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甲状腺功能减退对大鼠血管 125I-白蛋白渗透及血流的影响。

Effects of hypothyroidism on vascular 125I-albumin permeation and blood flow in rats.

作者信息

Tilton R G, Pugliese G, Chang K, Speedy A, Province M A, Kilo C, Williamson J R

机构信息

Department of Pathology, Washington University School of Medicine, St Louis, MO.

出版信息

Metabolism. 1989 May;38(5):471-8. doi: 10.1016/0026-0495(89)90201-1.

Abstract

Effects of hypothyroidism on vascular 125I-albumin permeation and on blood flow were assessed in multiple tissues of male Sprague-Dawley rats rendered hypothyroid by dietary supplementation with 0.5% (wt/wt) 2-thiouracil or by thyroidectomy. In both thiouracil-treated and thyroidectomized rats, body weights, kidney weight, arterial blood pressure, and pulse rate were decreased significantly v age-matched controls. After 10 to 12 weeks of thiouracil treatment, 125I-albumin permeation was increased significantly in the kidney, aorta, eye (anterior uvea, choroid, retina), skin, and new granulation tissue, remained unchanged in brain, sciatic nerve, and heart, and was decreased in forelimb skeletal muscle. A similar pattern was observed in thyroidectomized rats, except that increases in 125I-albumin permeation for all tissues were smaller than those observed in thiouracil-treated rats, and 125I-albumin permeation in retina did not differ from controls. In both thiouracil-treated and thyroidectomized rats, changes in blood flow (assessed with 15-microns, 85Sr-labeled microspheres) relative to the decrease in arterial blood pressure were indicative of a decrease in regional vascular resistance except in the choroid and in the kidney, in which vascular resistance was increased significantly. Glomerular filtration rate was decreased, but filtration fraction and urinary excretion of albumin remained unchanged by thiouracil treatment and thyroidectomy. These results indicate that vascular hemodynamics and endothelial cell barrier functional integrity are modulated in many different tissues by the thyroid. In view of the correspondence of hypothyroid- and diabetes-induced vascular permeability changes, these results raise the possibility that altered thyroid function in diabetes may play a role in the pathogenesis of diabetic vascular disease.

摘要

通过在雄性Sprague-Dawley大鼠的饮食中补充0.5%(重量/重量)的2-硫脲或进行甲状腺切除来制造甲状腺功能减退模型,评估甲状腺功能减退对雄性Sprague-Dawley大鼠多个组织中血管125I-白蛋白渗透及血流的影响。在硫脲处理组和甲状腺切除组大鼠中,其体重、肾脏重量、动脉血压和脉搏率均显著低于年龄匹配的对照组。硫脲处理10至12周后,肾脏、主动脉、眼睛(前葡萄膜、脉络膜、视网膜)、皮肤和新生肉芽组织中的125I-白蛋白渗透显著增加,大脑、坐骨神经和心脏中的125I-白蛋白渗透保持不变,前肢骨骼肌中的125I-白蛋白渗透则降低。甲状腺切除组大鼠也观察到类似模式,只是所有组织中125I-白蛋白渗透的增加幅度小于硫脲处理组大鼠,且视网膜中的125I-白蛋白渗透与对照组无差异。在硫脲处理组和甲状腺切除组大鼠中,相对于动脉血压下降,血流变化(用15微米、85Sr标记的微球评估)表明除脉络膜和肾脏外,局部血管阻力降低,而脉络膜和肾脏中的血管阻力显著增加。硫脲处理和甲状腺切除使肾小球滤过率降低,但滤过分数和白蛋白尿排泄保持不变。这些结果表明,甲状腺对许多不同组织中的血管血流动力学和内皮细胞屏障功能完整性具有调节作用。鉴于甲状腺功能减退和糖尿病引起的血管通透性变化具有相关性,这些结果提示糖尿病患者甲状腺功能改变可能在糖尿病血管疾病的发病机制中起作用。

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