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恶性腹水产生的机制。

Mechanisms of malignant ascites production.

作者信息

Garrison R N, Galloway R H, Heuser L S

出版信息

J Surg Res. 1987 Feb;42(2):126-32. doi: 10.1016/0022-4804(87)90109-0.

Abstract

The accumulation of malignant ascites is determined primarily by the obstruction of diaphragmatic lymphatics with tumor inhibiting the outflow of peritoneal fluid. An abnormal increase in peritoneal fluid production has been shown to contribute to ascites formation by a marked neovascularization of the parietal peritoneum. Cell-free malignant ascitic fluid obtained from rats with intra-abdominal Walker 256 carcinoma when infused into the peritoneal cavities of normal animals causes an increase in edema formation and an increase in the permeability of protein from normal omental vessels. Protamine sulfate, a known inhibitor of angiogenesis when infused into the peritoneal cavity along with cell free malignant ascitic fluid, significantly reduces the leak of protein from the intravascular space when compared to ascites alone. Persistent permeability changes continue to exist even after the inhibition of vessel proliferation. These results indicate that angiogenesis is responsible for a major portion of the increase in permeability caused by malignant ascitic fluids. Other tumor-induced factors may be present which alter vascular permeability by other mechanisms which remain to be elucidated.

摘要

恶性腹水的积聚主要由肿瘤阻塞膈淋巴管抑制腹腔液流出所致。研究表明,壁腹膜显著的新生血管形成导致腹腔液生成异常增加,从而促使腹水形成。从患有腹腔内Walker 256癌的大鼠获取的无细胞恶性腹水注入正常动物腹腔后,会导致水肿形成增加以及正常网膜血管的蛋白质通透性增加。硫酸鱼精蛋白是一种已知的血管生成抑制剂,当与无细胞恶性腹水一起注入腹腔时,与单独注入腹水相比,能显著减少血管内空间蛋白质的渗漏。即使血管增殖受到抑制,持续的通透性变化仍然存在。这些结果表明,血管生成是恶性腹水导致通透性增加的主要原因。可能还存在其他肿瘤诱导因子,它们通过其他尚待阐明的机制改变血管通透性。

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