Reduced numbers of calcitonin gene-related peptide-(CGRP-) and tachykinin-immunoreactive sensory neurones associated with greater enkephalin immunoreactivity in the dorsal horn of a mutant rat with hereditary sensory neuropathy

• Published in: Cell and tissue research Vol. 255; no. 2; p. 451
• Main Authors: Kar, S, Gibson, S J, Scaravilli, F, Jacobs, J M, Aber, V R, Polak, J M
• Format: Journal Article
• Language: English
• Published: Germany 01.02.1989
• Subjects: Animals; Calcitonin Gene-Related Peptide; Enkephalins - immunology; Enkephalins - metabolism; Female; Ganglia, Spinal - immunology; Ganglia, Spinal - metabolism; Ganglia, Spinal - pathology; Hereditary Sensory and Motor Neuropathy - immunology; Hereditary Sensory and Motor Neuropathy - pathology; Immunohistochemistry; Male; Neurons, Afferent - immunology; Neurons, Afferent - metabolism; Neurons, Afferent - pathology; Neuropeptide Y - immunology; Neuropeptide Y - metabolism; Neuropeptides - immunology; Neuropeptides - metabolism; Rats; Rats, Inbred Strains; Skin - innervation; Tachykinins - immunology; Tachykinins - metabolism
• ISSN: 0302-766X
• DOI: 10.1007/BF00224131

The mutilated foot rat is a mutant with autosomal recessive sensory neuropathy and frequent mutilation of the hindlimbs. Decreased numbers of dorsal root ganglion cells and diminished sensitivity to painful stimuli are characteristics of these animals. By use of immunocytochemistry, changes in the distributions of peptides involved in sensory and/or autonomic regulation, i.e., calcitonin gene-related peptide (CGRP), tachykinins, enkephalin and neuropeptide Y in spinal cord, dorsal root ganglia and skin of these animals, were studied. In comparison with normal litter-mate controls, the dorsal horn of mutilated foot rats contained substantially fewer CGRP- and tachykinin-immunoreactive fibres but more fibres immunoreactive for enkephalin. Many enkephalin-immunoreactive cell bodies were also found in the dorsal horn of the mutants, by contrast none were visible in control animals. Neuropeptide Y immunoreactivity was, however, unchanged in the spinal cord of the mutants. In the dorsal root ganglia of the mutants, the number of CGRP- or tachykinin-immunoreactive cells and their proportion to total neuronal numbers were significantly less in comparison with normal controls. The diameter range of CGRP- and tachykinin-immunoreactive cells shifted from small (15-25 microns) to medium size (25-45 microns) as revealed by frequency distribution histograms. The skin from the affected fore- and hindlimbs of the mutant rats, in keeping with fewer CGRP- and tachykinin-immunoreactive cells in the dorsal root ganglia, contained substantially less fibres immunoreactive for CGRP and tachykinins; a difference that was not seen in skin of unaffected areas (whiskers and snout). By contrast, neuropeptide Y-immunoreactive fibres showed a normal distribution around blood vessels and sweat glands of mutilated foot rats. The data suggest that diminished pain perception in the mutilated foot rat is related to loss of peptide-containing sensory neurones. Furthermore, the intraspinal increase of enkephalinergic neurons in the dorsal horn, concomitant with the decreased number of primary sensory neurones, may also play a contributory rôle in reducing pain thresholds.