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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Distributions of microvascular pressure in skeletal muscle of one-kidney, one clip, two-kidney, one clip, and deoxycorticosterone-salt hypertensive rats.
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Distributions of microvascular pressure in skeletal muscle of one-kidney, one clip, two-kidney, one clip, and deoxycorticosterone-salt hypertensive rats.

机译:一肾,一夹,二肾,一夹和脱氧皮质酮盐类高血压大鼠骨骼肌中微血管压力的分布。

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Studies were performed on the cremaster skeletal muscle in rats to investigate the microvascular changes that are associated with established one-kidney, one clip (1K1C) and two-kidney, one clip (2K1C) Goldblatt hypertension and with deoxycorticosterone (DOC)-salt hypertension. Rats were anesthetized with urethane and chloralose; and cremaster muscles with intact circulation and innervation were suspended in a controlled Krebs bath. Microvascular pressures and vessel diameters were measured at three consecutive arteriolar (A) and venular (V) branch levels. Arteriolar diameters (means +/- SEM) in normotensive (NT) rats were 119 +/- 7, 86 +/- 5, and 31 +/- 3 micron respectively for 1A, 2A, and 3A arterioles; and venule diameters were 218 +/- 12, 141 +/- 15, and 53 +/- 7 micron respectively for 1V, 2V, and 3V venules. As compared to NT rats, there was a selective decrease in lumen size (percent reduction from control) for 1A and 2A (23% to 38%) in 1K1C and 2K1C rats and for 1A, 2A, and 3A (42% to 44%) in DOC rats. Venule diameters were not significantly different between normotensive and hypertensive animals at any branch level. Femoral artery pressures were significantly elevated (greater than or equal to 43%) in all three forms of hypertension; however, this increase in pressure was not proportionally transmitted throughout the microcirculation. This was evidenced by normal pressure in 3A arterioles and in all venules for 1K1C and 2K1C rats and by normal pressures in 3V and larger venules for DOC rats. Our findings indicate that elevated arterial pressure in chronic renal hypertension is not transmitted uniformly across all microvascular segments.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:对大鼠的提睾骨骼肌进行了研究,以研究与既定的一肾,一夹(1K1C)和二肾,一夹(2K1C)Goldblatt高血压以及脱氧皮质酮(DOC)-盐高血压相关的微血管变化。大鼠用尿烷和氯醛麻醉。完整循环和神经支配的cremaster肌肉悬浮在受控的Krebs浴中。在三个连续的小动脉(A)和小静脉(V)分支水平测量微血管压力和血管直径。对于1A,2A和3A小动脉,正常血压(NT)大鼠的小动脉直径(平均值+/- SEM)分别为119 +/- 7、86 +/- 5和31 +/- 3微米;对于1V,2V和3V小静脉,小静脉直径分别为218 +/- 12、141 +/- 15和53 +/- 7微米。与NT大鼠相比,在1K1C和2K1C大鼠中1A和2A(23%至38%)以及1A,2A和3A(42%至44%)的管腔大小选择性减少(相对于对照减少的百分比) )在DOC大鼠中。正常血压和高血压动物在任何分支水平上的静脉直径均无显着差异。在所有三种形式的高血压中,股动脉压力均显着升高(大于或等于43%)。但是,这种压力增加并未在整个微循环中成比例地传递。 1K1C和2K1C大鼠的3A小动脉和所有小静脉中的正常压力以及DOC大鼠的3V和较大的小静脉中的正常压力证明了这一点。我们的研究结果表明,慢性肾高血压中的动脉压并非在所有微血管节段中均等地传播。(摘要截断为250字)

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