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血管加压素拮抗剂在下腔静脉缩窄中对水排泄的影响。

Effect of vasopressin antagonist on water excretion in inferior vena cava constriction.

作者信息

Ishikawa S, Saito T, Okada K, Tsutsui K, Kuzuya T

出版信息

Kidney Int. 1986 Jul;30(1):49-55. doi: 10.1038/ki.1986.149.

Abstract

Elevated levels of plasma arginine vasopressin (AVP) have been suggested to impair water excretion in congestive heart failure. In the present study, to determine a role for AVP in the impaired water excretion in rats with the inferior vena cava constriction (IVC), two AVP antagonists were used in the IVC rats at the proximal portion of the hepatic vein under the diaphragm and in sham-operated (control) rats. After surgery, 48 hrs were allowed before the experiments were started. A mean cardiac index of 260.0 +/- 12.3 ml/min/kg in the IVC rats was significantly lower than that in the control rats, 323.6 +/- 13.2 ml/min/kg (P less than 0.01). The rats were given an antidiuretic antagonist, [1-(beta-mercapto-beta, beta-cyclopentamethylenepropionic acid), 2-(O-ethyl)-D-tyrosine, 4-valine] AVP (30 micrograms/kg) or the antagonist vehicle, i.p., and 20 min later they were administered 30 ml/kg of water orally. Minimal urinary osmolality (Uosm) in the IVC rats receiving the vehicle was significantly greater than the control rats (292.7 +/- 53.1 vs. 97.8 +/- 10.6 mOsm/kg H2O, P less than 0.01). The administration of the antidiuretic antagonist in the IVC rats decreased minimal Uosm to 90.0 +/- 3.6 mOsm/kg H2O. This value was significantly lower than the vehicle rats (P less than 0.01), and was a comparable level to minimal Uosm of 82.1 +/- 3.7 mOsm/kg H2O in the control rats receiving the antidiuretic antagonist. The IVC rats excreted 51.4 +/- 5.9% of the water load in three hr, a value significantly less than that excreted by the control rats, 95.1 +/- 6.0% (P less than 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

血浆精氨酸血管加压素(AVP)水平升高被认为会损害充血性心力衰竭患者的水排泄功能。在本研究中,为了确定AVP在腔静脉缩窄(IVC)大鼠水排泄受损中的作用,在膈肌下方肝静脉近端对IVC大鼠和假手术(对照)大鼠使用了两种AVP拮抗剂。手术后,在开始实验前等待48小时。IVC大鼠的平均心脏指数为260.0±12.3 ml/min/kg,显著低于对照大鼠的323.6±13.2 ml/min/kg(P<0.01)。给大鼠腹腔注射抗利尿拮抗剂[1-(β-巯基-β,β-环戊亚甲基丙酸),2-(O-乙基)-D-酪氨酸,4-缬氨酸]AVP(30微克/千克)或拮抗剂载体,20分钟后经口给予它们30毫升/千克的水。接受载体的IVC大鼠的最低尿渗透压(Uosm)显著高于对照大鼠(292.7±53.1对97.8±10.6毫渗量/千克H2O,P<0.01)。在IVC大鼠中给予抗利尿拮抗剂可使最低Uosm降至90.0±3.6毫渗量/千克H2O。该值显著低于接受载体的大鼠(P<0.01),并且与接受抗利尿拮抗剂的对照大鼠的最低Uosm的82.1±3.7毫渗量/千克H2O相当。IVC大鼠在3小时内排泄了51.4±5.9%的水负荷,该值显著低于对照大鼠排泄的95.1±6.0%(P<0.01)。(摘要截短至250字)

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