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血管紧张素II会破坏抑制性回避记忆的提取。

Angiotensin II disrupts inhibitory avoidance memory retrieval.

作者信息

Bonini Juliana S, Bevilaqua Lia R, Zinn Carolina G, Kerr Daniel S, Medina Jorge H, Izquierdo Iván, Cammarota Martín

机构信息

Centro de Memória, Instituto de Pesquisas Biomédicas, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, RS, Brazil.

出版信息

Horm Behav. 2006 Aug;50(2):308-13. doi: 10.1016/j.yhbeh.2006.03.016. Epub 2006 May 12.

DOI:10.1016/j.yhbeh.2006.03.016
PMID:16697382
Abstract

The brain renin-angiotensin system (RAS) is involved in learning and memory, but the actual role of angiotensin II (A(II)) and its metabolites in this process has been difficult to comprehend. This has been so mainly due to procedural issues, especially the use of multi-trial learning paradigms and the utilization of pre-training intracerebroventricular infusion of RAS-acting compounds. Here, we specifically analyzed the action of A(II) in aversive memory retrieval using a hippocampal-dependent, one-trial, step-down inhibitory avoidance task (IA) in combination with stereotaxically localized intrahippocampal infusion of drugs. Rats bilaterally implanted with infusion cannulae aimed to the CA1 region of the dorsal hippocampus were trained in IA and tested for memory retention 24 h later. We found that when given into CA1 15 min before IA memory retention test, A(II), but not angiotensin IV or angiotensin(1-7) induced a dose-dependent and reversible amnesia without altering locomotor activity, exploratory behavior or anxiety state. The effect of A(II) was blocked in a dose-dependent manner by the A(II)-type 2 receptor (AT(2)) antagonist PD123319 but not by the A(II)-type 1 receptor (AT(1)) antagonist losartan. By themselves, neither PD123319 nor losartan had any effect on memory expression. Our data indicate that intra-CA1 A(II) hinders retrieval of avoidance memory through a process that involves activation of AT(2) receptors.

摘要

脑肾素-血管紧张素系统(RAS)参与学习和记忆,但血管紧张素II(A(II))及其代谢产物在此过程中的实际作用一直难以理解。主要原因在于实验程序问题,特别是多试验学习范式的使用以及在训练前脑室内注入RAS作用化合物。在此,我们使用海马依赖性单次递减抑制性回避任务(IA)并结合立体定位海马内药物注入,具体分析了A(II)在厌恶记忆提取中的作用。将双侧植入针对背侧海马CA1区的注入套管的大鼠进行IA训练,并在24小时后测试记忆保持情况。我们发现,在IA记忆保持测试前15分钟注入CA1时,A(II)而非血管紧张素IV或血管紧张素(1-7)可诱导剂量依赖性且可逆的失忆,同时不改变运动活性、探索行为或焦虑状态。A(II)型2受体(AT(2))拮抗剂PD123319可剂量依赖性地阻断A(II)的作用,但A(II)型1受体(AT(1))拮抗剂氯沙坦则无此作用。单独使用时,PD123319和氯沙坦对记忆表达均无任何影响。我们的数据表明,CA1区内的A(II)通过涉及AT(2)受体激活的过程阻碍回避记忆的提取。

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