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猪完全性上尿路梗阻4周后的肾血流量和肾盂压力。血栓素A2合成酶抑制剂对肾小体前主动血管收缩的影响。

Renal blood flow and pelvic pressure after 4 weeks of total upper urinary tract obstruction in the pig. The effect of a TxA2 synthetase inhibitor on active preglomerular vasoconstriction.

作者信息

Frøkiaer J, Tågehøj Jensen F, Husted S E, Mortensen J, Djurhuus J C

机构信息

Institute of Experimental Clinical Research, University of Aarhus, Denmark.

出版信息

Urol Res. 1988;16(3):167-71. doi: 10.1007/BF00256014.

Abstract

In 8 female pigs complete unilateral ureteral obstruction was investigated over a 4 weeks period. The pigs were monitored with intrapelvic pressure measurements and by 131-I-hippuran scintigraphy twice a week; one group without and one with TxA2 blocking, UK-38,485 [3-(1H-imidazol-1-yl-methyl)-2-methyl-1H-indol-1-propanoic acid], which is a well-known selective thromboxane synthetase inhibitor. During the course of obstruction there was an ipsilateral linear reduction of split function to background level and a net reduction in total hippuran clearance in both groups. On the obstructed side there was a linear reduction of hippuran clearance from 116 +/- 26 ml/min to 11 +/- 3 ml/min during the first 2 weeks of obstruction. The TxA2 synthetase inhibitor, 5 mg/kg reduced se-TxB2 to almost zero for at least one hour after i.v. administration. One week after obstruction the pelvic pressure was 45 +/- 5 cm H2O) administration of the TxA2 synthetase inhibitor. The pelvic pressure remained elevated throughout the period of observation. The study confirmed earlier work which showed that total ureteral obstruction caused complete cessation of kidney function within a few weeks, but contradicts previous studies because there was no increase in renal blood flow after thromboxane blockade. These differences may be explained by several mechanisms. The continuing increase in pelvic pressure suggested that it was not only a preglomerular vasoconstriction which was responsible for the renal flow reduction, but that there was also a postglomerular vasoconstriction.

摘要

在8只雌性猪身上,对完全性单侧输尿管梗阻进行了为期4周的研究。每周两次通过肾盂内压力测量和131-I-马尿酸闪烁扫描对猪进行监测;一组不使用TxA2阻断剂,另一组使用UK-38,485 [3-(1H-咪唑-1-基甲基)-2-甲基-1H-吲哚-1-丙酸],它是一种著名的选择性血栓素合成酶抑制剂。在梗阻过程中,两组的同侧分肾功能均呈线性下降至背景水平,总马尿酸清除率净下降。在梗阻的前2周,梗阻侧马尿酸清除率从116±26 ml/min线性下降至11±3 ml/min。静脉注射5 mg/kg的TxA2合成酶抑制剂后,至少1小时内可将se-TxB2降至几乎为零。梗阻1周后,肾盂压力为45±5 cm H2O(注射TxA2合成酶抑制剂后)。在整个观察期内,肾盂压力一直升高。该研究证实了早期的工作,即完全性输尿管梗阻在几周内会导致肾功能完全停止,但与之前的研究相矛盾,因为血栓素阻断后肾血流量没有增加。这些差异可能由多种机制解释。肾盂压力持续升高表明,导致肾血流量减少的不仅是肾小球前血管收缩,还存在肾小球后血管收缩。

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