可拉维铁改善慢性不可预测的轻度应激性焦虑和抑郁:参与HPA轴、抗氧化防御系统、胆碱能和BDNF信号

Q2 Pharmacology, Toxicology and Pharmaceutics Drug metabolism and personalized therapy Pub Date : 2022-02-24 DOI:10.1515/dmpt-2021-0125
I. Ishola, T. Olubodun-Obadun, Oluwasayo A. Bakre, E. Ojo, O. Adeyemi
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引用次数: 4

摘要

摘要目的本研究旨在探讨从藤黄籽中分离的科拉维铁(KV)(一种双类黄酮)对慢性不可预测的轻度应激(CUMS)诱导的焦虑和抑郁样行为的有益作用。方法雄性白化小鼠随机分为6组,每组8只;第一组:车控无应力;第二组:coms控制;III-V组:CUMS + KV分别为1、5或50 mg/kg, VI组:KV (50 mg/kg, p.o.)非应激小鼠。动物接受为期14天的CUMS,随后在14 - 16天对抑郁和焦虑样行为进行评估。随后进行氧化应激、下丘脑-垂体轴、胆碱能和BDNF信号的生化检测。结果经KV处理后,CUMS显著减少了小鼠在高架迷宫试验(EPM)中张开双臂的时间,并显著增加了悬尾试验(TST)和强迫游泳试验(FST)的静止时间。KV还能减弱cums诱导的丙二醛/亚硝酸盐的生成,并降低前额皮质和海马的抗氧化酶活性。CUMS增加了血清皮质酮、乙酰胆碱酯酶活性,降低了PFC和海马的BDNF水平。结论:KV通过增强抗氧化防御机制、神经营养因子和胆碱能系统来预防CUMS诱导的小鼠焦虑和抑郁样行为。
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Kolaviron ameliorates chronic unpredictable mild stress-induced anxiety and depression: involvement of the HPA axis, antioxidant defense system, cholinergic, and BDNF signaling
Abstract Objectives This study sought to investigate the beneficial effect of kolaviron (KV) (a biflavonoid) isolated from Garcinia kola seed on chronic unpredictable mild stress (CUMS)-induced anxiety- and depressive-like behavior. Methods Male albino mice were randomly divided into six groups (n=8) as follows; Group I: vehicle-control unstressed; Group II: CUMS-control; Group III-V: CUMS + KV 1, 5 or 50 mg/kg, respectively, Group VI: KV (50 mg/kg, p.o.) unstressed mice. Animals were subjected to CUMS for 14 days, followed by estimation of depressive- and anxiety-like behavior from days 14–16. This was followed by biochemical assays for oxidative stress, hypothalamo-pituitary axis, cholinergic, and BDNF signaling. Results CUMS caused significant reduction in time spent in open arms of elevated plus maze test (EPM) and increase in immobility time in tail suspension test (TST) and forced swim test (FST) ameliorated by KV treatments. KV administration also attenuated CUMS-induced malondialdehyde/nitrite generation and decrease in antioxidant enzymes activities in the prefrontal cortex and hippocampus. CUMS increased serum corticosterone, acetylcholinesterase activity, and reduced BDNF level in the PFC and hippocampus were attenuated by KV administration. Conclusions KV prevented CUMS induced anxiety- and depression-like behavior in mice through enhancement of antioxidant defense mechanisms, neurotrophic factors, and cholinergic systems.
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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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