Central projections of identified, unmyelinated (C) afferent fibers innervating mammalian skin.

Unmyelinated (C) fibers are the most numerous sensory elements of mammalian peripheral nerve and comprise many of those responsible for initiating pain and temperature reactions; however, direct evidence has been lacking as to where and how these fibers terminate in the central nervous system. A plant lectin (Phaseolus vulgaris leukoagglutinin) was applied intracellularly by iontophoresis as an immunocytochemical marker. This permitted visualization of the central terminations of cutaneous C sensory fibers that had been identified by the nature of stimuli that excited them. The central branch of C-fiber units arborized and terminated mainly in the superficial layers of the spinal dorsal horn in defined patterns that related to their functional attributes. Thus, the superficial dorsal horn seems to act as a processing station for signals from fine sensory fibers.

[1]  E. Perl,et al.  Synaptic complexes formed by functionally defined primary afferent units with fine myelinated fibers , 1982, The Journal of comparative neurology.

[2]  A. G. Brown,et al.  Morphology and organization of axon collaterals from afferent fibres of slowly adapting type I units in cat spinal cord. , 1978, The Journal of physiology.

[3]  E. Perl,et al.  Morphological features of functionally defined neurons in the marginal zone and substantia gelatinosa of the spinal dorsal horn , 1979, The Journal of comparative neurology.

[4]  S. Hsu,et al.  A comparative study of the peroxidase-antiperoxidase method and an avidin-biotin complex method for studying polypeptide hormones with radioimmunoassay antibodies. , 1981, American journal of clinical pathology.

[5]  H. Groenewegen,et al.  Phaseolus vulgaris leuco-agglutinin immunohistochemistry. A comparison between autoradiographic and lectin tracing of neuronal efferents , 1984, Brain Research.

[6]  Heinrich Lissauer The tract of lissauer and its possible relation to the pain pathway , 1952, The Journal of comparative neurology.

[7]  M. Réthelyi Preterminal and terminal axon arborizations in the substantia gelatinosa of cat's spinal cord , 1977, The Journal of comparative neurology.

[8]  A. Scheibel,et al.  Terminal patterns in cat spinal cord. 3. Primary afferent collaterals. , 1969, Brain research.

[9]  E. Perl,et al.  Sensory receptors with unmyelinated (C) fibers innervating the skin of the rabbit's ear. , 1985, Journal of neurophysiology.

[10]  S. Gobel,et al.  Degenerative changes in primary trigeminal axons and in neurons in nucleus caudalis following tooth pulp extirpations in the cat , 1977, Brain Research.

[11]  E. Perl,et al.  Spinal termination of functionally identified primary afferent neurons with slowly conducting myelinated fibers , 1979, The Journal of comparative neurology.

[12]  S. W. Ranson UNMYELINATED NERVE-FIBRES AS CONDUCTORS OF PROTOPATHIC SENSATION , 1915 .

[13]  S. W. Ranson The tract of Lissauer and the substantia gelatinosa Rolandi , 1914 .

[14]  B. Rexed The cytoarchitectonic organization of the spinal cord in the cat , 1952, The Journal of comparative neurology.

[15]  S. Hsu,et al.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[16]  J. Szentágothai,et al.  The large synaptic complexes of the substantia gelatinosa , 2004, Experimental Brain Research.