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Unmyelinated innervation of sinus hair follicles in rats

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Abstract

Unmyelinated nerve fibres comprise approximately one third of the innervation of rodent sinus hair follicles but their function is unknown. They may play a role as high-threshold sensory fibres, or may be autonomic efferents controlling the vascular sinus. In the present experiments capsaicin and surgical sympathectomy were used to establish whether these unmyelinated fibres are afferent fibres or autonomic efferents. The deep vibrissal nerves of mystacial follicles (C1 and C4) and a non-mystacial follicle (the postero-orbital, PO) were assessed in normal adult animals (n = 6) and compared with those treated with neonatal capsaicin (n = 6) or bilateral superior cervical ganglionectomy (n = 7). In capsaicin-treated animals, counts of fibres in the deep vibrissal nerves from all follicles showed normal numbers of myelinated axons, but approximately 80% reduction in unmyelinated fibres (normal mean ± SD: C1 94± 10, C4 89 ± 9, PO 85 ± 6; after neonatal capsaicin: C1 17 ± 8, C4 16 ± 6, PO 18 ± 6; n = 6, P < 0.001 for all follicles). After sympathectomy there was no significant reduction in myelinated or unmyelinated fibre numbers. Labelling of PO follicles with WGA-HRP showed minimal numbers of labelled cells (0–10) within the superior cervical ganglion, also suggesting minimal sympathetic innervation. This sparse sympathetic supply to the follicle was further demonstrated by a lack of tyrosine hydroxylase reactivity within the follicle complex; tissues outside the dermal capsule showed reactivity. It is concluded that most of the unmyelinated fibres entering sinus hair follicles are sensory in function. Moreover, the sparse autonomic innervation suggests minimal efferent control of the vascular sinus. Changes in vascular pressure are therefore unlikely to be a mechanism for regulating follicle sensitivity.

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References

  • Andres KH (1966) Uber die Feinstruktur der Rezeptoren an Sinushaaren. Z Zellforsch Mikrosk Anat 75:339–365

    Google Scholar 

  • Barasi S, Lynn B (1986) Effects of sympathetic stimulation on mechanoreceptive and nociceptive afferent units from the rabbit pinna. Brain Res 378:21–27

    Google Scholar 

  • Bereiter DA, Stanford LR, Barker DJ (1980) Hormone-induced enlargement of receptive fields in trigeminal mechanoreceptive neurons. II. Possible mechanisms. Brain Res 184:411–423

    Google Scholar 

  • Carriere R, Patterson D (1962) The counting of mono- and bi-nucleated cells in tissue sections. Anat Rec 142:443–456

    Google Scholar 

  • Crissman RS, Warden RJ, Siciliano DA, Klein BG, Renehan WE, Jacquin MF, Rhoades RW (1991) Numbers of axons innervating mystacial vibrissa follicles in newborn and adult rats. Somato Motor Res 8:103–109

    Google Scholar 

  • Dorfl J (1985) The innervation of the mystacial region of the white mouse. A topograghical study. J Anat 142:173–184

    Google Scholar 

  • Fitzgerald M (1983) Capsaicin and sensory neurones — a review. Pain 15:109–130

    Google Scholar 

  • Freeman B, Rowe M (1981) The effect of sympathetic nerve stimulation on responses of cutaneous Pacinian corpuscles in the cat. Neurosci Lett 22:145–150

    Google Scholar 

  • Fuxe K, Nilsson BY (1965) Mechanoreceptors and adrenergic nerve terminals. Experientia 21:641–642

    Google Scholar 

  • Gibbins IL (1990) Target-related patterns of co-oexistence of neuropeptide Y, vasoactive intestinal peptide, enkephalin and substance P in cranial parasympathetic neurons innervating the facial skin and exocrine glands of guinea-pigs. Neuroscience 38:541–560

    Google Scholar 

  • Hedger JH, Webber RH (1976) Anatomical study of the cervical sympathetic trunk and ganglia in the albino rat (Mus norvegicus albinus). Acta Anat 96:206–217

    Google Scholar 

  • Jacquin MF, Renehan WE, Klein BG, Mooney RD, Rhoades RW (1986a) Functional consequences of neonatal intraorbital nerve section in rat trigeminal ganglion. J Neurosci 6:3706–3720

    Google Scholar 

  • Jacquin MF, Renehan WE, Mooney RD, Rhoades RW (1986b) Structure-function relationships in rat medullary and cervical dorsal horns. I. Trigeminal primary afferents. J Neurophysiol 55:1153–1180

    Google Scholar 

  • Johansson K, Arvidsson J, Thomander L (1988) Sympathetic nerve fibers in peripheral sensory and motor nerves in the face of the rat. J Auton Nerv Syst 23:83–86

    Google Scholar 

  • Klein BG, Renehan WE, Jacquin MF, Rhoades RW (1988) Anatomical consequences of neonatal infraorbital nerve transection upon the trigeminal ganglion and vibrissa follicle nerves in the adult rat. J Comp Neurol 268:469–488

    Google Scholar 

  • Lichtenstein SH, Carvell GE, Simons DJ (1990) Responses of rat trigeminal ganglion neurons to movements of vibrissae in different directions. Somato Motor Res 7:47–65

    Google Scholar 

  • Marfurt CF (1988) Sympathetic innervation of the rat cornea as demonstrated by the retrograde and anterograde transport of HRP-WGA. J Comp Neurol 268:147–160

    Google Scholar 

  • Marotte LR, Rice FL, Waite PME (1992) The morphology and innervation of facial vibrissae in the tammar wallaby, Macropus eugenii. J Anat 180:401–417

    Google Scholar 

  • Mesulam MM (1982) Tracing neural connections with horseradish peroxidase. Wiley, Bath

    Google Scholar 

  • Melaragno HP, Montagna W (1953) The tactile hair follicles in the mouse. Anat Rec 115:129–142

    Google Scholar 

  • Messenger JF (1900) The vibrissae of certain mammals. J Comp Neurol 10:399–406

    Google Scholar 

  • Nagy JI, Hunt SP, Iversen LL, Emson PC (1981) Biochemical and anatomical observations on the degeneration of peptide-containing primary afferent neurons after neonatal capsaicin. Neuroscience 6:1923–1934

    Google Scholar 

  • Nilsson BY (1972) Effects of sympathetic stimulation on mechanoreceptors of cat vibrissae. Acta Physiol Scand 85:390–397

    Google Scholar 

  • Pierce JP, Roberts WJ (1981) Sympathetically induced changes in the responses of guard hair and type II receptors in the cat. J Physiol 314:411–428

    Google Scholar 

  • Renehan WE, Munger BL (1986) Degeneration and regeneration of peripheral nerve in the rat trigeminal system. I. Identification and characterization of the multiple afferent innervation of the mystacial vibrissae. J Comp Neurol 246:129–145

    Google Scholar 

  • Rice FL, Mance A, Munger BL (1986) A comparative light microscopic analysis of the sensory innervation of the mystacial pad. I. Innervation of vibrissal follicle-sinus complexes. J Comp Neurol 252:154–174

    Google Scholar 

  • Roberts WJ, Levitt GR (1982) Histochemical evidence for sympathetic innervation of hair receptor afferents in cat skin. J Comp Neurol 210:204–209

    Google Scholar 

  • Roth CD, Richardson KC (1969) Electron microscopical studies on axonal degeneration in the rat iris following ganglionectomy. Am J Anat 124:341–360

    Google Scholar 

  • Smolen AJ, Wright LL, Cunningham TJ (1983) Neuron numbers in the superior cervical sympathetic ganglion of the rat: a critical comparison of methods fof cell counting. J Neurocytol 12:739–750

    Google Scholar 

  • Stephens RJ, Beebe IJ, Poulter TC (1973) Innervation of the vibrissae of the California sea lion, Zalophus californianus. Anat Rec 176:421–442

    Google Scholar 

  • Van Horn RN (1970) Vibrissae structure in the rhesus monkey. Folia Primatol (Basel) 13:241–285

    Google Scholar 

  • Waite PME, Cragg BG (1982) The peripheral and central changes resulting from cutting or crushing the afferent nerve supply to the whiskers. Proc R Soc Lond [Biol] 214:191–211

    Google Scholar 

  • Waite PME, de Permentier P (1991) The rat's postero-orbital sinus hair: I. Brainstem projections and the effect of infraorbital nerve section at different ages. J Comp Neurol 312:325–340

    Google Scholar 

  • Waite PME, Jacquin MF (1992) Dual innervation of the rat vibrissa: responses of trigeminal ganglion cells projecting through deep or superficial nerves. J Comp Neurol 322:233–245

    Google Scholar 

  • Williams JB, de Permentier P, Waite PME (1992) The rat's posteroorbital sinus hair: II. Normal morphology and the increase in peripheral innervation with adjacent nerve section. J Comp Neurol 321:1–11

    Google Scholar 

  • Wineski LE (1985) Facial morphology and vibrissal movement in the golden hamster. J Morphol 183:199–217

    Google Scholar 

  • Woolsey TA, Durham D, Harris RM, Simons DJ, Valentino KL (1981) Somatosensory development. Dev Perception 1:259–292

    Google Scholar 

  • Yohro T (1977) Structure of the sinus hair follicle in the big-clawed shrew, Sorex unguiculatus. J Morphol 153:333–354

    Google Scholar 

  • Zucker E, Welker WI (1969) Coding of somatic sensory input by vibrissae neurons in the rat's trigeminal ganglion. Brain Res 12:138–156

    Google Scholar 

Download references

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Waite, P.M.E., Li, L. Unmyelinated innervation of sinus hair follicles in rats. Anat Embryol 188, 457–465 (1993). https://doi.org/10.1007/BF00190140

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