Additive effect of histamine and muscimol upon induction of antinociceptive and antidepressant effects in mice.

IF 1.6 4区 心理学 Q3 BEHAVIORAL SCIENCES Behavioural Pharmacology Pub Date : 2024-04-01 Epub Date: 2023-05-26 DOI:10.1097/FBP.0000000000000729
Matin Baghani, Farzan Fathalizade, Fatemeh Khakpai, Soheila Fazli-Tabaei, Mohammad-Reza Zarrindast
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Abstract

We investigated the effects of histamine and GABA A receptor agents on pain and depression-like behaviors and their interaction using a tail-flick test and the forced swimming test (FST) in male mice. Our data revealed that intraperitoneal administration of muscimol (0.12 and 0.25 mg/kg) increased the percentage of maximum possible effect (%MPE) and area under the curve (AUC) of %MPE, indicating an antinociceptive response. Intraperitoneal injection of bicuculline (0.5 and 1 mg/kg) decreased %MPE and AUC of %MPE, suggesting hyperalgesia. Moreover, muscimol by reducing the immobility time of the FST elicited an antidepressant-like response but bicuculline by enhancing the immobility time of the FST caused a depressant-like response. Intracerebroventricular (i.c.v.) microinjection of histamine (5 µg/mouse) enhanced %MPE and AUC of %MPE. i.c.v. infusion of histamine (2.5 and 5 µg/mouse) decreased immobility time in the FST. Co-administration of different doses of histamine along with a sub-threshold dose of muscimol potentiated antinociceptive and antidepressant-like responses produced by histamine. Cotreatment of different doses of histamine plus a noneffective dose of bicuculline reversed antinociception and antidepressant-like effects elicited by histamine. Cotreatment of histamine, muscimol, and bicuculline reversed antinociceptive and antidepressant-like behaviors induced by the drugs. The results demonstrated additive antinociceptive and antidepressant-like effects between histamine and muscimol in mice. In conclusion, our results indicated an interaction between the histaminergic and GABAergic systems in the modulation of pain and depression-like behaviors.

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组胺和麝香草酚对诱导小鼠产生抗痛觉和抗抑郁作用的叠加效应
我们用尾弹试验和强迫游泳试验(FST)研究了组胺和GABA A受体药物对雄性小鼠疼痛和抑郁样行为的影响及其相互作用。我们的数据显示,腹腔注射麝香草酚(0.12 和 0.25 毫克/千克)可提高最大可能效应百分比(%MPE)和%MPE 的曲线下面积(AUC),这表明存在抗痛觉反应。腹腔注射比库库林(0.5 和 1 毫克/千克)会降低最大可能效应百分比和最大可能效应百分比的曲线下面积,表明存在痛觉减退。此外,麝香草酚通过缩短FST的静止时间引起了类似抗抑郁的反应,但比古丁通过延长FST的静止时间引起了类似抑制的反应。脑室内显微注射组胺(5微克/只小鼠)可提高MPE%和MPE%的AUC。同时注射不同剂量的组胺和阈下剂量的麝香草酚可增强组胺产生的抗痛觉和抗抑郁样反应。不同剂量的组胺加上无效剂量的双胭脂虫碱进行共处理,可逆转组胺引起的抗痛觉和抗抑郁样反应。组胺、麝香草酚和双谷氨酸的共处理可逆转药物诱导的抗痛觉和抗抑郁样行为。结果表明组胺和麝香草酚对小鼠的抗痛觉和类抗抑郁作用具有叠加效应。总之,我们的研究结果表明组胺能系统和 GABA 能系统在调节疼痛和抑郁样行为方面存在相互作用。
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来源期刊
Behavioural Pharmacology
Behavioural Pharmacology 医学-行为科学
CiteScore
3.40
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Behavioural Pharmacology accepts original full and short research reports in diverse areas ranging from ethopharmacology to the pharmacology of schedule-controlled operant behaviour, provided that their primary focus is behavioural. Suitable topics include drug, chemical and hormonal effects on behaviour, the neurochemical mechanisms under-lying behaviour, and behavioural methods for the study of drug action. Both animal and human studies are welcome; however, studies reporting neurochemical data should have a predominantly behavioural focus, and human studies should not consist exclusively of clinical trials or case reports. Preference is given to studies that demonstrate and develop the potential of behavioural methods, and to papers reporting findings of direct relevance to clinical problems. Papers making a significant theoretical contribution are particularly welcome and, where possible and merited, space is made available for authors to explore fully the theoretical implications of their findings. Reviews of an area of the literature or at an appropriate stage in the development of an author’s own work are welcome. Commentaries in areas of current interest are also considered for publication, as are Reviews and Commentaries in areas outside behavioural pharmacology, but of importance and interest to behavioural pharmacologists. Behavioural Pharmacology publishes frequent Special Issues on current hot topics. The editors welcome correspondence about whether a paper in preparation might be suitable for inclusion in a Special Issue.
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