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酮色林和哌唑嗪对门静脉高压大鼠血流动力学反应的比较。

Comparison of the hemodynamic responses to ketanserin and prazosin in portal hypertensive rats.

作者信息

Cummings S A, Kaumann A J, Groszmann R J

机构信息

Public Health Service Liver Core Center, Veterans Administration Medical Center, West Haven, Connecticut 06516.

出版信息

Hepatology. 1988 Sep-Oct;8(5):1112-5. doi: 10.1002/hep.1840080523.

Abstract

Ketanserin, a serotonin antagonist, is effective in lowering portal pressure in a rat model of portal hypertension. As ketanserin has alpha 1-adrenoceptor-blocking properties in addition to its serotonin-blocking effects, we sought to define further the mechanism of ketanserin's portal pressure-lowering effect. We attempted to determine whether the portal pressure-reducing effect of ketanserin was due to the unspecific effect of arterial blood pressure reduction mediated by alpha 1-adrenoceptor blockade or to serotonin receptor-blocking properties of ketanserin. The hemodynamic action of prazosin and alpha 1-adrenoceptor antagonist and ketanserin were compared in portal hypertensive rats in which the arterial pressure was equally reduced by both agents. The portal pressure was significantly lower in the ketanserin-treated group (11.3 +/- 0.4 mm Hg) when compared to the saline-treated group (13.6 +/- 0.7 mm Hg). The portal pressure was not significantly lower in the prazosin-treated group when compared to the saline-treated group (12.3 +/- 0.5 vs. 13.6 +/- 0.7 mm Hg, respectively). The same relationship held true for portal venous inflow and cardiac output. For each measurement, results in the ketanserin group were significantly lower when compared to the saline-treated group. These data in the prazosin-treated group were similar to data in the saline-treated group. The differences between the effect of ketanserin and prazosin were obtained despite similar blood pressure decreases. Ketanserin produced an 18% decrease and prazosin a 14% decrease in blood pressure when values were compared to their preinjection baselines.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

酮色林是一种5-羟色胺拮抗剂,在门静脉高压大鼠模型中能有效降低门静脉压力。由于酮色林除了具有5-羟色胺阻断作用外,还具有α1-肾上腺素能受体阻断特性,我们试图进一步明确酮色林降低门静脉压力作用的机制。我们试图确定酮色林降低门静脉压力的作用是由于α1-肾上腺素能受体阻断介导的动脉血压降低的非特异性作用,还是由于酮色林的5-羟色胺受体阻断特性。在门静脉高压大鼠中比较了哌唑嗪(一种α1-肾上腺素能受体拮抗剂)和酮色林的血流动力学作用,这两种药物使动脉血压同等程度降低。与生理盐水治疗组(13.6±0.7mmHg)相比,酮色林治疗组的门静脉压力显著降低(11.3±0.4mmHg)。与生理盐水治疗组相比,哌唑嗪治疗组的门静脉压力没有显著降低(分别为12.3±0.5mmHg和13.6±0.7mmHg)。门静脉血流和心输出量也呈现相同的关系。对于每项测量,酮色林组的结果与生理盐水治疗组相比均显著降低。哌唑嗪治疗组的数据与生理盐水治疗组的数据相似。尽管血压下降程度相似,但仍可得出酮色林和哌唑嗪作用的差异。与注射前基线值相比,酮色林使血压下降18%,哌唑嗪使血压下降14%。(摘要截短至250字)

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