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维拉帕米、钙和镁离子诱导的心脏环磷酸腺苷与心肌收缩力之间的解离。

Dissociation between cardiac cyclic AMP and myocardial contractility induced by verapamil, calcium and magnesium ions.

作者信息

Hess M E, Gabel B E

出版信息

Cardiology. 1979;64(2):75-86. doi: 10.1159/000170581.

Abstract

Isolated, perfused rat hearts were used to study the effects of verapamil, excess calcium ions or excess magnesium ions on changes in heart cyclic AMP and myocardial force of contraction. Verapamil caused a dose-dependent decrease in force of contraction and a nondose-related reduction in cyclic AMP. Perfusion of hearts with medium containing 5 mM calcium produced a significant rise in cyclic AMP, but no change in contractile force. The depressant effects of verapamil on contractility and cyclic AMP were reversed by 5mM calcium; excess calcium in the perfusion fluid also containing verapamil prevented the myocardial depressant effects of verapamil. Acutely elevating the magnesium concentration in the perfusion medium decreased force of contraction, accentuated the negative inotropic effect of verapamil, but did not decrease cyclic AMP or enhance the verapamil-induced reduction in cyclic AMP.

摘要

采用离体灌注大鼠心脏来研究维拉帕米、过量钙离子或过量镁离子对心脏环磷酸腺苷(cAMP)变化及心肌收缩力的影响。维拉帕米可使收缩力呈剂量依赖性降低,且使环磷酸腺苷呈非剂量相关性减少。用含5 mM钙离子的培养基灌注心脏可使环磷酸腺苷显著升高,但收缩力无变化。5 mM钙离子可逆转维拉帕米对收缩性和环磷酸腺苷的抑制作用;灌注液中过量的钙离子(同时也含有维拉帕米)可防止维拉帕米对心肌的抑制作用。急性提高灌注培养基中的镁离子浓度可降低收缩力,增强维拉帕米的负性肌力作用,但不会降低环磷酸腺苷或增强维拉帕米引起的环磷酸腺苷减少。

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