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纤溶酶原激活物抑制剂2降低炎症状态下的腹膜纤溶活性。

Plasminogen activator inhibitor 2 reduces peritoneal fibrinolytic activity in inflammation.

作者信息

Whawell S A, Vipond M N, Scott-Coombes D M, Thompson J N

机构信息

Department of Surgery, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.

出版信息

Br J Surg. 1993 Jan;80(1):107-9. doi: 10.1002/bjs.1800800134.

Abstract

Fibrinolysis in peritoneal tissue may play a role in the development of intra-abdominal adhesions. The plasminogen-activating capacity of human peritoneum results largely from the presence of tissue plasminogen activator (tPA). Inflammation reduces peritoneal plasminogen-activating activity and leads to the appearance of plasminogen activator inhibitor (PAI) type 1. The role of PAI-2 in the inhibition of peritoneal fibrinolysis during inflammation was investigated in this study. The plasminogen-activating activity of peritoneal biopsy homogenates (seven inflamed, seven normal), measured using a fibrin plate technique, was reduced in inflamed compared with normal tissue (median < 0.07 versus 13.9 units/cm2, P < 0.01); tPA antigen levels were not significantly different (median 1.02 versus 1.34 ng/ml). PAI-1 and PAI-2 antigens were not detected in normal human peritoneum but were present in inflamed peritoneum (median concentration 8.8 ng/ml for PAI-1, 26.7 ng/ml for PAI-2). These inhibitors may be important factors in adhesion formation by contributing to the abolition of peritoneal plasminogen-activating activity.

摘要

腹膜组织中的纤维蛋白溶解可能在腹腔粘连的形成中起作用。人腹膜的纤溶酶原激活能力主要源于组织型纤溶酶原激活物(tPA)的存在。炎症会降低腹膜纤溶酶原激活活性,并导致1型纤溶酶原激活物抑制剂(PAI)的出现。本研究调查了PAI-2在炎症期间抑制腹膜纤维蛋白溶解中的作用。使用纤维蛋白平板技术测量,与正常组织相比,炎症腹膜活检匀浆(7例炎症组织,7例正常组织)的纤溶酶原激活活性降低(中位数<0.07对13.9单位/平方厘米,P<0.01);tPA抗原水平无显著差异(中位数1.02对1.34纳克/毫升)。正常人体腹膜中未检测到PAI-1和PAI-2抗原,但在炎症腹膜中存在(PAI-1中位数浓度8.8纳克/毫升,PAI-2为26.7纳克/毫升)。这些抑制剂可能是导致腹膜纤溶酶原激活活性丧失从而在粘连形成中起重要作用的因素。

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Peritoneal fibrinolytic activity in peritonitis.腹膜炎时的腹膜纤维蛋白溶解活性
Am J Surg. 2002 Jan;183(1):67-9. doi: 10.1016/s0002-9610(01)00850-9.

本文引用的文献

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Inhibitor of fibrinolysis from mesothelium.间皮细胞来源的纤溶抑制物。
Nature. 1969 Jan 18;221(5177):269-70. doi: 10.1038/221269a0.

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