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糖尿病大鼠新血管的白蛋白渗透增加。

Albumin permeation of new vessels is increased in diabetic rats.

作者信息

Kilzer P, Chang K, Marvel J, Rowold E, Jaudes P, Ullensvang S, Kilo C, Williamson J R

出版信息

Diabetes. 1985 Apr;34(4):333-6. doi: 10.2337/diab.34.4.333.

Abstract

125I-bovine serum albumin (BSA) permeation of the vasculature of 3-wk-old granulation tissue (induced by subcutaneous implantation of polyester fabric) formed in the diabetic milieu was assessed in female BB/W, spontaneously diabetic rats and in male, Sprague-Dawley rats with streptozocin-induced diabetes as well as in corresponding nondiabetic controls. Albumin permeation of new granulation tissue vessels was markedly increased in both groups of diabetic animals relative to that of nondiabetic controls, while albumin permeation of vessels in most other tissues did not differ for controls and diabetics. These observations indicate that the functional integrity of new vessels formed in the diabetic milieu is impaired: (1) to a greater extent than that of older vessels formed before induction of diabetes and (2) relative to new vessels in nondiabetics. The implication of these observations is that molecular constituents of vessels synthesized in the diabetic milieu are quantitatively and/or qualitatively abnormal and/or their incorporation into vessels is defective.

摘要

评估了在糖尿病环境中形成的3周龄肉芽组织(由皮下植入聚酯织物诱导)的血管对125I-牛血清白蛋白(BSA)的渗透情况,研究对象包括雌性自发糖尿病的BB/W大鼠、链脲佐菌素诱导糖尿病的雄性Sprague-Dawley大鼠以及相应的非糖尿病对照大鼠。与非糖尿病对照相比,两组糖尿病动物新形成的肉芽组织血管对白蛋白的渗透均显著增加,而大多数其他组织血管的白蛋白渗透在对照组和糖尿病组之间并无差异。这些观察结果表明,在糖尿病环境中形成的新血管的功能完整性受损:(1)受损程度大于糖尿病诱导前形成的较老血管;(2)相对于非糖尿病动物的新血管。这些观察结果的意义在于,在糖尿病环境中合成的血管分子成分在数量和/或质量上异常,和/或它们整合到血管中的过程存在缺陷。

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