Stress and glucocorticoids impair inhibitory avoidance memory retrieval and extinction in male mice: the ameliorative effect of Ginkgo biloba extract.

IF 1.6 4区 心理学 Q3 BEHAVIORAL SCIENCES
Neda Alizadeh, Fatemeh Dehbashi, Emad Gholami, Paria Tarahomi, Ali Rashidy-Pour, Abbas Ali Vafaei, Payman Raise-Abdullahi
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引用次数: 0

Abstract

Memory retrieval involves recalling previously consolidated information, while memory extinction refers to the gradual weakening of such memories after recall. Stress and glucocorticoids influence the retrieval and extinction of memory. This study employed a passive avoidance task to examine the impact of acute mild stress and equivalent doses of exogenous corticosterone on fear memory retrieval and extinction in male mice. Subsequently, we investigated the potential therapeutic effects of Ginkgo biloba extract, EGb 761, on memory impairments induced by stress and corticosterone. Corticosterone was administered systemically 30 min before memory reactivation to model glucocorticoid activity during retrieval. Mild acute stress, like the stress levels typically experienced before an exam, was induced through 20-min restraint immediately before reactivation in separate groups. EGb 761 was injected 30 min before corticosterone or stress exposure. Results demonstrated that both corticosterone and acute stress impaired context-specific fear memory retrieval and enhanced subsequent extinction. Pretreatment with EGb 761 inhibited these impairing effects of acute stress and corticosterone on avoidance memory retrieval and extinction. Our findings suggest that the glucocorticoid system and acute stress markedly influence avoidance memory retrieval and extinction. Ginkgo biloba may possess therapeutic and memory-enhancing effects, particularly in stressful situations.

应激和糖皮质激素损害雄性小鼠的抑制性回避记忆检索和消退:银杏叶提取物的改善作用
记忆检索是指唤起先前巩固的信息,而记忆消退是指唤起后这些记忆逐渐减弱。压力和糖皮质激素会影响记忆的检索和消退。本研究采用被动回避任务来研究急性轻度应激和同等剂量的外源性皮质酮对雄性小鼠恐惧记忆检索和消退的影响。随后,我们研究了银杏叶提取物 EGb 761 对应激和皮质酮引起的记忆损伤的潜在治疗作用。我们在记忆重新激活前30分钟全身注射皮质酮,以模拟检索过程中糖皮质激素的活性。在重新激活记忆前 20 分钟,分别给不同组的受试者施加轻度急性应激,就像考试前通常会经历的应激水平一样。在皮质酮或应激暴露前 30 分钟注射 EGb 761。结果表明,皮质酮和急性应激都会损害特定情境下的恐惧记忆检索,并增强随后的消退。EGb 761的预处理抑制了急性应激和皮质酮对回避记忆检索和消退的损害作用。我们的研究结果表明,糖皮质激素系统和急性应激明显影响回避记忆的检索和消退。银杏叶可能具有治疗和增强记忆的作用,尤其是在应激情况下。
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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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