Caffeic acid differentially modulates behavior and neurochemicals in chronic unpredictable mild stress and dexamethasone induced models of depression.

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES Pharmacology Biochemistry and Behavior Pub Date : 2025-02-01 Epub Date: 2024-12-05 DOI:10.1016/j.pbb.2024.173930
Hariom, Prerna Kumari, Sushma Chaturvedi, Sonika Shrivastav, Sushma Maratha, Vaibhav Walia
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Abstract

In the present study authors studied the effect of caffeic acid (CA) in chronic unpredictable mild stress (CUMS) and dexamethasone (DEXA) model of depression. CUMS (21 days) and DEXA (1.5 mg/kg × 21 days) was used for the induction of depression and anxiety related behavior. Locomotor activity was determined using actophotometer. Depression related behavior was determined using tail suspension test (TST) and forced swim test (FST) whereas for the determination of anxiety related behavior elevated plus maze (EPM) test was used. Following behavioral studies, mice were sacrificed by decapitation method. Hippocampus was dissected and was used for the neurochemical assays including 5-HT (serotonin), glutamate, nitrite and gamma-aminobutyric acid (GABA). The results obtained suggested that the CA (25-100 mg/kg, i.p.) did not affect the activity count in CUMS exposed and DEXA treated mice. CA (50 mg/kg) evoked anxiogenic reactions in CUMS model by increasing the hippocampal nitrite and glutamate level while CA (50 mg/kg) exerted anxiolysis in DEXA model by reducing the level of 5-HT. In CUMS model, CA exerted antidepressant like effect by increasing the hippocampal nitric oxide (NO) level, in DEXA model CA exerted antidepressant like effect by reducing the hippocampal glutamate level. CA failed to reverse DEXA mediated nNOS inhibition and therefore decreases hippocampal glutamate level to exert antidepressant like effect. Thus, CA modulate anxiety and depression related neurobehavioral alterations in both CUMS and DEXA models.

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咖啡酸在慢性不可预测的轻度应激和地塞米松诱导的抑郁症模型中差异调节行为和神经化学物质。
本研究探讨了咖啡酸(CA)在慢性不可预测轻度应激(CUMS)和地塞米松(DEXA)抑郁症模型中的作用。采用CUMS(21 d)和DEXA(1.5 mg/kg × 21 d)诱导抑郁和焦虑相关行为。运动活动测定采用光热计。抑郁相关行为采用悬尾测试(TST)和强迫游泳测试(FST),焦虑相关行为采用升高迷宫测试(EPM)。行为学研究后,采用断头法处死小鼠。解剖海马,进行5-羟色胺(5-羟色胺)、谷氨酸、亚硝酸盐和γ -氨基丁酸(GABA)的神经化学检测。结果表明,CA(25-100 mg/kg, i.p.)对CUMS暴露和DEXA处理小鼠的活性计数没有影响。CA(50 mg/kg)通过增加海马亚硝酸盐和谷氨酸水平引起CUMS模型的焦虑反应,CA(50 mg/kg)通过降低5-HT水平引起DEXA模型的焦虑反应。在CUMS模型中,CA通过提高海马一氧化氮(NO)水平发挥抗抑郁样作用;在DEXA模型中,CA通过降低海马谷氨酸水平发挥抗抑郁样作用。CA未能逆转DEXA介导的nNOS抑制,从而降低海马谷氨酸水平,发挥类似抗抑郁药的作用。因此,在CUMS和DEXA模型中,CA调节焦虑和抑郁相关的神经行为改变。
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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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