal tissue healing time or pain that lasts longer than six months. Approximately 14% of the US population suffers from chronic widespread muscle pain conditions such as fibromyalgia (FMS) . FMS is characterized by widespread pain, which includes the trunk, widespread tenderness to pressure stimuli, and morning stiffness. FMS is also associated with a number of other symptoms, including pronounced fatigue, sleep disturbances, and psychological disturbances (depression and/or anxiety) . The prevalence of co-morbid symptoms varies across the population, with pain and fatigue occurring in up to 100% of the population, sleep disturbances in 90% and depression or anxiety occurring in 40% .
While the underlying cause of FMS is unknown, it has become increasingly clear that a number of systems are altered in people with FMS. Several hypotheses have been proposed as the underlying pathophysiology of FMS: muscular dysfunction, central sensitization, alterations in the hypothalamic-pituitary-adrenal (HPA) axis, and deficits in endogenous pain-modulating systems .
Currently patients are managed in a multidisciplinary approach, but are rarely cured. Therefore, it is imperative that a greater understanding of potential causes and pathology in FMS be investigated to guide development of new therapeutics and enhance current treatment strategies. A series of basic pathological alterations have been shown in human subjects. Enhanced cortisol responses and abnormal growth hormone regulation implicate the HPA axis . Reduced serotonin, increased substance P and increased nerve growth factor found in the cerebrospinal fluid of patients with FMS suggest alterations in inhibitory and excitatory neurotransmitters in the central nervous system [3, 4]. Enhanced central amplification and reduced central inhibition of pain [3, 4] implicate alterations in the central neural response to pain. Additionally, there is a strong familial aggregation for FMS, and evidence for polymorphisms of genes in the serotoninergic, dopaminergic and catecholaminergic systems [3, 4]. Considering a number of multiple changes in different organic systems, it has been suggested that several factors contribute to FMS, which may be a manifestation of multiple syndromes with similar symptoms. The development of an animal model mimicking FMS is therefore difficult, though the use of animal models are substantially important to gain a better understanding of the development and maintenance of FMS and guide the development of new therapeutics.
Animal models of disease states are valuable tools for developing new treatments and investigating underlying mechanisms. They should mimic the symptoms and pathology of the disease and importantly be predictive of effective treatments. FMS is a differentiated pain syndrome as it is diagnosed by symptoms, not by pathological conditions. Thus, an animal model of FMS ideally should include widespread pain and the associated symptoms.
In this review, we present different animal models that mimic the signs and symptoms of FMS. These models produce widespread and long-lasting hyperalgesia without overt peripheral tissue damage and thus mimic the clinical presentation of FMS. For example, several of these models use multiple low-intensity insults to induce the widespread hyperalgesia (for example, multiple acid injections, fatigue with acid injections, hyperalgesic priming), while another uses disruption of biogenic amines in the central nervous system mimicking underlying changes observed in FMS. Lastly, several use unavoidable stress, a known trigger in people with FMS.
Challenges for developing fibromyalgia-like animal models
Main findings of different animal models of fibromyalgia according to central and peripheral factors
Repeated muscle insult
Acid saline induced pain
No peripheral damage 
Reversal of mechanical hyperalgesia by neurotrophin-3 
Muscle hyperalgesia is similarly developed if the first acid injection is performed in different muscles, such as right lateral gastrocnemius, right medial gastrocnemius or left lateral gastrocnemius, keeping the second injection at the same site for all 
ASIC3-/- mice do not develop hyperalgesia 
ASIC3-/- mice do not develop hyperalgesia or central neuron sensitization, localization of ASIC3 in muscle afferents 
Substance P mediates NK1 receptor pathway to block acid activation in muscle nociceptors 
Shift of the cardiac autonomic balance towards a sympathetic predominance and reduction in baroreceptor reflex sensitivity 
Aerobic exercise with treadmill running reduces cutaneous and muscle hyperalgesia and increases neurotrophin-3 levels in muscle 
Increased ERK activity in the amygdala, and increased post-synaptic excitatory transmission from parabrachial nucleus in amygdala 
T-type calcium channels mediate hyperalgesia supraspinally, increases in ERK in paraventricular thalamus that depend on activation of T-type calcium channels 
Local anesthetic in the RVM during the second injection prevents the development of muscle hyperalgesia and reverses existing hyperalgesia 
Increased release of glutamate and aspartate and decreased glycine in the RVM during the second injection 
Reversal of both cutaneous and muscle hyperalgesia through microinjection of NMDA receptor antagonists into the RVM, and only cutaneous hyperalgesia into the NGC 
Increased expression of NR1 subunit of NMDA receptor in the RVM produces muscle hyperalgesia; downregulation of NR1 subunit in RVM prevents development of muscle hyperalgesia 
Reversal and prevention of hyperalgesia by blockade of spinal NMDA and non-NMDA glutamate receptors 
Increased number of spinothalamic neurons expressing p-NR1 in lamina X of the spinal cord 
Increased number of spinothalamic neurons expressing p-NR1 in lamina X of the spinal cord 
Increased spinal glutamate and aspartate concentrations in the spinal cord in a calcium-dependent manner 
Phosphorylation of CREB through activation of the spinal cAMP pathway in a time-dependent manner 
Muscle stimulation produces Fos expression ipsilaterally in all regions of the dorsal horn; paw stimulation produces ipsilateral Fos expression in the superficial spinal laminae, and bilaterally in deep laminae 
Reversal of mechanical hyperalgesia by μ and δ opioid receptor agonist (but not κ), glutamate receptor antagonist, pregabalin, reuptake inhibitors, K+ channel opener, Na+ channel blocker, but not cyclooxygenase-2 inhibitor and benzodiazepine; co-administration of tramadol and milnancipran is more effective in reducing muscle hyperalgesia than tramadol alone [20, 25–28]
Low intensity exercise reduces mechanical hyperalgesia, which is attenuated by opioid receptor agonist ; regular exercises prevent the development of muscle pain and exercise-induced chronic muscle pain through the decrease of phosphorylation of the NR1 in the RVM 
Development of chronic muscle hyperalgesia (2 weeks) after acute muscle inflammation 
IL-6 in muscle primes response to subsequent PGE2, and antisense to IL-6 or gp130 prevents hyperalgesic priming 
Spinal pretreatment with oligodeoxynucleotide antisense to PKCϵ reduces muscle hyperalgesia 
Cutaneous inflammation primes the hyperalgesic response to a subsequent injection of PGE2, 5-HT, or A2 agonist; PKCϵ inhibitor prevents priming effect 
αCaMKII produces hyperalgesic priming; inhibition of αCaMKII prevents activation of PKCϵ-induced priming; activation of αCaMKII produces priming that is not prevented by pretreatment with PKCϵ antisense 
Inhibitors of enzymes implicated in the metabolism of cyclic nucleotides to adenosine; A1 adenosine receptors block late phase of PGE2-induced muscle hyperalgesia 
Pretreatment with a selective neurotoxin (IB4-saporin) prevents GDNF-induced hyperalgesia; NGF and PsiepsilonRACK produce muscle hyperalgesia 
Hyperalgesic priming is reversed through the inhibition of translation in the peripheral terminal of the nociceptor 
Fatigue enhanced muscle pain
Female mice show greater enhancement of hyperalgesia that is prevented by ovariectomy (whole body fatigue); greater time-window, greater spatial window for induction of hyperalgesia, and longer lasting hyperalgesia not affected by ovariectomy (single-muscle fatigue) [39, 41]
Blockade of RVM NMDA receptors during fatigue prevents development of hyperalgesia 
Prevention of hyperalgesia and enhanced p-NR1 in RVM by regular physical activity 
Biogenic amine depletion
Reduction of levels of biogenic amines in central nervous system 
Increased time of immobility as a measure of depression 
Enhanced sensitivity to muscle and cold stimuli after reserpine; no pathology in peripheral nerves or brain 
Depletion of biogenic amines with reserpine leads to development of muscle hyperalgesia that is reversed by pregabalin, duloxetine, and pramipexol, but not diclofenac; 5HT2C receptor agonists reverse muscle hyperalgesia induced by reserpine; NSAIDs have no effect [43, 45]
Increased plasma corticosterone concentration; no change in anxiety or depression-like behaviors 
Decreased serotonin and its metabolites in brain and spinal cord after repeated cold stress 
Decreased morphine analgesia; increased U50,488 analgesia; decreased DAMGO analgesia when given supraspinally; diazepam prevented the decreased DAMGO analgesia 
Post-translational changes in proteins supraspinally after stress 
Widespread hyperalgesia of paw, viscera and jaw muscle 
Increased anxiety 
IL-6 downregulation on primary afferents prevents hyperalgesia dependent on glucocorticoids and catecholamines 
Subchronic swimming stress
Enhanced c-fos expression in response to formalin spinally 
Fibromyalgia-like animal models
The models outlined below primarily develop in response to repeated stimuli applied to the muscle, or stress combined with nociceptive stimuli applied to the muscle. In fact, these stimuli are often below threshold or produce a short lived response hyperalgesia in the animal, but when combined can produce a much longer-lasting hyperalgesia. While the duration of the hyperalgesia varies between models, and in some cases between sexes, the common theme of repeated insults to the organism remains. The combination of repeated insults is time-dependent with an ‘ideal’ window separating the multiple insults for the hyperalgesia to develop [5, 39]. It is also clear that, in some of the models, the noxious stimuli can be given in distinctly different regions of the body and still produce hyperalgesia [9, 39]. Combinations of stress along with muscle insult can prolong the duration of hyperalgesia. How this relates to the etiology of FMS is not entirely clear, but it may be that a combination of multiple stressors to the organism is necessary for widespread, long-lasting hyperalgesia to occur. These stressors could be repeated low-intensity localized insults, or could be more widespread and include conditions such as a sedentary lifestyle, stress, fatigue, obesity, or sex. These factors can result in molecular and cellular changes in both nociceptors and in central neurons that result in sensitization to maintain the pain. Further, the peripheral and central pathways can interact to further enhance the observed molecular and cellular changes to enhance the pain. Future studies will be required to translate these findings from animal models to human subjects.
Repeated muscle insult models: priming
Acid saline-induced pain model
The non-inflammatory pain model induced by repeated intramuscular acid injections in rodents has been suggested to have face validity to chronic widespread pain conditions (such as FMS) in humans. In this model, two injections of acid saline (pH 4.0) separated by 2 to 5 days, given unilaterally into the gastrocnemius muscle, produce a bilateral decrease in hindpaw and muscle mechanical withdrawal thresholds that lasts for 4 weeks (male and female rats and mice) [5, 24, 25]. Further, there is enhanced visceral (secondary) hyperalgesia and reduced physical activity (male rats and mice) [6, 7]. Administrating the first acid injection into one gastrocnemius muscle and the second to the contralateral gastrocnemius muscle produces comparable hyperalgesia to that produced by both acid injections in the same muscle (male rats) . There is also modulation of the cardiac autonomic system after the development of mechanical hyperalgesia, shifting the autonomic balance towards a sympathetic predominance and reduction in baroreceptor reflex sensitivity (male rats) . This experimental pre-clinical finding reinforces the hypothesis that different organic systems present simultaneous dysfunctions in FMS.
In this model hyperalgesia develops similarly between male and female mice , and shows similar results between rats and mice [5, 10]. Morphological analysis of the injected muscle reveals no obvious muscle damage or inflammation associated with acidic saline injections, and removal of afferent input from the injected site has no effect on the contralateral hypersensitivity (male rats) . On the other hand, the hypersensitivity once developed is reversed by blockade of excitatory activity spinally or supraspinally (male rats) [16, 18, 20, 23]. Together, these data suggest that once developed, this model is maintained primarily by central mechanisms and is independent of a nociceptive drive. It further mimics the clinical presentation of signs and symptoms observed in FMS with widespread hyperalgesia, minimal muscle tissue damage, alterations in central nociceptive processing, and alterations in cardiovascular autonomic balance.
Induction of hyperalgesia Peripheral, spinal and supraspinal mechanisms are all involved in the induction of the hyperalgesia in this repeated acid model. Induction of the model requires activation of acid sensing ion channel (ASIC)3 in muscle afferents as ASIC3-/- mice do not develop hyperalgesia (male and female) , suggesting activation of muscle afferents initiates the hyperalgesia. In human subjects, infusion of acidic buffer into the muscle produces pain and hyperalgesia, with females being more likely to develop referred pain than males [64, 65].
Neurotrophin (NT)-3 overexpression in muscle prevents chronic secondary hyperalgesia induced by acid saline injection (male and female mice) . Further, spinal increases in c-fos after repeated acid injection are prevented by NT-3 overexpression , further supporting that initial activation of muscle afferents drives central changes.
Interestingly, muscle hyperalgesia is produced by a single acid injection in mice with a deletion of the tachykinin precursor 1 (Tac1) gene or those given a co-administration of neurokinin 1 (NK1) receptor antagonists at the time of induction, suggesting that substance P may play a role in inhibiting the development of widespread pain . Substance P inhibits acid activation of ASIC3-muscle nociceptors and this may play a role in regulating development of chronic widespread pain .
Central mechanisms involving the spinal cord, brainstem and cortex have also been implicated in the development of hyperalgesia in this repeated acid model. Development of acid-induced hyperalgesia can be prevented by blockade of neuronal activity in the rostroventral medial medulla (RVM), a site known to facilitate nociception, during the second acidic saline injection, but not during the first, suggesting alterations in the RVM in response to the first injection (male rats) . Indeed, during the second acidic saline injection, excitatory neurotransmitter release increases and inhibitory neurotransmitter release decreases in the RVM (male rats) . Thus, alterations in excitatory and inhibitory balance in the RVM could potentially trigger development of widespread hyperalgesia.
Spinally, development of hyperalgesia is delayed by blockade of NMDA-glutamate receptors during the second injection but not the first (male rats) . In parallel there is an increase in release of the excitatory neurotransmitter glutamate in the spinal cord during the second but not the first acid injection (male rats) . Similar to the RVM, glycine is decreased in response to the second acidic saline injection . Thus, as in the RVM, alterations in excitatory and inhibitory balance can trigger development of hyperalgesia.
Little is known about cortical sites in this model despite evidence from imaging studies implicating several cortical areas in abnormal processing of nociceptive input in people with FMS . Recently, however, Cheng and colleagues  have investigated cortical and thalamic sites; there are increases in phosphorylation of ERK and there is enhanced postsynaptic excitatory transmission from the parabrachial nucleus in the central nucleus of the amygdala (male and female mice). Increases in phosphorylation of ERK also occur in the paraventricular thalamus after repeated acid injections (male and female mice) . The hyperalgesia and the increases in phosphorylation of ERK are prevented by intracerebroventricular blockade of T-type Ca2+ channels (T-channels) . Conversely, if ERK is not phosphorylated, hyperalgesia is not prevented . Together these data suggest that cortical sites are altered by repeated acid injections. Future studies should continue to examine cortical sites and connections between cortical sites and brainstem sites to gain an understanding of this pain condition.
Maintenance of hyperalgesia The hyperalgesia in this model appears to be independent of continued afferent input as removal of muscle afferents or blockade of ASICs has no effect on it once developed (male mice and rats) [5, 67, 68]. Furthermore, expression of ASIC-like currents or their properties in labeled muscle dorsal root ganglion neurons are not altered following repeated acid injections, suggesting that hyperalgesia is not related to changes in ASIC expression in this model (male mice) . Indeed, maintenance of the hyperalgesia once developed involves activation of spinal and supraspinal mechanisms.
In the spinal cord, recordings from nociceptive spinal neurons show enhanced sensitivity to innocuous and noxious mechanical stimuli bilaterally along with a bilateral spread of receptive fields (male and female mice) . Spinally, after development of hyperalgesia there are increases in concentrations of glutamate, increases in phosphorylation of the NR1 subunit of the NDMA receptor in spinothalamic tract neurons, and increases in phosphorylation of the transcription factor CREB (male rats) [21–23], all suggesting increased excitatory activity in the spinal cord. Blockade of NMDA or non-NMDA glutamate receptors, or the cAMP pathway reverse the already developed hyperalgesia (male rats) [20, 23]. Interestingly, spinal activation of the protein kinase C (PKC) pathway produces mechanical hyperalgesia that is prevented by blocking PKC, NMDA, or AMPA/kainite receptors. Nonetheless, PKC is not used for maintaining chronic hyperalgesia in this model (male rats) .
The RVM appears to be integral to the maintenance of chronic widespread pain after repeated acid injections. Blockade of neuron activity in the RVM reverses the acid-induced muscle hyperalgesia, suggesting the RVM plays a key role in maintaining hyperalgesia once developed (male rats) . NMDA receptors in the RVM play a key role in the hyperalgesia induced by repeated acid injections. Over-expression of the NR1 subunit of the NMDA receptor in the RVM produces hyperalgesia; downregulation of NR1 in the RVM reduces hyperalgesia; there is enhanced phosphorylation of NR1 in the RVM; and blockade of NMDA receptors in the RVM reverses the existing hyperalgesia (male rats) [18, 19].
Thus, repeated intramuscular injections require muscle afferents and central mechanisms for induction of hyperalgesia; and central mechanisms for maintenance. A variety of excitatory and inhibitory neurotransmitters, receptors, and pathways are involved in this process. Future investigations should expand on these studies in the spinal cord and brainstem, and begin to look for changes in cortical areas that process pain.
This model shows a similar pharmacological management profile to clinical treatment of FMS: reductions in pain and hyperalgesia by antidepressants, anticonvulsants, opioids, glutamate receptor antagonists, K+ channel openers, Na+ channel blocker and exercise, but not non-steroidal anti-inflammatory drugs (NSAIDS; male rats) [13, 25–29, 70]. Administration of alosetron (5-HT3 receptor antagonist), either intravenously or intrathecally, reverses the mechanical hypersensitivity observed after acid saline injections and prevents the development of visceral hyperalgesia (male rats) . Pregabalin (anticonvulsant drug) decreases both cutaneous and deep tissue hyperalgesia (male rats) . Moreover, tramadol (a centrally acting synthetic opioid analgesic used to treat moderate to moderately severe pain) and milnacipran (a serotonin-norepinephrine reuptake inhibitor used in the clinical treatment of FMS) showed a potent antihyperalgesic effect when administered together (male rats) . Taken together, acid-induced hyperalgesia is able to be reversed by a series of analgesic strategies commonly used clinically in FMS.
Exercise is an effective treatment clinically for FMS . Similarly, in the repeated acid model mechanical hyperalgesia is reversed or prevented with different exercise protocols. Low intensity exercise (walking on a treadmill for 5 consecutive days) reverses hyperalgesia in an opioid-dependent manner (male rats) . Moderate-intensity exercise training (walking on a treadmill for 5 days per week for 3 weeks) decreases cutaneous and deep tissue acid saline-induced mechanical hyperalgesia and increases NT-3 in muscle (female mice) , suggesting the reduction in mechanical hyperalgesia after exercise may be a result of elevated levels of NT-3 protein. Regular exercise training in running wheels (8 weeks) prevents the development of chronic muscle hyperalgesia in mice (male mice) . In parallel, the increase in phosphorylation of NR1 that normally occurs after repeated acid injections does not occur in animals that were physically active (running wheels) . Thus, the model is responsive to exercise as well as pharmacological management.
Limitations and future directions
The hyperalgesia that develops in this model is generally considered widespread and includes bilateral hindlimb muscles, paw and viscera [6, 25]; however, it is unclear if there are changes in other areas of the body, such as the forelimbs. The model does show reduced activity levels, and develops in sedentary but not physically active animals [7, 72] and thus mimics the reduced activity and enhanced prevalence of chronic pain in people with FMS [73, 74]. Future studies should confirm the prevention of chronic pain in human populations with acute pain by improving activity levels. It is unclear if there are co-morbid symptoms of depression, anxiety, fatigue or sleep disturbances in this model, and future studies should assess these co-morbidities. While the pharmacological profile of this model generally matches that of people with FMS, the model is sensitive to opioids delivered intrathecally , which is different from the clinical picture of those with FMS ; however, it should be noted that tramadol, a weak opioid agonist combined with a reuptake inhibitor, is effective in people with FMS . Lastly, most studies were performed in male mice or rats despite the fact that FMS occurs more frequently in females; future studies should perform mechanistic studies in both males and females.
Hyperalgesic priming model
Another model with multiple insults uses an acute inflammatory insult or mediator to induce hyperalgesia. After the hyperalgesia resolves, prostaglandin E2 (PGE2) injected into the same muscle results in a muscle hyperalgesia that lasts for at least 14 days as compared to hours in controls that did not receive the inflammatory insult (carrageenan or IL-6) (male rats) [31, 33]. Similarly, priming of the skin with carrageenan injected intradermally to the hindpaw results in a prolonged response to PGE2 lasting over 24 hours compared to less than 4 hours in naive animals (male rats) [32, 34, 37].
Induction of hyperalgesia
Peripheral mechanisms have been extensively studied in this model. Specifically, depletion of IB4(+) nociceptors with the neurotoxin IB4-saporin prevents the development of the hyperalgesia (male rats) . Further, depletion of the second messenger PKCϵ (with an oligodeoxynucleotide antisense) also prevents the development of the hyperalgesia (male rats) . Conversely, PsiepsilonRACK, which selectively activates PKCϵ, induces muscle hyperalgesia (male rats) . Inhibiting α calmodulin-dependent protein kinase II prevents activation of PKCϵ-induced priming (male and female rats) . Thus, these data show that IB4+ nociceptors and PKCϵ along with α calmodulin-dependent protein kinase II play a significant role in the priming model of muscle hyperalgesia.
The maintenance of the hyperalgesia in this priming model also involves peripheral nociceptors. Hyperalgesic priming is reversed through the inhibition of translation in the peripheral terminal of the nociceptor by injecting either rapamycin or cordycepin into muscle (male rats) . In inflammation-pretreated animals, the late phase of PGE2-induced hyperalgesia, but not the early, was blocked by injecting inhibitors of enzymes that block the metabolism of cyclic nucleotides to adenosine, and by blockade of A1 adenosine receptors (male rats) . Thus, once developed, changes in nociceptors that are related to increased gene production, activation of PKCϵ and adenosine may maintain the hyperalgesia in the hyperalgesic priming model.
Limitations and future directions
The hyperalgesia that develops in this model lasts for at least 2 weeks after induction ; it is unclear how long this hyperalgesia continues. It is clear that the hyperalgesia is longer-lasting than when the same stimuli are applied to the skin  and may indicate differential processing of muscle and cutaneous pain either peripherally or centrally. Standard pharmacological and non-pharmacological treatments for FMS, co-morbid symptoms of FMS, and changes in central processing have yet to be studied in this model. Again, most studies were performed in males and future studies should perform experiments in both sexes to ensure mechanisms are similar.
Fatigue-enhanced muscle pain
Combining a muscle fatiguing task with a low-intensity muscle insult results in long-lasting and widespread hyperalgesia. Muscle fatigue has been produced by either having animals run in a running wheel for 2 hours prior to the muscle insult or by direct electrical stimulation of the muscle. The whole-body fatiguing task has been followed by either two intramuscular injections of pH 5.0 saline or one intramuscular injection of 0.03% carrageenan (male and female mice) [40–42]. Long-lasting muscle and cutaneous hyperalgesia develop after the muscle insult combined with whole-body fatigue. There is no muscle damage, no change in muscle lactate, pCO2, pO2, creatinine kinase, phosphate, or histology in whole-body fatigued animals. Further, in this whole-body fatigue model, there is an enhanced hyperalgesia (carrageenan plus fatigue) in female mice compared to male mice that is dependent on estrogen .
A single muscle fatigue task, induced by electrical stimulation, in combination with two injections of pH 5.0 saline, also enhances the hyperalgesia in a sex-dependent manner (male and female mice) . Specifically, male and female mice, fatigued immediately prior to muscle insult in the same muscle, develop similar muscle hyperalgesia 24 hours later. However, female mice develop hyperalgesia contralaterally and the hyperalgesia lasts longer. Further hyperalgesia is easier to induce in female mice: females develop hyperalgesia when the muscle fatigue and muscle insult occur in different muscles, and when muscle insult is administered 24 hours after fatigue. The muscle insult with or without muscle fatigue results in minimal inflammatory changes in the muscle itself, and sex differences are not related to estradiol (ovariectomy) or changes in brainstem activity (pNR1) .
For the whole-body fatigue task, there is increased activation of neurons in the brainstem RVM: nucleus raphe pallidus, obscurus, and magnus as measured by c-fos expression in response to the fatigue task. Further, there is increased phosphorylation of the NR1 subunit of the NMDA receptor in the RVM after the whole-body fatigue task combined with muscle insult (male and female mice) [42, 72], and blockade of NMDA receptors in the RVM during the fatigue task prevents the development of the hyperalgesia (male and female mice) . In contrast, the single-muscle fatigue task combined with muscle insult has no effect on the phosphorylation of NR1 in the RVM (male and female mice) . It appears that the whole-body fatigue model involves central changes in the brainstem in sites involved in both pain and fatigue while the single muscle fatigue model may involve different mechanisms. Future studies are needed to understand in more detail the underlying mechanisms of these models.
Limitations and future directions
The hyperalgesia that develops in the fatigue-induced models lasts for between 7 days (males) and 35 days (females) . It is clear that muscle fatigue can enhance the hyperalgesia produced by low-intensity muscle insult, as observed in people with FMS . However, how this muscle fatigue relates to symptoms of fatigue in people with FMS is unclear. Standard pharmacological and non-pharmacological treatments for FMS and co-morbid symptoms of FMS are yet to be determined.
Biogenic amine depletion model
Description and pathophysiology
For this animal model, biogenic amines are depleted systemically by reserpine to mimic the alterations in biogenic amines observed clinically in FMS (male rats) [43–45]. Repeated administration of reserpine (1 mg/kg subcutaneously, once daily, for three consecutive days) causes long-lasting widespread muscle and cutaneous hyperalgesia that is sustained for at least 1 week in both male and female rats. This treatment regimen decreases the amount of biogenic amines (dopamine, norepinephrine, and 5-hydroxytryptamine) in the spinal cord, thalamus, and prefrontal cortex. There is also an increase in immobility time in the forced swim test, a test for depression, which is a common co-morbid symptom of FMS (male rats) .
Reserpine-induced mechanical hyperalgesia is reduced by administration of anticonvulsants, serotonin-norepinephrine reuptake inhibitors, and dopamine agonist drugs, but not by NSAIDs. Lorcaserin, YM-348 and vabicaserin, all 5HT2C receptor agonists, also reverse the hyperalgesia induced by reserpine (male rats) . The lack of NSAID-induced analgesia, and the modulation amines, matches the pharmacological profile for managing chronic pain in FMS [78, 79].
Limitations and future directions
While this model has been characterized pharmacologically, and animals show signs of the co-morbid symptom of depression, future studies are needed to determine how alterations of the serotonergic system contribute to the development and maintenance of hyperalgesia. Further, all the studies so far have been performed in males and future studies should confirm these effects in females and examine if there are differences in the mechanisms between males and females.
Intermittent cold stress (ICS), also referred to as repeated cold stress, is used as a procedure for a mouse model that mimics symptoms of chronic widespread pain. In the ICS model, mice are kept in a cold room (-3 to +4°C) overnight for 3 days, and transferred between normal room temperature (24°C) and a cold room every 30 minutes during the day (male rats) . Muscle hyperalgesia lasts at least 3 weeks after repeated cold stress and was longer and more severe after stress at -3°C than at 4°C. Cutaneous hyperalgesia was observed after stress at -3°C, but not at 4°C (male rats) . This model has several advantages, as no specific apparatus, except for a conventional refrigerator, is necessary, and the short period of stress application (three nights) is sufficient to cause hyperalgesia. While plasma corticosterone concentration is increased after ICS stimulus, anxiety and depression-like behaviors do not develop .
Supraspinal and spinal nociceptive processing is altered in the cold stress-induced myalgia . Supraspinally, an ICS-induced impairment in the descending inhibitory system has been reported. There is a reduction of both serotonin (5-HT) and 5-hydroxy indoleacetic acid (5-HIAA) levels in supraspinal regions, such as hypothalamus, thalamus, midbrain, and pons plus medulla oblongata, in repeatedly cold-stressed rats (male rats) . ICS-induced hyperalgesia is reduced by spinal blockade of substance P, calcitonin-gene-related peptide, NMDA-glutamate receptors and neurokinin-1 receptors (male rats) [51–53]. Further, there are alterations in the opioid system in the spinal cord in ICS-treated rats with decreases in mu-opioid agonist antinociception, and increases in antinociception by kappa-opioid receptors (male mice) . In addition, post-translational changes in proteins have been observed supraspinally after ICS (male rats) . Thus, spinal and supraspinal changes in both excitatory and inhibitory systems are observed and may underlie the development and maintenance of the hyperalgesia in this model.
Anticonvulsant and antidepressant drugs reduce ICS-induced hyperalgesia. Specifically, systemic gabapentin reverses hyperalgesia at the one-tenth dose for neuropathic pain-induced rats, and central gabapentin produced long-lasting analgesia (4 to 5 days) in the stress-induced hyperalgesia model, but not in the neuropathic pain model (male and female mice) . A single or repeated intrathecal administration of the antidepressant (milnacipran, amitriptyline, mianserin or paroxetine) reduces hyperalgesia (male mice) . Morphine produces analgesia in ICS mice when injected spinally or peripherally, but not systemically or supraspinally, suggesting that supraspinal sites do not contribute to the analgesia of morphine in this model (male mice) . One hypothesis proposed by the authors is that the lack of morphine-induced analgesia supraspinally could be explained by a loss of descending pain-inhibitory activation, as periaqueductal gray-RVM-spinal cord interconnection areas are important sites for morphine analgesia (male mice) .
Limitations and future directions
The hyperalgesia that develops in this model lasts for at least 3 weeks after induction ; it is unclear how long this hyperalgesia continues. Standard pharmacological agents effective in FMS are also effective in this model; however, differing from FMS  opioids reduce the hyperalgesia in the cold-stress model. Co-morbid anxiety and depressive-like behaviors do not develop in this model, differing from people with FMS; other co-morbid symptoms have not been tested. Again, most studies have been performed in males and future studies should include females and confirm the mechanisms are similar between males and females.
Sound stress model
In this model, animals are exposed to sound stress over 4 days. Animals are placed in a cage placed 25 cm from a speaker that emits 4 pure tones (5, 11, 15, and 19 kHz). Amplitudes vary through time independently from 20 to 110 dB level at random times each minute, lasting 5 or 10 seconds. Animals are exposed to the sound stressor on days 1, 3, and 4 (male rats) . Sound stress by itself has no effect on mechanical sensitivity in rats. However, there is an increase and more prolonged cutaneous hyperalgesia in response to local injections of PGE2 or epinephrine . There is also an increase in visceral sensitivity and hyperalgesia of the masseter muscle after intraplantar PGE2 in animals exposed to sound stress, showing the widespread nature of the hyperalgesia (male rats) . Further, animals show increases in the anxiety index on the elevated plus maze, suggesting animals show a co-morbid anxiety . Together these symptoms of widespread hyperalgesia (paw, viscera, jaw) and anxiety mimic clinical symptoms and co-morbidities in FMS patients who have widespread pain, and a higher incidence of irritable bowel syndrome, temporomandibular disorder, and anxiety.
The repeated exposure to sound stress leads to long-lasting increased activity of catecholamine synthesizing enzymes in the adrenal medulla (male rats) [55, 58] that results in increased plasma levels of epinephrine for at least 28 days after the last exposure to sound stress , suggesting that a long-lasting stress-induced alteration in the animal persists well beyond exposure to the starting stress factor. After sound stress, lipopolysaccharide injected into skeletal muscle results in long-lasting mechanical hyperalgesia. Treatment with antisense oligodeoxynucleotide to decrease expression of IL-6 receptor on primary afferent neurons blocked lipopolysaccharide-induced hyperalgesia in stressed rats, but did not attenuate it in non-stressed rats (male rats) . Thus, alterations in cytokines and the HPA axis may underlie stress-induced enhancement of hyperalgesia.
Limitations and future directions
The duration of hyperalgesia and the responsiveness of the hyperalgesia to clinical pharmacological agents used to treat FMS should help to characterize and validate the model. Co-morbid anxiety develops in this model and future studies could confirm other co-morbid symptoms like depression, fatigue, or sleep disturbances. Again the studies were performed only in male rats and thus future studies should include females and confirm mechanisms are similar between males and females.
Subchronic swim stress
In the subchronic swim stress model, rats are forced to swim in water at room temperature for 10 to 20 minutes per day for 3 days (male rats) . Animals develop hyperalgesia to thermal stimulus (hot plate), decreases in grip force lasting for up to 9 days and enhanced response to inflammatory stimuli (formalin and carrageenan) (male rats) [59–61]. Changes in the spinal cord have been observed in this model with enhanced c-fos expression in response to formalin, decreased basal and evoked release of the inhibitory neurotransmitter GABA and enhanced basal and evoked release of glutamate (male rats) [60, 62, 63], suggesting both enhanced central excitability and reduced central inhibition. Pharmacological validation of the model has been done by showing efficacy to reuptake inhibitors (clomipramine, fluoexite, milnacipran), the serotonin precursor tryptophan, and diazepam (male rats) [59, 61, 62].
Limitations and future directions
This model has only begun to be characterized and future studies can begin to examine underlying mechanisms. It is unclear if there is enhanced widespread hyperalgesia to mechanical stimuli as well as thermal stimuli, if there are alterations in peripheral and supraspinal nociceptive pathways, if there are sex differences in the induction or presentation of the model, or if there are co-morbid symptoms.
Other emerging stress models
Other models combining stress with a peripheral insult have recently emerged and may prove useful in the study of FMS. These include the restraint-stress model where rats are restrained in plexiglass tubes (1 hour per day, daily for 6 weeks) that eliminate movement (male rats) . These animals show signs of hyperalgesia to mechanical, heat and cold stimuli within a week that remains through the 6 weeks of stress, and enhanced response to formalin . Using ultrasonic vocalization as a sign of stress, rats were subjected to unavoidable scrambled foot shock-light stimuli. In this model there is enhanced response to formalin that is reduced by pregabaline and reuptake inhibitors (male rats) .
The current available animal models of chronic widespread pain have been induced by different means, including repeated muscle insults (priming techniques), depletion of biogenic amines, and stress with or without muscle insult. Similarities in presentation with widespread hyperalgesia and minimal peripheral tissue damage are found in nearly every model. However, there are clear peripheral and central nervous system changes that may be dependent on the individual model. These models are all relatively new and are currently being explored in more detail. Several questions arise from each of these models and there are some central themes to each. Which models result in peripheral sensitization? Which models result in central sensitization? Is there a continued afferent driver in some conditions? Is there a central driver in others? Are excitatory neurotransmitters, such as substance P, glutamate, or neurotrophic factors, altered peripherally or centrally? Is there involvement in other systems such as the immune system, endocrine system, or the hypothalamic-pituitary axis? How does each of these models differ and how are they similar? Do these models show a similar pharmacological and non-pharmacological treatment profile to people with chronic widespread pain? Will these models be predictive of future treatments and be useful for drug development?
So far, studies on animal models of FMS included in this review have essentially focused on sensory changes such as mechanical and thermal hyperalgesia for characterizing those models. This is an excellent start and completely comprehensible as widespread pain is the main symptom in FMS . However, effects on physical activity levels, quality of life and non-reflexive behavioral tests should also be considered. In addition, co-morbid symptoms such as fatigue or sleep disturbances, as well as emotional dysfunction, including anxiety, depression and mood should be investigated. Interestingly, while FMS is predominately a female disease, most studies were done on males. Future studies should at minimum include female mice in the dataset and examine for potential sexual dimorphisms.
The animal models reviewed in this manuscript are diverse in terms of induction, and diverse in terms of potential underlying mechanisms. No one model is likely the ‘ideal’ or ‘best’ model to mimic FMS. As FMS is also a diverse syndrome that likely has multiple etiologies and multiple subtypes, these models may be useful to ascertain particular pathways and mechanisms that could be altered to result in the manifestation of chronic widespread pain. A mixture of diverse animal models of FMS, each mimicking particular biomarkers and clinical conditions observed in FMS, may contribute to the comprehension of its pathophysiology and improvement of its management.
This article is part of the series on New perspectives in fibromyalgia, edited by Daniel Clauw. Other articles in this series can be found at http://arthritis-research.com/series/fibromyalgia
Acid sensing ion channel
Intermittent cold stress
Non-steroidal anti-inflammatory drug
Protein kinase C
Rostroventral medial medulla.
Supported by NIH AR061371.
- Gaskin DJ, Richard P: The economic costs of pain in the United States. J Pain. 2012, 13: 715-724. 10.1016/j.jpain.2012.03.009.View ArticlePubMed
- Clauw DJ, Crofford LJ: Chronic widespread pain and fibromyalgia: what we know, and what we need to know. Best Pract Res Clin Rheumatol. 2003, 17: 685-701. 10.1016/S1521-6942(03)00035-4.View ArticlePubMed
- Sluka KA: Pain syndromes: myofascial pain and fibromyalgia. Mechanisms and Management of Pain for the Physical Therapist. Edited by: Sluka KA. 2009, Seattle: IAPS Press, 279-297.
- Dadabhoy D, Crofford LJ, Spaeth M, Russell IJ, Clauw DJ: Biology and therapy of fibromyalgia. Evidence-based biomarkers for fibromyalgia syndrome. Arthritis Res Ther. 2008, 10: 211-10.1186/ar2443.PubMed CentralView ArticlePubMed
- Sluka KA, Kalra A, Moore SA: Unilateral intramuscular injections of acidic saline produce a bilateral, long-lasting hyperalgesia. Muscle Nerve. 2001, 24: 37-46. 10.1002/1097-4598(200101)24:1<37::AID-MUS4>3.0.CO;2-8.View ArticlePubMed
- Miranda A, Peles S, Rudolph C, Shaker R, Sengupta JN: Altered visceral sensation in response to somatic pain in the rat. Gastroenterology. 2004, 126: 1082-1089. 10.1053/j.gastro.2004.01.003.View ArticlePubMed
- Pratt D, Fuchs PN, Sluka KA: Assessment of avoidance behaviors in mouse models of muscle pain. Neurosci. 2013, 248C: 54-60.View Article
- Gandhi R, Ryals JM, Wright DE: Neurotrophin-3 reverses chronic mechanical hyperalgesia induced by intramuscular acid injection. J Neurosci. 2004, 24: 9405-9413. 10.1523/JNEUROSCI.0899-04.2004.View ArticlePubMed
- Jasper LL, MacNeil BJ: Diverse sensory inputs permit priming in the acidic saline model of hyperalgesia. Eur J Pain. 2012, 16: 966-973. 10.1002/j.1532-2149.2011.00103.x.PubMed CentralView ArticlePubMed
- Sluka KA, Price MP, Breese NM, Stucky CL, Wemmie JA, Welsh MJ: Chronic hyperalgesia induced by repeated acid injections in muscle is abolished by the loss of ASIC3, but not ASIC1. Pain. 2003, 106: 229-239. 10.1016/S0304-3959(03)00269-0.View ArticlePubMed
- Lin CC, Chen WN, Chen CJ, Lin YW, Zimmer A, Chen CC: An antinociceptive role for substance P in acid-induced chronic muscle pain. Proc Natl Acad Sci U S A. 2012, 109: E76-E83. 10.1073/pnas.1108903108.PubMed CentralView ArticlePubMed
- Oliveira LR, de Melo VU, Macedo FN, Barreto AS, Badaue-Passos D, Viana dos Santos MR, Dias DP, Sluka KA, DeSantana JM, Santana-Filho VJ: Induction of chronic non-inflammatory widespread pain increases cardiac sympathetic modulation in rats. Auton Neurosci. 2012, 167: 45-49. 10.1016/j.autneu.2011.12.004.View ArticlePubMed
- Sharma NK, Ryals JM, Gajewski BJ, Wright DE: Aerobic exercise alters analgesia and neurotrophin-3 synthesis in an animal model of chronic widespread pain. Phys Ther. 2010, 90: 714-725. 10.2522/ptj.20090168.PubMed CentralView ArticlePubMed
- Cheng SJ, Chen CC, Yang HW, Chang YT, Bai SW, Chen CC, Yen CT, Min MY: Role of extracellular signal-regulated kinase in synaptic transmission and plasticity of a nociceptive input on capsular central amygdaloid neurons in normal and acid-induced muscle pain mice. J Neurosci. 2011, 31: 2258-2270. 10.1523/JNEUROSCI.5564-10.2011.View ArticlePubMed
- Chen WK, Liu IY, Chang YT, Chen YC, Chen CC, Yen CT, Shin HS, Chen CC: Ca(v)3.2 T-type Ca2+ channel-dependent activation of ERK in paraventricular thalamus modulates acid-induced chronic muscle pain. J Neurosci. 2010, 30: 10360-10368. 10.1523/JNEUROSCI.1041-10.2010.View ArticlePubMed
- Tillu DV, Gebhart GF, Sluka KA: Descending facilitatory pathways from the RVM initiate and maintain bilateral hyperalgesia after muscle insult. Pain. 2008, 136: 331-339. 10.1016/j.pain.2007.07.011.PubMed CentralView ArticlePubMed
- Radhakrishnan R, Sluka KA: Increased glutamate and decreased glycine release in the rostral ventromedial medulla during induction of a pre-clinical model of chronic widespread muscle pain. Neurosci Lett. 2009, 457: 141-145. 10.1016/j.neulet.2009.03.086.PubMed CentralView ArticlePubMed
- da Silva LFS, DeSantana JM, Sluka KA: Activation of NMDA receptors in the brainstem, rostral ventromedial medulla, and nucleus reticularis gigantocellularis mediates mechanical hyperalgesia produced by repeated intramuscular injections of acidic saline in rats. Pain. 2010, 11: 378-387. 10.1016/j.jpain.2009.08.006.View Article
- da Silva LFS, Walder RY, Davidson BL, Wilson SP, Sluka KA: Changes in expression of NMDA-NR1 receptor subunits in the rostral ventromedial medulla modulates pain behaviors. Pain. 2010, 151: 155-161. 10.1016/j.pain.2010.06.037.PubMed CentralView ArticlePubMed
- Skyba DA, King EW, Sluka KA: Effects of NMDA and non-NMDA ionotropic glutamate receptor antagonists on the development and maintenance of hyperalgesia induced by repeated intramuscular injection of acidic saline. Pain. 2002, 98: 69-78. 10.1016/S0304-3959(01)00471-7.View ArticlePubMed
- Bement MK, Sluka KA: Co-localization of p-CREB and p-NR1 in spinothalamic neurons in a chronic muscle pain model. Neurosci Lett. 2007, 418: 22-27. 10.1016/j.neulet.2007.02.078.View ArticlePubMed
- Skyba DA, Lisi TL, Sluka KA: Excitatory amino acid concentrations increase in the spinal cord dorsal horn after repeated intramuscular injection of acidic saline. Pain. 2005, 119: 142-149. 10.1016/j.pain.2005.09.025.View ArticlePubMed
- Hoeger-Bement MK, Sluka KA: Phosphorylation of CREB and mechanical hyperalgesia is reversed by blockade of the cAMP pathway in a time-dependent manner after repeated intramuscular acid injections. J Neurosci. 2003, 23: 5437-5445.PubMed
- Sharma NK, Ryals JM, Liu H, Liu W, Wright DE: Acidic saline-induced primary and secondary mechanical hyperalgesia in mice. J Pain. 2009, 10: 1231-1241. 10.1016/j.jpain.2009.04.014.PubMed CentralView ArticlePubMed
- Yokoyama T, Audette KM, Sluka KA: Pregabalin reduces muscle and cutaneous hyperalgesia in two models of chronic muscle pain in rats. J Pain. 2007, 8: 422-429. 10.1016/j.jpain.2006.11.007.View ArticlePubMed
- Sluka KA, Rohlwing JJ, Bussey RA, Eikenberry SA, Wilken JM: Chronic muscle pain induced by repeated acid injection is reversed by spinally administered μ-, and δ-, but not κ-, opioid receptor agonists. J Pharmacol Exp Ther. 2002, 302: 1146-1150. 10.1124/jpet.102.033167.View ArticlePubMed
- Kim SH, Song J, Mun H, Park KU: Effect of the combined use of tramadol and milnacipran on pain threshold in an animal model of fibromyalgia. Korean J Intern Med. 2009, 24: 139-142. 10.3904/kjim.2009.24.2.139.PubMed CentralView ArticlePubMed
- Nielsen AN, Mathiesen C, Blackburn-Munro G: Pharmacological characterisation of acid-induced muscle allodynia in rats. Eur J Pharmacol. 2004, 487: 93-103. 10.1016/j.ejphar.2004.01.017.View ArticlePubMed
- Bement MK, Sluka KA: Low-intensity exercise reverses chronic muscle pain in the rat in a naloxone-dependent manner. Arch Phys Med Rehabil. 2005, 86: 1736-1740. 10.1016/j.apmr.2005.03.029.View ArticlePubMed
- Sluka KA, O’Donnell JM, Danielson J, Rasmussen LA: Regular physical activity prevents development of chronic pain and activation of central neurons. J Appl Physiol. 2013, 114: 725-733. 10.1152/japplphysiol.01317.2012.PubMed CentralView ArticlePubMed
- Dina OA, Levine JD, Green PG: Muscle inflammation induces a protein kinase C epsilon-dependent chronic-latent muscle pain. J Pain. 2008, 9: 457-462. 10.1016/j.jpain.2008.01.328.PubMed CentralView ArticlePubMed
- Parada CA, Reichling DB, Levine JD: Chronic hyperalgesic priming in the rat involves a novel interaction between cAMP and PKCepsilon second messenger pathways. Pain. 2005, 113: 185-190. 10.1016/j.pain.2004.10.021.View ArticlePubMed
- Dina OA, Green PG, Levine JD: Role of interleukin-6 in chronic muscle hyperalgesic priming. Neurosci. 2008, 152: 521-525. 10.1016/j.neuroscience.2008.01.006.View Article
- Aley KO, Messing RO, Mochly-Rosen D, Levine JD: Chronic hypersensitivity for inflammatory nociceptor sensitization mediated by the epsilon isozyme of protein kinase C. J Neurosci. 2000, 20: 4680-4685.PubMed
- Ferrari LF, Bogen O, Levine JD: Role of nociceptor alphaCaMKII in transition from acute to chronic pain (hyperalgesic priming) in male and female rats. J Neurosci. 2013, 33: 11002-11011. 10.1523/JNEUROSCI.1785-13.2013.PubMed CentralView ArticlePubMed
- Ferrari LF, Levine E, Levine JD: Role of a novel nociceptor autocrine mechanism in chronic pain. Eur J Neurosci. 2013, 37: 1705-1713. 10.1111/ejn.12145.View ArticlePubMed
- Joseph EK, Levine JD: Hyperalgesic priming is restricted to isolectin B4-positive nociceptors. Neurosci. 2010, 169: 431-435. 10.1016/j.neuroscience.2010.04.082.View Article
- Ferrari LF, Bogen O, Chu C, Levine JD: Peripheral administration of translation inhibitors reverses increased hyperalgesia in a model of chronic pain in the rat. J Pain. 2013, 14: 731-738. 10.1016/j.jpain.2013.01.779.PubMed CentralView ArticlePubMed
- Gregory NS, Gibson-Corley K, Frey-Law L, Sluka KA: Fatigue-enhanced hyperalgesia in response to muscle insult: induction and development occur in a sex-dependent manner. Pain. 2013
- Yokoyama T, Lisi TL, Moore SA, Sluka KA: Muscle fatigue increases the probability of developing hyperalgesia in mice. J Pain. 2007, 8: 692-699. 10.1016/j.jpain.2007.05.008.PubMed CentralView ArticlePubMed
- Sluka KA, Rasmussen LA: Fatiguing exercise enhances hyperalgesia to muscle inflammation. Pain. 2010, 148: 188-197. 10.1016/j.pain.2009.07.001.PubMed CentralView ArticlePubMed
- Sluka KA, Danielson J, Rasmussen L, Dasilva LF: Exercise-induced pain requires NMDA receptor activation in the medullary raphe nuclei. Med Sci Sports Exerc. 2012, 44: 420-427. 10.1249/MSS.0b013e31822f490e.PubMed CentralView ArticlePubMed
- Nagakura Y, Oe T, Aoki T, Matsuoka N: Biogenic amine depletion causes chronic muscular pain and tactile allodynia accompanied by depression: a putative animal model of fibromyalgia. Pain. 2009, 146: 26-33. 10.1016/j.pain.2009.05.024.View ArticlePubMed
- Nagakura Y, Takahashi M, Noto T, Sekizawa T, Oe T, Yoshimi E, Tamaki K, Shimizu Y: Different pathophysiology underlying animal models of fibromyalgia and neuropathic pain: comparison of reserpine-induced myalgia and chronic constriction injury rats. Behav Brain Res. 2012, 226: 242-249. 10.1016/j.bbr.2011.09.023.View ArticlePubMed
- Ogino S, Nagakura Y, Tsukamoto M, Watabiki T, Ozawa T, Oe T, Shimizu Y, Ito H: Systemic administration of 5-HT(2C) receptor agonists attenuates muscular hyperalgesia in reserpine-induced myalgia model. Pharmacol Biochem Behav. 2013, 108: 8-15.View ArticlePubMed
- Nishiyori M, Uchida H, Nagai J, Araki K, Mukae T, Kishioka S, Ueda H: Permanent relief from intermittent cold stress-induced fibromyalgia-like abnormal pain by repeated intrathecal administration of antidepressants. Mol Pain. 2011, 7: 69-10.1186/1744-8069-7-69.PubMed CentralView ArticlePubMed
- Nasu T, Taguchi T, Mizumura K: Persistent deep mechanical hyperalgesia induced by repeated cold stress in rats. Eur J Pain. 2010, 14: 236-244. 10.1016/j.ejpain.2009.05.009.View ArticlePubMed
- Hata T, Itoh E, Kawabata A: Changes in CNS levels of serotonin and its metabolite in SART-stressed (repeatedly cold-stressed) rats. Jpn J Pharmacol. 1991, 56: 101-104. 10.1254/jjp.56.101.View ArticlePubMed
- Omiya Y, Goto K, Ishige A, Komatsu Y: Changes in analgesia-producing mechanism of repeated cold stress loading in mice. Pharmacol Biochem Behav. 2000, 65: 261-266. 10.1016/S0091-3057(99)00215-4.View ArticlePubMed
- Fujisawa H, Ohtani-Kaneko R, Naiki M, Okada T, Masuko K, Yudoh K, Suematsu N, Okamoto K, Nishioka K, Kato T: Involvement of post-translational modification of neuronal plasticity-related proteins in hyperalgesia revealed by a proteomic analysis. Proteomics. 2008, 8: 1706-1719. 10.1002/pmic.200700928.View ArticlePubMed
- Satoh M, Kuraishi Y, Kawamura M: Effects of intrathecal antibodies to substance-P, calcitonin gene-related peptide and galanin on repeated cold stress-induced hyperalgesia - comparison with carrageenan-induced hyperalgesia. Pain. 1992, 49: 273-278. 10.1016/0304-3959(92)90151-Z.View ArticlePubMed
- Kuraishi Y, Satoh M: Participation of spinal cord substance P in hyperalgesia induced by repeated cold stress. Regul Pept. 1993, 46: 405-406. 10.1016/0167-0115(93)90101-D.View ArticlePubMed
- Okano K, Kuraishi Y, Satoh M: Effects of intrathecally injected glutamate and substance P antagonists on repeated cold stress-induced hyperalgesia in rats. Biol Pharm Bull. 1995, 18: 42-44. 10.1248/bpb.18.42.View ArticlePubMed
- Nishiyori M, Ueda H: Prolonged gabapentin analgesia in an experimental mouse model of fibromyalgia. Mol Pain. 2008, 4: 52-10.1186/1744-8069-4-52.PubMed CentralView ArticlePubMed
- Khasar SG, Dina OA, Green PG, Levine JD: Sound stress-induced long-term enhancement of mechanical hyperalgesia in rats is maintained by sympathoadrenal catecholamines. J Pain. 2009, 10: 1073-1077. 10.1016/j.jpain.2009.04.005.PubMed CentralView ArticlePubMed
- Dina OA, Levine JD, Green PG: Enhanced cytokine-induced mechanical hyperalgesia in skeletal muscle produced by a novel mechanism in rats exposed to unpredictable sound stress. Eur J Pain. 2011, 15: 796-800. 10.1016/j.ejpain.2011.02.005.PubMed CentralView ArticlePubMed
- Green PG, Alvarez P, Gear RW, Mendoza D, Levine JD: Further validation of a model of fibromyalgia syndrome in the rat. J Pain. 2011, 12: 811-818. 10.1016/j.jpain.2011.01.006.PubMed CentralView ArticlePubMed
- Khasar SG, Burkham J, Dina OA, Brown AS, Bogen O, Alessandri-Haber N, Green PG, Reichling DB, Levine JD: Stress induces a switch of intracellular signaling in sensory neurons in a model of generalized pain. J Neurosci. 2008, 28: 5721-5730. 10.1523/JNEUROSCI.0256-08.2008.PubMed CentralView ArticlePubMed
- Quintero L, Moreno M, Avila C, Arcaya J, Maixner W, Suarez-Roca H: Long-lasting delayed hyperalgesia after subchronic swim stress. Pharmacol Biochem Behav. 2000, 67: 449-458. 10.1016/S0091-3057(00)00374-9.View ArticlePubMed
- Quintero L, Cuesta MC, Silva JA, Arcaya JL, Pinerua-Suhaibar L, Maixner W, Suarez-Roca H: Repeated swim stress increases pain-induced expression of c-Fos in the rat lumbar cord. Brain Res. 2003, 965: 259-268. 10.1016/S0006-8993(02)04224-5.View ArticlePubMed
- Suarez-Roca H, Quintero L, Arcaya JL, Maixner W, Rao SG: Stress-induced muscle and cutaneous hyperalgesia: differential effect of milnacipran. Physiol Behav. 2006, 88: 82-87. 10.1016/j.physbeh.2006.03.010.View ArticlePubMed
- Suarez-Roca H, Leal L, Silva JA, Pinerua-Shuhaibar L, Quintero L: Reduced GABA neurotransmission underlies hyperalgesia induced by repeated forced swimming stress. Behav Brain Res. 2008, 189: 159-169. 10.1016/j.bbr.2007.12.022.View ArticlePubMed
- Quintero L, Cardenas R, Suarez-Roca H: Stress-induced hyperalgesia is associated with a reduced and delayed GABA inhibitory control that enhances post-synaptic NMDA receptor activation in the spinal cord. Pain. 2011, 152: 1909-1922. 10.1016/j.pain.2011.04.017.View ArticlePubMed
- Frey Law LA, Sluka KA, McMullen T, Lee J, rendt-Nielsen L, Graven-Nielsen T: Acidic buffer induced muscle pain evokes referred pain and mechanical hyperalgesia in humans. Pain. 2008, 140: 254-264. 10.1016/j.pain.2008.08.014.View ArticlePubMed
- Issberner U, Reeh PW, Steen KH: Pain due to tissue acidosis: a mechanism for inflammatory and ischemic myalgia?. Neurosci Lett. 1996, 208: 191-194. 10.1016/0304-3940(96)12576-3.View ArticlePubMed
- Gracely RH, Petzke F, Wolf JM, Clauw DJ: Functional magnetic resonance imaging evidence of augmented pain processing in fibromyalgia. Arthritis Rheum. 2002, 46: 1333-1343. 10.1002/art.10225.View ArticlePubMed
- Gautam M, Benson CJ, Ranier JD, Light AR, Sluka KA: ASICs do not play a role in maintaining hyperalgesia induced by repeated intramuscular acid injections. Pain Res Treat. 2012, 2012: 817347-PubMed CentralPubMed
- Karczewski J, Spencer RH, Garsky VM, Liang A, Leitl MD, Cato MJ, Cook SP, Kane S, Urban MO: Reversal of acid-induced and inflammatory pain by the selective ASIC3 inhibitor, APETx2. Br J Pharmacol. 2010, 161: 950-960. 10.1111/j.1476-5381.2010.00918.x.PubMed CentralView ArticlePubMed
- Sluka KA, Audette KM: Activation of protein kinase C in the spinal cord produces mechanical hyperalgesia by activating glutamate receptors, but does not mediate chronic muscle-induced hyperalgesia. Mol Pain. 2006, 2: 13-10.1186/1744-8069-2-13.PubMed CentralView ArticlePubMed
- Miranda A, Peles S, McLean PG, Sengupta JN: Effects of the 5-HT3 receptor antagonist, alosetron, in a rat model of somatic and visceral hyperalgesia. Pain. 2006, 126: 54-63. 10.1016/j.pain.2006.06.014.View ArticlePubMed
- Busch AJ, Barber KA, Overend TJ, Peloso PM, Schachter CL: Exercise for treating fibromyalgia syndrome. Cochrane Database Syst Rev. 2007, CD003786-
- Sluka KA, O’Donnell JM, Danielson J, Rasmussen LA: Regular physical activity prevents development of chronic pain and activation of central neurons. J Appl Physiol. 2012, 114: 725-733.PubMed CentralView ArticlePubMed
- Ellingson LD, Shields MR, Stegner AJ, Cook DB: Physical activity, sustained sedentary behavior, and pain modulation in women with fibromyalgia. J Pain. 2012, 13: 195-206. 10.1016/j.jpain.2011.11.001.PubMed CentralView ArticlePubMed
- Landmark T, Romundstad P, Borchgrevink PC, Kaasa S, Dale O: Associations between recreational exercise and chronic pain in the general population: evidence from the HUNT 3 study. Pain. 2011, 152: 2241-2247. 10.1016/j.pain.2011.04.029.View ArticlePubMed
- Painter JT, Crofford LJ: Chronic opioid use in fibromyalgia syndrome: a clinical review. J Clin Rheumatol. 2013, 19: 72-77. 10.1097/RHU.0b013e3182863447.View ArticlePubMed
- Biasi G, Manca S, Manganelli S, Marcolongo R: Tramadol in the fibromyalgia syndrome: a controlled clinical trial versus placebo. Int J Clin Pharmacol Res. 1998, 18: 13-19.PubMed
- Light AR, White AT, Hughen RW, Light KC: Moderate exercise increases expression for sensory, adrenergic, and immune genes in chronic fatigue syndrome patients but not in normal subjects. J Pain. 2009, 10: 1099-1112. 10.1016/j.jpain.2009.06.003.PubMed CentralView ArticlePubMed
- Yunus MB, Masi AT, Aldag JC: Short term effects of ibuprofen in primary fibromyalgia syndrome: a double blind, placebo controlled trial. J Rheumatol. 1989, 16: 527-532.PubMed
- Arnold LM: The pathophysiology, diagnosis and treatment of fibromyalgia. Psychiatr Clin North Am. 2010, 33: 375-408. 10.1016/j.psc.2010.01.001.View ArticlePubMed
- Nishiyori M, Nagai J, Nakazawa T, Ueda H: Absence of morphine analgesia and its underlying descending serotonergic activation in an experimental mouse model of fibromyalgia. Neurosci Lett. 2010, 472: 184-187. 10.1016/j.neulet.2010.01.080.View ArticlePubMed
- Bardin L, Malfetes N, Newman-Tancredi A, Depoortere R: Chronic restraint stress induces mechanical and cold allodynia, and enhances inflammatory pain in rat: relevance to human stress-associated painful pathologies. Behav Brain Res. 2009, 205: 360-366. 10.1016/j.bbr.2009.07.005.View ArticlePubMed
- Bardin L, Gregoire S, Aliaga M, Malfetes N, Vitton O, Ladure P, Newman-Tancredi A, Depoortere R: Comparison of milnacipran, duloxetine and pregabalin in the formalin pain test and in a model of stress-induced ultrasonic vocalizations in rats. Neurosci Res. 2010, 66: 135-140. 10.1016/j.neures.2009.10.009.View ArticlePubMed
- Gregory NS, Harris AL, Robinson CR, Dougherty PM, Fuchs PN, Sluka KA: An overview of animal models of pain: disease models and outcome measures. J Pain. 2013, 14: 1255-1269. 10.1016/j.jpain.2013.06.008.View ArticlePubMed