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木耳(木耳科)水提取物通过减轻大鼠氧化应激对氟哌啶醇诱导的僵住症的作用。

Role of Aqueous Extract of the Wood Ear Mushroom, Auricularia polytricha (Agaricomycetes), in Avoidance of Haloperidol-lnduced Catalepsy via Oxidative Stress in Rats.

作者信息

Liu Xiaohong, Sharma Rakesh Kumar, Mishra Anurag, Chinnaboina Gopala Krishna, Gupta Gaurav, Singh Mahaveer

机构信息

Pharmacy, Ji'an Central People's Hospital, Ji'an Affiliated Hospital of Nanchang University, Ji'an, Jiangxi, China.

School of Pharmacy, Suresh Gyan Vihar University, Jagatpura, Jaipur, India.

出版信息

Int J Med Mushrooms. 2019;21(4):323-330. doi: 10.1615/IntJMedMushrooms.2019030351.

DOI:10.1615/IntJMedMushrooms.2019030351
PMID:31002628
Abstract

Haloperidol-induced catalepsy is an animal model of a psychotic disorder that may be associated with neurodegeneration and free radical damage. Auricularia polytricha is effective in both prevention and treatment of numerous types of neurological disorders. In the present study, anticataleptic activity of aqueous extract of A polytricha (AEAP) at different doses (400 and 600 mg/kg, respectively, p.o.) was studied using haloperidol-induced (1 mg/ kg, i.p.) catalepsy in rats. Repeated treatment with haloperidol (1 mg/kg, i.p.) on each other day for 15 days (days 5, 10, and 15) significantly induced catalepsy in rats. The effect of AEAP at different doses (400 and 600 mg/kg, p.o.) on levels of superoxide dismutase, catalase, and glutathione reductase as well as inhibition of lipid peroxidation in the forebrain region was assessed. After 15 days of treatment, AEAP (400 and 600 mg/kg) significantly inhibited haloperidol-induced catalepsy. Treatment with AEAP (400 and 600 mg/kg) exhibited significant elevation in the levels of superoxide dismutase, catalase, and glutathione reductase as well as lipid peroxidation in the forebrain region compared to the haloperidol-treated group. The study concludes that AEAP (400 and 600 mg/kg) significantly protects animals against haloperidol-induced catalepsy.

摘要

氟哌啶醇诱导的僵住症是一种可能与神经退行性变和自由基损伤相关的精神障碍动物模型。木耳对多种类型的神经障碍具有预防和治疗作用。在本研究中,使用氟哌啶醇(1mg/kg,腹腔注射)诱导大鼠产生僵住症,研究了不同剂量(分别为400和600mg/kg,口服)的木耳水提取物(AEAP)的抗僵住症活性。每隔一天用氟哌啶醇(1mg/kg,腹腔注射)重复处理15天(第5、10和15天)可显著诱导大鼠产生僵住症。评估了不同剂量(400和600mg/kg,口服)的AEAP对前脑区域超氧化物歧化酶、过氧化氢酶和谷胱甘肽还原酶水平以及脂质过氧化抑制的影响。治疗15天后,AEAP(400和600mg/kg)显著抑制了氟哌啶醇诱导的僵住症。与氟哌啶醇治疗组相比,AEAP(400和600mg/kg)治疗使前脑区域超氧化物歧化酶、过氧化氢酶和谷胱甘肽还原酶水平以及脂质过氧化显著升高。该研究得出结论,AEAP(400和600mg/kg)可显著保护动物免受氟哌啶醇诱导的僵住症影响。

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