Early Onset of Spontaneous Activity in Uninjured C-Fiber Nociceptors after Injury to Neighboring Nerve Fibers

Ligation and transection of the L5 spinal nerve in the rat lead to behavioral signs of pain and hyperalgesia. Discharge of injured nociceptors has been presumed to play a role in generating the pain. However, A fibers, but not C fibers, in the injured L5 spinal nerve have been shown to develop spontaneous activity. Moreover, an L5 dorsal root rhizotomy does not reverse this pain behavior, suggesting that signals from other uninjured spinal nerves are involved. We asked if abnormal activity develops in an adjacent, uninjured root. Single nerve fiber recordings were made from the L4 spinal nerve after ligation and transection of the L5 spinal nerve. Within 1 d of the lesion, spontaneous activity developed in approximately half of the C fiber afferents. This spontaneous activity was at a low level (median rate, seven action potentials/5 min), originated distal to the dorsal root ganglion, and was present in nociceptive fibers with cutaneous receptive fields. The incidence and level of spontaneous activity were similar 1 week after injury. The early onset of spontaneous activity in uninjured nociceptive afferents could be the signal that produces the central sensitization responsible for the development of mechanical hyperalgesia. Because L4 afferents comingle with degenerating L5 axons in the peripheral nerve, we hypothesize that products associated with Wallerian degeneration lead to an alteration in the properties of the adjacent, uninjured afferents.

[1]  Richard A. Meyer,et al.  A Laser Stimulator for the Study of Cutaneous Thermal and Pain Sensations , 1976, IEEE Transactions on Biomedical Engineering.

[2]  W D Willis,et al.  Cutaneous sensory receptors in the rat foot. , 1993, Journal of neurophysiology.

[3]  R. Meyer,et al.  Ectopic excitability of injured nerves in monkey: entrained responses to vibratory stimuli. , 1991, Journal of neurophysiology.

[4]  W. Jänig,et al.  Axotomized and Intact Muscle Afferents But No Skin Afferents Develop Ongoing Discharges of Dorsal Root Ganglion Origin after Peripheral Nerve Lesion , 2000, The Journal of Neuroscience.

[5]  M. Koltzenburg,et al.  Nociceptor modulated central sensitization causes mechanical hyperalgesia in acute chemogenic and chronic neuropathic pain. , 1994, Brain : a journal of neurology.

[6]  W. Jänig,et al.  Discharge pattern of afferent fibers from a neuroma , 1984, Pain.

[7]  Jin Mo Chung,et al.  An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat , 1992, PAIN.

[8]  R. Meyer,et al.  Neural activity originating from a neuroma in the baboon , 1985, Brain Research.

[9]  K. D. Davis,et al.  Mechanically insensitive afferents (MIAs) in cutaneous nerves of monkey , 1990, Pain.

[10]  R. Meyer,et al.  Sensitization of unmyelinated nociceptive afferents in monkey varies with skin type. , 1983, Journal of neurophysiology.

[11]  S. Kilo,et al.  Unresponsive afferent nerve fibres in the sural nerve of the rat. , 1991, The Journal of physiology.

[12]  R. Gilbert,et al.  Development of secondary hyperalgesia following non-painful thermal stimulation of the skin: a psychophysical study in man , 1993, Pain.

[13]  H O Handwerker,et al.  Different patterns of hyperalgesia induced by experimental inflammation in human skin. , 1994, Brain : a journal of neurology.

[14]  J. McArthur,et al.  Sensory and Motor Denervation Influence Epidermal Thickness in Rat Foot Glabrous Skin , 1997, Experimental Neurology.

[15]  W. Jänig,et al.  Dorsal root section elicits signs of neuropathic pain rather than reversing them in rats with L5 spinal nerve injury , 2000, Pain.

[16]  R. Meyer,et al.  Mechanical hyperalgesia after an L5 spinal nerve lesion in the rat is not dependent on input from injured nerve fibers , 2000, Pain.

[17]  S. McMahon,et al.  Potent analgesic effects of GDNF in neuropathic pain states. , 2000, Science.

[18]  R M Eglen,et al.  A comparison of the potential role of the tetrodotoxin-insensitive sodium channels, PN3/SNS and NaN/SNS2, in rat models of chronic pain. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[19]  M. Rowbotham,et al.  Postherpetic Neuralgia: Irritable Nociceptors and Deafferentation , 1998, Neurobiology of Disease.

[20]  P. Wall,et al.  Tactile allodynia in the absence of C-fiber activation: altered firing properties of DRG neurons following spinal nerve injury , 2000, Pain.

[21]  T. Fukuoka,et al.  Change in mRNAs for neuropeptides and the GABAA receptor in dorsal root ganglion neurons in a rat experimental neuropathic pain model , 1998, Pain.

[22]  R. Meyer,et al.  Uninjured C-fiber nociceptors develop spontaneous activity and alpha-adrenergic sensitivity following L6 spinal nerve ligation in monkey. , 1999, Journal of neurophysiology.