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一氧化氮介导腺苷对离体兔房室结细胞钙电流的抗肾上腺素能作用。

Nitric oxide mediates the anti-adrenergic effect of adenosine on calcium current in isolated rabbit atrioventricular nodal cells.

作者信息

Martynyuk A E, Kane K A, Cobbe S M, Rankin A C

机构信息

Department of Medical Cardiology, Royal Infirmary, Glasgow, UK.

出版信息

Pflugers Arch. 1996 Jan;431(3):452-7. doi: 10.1007/BF02207285.

Abstract

The aim of this study was to determine if adenosine exerts an anti-adrenergic effect on rabbit isolated atrioventricular (AV) nodal cells and, if so, the dependence of this effect on nitric oxide (NO) production. Inward Ca current, ICa, was measured in AV nodal cells, enzymatically isolated from rabbit hearts. Isoprenaline (0.1 microM) increased ICa from 676 +/-59 to 1102 +/-86 pA (n =25). This isoprenaline-induced increase in ICa(178 +/-15% of control) was abolished in the presence of 10 microM adenosine (ICa100 +/-2% of control, n =9, P <0.05). This effect of adenosine was completely blocked by the A1 receptor antagonist CPDPX (8-cyclopentyl l, 3-dipropylxanthine, 0.1 microM). In cells pre-treated with the NO synthase inhibitor, L-nitro-arginine methyl ester (L-NAME, 1 mM) the isoprenaline-induced increase in ICa(208 +/-39% of control, n=7) was not reduced by the addition of 10 microM adenosine (195 +/-32% of control). Co-incubation of cells in L-NAME with L-arginine (1 mM, the endogenous substrate of NO synthase) restored the adenosine-induced attenuation of ICa. In these cells, isoprenaline increased ICa (157 +/-7% of control, n =6), and, following addition of adenosine (10 microM) ICa was reduced to 107 +/-8% (P <0.05). The NO-releasing agent SIN-1 (3-morpholino-sydnonimine, 100 microM), inhibited ICa augmented by isoprenaline (n=5). It is concluded that adenosine exerts an anti-adrenergic effect on the AV node via A1 receptors to attenuate a catecholamine-stimulated increase in ICa and that this action involves the intracellular production of NO.

摘要

本研究的目的是确定腺苷是否对兔离体房室(AV)结细胞发挥抗肾上腺素能作用,如果是,该作用对一氧化氮(NO)生成的依赖性。从兔心脏酶解分离的AV结细胞中测量内向钙电流(ICa)。异丙肾上腺素(0.1微摩尔)使ICa从676±59皮安增加到1102±86皮安(n = 25)。在10微摩尔腺苷存在时,异丙肾上腺素诱导的ICa增加(为对照的178±15%)被消除(ICa为对照的100±2%,n = 9,P <0.05)。腺苷的这种作用被A1受体拮抗剂CPDPX(8-环戊基-1,3-二丙基黄嘌呤,0.1微摩尔)完全阻断。在用一氧化氮合酶抑制剂L-硝基-精氨酸甲酯(L-NAME,1毫摩尔)预处理的细胞中,添加10微摩尔腺苷并未降低异丙肾上腺素诱导的ICa增加(为对照的208±39%,n = 7)(为对照的195±32%)。将细胞与L-NAME和L-精氨酸(1毫摩尔,一氧化氮合酶的内源性底物)共同孵育可恢复腺苷诱导的ICa衰减。在这些细胞中,异丙肾上腺素增加ICa(为对照的157±7%,n = 6),添加腺苷(10微摩尔)后ICa降至107±8%(P <0.05)。释放NO的试剂SIN-1(3-吗啉代-西多胺,100微摩尔)抑制异丙肾上腺素增强的ICa(n = 5)。得出的结论是,腺苷通过A1受体对房室结发挥抗肾上腺素能作用,以减弱儿茶酚胺刺激引起的ICa增加,且该作用涉及细胞内NO的生成。

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