| Literature DB >> 29340845 |
Xiaofan Yang1, Pingping Xue2, Ruozheng Wei3, Xin Liu4, Xiang Xu1, Zhenyu Liu1, Yanhua Chen1, Zhenbing Chen5.
Abstract
Neuroactive steroids such as progesterone, testosterone, and their derivatives have been widely studied for their neuroprotective roles in the nervous system. Autologous nerve transplantation is considered as the gold standard repair technique when primary suture is impossible; nevertheless, this method is far from ideal. In this study, we aimed to explore the impact of dihydrotestosterone (DHT), a 5α-reduced derivative of testosterone, on the recovery of peripheral nerve injury treated with autologous nerve transplantation. Sprague-Dawley rats were subjected to a 10-mm right side sciatic nerve reversed autologous nerve transplantation and randomly divided into groups that received DHT or DHT + flutamide (an androgen receptor blocker) daily for 8 weeks after operation. Our results demonstrated that DHT could speed up the rate of axonal regeneration and increase the expression of myelin protein zero (P0) in autograft reversal sciatic nerves. Thus, our study provided new insights into improving the prognosis of patients with long gap peripheral nerve defects.Entities:
Keywords: Androgen receptor; Autologous nerve transplantation; Dihydrotestosterone; Myelin protein zero; Peripheral nerve injury
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Year: 2018 PMID: 29340845 DOI: 10.1007/s11064-018-2466-2
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996