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持续输注内毒素诱导的弥散性血管内凝血实验模型

Experimental model of disseminated intravascular coagulation induced by sustained infusion of endotoxin.

作者信息

Yoshikawa T, Furukawa Y, Murakami M, Takemura S, Kondo M

出版信息

Res Exp Med (Berl). 1981;179(3):223-8. doi: 10.1007/BF01851619.

Abstract

Experimental disseminated intravascular coagulation (DIC) was induced by sustained infusion of endotoxin into the femoral vein in rats. The severity of DIC was determined with reference to various parameters, such as fibrinogen and fibrin degradation products (FDP), prothrombin time (PT), partial thromboplastin time (PTT), platelet count, and number of renal glomeruli having fibrin thrombi. Experimental DIC could be induced by a 4-h sustained infusion of endotoxin in a dose of 100 mg/kg. The DIC induced in rats showed a close resemblance to human DIC as judged from such changes as an elevation in FDP, prolongation of PT and PTT, depression in fibrinogen and platelet count, and increase in glomeruli having fibrin thrombi. This experimental model has an advantage in that severity of DIC can be determined by measuring various parameters. It will be of use in the studies aimed at the establishment of a therapy for DIC as well as in the studies on DIC in rats.

摘要

通过向大鼠股静脉持续输注内毒素诱导实验性弥散性血管内凝血(DIC)。参照各种参数来确定DIC的严重程度,这些参数包括纤维蛋白原和纤维蛋白降解产物(FDP)、凝血酶原时间(PT)、部分凝血活酶时间(PTT)、血小板计数以及有纤维蛋白血栓形成的肾小球数量。通过以100mg/kg的剂量持续输注4小时内毒素可诱导实验性DIC。从FDP升高、PT和PTT延长、纤维蛋白原和血小板计数降低以及有纤维蛋白血栓形成的肾小球数量增加等变化判断,大鼠诱导的DIC与人类DIC极为相似。该实验模型的优点在于可通过测量各种参数来确定DIC的严重程度。它将有助于旨在建立DIC治疗方法的研究以及大鼠DIC的研究。

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