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血栓素合成酶抑制剂对未麻醉绵羊肾功能的急性影响。

Acute effect of a thromboxane synthetase inhibitor on renal function in unanaesthetized sheep.

作者信息

Cumming A D, Lindsay R M, McDonald J W, Linton A L

机构信息

Department of Medicine, University of Western Ontario, London, Canada.

出版信息

Clin Sci (Lond). 1987 Aug;73(2):171-6. doi: 10.1042/cs0730171.

Abstract
  1. Eleven healthy, unanaesthetized sheep were given either a single intravenous bolus infusion of U63,577A (Upjohn), a selective thromboxane synthetase inhibitor, at a dose of 30 mg/kg (group 1, n = 6), or vehicle alone (group 2, n = 5). Animals were maintained in metabolic cages during the study, and received 150 ml of water/h and 7.5 mmol of sodium/h as Ringers lactate by intravenous infusion for 24 h before and during the study. During two 1 h control urine collections via bladder catheter, urine volume and sodium excretion closely paralleled these infusion rates. 2. In the first hour after injection of U63,577A, there were significant two- to three-fold increases in urine volume, urinary sodium excretion and fractional sodium excretion, compared with the control collections. During the subsequent 4 h, urine volume, urinary sodium excretion, and fractional sodium excretion fell to values significantly lower than in the control period. Creatinine clearance was reduced 1, 2 and 4 h post injection and returned to control values at 5 h. Urinary excretion of thromboxane B2 was significantly reduced compared with control values during the 5 h after injection of U63,577A. Excretion of 6-keto-prostaglandin F1 alpha did not change. Plasma renin activity was significantly increased 1, 3 and 5 h after injection of U63,577A. Vehicle controls showed no change in any of the above parameters. 3. The results indicate that in healthy conscious sheep, sodium and water replete, U63,577A has a transient but significant diuretic and natriuretic effect, followed by sodium and water retention and increased plasma renin activity.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 给11只健康、未麻醉的绵羊静脉注射一次大剂量的U63,577A(Upjohn公司生产,一种选择性血栓素合成酶抑制剂),剂量为30毫克/千克(第1组,n = 6),或仅注射赋形剂(第2组,n = 5)。在研究期间,动物饲养在代谢笼中,在研究前和研究期间通过静脉输注每小时给予150毫升水和7.5毫摩尔钠的乳酸林格氏液,持续24小时。在通过膀胱导管进行的两次1小时对照尿液收集期间,尿量和钠排泄量与这些输注速率密切平行。2. 在注射U63,577A后的第一小时,与对照收集相比,尿量、尿钠排泄量和钠排泄分数显著增加了两到三倍。在随后的4小时内,尿量、尿钠排泄量和钠排泄分数降至显著低于对照期的值。注射后1小时、2小时和4小时肌酐清除率降低,5小时恢复到对照值。注射U63,577A后5小时内,血栓素B2的尿排泄量与对照值相比显著降低。6-酮-前列腺素F1α的排泄量没有变化。注射U63,577A后1小时、3小时和5小时血浆肾素活性显著增加。赋形剂对照组上述参数均无变化。3. 结果表明,在健康、清醒、钠和水充足的绵羊中,U63,577A具有短暂但显著的利尿和利钠作用,随后是钠和水潴留以及血浆肾素活性增加。(摘要截短至250字)

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