TY - JOUR
T1 - Enhancement of rat hypoglossal nerve regeneration by chitin sheet plus gangliosides
AU - Itoh, Michi ichirou
AU - Baba, Nobuyuki
AU - Cho, Ryong Ho
AU - Kuga, Yoshihiro
AU - Mizuno, Akio
AU - Fukumoto, Satoshi
AU - Furukawa, Koichi
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2000
Y1 - 2000
N2 - The effects of chitin sheet interposition with and without brain gangliosides on the regeneration of hypoglossal nerve fibres was studied in the rat following resection of a 5 mm length of the nerve. At 10 weeks after operation, the number of horseradish peroxidase (HRP)-labelled motor neurones, indicative of the axonal repair process, on the side treated with chitin and gangliosides was higher than on the control side (where 5 mm of the nerve was simply resected). The ratios of HRP-positive neurones in the right hypoglossal nucleus (treated side)/left hypoglossal nucleus (intact side) was 0 in the 5 mm-resected group, 53% in the chitin-grafted group, 88% in the ganglioside (0.2 μg)-injected group, 90% in the ganglioside (2 μg)-injected group, 91% in the chitin with ganglioside (0.2 μg)-injected group, 91% in the chitin with ganglioside (2 μg)-injected group and 85% in the autograft group, respectively. There were significant differences between the 5 mm-resected group and chitin-grafted group, ganglioside-injected group, chitin with ganglioside group and autograft group, and between the chitin-grafted group and ganglioside-injected, chitin with ganglioside and autograft groups (P < 0.005, respectively). Our results indicated that the use of chitin and gangliosides stimulated the regeneration of severed motor nerve fibres. These findings suggest that chitin and gangliosides might be therapeutically useful for treatment of neuronal degeneration. (C) 2000 The British Association of Plastic Surgeons.
AB - The effects of chitin sheet interposition with and without brain gangliosides on the regeneration of hypoglossal nerve fibres was studied in the rat following resection of a 5 mm length of the nerve. At 10 weeks after operation, the number of horseradish peroxidase (HRP)-labelled motor neurones, indicative of the axonal repair process, on the side treated with chitin and gangliosides was higher than on the control side (where 5 mm of the nerve was simply resected). The ratios of HRP-positive neurones in the right hypoglossal nucleus (treated side)/left hypoglossal nucleus (intact side) was 0 in the 5 mm-resected group, 53% in the chitin-grafted group, 88% in the ganglioside (0.2 μg)-injected group, 90% in the ganglioside (2 μg)-injected group, 91% in the chitin with ganglioside (0.2 μg)-injected group, 91% in the chitin with ganglioside (2 μg)-injected group and 85% in the autograft group, respectively. There were significant differences between the 5 mm-resected group and chitin-grafted group, ganglioside-injected group, chitin with ganglioside group and autograft group, and between the chitin-grafted group and ganglioside-injected, chitin with ganglioside and autograft groups (P < 0.005, respectively). Our results indicated that the use of chitin and gangliosides stimulated the regeneration of severed motor nerve fibres. These findings suggest that chitin and gangliosides might be therapeutically useful for treatment of neuronal degeneration. (C) 2000 The British Association of Plastic Surgeons.
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U2 - 10.1054/bjps.2000.3393
DO - 10.1054/bjps.2000.3393
M3 - Article
C2 - 11000078
AN - SCOPUS:0033778380
SN - 1748-6815
VL - 53
SP - 607
EP - 611
JO - Journal of Plastic, Reconstructive and Aesthetic Surgery
JF - Journal of Plastic, Reconstructive and Aesthetic Surgery
IS - 7
ER -