Inhibition of central angiotensin II enhances memory function and reduces oxidative stress status in rat hippocampus

被引:75
作者
Bild, Walther [1 ,3 ]
Hritcu, Lucian [2 ]
Stefanescu, Cristinel [1 ]
Ciobica, Alin [2 ,3 ]
机构
[1] Gr T Popa Univ Med & Pharm, Iasi 700115, Romania
[2] Alexandru Ioan Cuza Univ, Iasi 700506, Romania
[3] Romanian Acad, Ctr Biomed Res, Iasi Branch, Iasi, Romania
关键词
Angiotensin II; Memory; Oxidative stress; CONVERTING ENZYME-INHIBITORS; MILD COGNITIVE IMPAIRMENT; CEREBRAL-BLOOD-FLOW; ALZHEIMERS-DISEASE; ANTIHYPERTENSIVE TREATMENTS; RECEPTOR ANTAGONISTS; VASCULAR DEMENTIA; AT(1) RECEPTOR; DEFICIENT MICE; MOTOR-ACTIVITY;
D O I
10.1016/j.pnpbp.2012.12.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
While it is now well established that the independent brain renin-angiotensin system (RAS) has some important central functions besides the vascular ones, the relevance of its main bioactive peptide angiotensin II (Ang II) on the memory processes, as well as on oxidative stress status is not completely understood. The purpose of the present work was to evaluate the effects of central Ang II administration, as well as the effects of Mg II inhibition with either AT1 and AT 2 receptor specific blockers (losartan and PD-123177, respectively) or an angiotensin-converting enzyme (ACE) inhibitor (captopril). These effects were studied on the short-term memory (assessed through Y-maze) or long-term memory (as determined in passive avoidance) and on the oxidative stress status of the hippocampus. Our results demonstrate memory deficits induced by the administration of Ang II, as showed by the significant decrease of the spontaneous alternation in Y-maze (p = 0.015) and latency-time in passive avoidance task (p = 0.001) when compared to saline. On the other side, the administration of all the aforementioned Ang II blockers significantly improved the spontaneous alternation in Y-maze task, while losartan also increased the latency time as compared to saline in step-through passive avoidance (p = 0.042). Also, increased oxidative stress status was induced in the hippocampus by the administration of Ang II, as demonstrated by increased levels of lipid peroxidation markers (malondialdehyde-MDA concentration) (p<0.0001) and a decrease in both antioxidant enzymes determined: superoxide dismutase-SOD (p<0.0001) and glutathione peroxidase-GPX (p = 0.01), as compared to saline. Additionally, the administration of captopril resulted in an increase of both antioxidant enzymes and decreased levels of lipid peroxidation (p = 0.001), while PD-123177 significantly decreased MDA concentration (p>0.0001) vs. saline. Moreover, significant correlations were found between all of the memory related behavioral parameters and the main oxidative stress markers from the hippocampus, which is known for its implication in the processes of memory and also where RAS components are well expressed. This could be relevant for the complex interactions between Ang II, behavioral processes and neuronal oxidative stress, and could generate important therapeutic approaches. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:79 / 88
页数:10
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