Using c-fos as a Neural Marker of Pain

Just over a decade has past since Hunt et al. reported that the gene c-fos and its protein product Fos are expressed in the spinal cord of rats subjected to peripheral noxious stimulation. These authors showed that noxious stimulation (application of radiant heat or mustard oil) to the hind paw resulted in a massive increase in the expression of Fos in neurons in the dorsal horn of the lumbar spinal cord. Since then, there has been an explosion of studies in which c-fos has been used to study nociception (pain), and the number of such studies increases each year. The net result has been to establish c-fos expression as a valuable tool in pain research. Moreover, recent studies have provided evidence identifying the role of c-fos expression in spinal nociceptive processes. However, there are several important limitations to the practice of using c-fos to study nociception, and these limitations can be easily overlooked as the practice graduates to the status of an established technique. The increasing use of c-fos to study nociception necessitates a critical review of the practice, identifying the shortcomings as well as the strengths of this tool.

[1]  K. Tarczy-Hornoch,et al.  Differential effects of morphine on noxious stimulus-evoked fos-like immunoreactivity in subpopulations of spinoparabrachial neurons , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  R. Blair,et al.  Noxious heat‐evoked Fos–like immunoreactivity in the rat medulla, with emphasis on the catecholamine cell groups , 1995, The Journal of comparative neurology.

[3]  K. D. Cliffer,et al.  Direct somatosensory projections from the spinal cord to the hypothalamus and telencephalon , 1987 .

[4]  D. Menétrey,et al.  Lumbar cord neurons at the origin of the spinothalamic tract in the rat , 1976, Brain Research.

[5]  D. Lima,et al.  Neurons in the superficial dorsal horn of the rat spinal cord projecting to the medullary ventrolateral reticular formation express c-fos after noxious stimulation of the skin , 1993, Brain Research.

[6]  M. Iadarola,et al.  Differential activation of spinal cord dynorphin and enkephalin neurons during hyperalgesia: evidence using cDNA hybridization , 1988, Brain Research.

[7]  P. Wall,et al.  Textbook of pain , 1989 .

[8]  R. Yezierski Spinomesencephalic tract: Projections from the lumbosacral spinal cord of the rat, cat, and monkey , 1988, The Journal of comparative neurology.

[9]  J. Besson,et al.  Carrageenin-evoked c-Fos expression in rat lumbar spinal cord: the effects of indomethacin. , 1995, European journal of pharmacology.

[10]  G. Wilcox,et al.  A nitric oxide synthesis inhibitor (L-NAME) reduces licking behavior and Fos-labeling in the spinal cord of rats during formalin-induced inflammation , 1996, PAIN®.

[11]  E. Carstens,et al.  Brainstem neurons expressing c-Fos immunoreactivity following irritant chemical stimulation of the rat's tongue , 1995, Neuroscience.

[12]  D. Lima A spinomedullary projection terminating in the dorsal reticular nucleus of the rat , 1990, Neuroscience.

[13]  P. Wall,et al.  A system of rat spinal cord lamina 1 cells projecting through the contralateral dorsolateral funiculus , 1983, The Journal of comparative neurology.

[14]  M. Heinrich Sensory mechanisms of the spinal cord, ed 2. By William D. Willis, Jr, and Richard E. Coggeshall New York, Plenum Publishing, I991 575 pp, illustrated, $89.50 , 1992 .

[15]  J. Besson,et al.  The contribution of NMDA receptor activation to spinal c‐Fos expression in a model of inflammatory pain , 1995, British journal of pharmacology.

[16]  A. Pertovaara,et al.  Cocaine‐induced effects on pain behavior and C‐fos expression in the spinal dorsal horn of the rat , 1996 .

[17]  A. Herz,et al.  Spinal cord dynorphin may modulate nociception via a ℵ-opioid receptor in chronic arthritic rats , 1985, Brain Research.

[18]  A. Beitz,et al.  Altered c‐fos expression in the parabrachial nucleus in a rodent model of CFA‐induced peripheral inflammation , 1996, The Journal of comparative neurology.

[19]  M. Peschanski,et al.  Electrophysiological evidence for a role of the anterolateral quadrant of the spinal cord in the transmission of noxious messages to the thalamic ventrobasal complex in the rat , 1985, Brain Research.

[20]  J E Swett,et al.  The somatotopic organization of primary afferent terminals in the superficial laminae of the dorsal horn of the rat spinal cord , 1985, The Journal of comparative neurology.

[21]  M. Tohyama,et al.  Histamine-caused itch induces Fos-like immunoreactivity in dorsal horn neurons: effect of morphine pretreatment , 1992, Brain Research.

[22]  S. Hunt,et al.  Induction of c-fos-like protein in spinal cord neurons following sensory stimulation , 1987, Nature.

[23]  C. Woolf,et al.  Proceedings of the 11th World Congress on Pain , 1991 .

[24]  T. Day,et al.  c-Fos expression in hypothalamic neurosecretory and brainstem catecholamine cells following noxious somatic stimuli , 1994, Neuroscience.

[25]  J. Besson,et al.  [Peripheral and spinal mechanisms of nociception]. , 1986, Revue neurologique.

[26]  A. Pertovaara,et al.  Induction and suppression of immediate-early genes in the rat brain by a selective alpha-2-adrenoceptor agonist and antagonist following noxious peripheral stimulation , 1993, Neuroscience.

[27]  E. Weihe,et al.  Induction of the gene encoding pro-dynorphin by experimentally induced arthritis enhances staining for dynorphin in the spinal cord of rats , 1989, Neuroscience.

[28]  James I. Morgan,et al.  Stimulus-transcription coupling in neurons: role of cellular immediate-early genes , 1989, Trends in Neurosciences.

[29]  D. Bereiter,et al.  Differential distribution of fos-like immunoreactivity in the spinal trigeminal nucleus after noxious and innocuous thermal and chemical stimulation of rat cornea , 1996, Neuroscience.

[30]  J. Weil-Fugazza,et al.  Hindbrain structures involved in pain processing as revealed by the expression of c-Fos and other immediate early gene proteins , 1994, Neuroscience.

[31]  E. Bullitt,et al.  The effect of stimulus duration on noxious-stimulus induced c-fos expression in the rodent spinal cord , 1992, Brain Research.

[32]  J. Lucas,et al.  Co-induction of jun B and c-fos in a subset of neurons in the spinal cord. , 1991, Oncogene.

[33]  M. Iadarola,et al.  Temporal analysis of increases in c-fos, preprodynorphin and preproenkephalin mRNAs in rat spinal cord. , 1989, Brain research. Molecular brain research.

[34]  A. Herz,et al.  A model of chronic pain in the rat: response of multiple opioid systems to adjuvant-induced arthritis , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  W D Willis,et al.  The pain system. The neural basis of nociceptive transmission in the mammalian nervous system. , 1985, Pain and headache.

[36]  M. Zimmermann,et al.  Control of gene transcription by Jun and Fos proteins in the nervous system , 1994 .

[37]  R. Faull,et al.  The use of c-fos as a metabolic marker in neuronal pathway tracing , 1989, Journal of Neuroscience Methods.

[38]  R. Bandler,et al.  Deep and superficial noxious stimulation increases Fos-like immunoreactivity in different regions of the midbrain periaqueductal grey of the rat , 1993, Neuroscience Letters.

[39]  A. Coimbra,et al.  C-fos expression in the hypothalamo-pituitary system induced by electroacupuncture or noxious stimulation. , 1994, Neuroreport.

[40]  J. Besson,et al.  Ketoprofen produces profound inhibition of spinal c-Fos protein expression resulting from an inflammatory stimulus but not from noxious heat , 1996, Pain.

[41]  K. D. Cliffer,et al.  Physiological characterization of spinohypothalamic tract neurons in the lumbar enlargement of rats. , 1991, Journal of neurophysiology.

[42]  A I Basbaum,et al.  Systemic morphine suppresses noxious stimulus-evoked Fos protein-like immunoreactivity in the rat spinal cord , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[43]  K. D. Cliffer,et al.  Direct somatosensory projections from the spinal cord to the hypothalamus and telencephalon R. Burstein, K.D. Cliffer and G.J. Giesler Jr., J. Neurosci., 7 (1987) 4159–4164 , 1988, Pain.

[44]  L. Jasmin,et al.  Walking evokes a distinctive pattern of Fos-like immunoreactivity in the caudal brainstem and spinal cord of the rat , 1994, Neuroscience.

[45]  C. Woolf,et al.  Basal and touch-evoked fos-like immunoreactivity during experimental inflammation in the rat , 1996, Pain.

[46]  E. Bullitt Induction of c-fos-like protein within the lumbar spinal cord and thalamus of the rat following peripheral stimulation , 1989, Brain Research.

[47]  W. Zieglgänsberger,et al.  Opiates modify induction of c-fos proto-oncogene in the spinal cord of the rat following noxious stimulation , 1990, Neuroscience Letters.

[48]  S. Jones Noradrenergic modulation of noxious heat‐evoked fos‐like immunoreactivity in the dorsal horn of the rat sacral spinal cord , 1992, The Journal of comparative neurology.

[49]  Fos expression in the spinal cord is suppressed in rats displaying conditioned hypoalgesia. , 1995, Behavioral neuroscience.

[50]  A. Todd,et al.  Some inhibitory neurons in the spinal cord develop c-fos-immunoreactivity after noxious stimulation , 1994, Neuroscience.

[51]  P. Wall,et al.  Electrophysiological mapping of brainstem projections of spinal cord lamina I cells in the rat , 1985, Brain Research.

[52]  D. G. Herrera,et al.  Activation of c-fos in the brain , 1996, Progress in Neurobiology.

[53]  A I Basbaum,et al.  Differential origins of spinothalamic tract projections to medial and lateral thalamus in the rat , 1979, The Journal of comparative neurology.

[54]  P. Redgrave,et al.  Analysis of nociceptive neurones in the rat superior colliculus using c‐fos immunohistochemistry , 1996, The Journal of comparative neurology.

[55]  E. Bullitt Expression of C‐fos‐like protein as a marker for neuronal activity following noxious stimulation in the rat , 1990, The Journal of comparative neurology.

[56]  T. Curran,et al.  Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. , 1991, Annual review of neuroscience.

[57]  R. F. Westbrook,et al.  The formalin test: scoring properties of the first and second phases of the pain response in rats , 1995, Pain.

[58]  J. C. Hunter,et al.  C-fos antisense oligodeoxynucleotide increases formalin-induced nociception and regulates preprodynorphin expression , 1995, Neuroscience.

[59]  K. D. Cliffer,et al.  Distributions of spinothalamic, spinohypothalamic, and spinotelencephalic fibers revealed by anterograde transport of PHA-L in rats , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[60]  E. Bullitt,et al.  Somatotopy of spinal nociceptive processing , 1991, The Journal of comparative neurology.

[61]  B. Chiasson,et al.  Antisense oligonucleotide eliminates in vivo expression of c-fos in mammalian brain. , 1992, European journal of pharmacology.

[62]  A. Light,et al.  Electrical stimulation in the medullary nucleus raphe magnus inhibits noxious heat-evokedfos protein-like immunoreactivity in the rat lumbar spinal cord , 1990, Brain Research.

[63]  J. Besson,et al.  A spino-reticulo-thalamic pathway in the rat: An anatomical study with reference to pain transmission , 1984, Neuroscience.

[64]  R. Traub,et al.  Dynorphin expression and Fos-like immunoreactivity following inflammation induced hyperalgesia are colocalized in spinal cord neurons. , 1991, Brain research. Molecular brain research.

[65]  A. Coimbra,et al.  Activation of anterior lobe corticotrophs by electroacupuncture or noxious stimulation in the anaesthetized rat, as shown by colocalization of fos protein with ACTH and β-endorphin and increased hormone release , 1996, Brain Research Bulletin.

[66]  J. Besson,et al.  Spinal afferents to the ventrobasal thalamic complex in the rat: an anatomical study using wheat-germ agglutinin conjugated to horseradish peroxidase , 1983, Brain Research.

[67]  S. P. Hunt,et al.  Changing patterns of c-fos induction in spinal neurons following thermal cutaneous stimulation in the rat , 1990, Neuroscience.

[68]  Patrick D. Wall,et al.  Central hyperexcitability triggered by noxious inputs , 1993, Current Opinion in Neurobiology.

[69]  M. Iadarola,et al.  In situ hybridization histochemistry and immunocytochemistry reveal an increase in spinal dynorphin biosynthesis in a rat model of peripheral inflammation and hyperalgesia. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[70]  W. Willis,et al.  Sensory Mechanisms of the Spinal Cord , 1991, Springer US.

[71]  A. Basbaum,et al.  The antinociceptive action of supraspinal opioids results from an increase in descending inhibitory control: Correlation of nociceptive behavior and c-fos expression , 1991, Neuroscience.

[72]  J. Sandkühler,et al.  Map of spinal neurons activated by chemical stimulation in the nucleus raphe magnus of the unanesthetized rat , 1995, Neuroscience.

[73]  G. Paxinos The Rat nervous system , 1985 .

[74]  R. Dubner,et al.  Enhancement of dynorphin gene expression in spinal cord following experimental inflammation: stimulus specificity, behavioral parameters and opioid receptor binding , 1988, Pain.

[75]  O. Hermanson,et al.  Subnuclear localization of FOS‐like immunoreactivity in the rat parabrachial nucleus after nociceptive stimulation , 1996, The Journal of comparative neurology.

[76]  M. Bentivoglio,et al.  C‐fos mRNA is Spontaneously Induced in the Rat Brain During the Activity Period of the Circadian Cycle , 1993, European Journal of Neuroscience.

[77]  W. Zieglgänsberger,et al.  C-fos induction in the spinal cord following noxious stimulation: Prevention by opiates but not by nmda antagonists , 1990, Pain.

[78]  K. Elliott,et al.  Dextromethorphan suppresses both formalin-induced nociceptive behavior and the formalin-induced increase in spinal cord c-fos mRNA , 1995, Pain.

[79]  A. Basbaum,et al.  Diffuse noxious inhibitory controls reduce the expression of noxious stimulus-evoked fos-like immunoreactivity in the superficial and deep laminae of the rat spinal cord , 1994, Pain.

[80]  A. Beitz,et al.  Electroacupuncture modifies the expression of c-fos in the spinal cord induced by noxious stimulation , 1992, Brain Research.

[81]  W. Willis,et al.  Sensory Mechanisms of the Spinal Cord , 1979, Springer US.

[82]  D. Lima,et al.  Spinal c-fos expression is differentially induced by brief or persistent noxious stimulation. , 1994, Neuroreport.

[83]  K. D. Cliffer,et al.  Cells of origin of the spinohypothalamic tract in the rat , 1990, The Journal of comparative neurology.

[84]  D. Menétrey,et al.  Spinal neurons reaching the lateral reticular nucleus as studied in the rat by retrograde transport of horseradish peroxidase , 1983, The Journal of comparative neurology.

[85]  D. Menétrey,et al.  Expression of c‐fos protein in interneurons and projection neurons of the rat spinal cord in response to noxious somatic, articular, and visceral stimulation , 1989, The Journal of comparative neurology.