Zingiber officinale (Ginger) hydroalcoholic extract improved avoidance memory in rat model of streptozotocin-induced diabetes by regulating brain oxidative stress

丙二醛 链脲佐菌素 氧化应激 糖尿病 超氧化物歧化酶 生姜 医学 过氧化氢酶 抗氧化剂 内分泌学 药理学 内科学 化学 传统医学 生物化学
作者
Narges Marefati,Tara Abdi,Farimah Beheshti,Farzaneh Vafaee,Maryam Mahmoudabady,Mahmoud Hosseini
出处
期刊:Hormone Molecular Biology and Clinical Investigation [De Gruyter]
卷期号:43 (1): 15-26 被引量:9
标识
DOI:10.1515/hmbci-2021-0033
摘要

Abstract Objectives Diabetes mellitus associated cognitive impairment is suggested to be due to oxidative stress. Considering the anti-diabetic, antioxidant, antihyperlipidemic, and anti-inflammatory effects of Zingiber officinale , the present study aimed to investigate its effect on memory and oxidative stress factors in streptozotocin (STZ)-induced diabetic rats. Methods The rats were allocated into five groups: Control, Diabetic, Diabetic + Ginger 100, Diabetic + Ginger 200, and Diabetic + Ginger 400. Following diabetes induction by STZ (60 mg/kg), 100, 200, or 400 mg/kg Ginger was given for eight weeks. Passive avoidance test (PA) was done and thiol, malondialdehyde (MDA), superoxide dismutase (SOD), and catalase (CAT) measurements were carried out in the brain. Results The latency into the dark compartment decreased (p<0.001) and the number of entries and time spent in the dark chamber increased in the Diabetic group compared to the Control (p<0.001 for all). All three doses of extract improved performance of the rats in the PA test (p<0.001 for all). The hippocampal and cortical MDA level was higher (p<0.001) while CAT, SOD, and total thiol were lower (p<0.01–p<0.001) in the Diabetic group than the Control. Treatment with 200 and 400 mg/kg Z. officinale extract reduced hippocampal and cortical MDA (p<0.001) and improved CAT (p<0.001) while, just the dose of 400 mg/kg of the extract increased SOD and total thiol in hippocampal and cortical tissues (p<0.001) compared with Diabetic group. Conclusions Z. officinale extract could improve memory by reducing the oxidative stress in STZ-induced diabetes model.
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