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多巴胺D1受体激动剂A77636或SKF81297对老年猴子空间工作记忆的剂量依赖性影响。

Dose-dependent effects of the dopamine D1 receptor agonists A77636 or SKF81297 on spatial working memory in aged monkeys.

作者信息

Cai J X, Arnsten A F

机构信息

Kunming Institute of Zoology, The Chinese Academy of Sciences, Yunnan.

出版信息

J Pharmacol Exp Ther. 1997 Oct;283(1):183-9.

PMID:9336323
Abstract

With advancing age, monkeys develop deficits in spatial working memory resembling those induced by lesions of the prefrontal cortex (PFC). Aged monkeys also exhibit marked loss of dopamine from the PFC, a transmitter known to be important for proper PFC cognitive function. Previous results suggest that D1 agonist treatment can improve spatial working memory abilities in aged monkeys. However, this research was limited by the use of drugs with either partial agonist actions or significant D2 receptor actions. In our study, the selective dopamine D1 receptor full agonists A77636 and SKF81297 were examined in aged monkeys for effects on the working memory functions of the PFC. Both compounds produced a significant, dose-related effect on delayed response performance without evidence of side effects: low doses improved performance although higher doses impaired or had no effect on performance. Both the improvement and impairment in performance were reversed by pretreatment with the D1 receptor antagonist, SCH23390. These findings are consistent with previous results demonstrating that there is a narrow range of D1 receptor stimulation for optimal PFC cognitive function, and suggest that very low doses of D1 receptor agonists may have cognitive-enhancing actions in the elderly.

摘要

随着年龄的增长,猴子在空间工作记忆方面会出现缺陷,类似于前额叶皮层(PFC)损伤所导致的情况。老年猴子的PFC中多巴胺也显著减少,多巴胺是一种已知对PFC正常认知功能很重要的神经递质。先前的研究结果表明,D1激动剂治疗可以改善老年猴子的空间工作记忆能力。然而,这项研究受到使用具有部分激动剂作用或显著D2受体作用药物的限制。在我们的研究中,对老年猴子进行了选择性多巴胺D1受体完全激动剂A77636和SKF81297的实验,以观察其对PFC工作记忆功能的影响。两种化合物对延迟反应表现均产生了显著的、剂量相关的影响,且无副作用迹象:低剂量改善了表现,而高剂量则损害表现或对表现无影响。表现的改善和损害都可通过用D1受体拮抗剂SCH23390预处理来逆转。这些发现与先前的结果一致,即表明存在一个狭窄的D1受体刺激范围以实现最佳的PFC认知功能,并表明极低剂量的D1受体激动剂可能对老年人具有认知增强作用。

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