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Study on the Mechanism of Improvement Effects of Gastrodin Injection on Methamphetamine Induced Neurotoxic Damage in Rats via nNOS Pathway / 中国药房
China Pharmacy ; (12): 1171-1178, 2020.
Article in Chinese | WPRIM | ID: wpr-821602
ABSTRACT
OBJECTIVE:To stu dy the mechanism of improvement effects of Gastrodin injection on methamphetamine induced neurotoxic damage in rats via nNOS pathway. METHODS :SD rats were randomly divided into control groupmethamphetamine group,regular-dose of gastrodin group ,double-dose of gastrodin group ,negative control (NC)adenovirus group ,NC adenovirus+ methamphetamine group ,NC adenovirus+gastrodin group and nNOS adenovirus+gastrodin group ,with 10 rats in each group. Control group was given normal saline intraperitoneally ,twice a day. Methamphetamine group was given methamphetamine intraperitoneally(7.5 mg/kg),twice a day. Regular-dose and double-dose of gastrodin groups were respectively given different doses of Gastrodin injection (10,20 mg/kg)intraperitoneally 30 min earlier ,once a day ,and then given methamphetamine intraperitoneally by the same way as methamphetamine group. NC adenovirus group was given NC adenovirus (4.8×107 PFU)3 μL once in the striatum and normal saline intraperitoneally ,twice a day. NC adenovirus+methamphetamine group was given NC adenovirus by the same way and methamphetamine (7.5 mg/kg)intraperitoneally,twice a day. NC adenovirus+gastrodin group was given NC adenovirus+methamphetamine by the same way ,meanwhile given Gastrodin injection intraperitoneally (20 mg/kg)30 min before methamphetamine ,once a day. nNOS adenovirus+gastrodin group was given nNOS adenovirus and methamphetamine by the same way ,meanwhile given Gastrodin injection intraperitoneally (20 mg/kg)30 min before methamphetamine ,once a day. Each group was given relevant medicine intraperitoneally 1 mL/100 g,for consecutive 3 days. The stereotyped behavior of rats were observed and scored ;the apoptotic rate ,the protein expression of apoptotic factors (Bcl-2,Bax,Cleaved caspase- 3),the levels of oxidative stress factors (MDA,SOD,GPx) and NO ,the protein expression of nNOS were detected. RESULTS : Compared with control groupstereotyped behavior score ,cell apoptosis rate of striatum ,protein expression of Bax ,Cleaved caspase-3 and nNOS ,the levels of MDA and NO were increased significantly in methamphetamine group ;while the protein expression of Bcl- 2 and the levels of SOD and GPx were decreased significantly (P<0.05 or P<0.01). Compared with methamphetamine group ,stereotyped behavior score ,cell apoptosis rate of striatum ,protein expression of Bax ,Cleaved caspase- 3 and nNOS ,the levels of MDA and NO were decreased significantly in regular-dose and double-dose of gastrodin groups ;while the protein expression of Bcl- 2,the levels of SOD and GPx were increased significantly ,and most above indexes in double-dose of gastradin group were better than regular-dose of gastrodin group (P<0.05 or P<0.01). Compared with NC adenovirus group ,cell apoptosis rate of striatum ,protein expression of Bax ,Cleaved caspase- 3 and nNOS ,the levels of MDA and NO were increased significantly in NC adenovirus+methamphetamine group ;while the protein expression of Bcl- 2,the levels of SOD and GPx were decreased significantly (P<0.01). Compared with NC adenovirus+methamphetamine group ,cell apoptosis rate of striatum ,protein expression of Bax ,Cleaved caspase- 3 and nNOS ,the levels of MDA and NO were decreased significantly in NC adenovirus+ gastrodin group ;while the protein expression of Bcl- 2,the levels of SOD and GPx were increased significantly (P<0.01). Compared with NC adenovirus+gastrodin group ,cell apoptosis rate of striatum ,protein expression of Bax ,Cleaved caspase- 3 and nNOS,the levels of MDA and NO were increased significantly in nNOS adenovirus+gastrodin group ;while the protein expression of Bcl- 2,the levels of SOD and GPx were decreased significantly (P<0.01). CONCLUSIONS :Gastrodin injection can protect rats against neurotoxic damage induced by methamphetamine ,and the effect is related to the inhibition of nNOS-mediated apoptosis and oxidative stress.

Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: China Pharmacy Year: 2020 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: China Pharmacy Year: 2020 Type: Article