Pathology of Nerve Terminal Degeneration in the Skin

To characterize the pathology of epidermal nerve degeneration and regeneration, we investigated temporal and spatial changes in skin innervation of the mouse footpad. Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epiderm...

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Veröffentlicht in:Journal of neuropathology and experimental neurology 2000-04, Vol.59 (4), p.297-307
Hauptverfasser: HSIEH, SUNG-TSANG, CHIANG, HOU-YU, LIN, WHEI-MIN
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CHIANG, HOU-YU
LIN, WHEI-MIN
description To characterize the pathology of epidermal nerve degeneration and regeneration, we investigated temporal and spatial changes in skin innervation of the mouse footpad. Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p < 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p < 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. In contrast, 3 months after nerve crushing, the epidermis on the surgery side resumed a normal innervation pattern as the epidermis on the control side (10.3 ± 3.9 vs 10.6 ± 1.5 fibers/mm, p = 0.1). This study demonstrates the characteristics of degenerating and regenerating nerves, and suggests that successful reinnervation mainly originates from regenerating nerves of the original nerve trunks. All these findings provide qualitative and quantitative information for interpreting the pathology of cutaneous nerves.
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Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p &lt; 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p &lt; 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. In contrast, 3 months after nerve crushing, the epidermis on the surgery side resumed a normal innervation pattern as the epidermis on the control side (10.3 ± 3.9 vs 10.6 ± 1.5 fibers/mm, p = 0.1). This study demonstrates the characteristics of degenerating and regenerating nerves, and suggests that successful reinnervation mainly originates from regenerating nerves of the original nerve trunks. 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Within 24 hours after sciatic nerve axotomy, terminals of epidermal nerves appeared swollen and there was a mild reduction in epidermal nerve density (5.7 ± 2.8 vs 12.7 ± 2.2 fibers/mm, p &lt; 0.04). Epidermal nerves completely disappeared by 48 hours (0.2 ± 0.2 vs 14.2 ± 0.9 fibers/mm, p &lt; 0.001). Concomitant with the disappearance of epidermal nerves, the immunocytochemical pattern of the subepidermal nerve plexus became fragmented. At the electron microscopic level, the axoplasm of degenerating dermal nerves was distended with organelles and later became amorphous. Beginning from day 28 after axotomy, collateral sprouts from the adjacent saphenous nerve territory extended into the denervated area with a beaded appearance. They never penetrated the epidermal-dermal junction to innervate the epidermis. 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Diseases due to physical agents</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Nerve Crush</subject><subject>Nerve Endings - metabolism</subject><subject>Nerve Endings - pathology</subject><subject>Nerve Endings - ultrastructure</subject><subject>Nerve Regeneration - physiology</subject><subject>Physiological aspects</subject><subject>Sciatic Nerve - metabolism</subject><subject>Sciatic Nerve - physiology</subject><subject>Sciatic Nerve - surgery</subject><subject>Sciatic Nerve - ultrastructure</subject><subject>Skin</subject><subject>Skin - innervation</subject><subject>Skin - pathology</subject><subject>Skin - ultrastructure</subject><subject>Thiolester Hydrolases - metabolism</subject><subject>Traumas. 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subjects Animals
Axons - ultrastructure
Axotomy
Biological and medical sciences
Cytochemistry
Denervation
Hindlimb - innervation
Immunohistochemistry
Injuries of the nervous system and the skull. Diseases due to physical agents
Male
Medical sciences
Mice
Mice, Inbred ICR
Nerve Crush
Nerve Endings - metabolism
Nerve Endings - pathology
Nerve Endings - ultrastructure
Nerve Regeneration - physiology
Physiological aspects
Sciatic Nerve - metabolism
Sciatic Nerve - physiology
Sciatic Nerve - surgery
Sciatic Nerve - ultrastructure
Skin
Skin - innervation
Skin - pathology
Skin - ultrastructure
Thiolester Hydrolases - metabolism
Traumas. Diseases due to physical agents
Tropical medicine
Ubiquitin Thiolesterase
Wallerian Degeneration - pathology
title Pathology of Nerve Terminal Degeneration in the Skin
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