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Diosgenin improves functional recovery from sciatic crushed nerve injury in rats

Authors
Lee, Byung-KiKim, Chang-JuShin, Mal-SoonCho, Young Sam
Issue Date
8월-2018
Publisher
KOREAN SOC EXERCISE REHABILITATION
Keywords
Sciatic nerve injury; Functional recovery; Diosgenin; c-Fos; Brained-derived neurotrophic factor
Citation
JOURNAL OF EXERCISE REHABILITATION, v.14, no.4, pp.566 - 572
Indexed
SCOPUS
KCI
Journal Title
JOURNAL OF EXERCISE REHABILITATION
Volume
14
Number
4
Start Page
566
End Page
572
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/73862
DOI
10.12965/jer.1836340.170
ISSN
2288-176X
Abstract
Peripheral nerve injuries are commonly encountered clinical problem and often result in chronic pain and severe functional deficit. Diosgenin is a plant steroidal saponin and has anti-inflammatory and anticancer effects. In the present study, we investigated the effect of diosgenin on functional recovery following sciatic crushed nerve injury in rats. Walking track analysis for the functional recovery which can be quantified with the sciatic function index (SFI) was conducted. Immunohistochemistry for c-Fos in the ventrolateral periaqueductal gray (vlPAG) and paraventricular nucleus (PVN) and western blot for brain-derived neurotrophic factor (BDNF), tyrosine kinase B (TrkB), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthesis (iNOS) in the sciatic nerve were performed. The right sciatic nerve was crushed for 30 sec using a surgical clip. The animals in the diosgenin-treated groups received orally once a day at the respective doses for 7 consecutive days, starting one day after surgery. Sciatic crushed nerve injury showed characteristic gait changes showing decrease of SFI value. Diosgenin treatment increased the SFI value and suppressed nerve injury-induced c-Fos expression in the vlPAG and PVN. Diosgenin treatment inhibited nerve injury- induced increase of BDNF, TrkB, COX-2, and iNOS expressions. It is possible that diosgenin can be used as the new therapeutic agent for pain control and functional recovery following peripheral nerve injury.
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