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腺苷受体在异丙肾上腺素输注期间大鼠对下腔静脉阻塞的反常心动过缓反应中的作用。

Role of adenosine receptors in the paradoxic bradycardia response of rats to inferior vena cava occlusion during an infusion of isoproterenol.

作者信息

Waxman M B, Asta J A

机构信息

Department of Medicine of the University of Toronto and the Division of Cardiology of the Toronto Hospital, Ontario, Canada.

出版信息

Circulation. 1998 Sep 22;98(12):1228-35. doi: 10.1161/01.cir.98.12.1228.

Abstract

BACKGROUND

In susceptible humans, vasodepressor reactions are induced by restriction of venous return (upright tilting) and administration of isoproterenol. Because paradoxic bradycardia is a major manifestation of vasodepressor reactions, and allowing for extrapolation between paradoxic bradycardia in rats and vasodepressor reactions, we examined whether adenosine receptors mediate the paradoxic bradycardia reaction.

METHODS AND RESULTS

Paradoxic bradycardia was induced in rats by inferior vena cava occlusion during an isoproterenol infusion. We studied whether dipyridamole, an adenosine transport inhibitor, and aminophylline (nonselective) or DPCPX (selective) A1 antagonists augmented or inhibited paradoxic bradycardia, respectively, during inferior vena cava occlusion. The maximum changes in R-R during 60 seconds of inferior vena cava occlusion were that (1) in control, the rate accelerated (DeltaR-R, -9.7+/-0.8 ms, P<0.001); (2) during isoproterenol (0.8 microg . min-1), paradoxic bradycardia occurred (DeltaR-R, +92.0+/-32.0 ms, P<0.001); (3) during isoproterenol but after dipyridamole, paradoxic bradycardia occurred at a much lower dose of isoproterenol (0.2 microg . min-1), and the magnitude was increased at all doses (at 0.8 microg . min-1 isoproterenol, DeltaR-R, +195.6+/-27.6 ms, P<0.001 versus isoproterenol alone, DeltaR-R, +92.0+/-32 ms); (4) during isoproterenol and dipyridamole, atropine did not block paradoxic bradycardia, but cervical vagotomy inhibited paradoxic bradycardia (DeltaR-R, +5.6+/-1.8 ms, P<0.001 compared with isoproterenol and dipyridamole alone); and (5) during isoproterenol alone, aminophylline or DPCPX blocked paradoxic bradycardia (DeltaR-R, -5.4+/-1.0 ms, and DeltaR-R, -2.6+/-0.5 ms, respectively, each P<0.001 compared with isoproterenol alone).

CONCLUSIONS

The adenosine A1 receptor mediates the paradoxic bradycardia reflex during inferior vena cava occlusion in the face of isoproterenol via vagal afferents.

摘要

背景

在易患人群中,静脉回流受限(直立倾斜)和给予异丙肾上腺素可诱发血管减压反应。由于反常性心动过缓是血管减压反应的主要表现,并且考虑到大鼠的反常性心动过缓和血管减压反应之间的推断关系,我们研究了腺苷受体是否介导反常性心动过缓反应。

方法与结果

在输注异丙肾上腺素期间,通过下腔静脉闭塞在大鼠中诱发反常性心动过缓。我们研究了腺苷转运抑制剂双嘧达莫以及氨茶碱(非选择性)或DPCPX(选择性)A1拮抗剂在大鼠下腔静脉闭塞期间分别增强或抑制反常性心动过缓的情况。在下腔静脉闭塞60秒期间R-R的最大变化如下:(1)在对照组中,心率加快(R-R变化量,-9.7±0.8毫秒,P<0.001);(2)在异丙肾上腺素(0.8微克·分钟-1)期间,出现反常性心动过缓(R-R变化量,+92.0±32.0毫秒,P<0.001);(3)在异丙肾上腺素期间但在双嘧达莫之后,在更低剂量的异丙肾上腺素(0.2微克·分钟-1)时就出现反常性心动过缓,并且在所有剂量下幅度都增加(在异丙肾上腺素0.8微克·分钟-1时,R-R变化量,+195.6±27.6毫秒,与单独使用异丙肾上腺素相比,P<0.001,单独使用异丙肾上腺素时R-R变化量,+92.0±32毫秒);(4)在异丙肾上腺素和双嘧达莫期间,阿托品不能阻断反常性心动过缓,但颈迷走神经切断术可抑制反常性心动过缓(R-R变化量,+5.6±1.8毫秒,与单独使用异丙肾上腺素和双嘧达莫相比,P<0.001);(5)在单独使用异丙肾上腺素期间,氨茶碱或DPCPX可阻断反常性心动过缓(R-R变化量分别为-5.4±1.0毫秒和-2.6±0.5毫秒,与单独使用异丙肾上腺素相比,各P<0.001)。

结论

腺苷A1受体通过迷走神经传入纤维介导了在异丙肾上腺素存在的情况下下腔静脉闭塞期间的反常性心动过缓反射。

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