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去纤苷对猫致死性急性心肌缺血的保护作用。

Protective activity of defibrotide against lethal acute myocardial ischemia in the cat.

作者信息

Niada R, Porta R, Pescador R, Mantovani M, Prino G

出版信息

Thromb Res. 1986 May 1;42(3):363-74. doi: 10.1016/0049-3848(86)90265-3.

Abstract

Defibrotide (D) is a natural polydeoxyribonucleotide from mammalian lungs with profibrinolytic and antithrombotic activities. D also has PGI2-stimulating and tissue plasminogen activator (TPA)-releasing activities, but has no anticoagulant properties. The protective effects of D were demonstrated very recently in a model for non-lethal ischemia in the cat. In the experiments reported here Defibrotide was tested in a model for acute myocardial ischemia leading to ventricular fibrillation (VF) and death of the cat. Occlusion of the coronary artery (LAD) at its origin induced VF and death in 17 of 20 control cats. When cats were treated with D (32 mg Kg-1, bolus i.v., + 32 mg Kg-1 h-1, i.v., after LAD occlusion) 19 of 20 animals survived until the end of experiments. D also prevented changes in plasma and myocardial CPK, hemodynamics and ECG. D was compared with a variety of pharmacological agents which are used clinically for specific cardiovascular diseases. The ability of D to promote considerable generation of PGI2 from vascular walls plus its ability to prevent the decreases in CPK-activity and ATP in the myocardial tissue may have roles in its beneficial effects against ischemic heart in the cat. However, the mechanism/s of the substantial protective effect of D against cardiac death has still to be clarified.

摘要

去纤苷(D)是一种从哺乳动物肺中提取的天然多脱氧核糖核苷酸,具有促纤溶和抗血栓活性。D还具有刺激前列环素(PGI2)生成和释放组织纤溶酶原激活物(TPA)的活性,但没有抗凝特性。最近在猫的非致死性缺血模型中证实了D的保护作用。在本文报道的实验中,对去纤苷在导致猫心室颤动(VF)和死亡的急性心肌缺血模型中进行了测试。在20只对照猫中,冠状动脉(左前降支,LAD)起始处闭塞导致17只猫发生VF和死亡。当猫接受D治疗(32mg·kg-1,静脉推注,+32mg·kg-1·h-1,LAD闭塞后静脉输注)时,20只动物中有19只存活至实验结束。D还可防止血浆和心肌肌酸磷酸激酶(CPK)、血流动力学和心电图的变化。将D与临床上用于特定心血管疾病的多种药物进行了比较。D促进血管壁大量生成PGI2的能力及其防止心肌组织中CPK活性和三磷酸腺苷(ATP)降低的能力,可能在其对猫缺血性心脏的有益作用中发挥了作用。然而,D对心脏死亡的显著保护作用机制仍有待阐明。

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