School of Medicine, Campus USP, Ribeirão Preto, SP 14049-900, Brazil.
School of Medicine, Campus USP, Ribeirão Preto, SP 14049-900, Brazil; State University of Mato Grosso do Sul-Medicine UEMS, Brazil.
Pharmacol Biochem Behav. 2022 Jul;218:173425. doi: 10.1016/j.pbb.2022.173425. Epub 2022 Jul 4.
Re-exposure of rats to a previously fear-conditioned environment arouses great alterations in behavioral and cardiovascular parameters. Pieces of works provide putative evidence for the contribution of the dorsal hippocampus (dHC) to contextual conditioning. dHC gathers massive cholinergic inputs from the basal forebrain, and dHC acetylcholine (ACh) is often described as triggering the retrieval of defensive behavior. ACh acts partially through muscarinic receptors (mAChRs) M1R and M3R subtypes. Hence, activation of mAChRs facilitates autonomic and behavioral responses associated with threats and dangers. Therefore, this study explored the likely involvement of M1R and M3R in rat dHC to establish the behavioral and autonomic changes associated with contextual fear retrieval. Male Wistar rats had stainless steel guide cannula implanted into the dHC before being submitted to contextual fear conditioning (6 footshocks, 1.5 mA, 3 s). A catheter placed within the femoral artery allowed autonomic recordings. A variety of drugs were delivered into the dHC 10 min before contextual re-exposure. The choline reuptake inhibitor hemicholinium induced a decrease of the fear conditioned responses, while did not modify it in non-conditioned animals. The non-selective mAChR antagonist atropine also reduced the fear-conditioned responses, as did the selective M1/M3 mAChRs antagonist fumarate. On the other hand, the M1 selective mAChR antagonist pirenzepine inhibited all the autonomic fear responses without affecting animal freezing. These findings support that cholinergic neurotransmission present in the dHC acts through mAChRs to coordinate the expression of fear evoked by contextual conditioning.
大鼠重新暴露于先前恐惧条件的环境中会引起行为和心血管参数的巨大变化。一些研究工作为背侧海马(dHC)对情境条件作用的贡献提供了推测性证据。dHC 从基底前脑接收大量胆碱能输入,dHC 乙酰胆碱(ACh)常被描述为触发防御行为的检索。ACh 通过毒蕈碱型乙酰胆碱受体(mAChRs)M1R 和 M3R 亚类发挥部分作用。因此,mAChRs 的激活促进了与威胁和危险相关的自主和行为反应。因此,本研究探索了 M1R 和 M3R 在大鼠 dHC 中的可能参与,以确定与情境恐惧检索相关的行为和自主变化。雄性 Wistar 大鼠在进行情境恐惧条件作用(6 次电击,1.5 mA,3 s)之前,将不锈钢引导套管植入 dHC。放置在股动脉内的导管允许进行自主记录。在重新暴露于情境之前 10 分钟,将各种药物递送至 dHC。胆碱重摄取抑制剂 hemicholinium 诱导恐惧条件反应减少,而在未驯化动物中不改变。非选择性 mAChR 拮抗剂阿托品也降低了恐惧条件反应,而选择性 M1/M3 mAChRs 拮抗剂富马酸也是如此。另一方面,M1 选择性 mAChR 拮抗剂哌仑西平抑制了所有自主恐惧反应,而不影响动物的冻结。这些发现支持 dHC 中存在的胆碱能神经传递通过 mAChRs 作用,以协调由情境条件作用引起的恐惧表达。