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高渗甘露醇在心肌缺血和坏死中的保护作用。

The protective effect of hyperosmotic mannitol in myocardial ischemia and necrosis.

作者信息

Powell W J, DiBona D R, Flores J, Leaf A

出版信息

Circulation. 1976 Oct;54(4):603-15. doi: 10.1161/01.cir.54.4.603.

Abstract

Morphologic and hemodynamic changes that occur following coronary occlusion are examined. The effectiveness of hyperosmotic mannitol in lessening the extent of myocardial damage is assessed and mechanisms for its action discussed. Forty and 60 min of coronary vascular occlusion followed by 15 and 45 min of reflow were associated with a persistence of ischemia following reflow of blood, as established by infusions of silastic into the aortic root. Electron microscopic studies demonstrated myocardial and endothelial cell swelling at the end of the reflow period. The process of cell swelling appeared to be initiated during the period of arterial occlusion. This cell swelling was reduced by elevation of serum osmolality by 30-40 mOsm above control with the administration of mannitol during and following occlusion. There was an associated 40-50% reduction of vascular resistance following occlusion if mannitol was administered. In addition, the extent of necrosis, which was widespread in untreated hearts 12 hours after occlusion, was strikingly less in the hearts of dogs which received mannitol. Thus, in ischemic myocardium, elevation of osmolality by mannitol reduces myocardial necrosis, probably through its restoration of normal cell volume.

摘要

研究了冠状动脉闭塞后发生的形态学和血流动力学变化。评估了高渗甘露醇在减轻心肌损伤程度方面的有效性,并讨论了其作用机制。通过将硅橡胶注入主动脉根部确定,冠状动脉血管闭塞40分钟和60分钟后再灌注15分钟和45分钟,再灌注后缺血持续存在。电子显微镜研究显示再灌注期末心肌和内皮细胞肿胀。细胞肿胀过程似乎在动脉闭塞期开始。在闭塞期间及之后给予甘露醇,使血清渗透压比对照升高30 - 40 mOsm,可减轻这种细胞肿胀。如果给予甘露醇,闭塞后血管阻力会降低40 - 50%。此外,闭塞12小时后,未治疗的心脏广泛出现坏死,而接受甘露醇治疗的犬心脏坏死程度明显减轻。因此,在缺血心肌中,甘露醇提高渗透压可能通过恢复正常细胞体积来减少心肌坏死。

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