C-fiber depletion alters response properties of neurons in trigeminal nucleus principalis.

The effects of C-fiber depletion induced by neonatal capsaicin treatment on the functional properties of vibrissa-sensitive low-threshold mechanoreceptive (LTM) neurons in the rat trigeminal nucleus principalis were examined in adult rats. Neonatal rats were injected either with capsaicin or its vehicle within 48 h of birth. The depletion of unmyelinated afferents was confirmed by the significant decrease in plasma extravasation of Evan's blue dye induced in the hindlimb skin of capsaicin-treated rats by cutaneous application of mustard oil and by the significant decrease of unmyelinated fibers in both the sciatic and infraorbital nerves. The mechanoreceptive field (RF) and response properties of 31 vibrissa-sensitive neurons in capsaicin-treated rats were compared with those of 32 vibrissa-sensitive neurons in control (untreated or vehicle-treated) rats. The use of electronically controlled mechanical stimuli allowed quantitative analysis of response properties of vibrissa-sensitive neurons; these included the number of center- and surround-RF vibrissae within the RF (i.e., those vibrissae which when stimulated elicited >/=1 and <1 action potential per stimulus, respectively), the response magnitude and latency, and the selectivity of responses to stimulation of vibrissae in different directions with emphasis on combining both the response magnitude and direction of vibrissal deflection in a vector analysis. Neonatal capsaicin treatment was associated with significant increases in the total number of vibrissae, in the number of center-RF vibrissae per neuronal RF, and in the percentage of vibrissa-sensitive neurons that also responded to stimulation of other types of orofacial tissues. Compared with control rats, capsaicin-treated rats showed significant increases in the response magnitude to stimulation of surround-RF vibrissae as well as in response latency variability to stimulation of both center- and surround-RF vibrissae. C-fiber depletion also significantly altered the directional selectivity of responses to stimulation of vibrissae. For neurons with multiple center-RF vibrissae, the proportion of center-RF vibrissae with net vector responses oriented toward the same quadrant was significantly less in capsaicin-treated compared with control rats. These changes in the functional properties of principalis vibrissa-sensitive neurons associated with marked depletion of C-fiber afferents are consistent with similarly induced alterations in LTM neurons studied at other levels of the rodent somatosensory system, and indeed may contribute to alterations previously described in the somatosensory cortex of adult rodents. Furthermore, these results provide additional support to the view that C fibers may have an important role in shaping the functional properties of LTM neurons in central somatosensory pathways.

[1]  I. Darian‐Smith Neural mechanisms of facial sensation. , 1966, International review of neurobiology.

[2]  J. Szolcsányi,et al.  Direct evidence for neurogenic inflammation and its prevention by denervation and by pretreatment with capsaicin. , 1967, British journal of pharmacology and chemotherapy.

[3]  P. Rakić Local circuit neurons. , 1975, Neurosciences Research Program bulletin.

[4]  Barry J. Sessle,et al.  Inputs to trigeminal brain stem neurones from facial, oral, tooth pulp and pharyngolaryngeal tissues: II. Role of trigeminal nucleus caudalis in modulating responses to innocuous and noxious stimuli , 1976, Brain Research.

[5]  M. Wong-Riley Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry , 1979, Brain Research.

[6]  F. Lembeck,et al.  DECREASE OF SUBSTANCE P IN PRIMARY AFFERENT NEURONES AND IMPAIRMENT OF NEUROGENIC PLASMA EXTRAVASATION BY CAPSAICIN , 1980, British journal of pharmacology.

[7]  J. Dostrovsky,et al.  Functional properties of neurons in cat trigeminal subnucleus caudalis (medullary dorsal horn). I. Responses to oral-facial noxious and nonnoxious stimuli and projections to thalamus and subnucleus oralis. , 1981, Journal of neurophysiology.

[8]  P. Wall,et al.  Somatotopic maps are disorganized in adult rodents treated neonatally with capsaicin , 1982, Nature.

[9]  J. M. Gibson,et al.  Comparison of response properties of cerebellar- and thalamic-projecting interpolaris neurons. , 1982, Journal of neurophysiology.

[10]  P. Kenins Responses of single nerve fibres to capsaicin applied to the skin , 1982, Neuroscience Letters.

[11]  D. Simons Multi-whisker stimulation and its effects on vibrissa units in rat Sml barrel cortex , 1983, Brain Research.

[12]  J. Nagy,et al.  The termination of primary afferents within the rat dorsal horn: Evidence for rearrangement following capsaicin treatment , 1983, The Journal of comparative neurology.

[13]  Maria Fitzgerald,et al.  Capsaicin and sensory neurones — a review , 1983, Pain.

[14]  P. Wall,et al.  Plasticity in the nucleus gracilis of the rat , 1983, Experimental Neurology.

[15]  D. van der Kooy,et al.  Effects of neonatal capsaicin treatment on nociceptive thresholds in the rat , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  Grace Yang,et al.  Organization of the infraorbital nerve in rat: a quantitative electron microscopic study , 1984, Brain Research.

[17]  D. Simons Temporal and spatial integration in the rat SI vibrissa cortex. , 1985, Journal of neurophysiology.

[18]  P. Wall,et al.  Expansion of receptive fields in the mouse cortical barrelfield after administration of capsaicin to neonates or local application on the infraorbital nerve in adults , 1985, Brain Research.

[19]  P. Reeh,et al.  Does neurogenic inflammation alter the sensitivity of unmyelinated nociceptors in the rat? , 1986, Brain Research.

[20]  T F Burks,et al.  The neuropharmacology of capsaicin: review of some recent observations. , 1986, Pharmacological reviews.

[21]  J. Ygge,et al.  A quantitative study of the effects of neonatal capsaicin treatment and of subsequent peripheral nerve transection in the adult rat , 1986, Brain Research.

[22]  H. Schmalbruch,et al.  Fiber composition of the rat sciatic nerve , 1986, The Anatomical record.

[23]  J. Dostrovsky,et al.  Tooth pulp deafferentation is associated with functional alterations in the properties of neurons in the trigeminal spinal tract nucleus. , 1986 .

[24]  M. Armstrong‐James,et al.  Spatiotemporal convergence and divergence in the rat S1 “Barrel” cortex , 1987, The Journal of comparative neurology.

[25]  M. Jacquin,et al.  Structure and function of barrel 'precursor' cells in trigeminal nucleus principalis. , 1988, Brain research.

[26]  P W Mantyh,et al.  Distribution of calcitonin gene‐related peptide immunoreactivity in relation to the rat central somatosensory projection , 1988, The Journal of comparative neurology.

[27]  L. Kruger,et al.  Morphological features of thin sensory afferent fibers: a new interpretation of 'nociceptor' function. , 1988, Progress in brain research.

[28]  H. Handwerker,et al.  Selective excitation by capsaicin of mechano-heat sensitive nociceptors in rat skin , 1988, Brain Research.

[29]  M. Jacquin,et al.  Structure‐function relationships in rat brainstem subnucleus interpolaris: III. Local circuit neurons , 1989, The Journal of comparative neurology.

[30]  D. Simons,et al.  Thalamocortical response transformation in the rat vibrissa/barrel system. , 1989, Journal of neurophysiology.

[31]  B. Sessle,et al.  Properties of nociceptive and non-nociceptive neurons in trigeminal subnucleus oralis of the rat , 1990, Brain Research.

[32]  C. Woolf,et al.  Neonatal capsaicin treatment induces invasion of the substantia gelatinosa by the terminal arborizations of hair follicle afferents in the rat dorsal horn , 1990, The Journal of comparative neurology.

[33]  M F Jacquin,et al.  Structure-function relationships in rat brain stem subnucleus interpolaris. IX. Inputs from subnucleus caudalis. , 1990, Journal of neurophysiology.

[34]  P. Holzer Capsaicin: cellular targets, mechanisms of action, and selectivity for thin sensory neurons. , 1991, Pharmacological reviews.

[35]  M. Calford,et al.  C-fibres provide a source of masking inhibition to primary somatosensory cortex , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[36]  J. Wall,et al.  Current hypotheses of structural pattern formation in the somatosensory system and their potential relevance to humans , 1992, Brain Research.

[37]  D. Haas,et al.  Development of an orofacial model of acute inflammation in the rat. , 1992, Archives of oral biology.

[38]  C. Hildebrand,et al.  Ventral root afferents are not capsaicin-sensitive and fail to induce extravasation from pial vessels , 1993 .

[39]  M F Jacquin,et al.  Morphology and topography of identified primary afferents in trigeminal subnuclei principalis and oralis. , 1993, Journal of neurophysiology.

[40]  M. Jacquin,et al.  Organization of the proximal, orbital segment of the infraorbital nerve at multiple intervals after axotomy at birth: A quantitative electron microscopic study in rat , 1993, The Journal of comparative neurology.

[41]  C. L. Kwan,et al.  Effects of tooth pulp deafferentation on brainstem neurons of the rat trigeminal subnucleus oralis. , 1993, Somatosensory & motor research.

[42]  C. Woolf,et al.  The contribution of GABAA and glycine receptors to central sensitization: disinhibition and touch-evoked allodynia in the spinal cord. , 1994, Journal of neurophysiology.

[43]  R. Dubner,et al.  Inflammation and hyperalgesia in rats neonatally treated with capsaicin: effects on two classes of nociceptive neurons in the superficial dorsal horn , 1994, Pain.

[44]  M. Zhuo,et al.  Effects of neonatal capsaicin treatment on descending modulation of spinal nociception from the rostral, medial medulla in adult rat , 1994, Brain Research.

[45]  Sk Hong,et al.  Critical role of the capsaicin-sensitive nerve fibers in the development of the causalgic symptoms produced by transecting some but not all of the nerves innervating the rat tail , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  D J Simons,et al.  Quantitative effects of GABA and bicuculline methiodide on receptive field properties of neurons in real and simulated whisker barrels. , 1996, Journal of neurophysiology.

[47]  H. Schwark,et al.  Capsaicin-induced rapid receptive field reorganization in cuneate neurons. , 1996, Journal of neurophysiology.

[48]  C. L. Kwan,et al.  Neuroplastic effects of neonatal capsaicin on neurons in adult rat trigeminal nucleus principalis and subnucleus oralis. , 1996, Journal of neurophysiology.

[49]  Jon H. Kaas,et al.  Central reorganization of sensory pathways following peripheral nerve regeneration in fetal monkeys , 1996, Nature.

[50]  T. Sugimoto,et al.  Trigeminal primary projection to the rat brain stem sensory trigeminal nuclear complex and surrounding structures revealed by anterograde transport of cholera toxin B subunit-conjugated and Bandeiraea simplicifolia isolectin B4-conjugated horseradish peroxidase , 1997, Neuroscience Research.

[51]  B. Sessle,et al.  NMDA receptor involvement in neuroplastic changes induced by neonatal capsaicin treatment in trigeminal nociceptive neurons. , 1997, Journal of neurophysiology.

[52]  T. Sugimoto,et al.  c-fos induction in the subnucleus oralis following trigeminal nerve stimulation , 1998, Brain Research.