Influence of hippocampal GABAB receptor inhibition on memory in rats with acute β-amyloid toxicity

被引:27
作者
Almasi, Azam [1 ]
Zarei, Mohammad [1 ]
Raoufi, Safoura [1 ]
Sarihi, Abdolrahman [1 ]
Salehi, Iraj [1 ]
Komaki, Alireza [1 ]
Hashemi-Firouzi, Nasrin [1 ]
Shahidi, Siamak [1 ]
机构
[1] Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
关键词
Alzheimer disease; Dentate gyrus; Recognition; beta-Amyloid; GABA; LONG-TERM POTENTIATION; CGP; 36; 742; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; OBJECT RECOGNITION; DENTATE GYRUS; PASSIVE-AVOIDANCE; ADULT HIPPOCAMPUS; OXIDATIVE STRESS; PERFORANT PATH;
D O I
10.1007/s11011-018-0292-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The neurotransmitter gamma-aminobutyric acid (GABA) is involved in the process of memory. It has been reported that the inhibition of GABA(B) receptors has beneficial effects on cognition. The aim of this study was to investigate the role of CGP35348 (a GABA(B) receptor antagonist) on dentate gyrus GABA(B) receptor inhibition and its effects on learning and memory impairments that had been induced in adult male rats by microinjection of beta-amyloid (A beta). Seventy Wistar male rats were randomly divided into seven groups: control, sham (receiving the A beta vehicle only), A beta, A beta + CGP35348 (1, 10, and 100 mu g/mu L), and CGP35348 alone (10 mu g/mu L). Memory impairment was induced by unilateral interventricular microinjection of A beta (6 mu g/6 mu L). Rats were cannulated bilaterally in the dentate gyrus, and then, they were treated for 20 consecutive days. Learning and memory were assessed using the novel object recognition and passive avoidance learning tests. The discrimination index and the step-through latency were significantly increased in the A beta + CGP35348 group in comparison to the A beta only group (P < 0.05 and P < 0.01, respectively). Data showed that the discrimination index was decreased in the A beta + CGP35348 group in comparison with the control group (P < 0.05) and sham group (P < 0.01). Moreover, the step-through latency was significantly decreased in the A beta + CGP35348 group in comparison to the control and sham groups (P < 0.01). Data from this study indicated that intra-hippocampal microinjection of the GABA(B) receptor antagonist counteracts the learning, memory, and cognitive impairments induced by A beta. It can be concluded that the GABA(B) receptor antagonist is a possible therapeutic agent against the progression of acute A beta toxicity-induced memory impairment.
引用
收藏
页码:1859 / 1867
页数:9
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