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腺嘌呤二核苷酸对大鼠海马脑片CA3区癫痫样活动的影响。

The effects of adenine dinucleotides on epileptiform activity in the CA3 region of rat hippocampal slices.

作者信息

Ross F M, Brodie M J, Stone T W

机构信息

Institute of Biomedical and Life Sciences, Division of Neuroscience and Biomedical Systems, University of Glasgow, UK.

出版信息

Neuroscience. 1998 Jul;85(1):217-28. doi: 10.1016/s0306-4522(97)00619-2.

Abstract

Alpha, omega-adenine dinucleotides (Ap(n)A) consist of two adenosine molecules linked at the 5' position by phosphate groups, the number of which is denoted by n and can range from 2 to 6. The aim of this study was to investigate the effect of Ap4A and Ap5A on the rate of epileptiform activity. Hippocampal slices (450 microm), when perfused with a medium containing no added magnesium and 4-aminopyridine (50 microM), generate epileptiform activity of an interictal nature. Ap4A and Ap5A at 1 microM depressed the discharge rate to a significant extent. At this concentration adenosine (1 microM) did not produce any effect. However at 10 microM adenosine, Ap4A and Ap5A all decreased the burst frequency. Adenosine deaminase (0.2 U/ml) totally annulled the inhibition of epileptiform activity produced by 10 microM adenosine or 1 microM Ap4A and Ap5A. Adenosine deaminase did not significantly change the maximum depression of activity produced by 10 microM Ap4A and Ap5A. 8-cyclopentyl-1,3-dimethylxanthine, an A1, receptor antagonist, increased the basal rate of epileptiform activity and prevented the depression of burst discharges by Ap4A. 5'-adenylic acid deaminase converts AMP into IMP which is inactive. 5'-adenylic acid deaminase did not prevent the inhibitory effects of Ap4A. The results suggests that in the CA3 region of the hippocampus, Ap4A and Ap5A act partly by stimulating xanthine-sensitive receptors directly and partly through the formation of the metabolite, adenosine.

摘要

α,ω-腺嘌呤二核苷酸(Ap(n)A)由两个腺苷分子通过磷酸基团在5'位相连组成,磷酸基团的数量用n表示,范围为2至6。本研究的目的是研究Ap4A和Ap5A对癫痫样活动速率的影响。海马切片(450微米)在灌注不含添加镁和4-氨基吡啶(50微摩尔)的培养基时,会产生发作间期性质的癫痫样活动。1微摩尔的Ap4A和Ap5A能显著降低放电速率。在此浓度下,腺苷(1微摩尔)没有任何作用。然而,在10微摩尔腺苷时,Ap4A和Ap5A均降低了爆发频率。腺苷脱氨酶(0.2单位/毫升)完全消除了10微摩尔腺苷或1微摩尔Ap4A和Ap5A对癫痫样活动的抑制作用。腺苷脱氨酶并没有显著改变10微摩尔Ap4A和Ap5A所产生的最大活动抑制程度。8-环戊基-1,3-二甲基黄嘌呤,一种A1受体拮抗剂,增加了癫痫样活动的基础速率,并阻止了Ap4A对爆发放电的抑制作用。5'-腺苷酸脱氨酶将AMP转化为无活性的IMP。5'-腺苷酸脱氨酶并没有阻止Ap4A的抑制作用。结果表明,在海马体的CA3区域,Ap4A和Ap5A部分通过直接刺激对黄嘌呤敏感的受体起作用,部分通过代谢产物腺苷的形成起作用。

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