Effect of captopril on serotonergic mechanisms in two-kidney, one-clip renal hypertensive rats.

D Morelowska, E Chabielska, D Pawlak, A Azzadin, A Białkowska, D Krygicz, W Buczko
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Abstract

In 2K,1C-RHR (two-kidney, one-clip hypertensive rats) serotonergic mechanisms in blood platelets were studied. The endogenous serotonin (5-HT) concentration in whole blood and in platelets remained unchanged in relation to the sham operated rats. Also the uptake of labelled 5-HT in rats with renal hypertension was not altered. However platelets aggregability was increased in 2K,1C-RHR. Acute administration of captopril (10 mg/kg and 100 mg/kg po) diminished blood pressure but did not change either the concentration of 5-HT in whole blood and in platelets of hypertensive rats or the uptake of this amine. Platelets aggregation and the amplifying effect of 5-HT in hypertensive rats were also unchanged after acute captopril administration. Similar results were observed after its administration in a dose of 30 mg/kg for one week. Our results indicate that captopril did not affect the platelets serotonergic mechanisms in 2K,1C-RHR.

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卡托普利对双肾单夹肾性高血压大鼠血清素能机制的影响。
研究了2K、1C-RHR(双肾单夹高血压大鼠)血清素在血小板中的作用机制。假手术大鼠全血和血小板内源性5-羟色胺(5-HT)浓度保持不变。肾性高血压大鼠对标记5-羟色胺的摄取也没有改变。然而,血小板聚集性在2K、1C-RHR中增加。急性给药卡托普利(10mg /kg和100mg /kg)降低血压,但没有改变高血压大鼠全血和血小板中5-羟色胺的浓度,也没有改变这种胺的摄取。急性卡托普利给药后高血压大鼠的血小板聚集和5-羟色胺的放大作用也没有改变。以30 mg/kg剂量给药一周后,观察到类似的结果。我们的结果表明卡托普利不影响血小板血清素能机制在2K,1C-RHR。
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