首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >In vitro vascular effects of cicletanine in pregnancy-induced hypertension.
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In vitro vascular effects of cicletanine in pregnancy-induced hypertension.

机译:喜乐丹宁在妊娠性高血压中的体外血管作用。

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摘要

1. The vascular effects of cicletanine have been studied in vitro on ring preparations of inferior epigastric arteries from normotensive human females and human females with pregnancy-induced hypertension (preeclampsia). 2. Cicletanine (10(-7)-10(-3) M) elicited concentration-dependent relaxation of vessels precontracted with 10(-7) M noradrenaline (NA) or 60 mM K+ but was more potent in the former. Relaxation was significantly greater in rings from preeclamptic patients and was uninfluenced by endothelium removal. 3. The intracellular Ca-dependent contractile responses to 10(-5) M NA in Ca-free medium as well as the subsequent extracellular Ca-dependent contractions (on restoration of external Ca) were significantly attenuated dose-dependently by cicletanine (10(-5) M, 3 x 10(-4) M) in arterial rings from both normotensive and preeclamptic patients. Cicletanine also relaxed rings precontracted by 25 mM K+ but was ineffective against 80 mM K(+)-induced contractions. 4. The inhibition of intracellular Ca-dependent contractions was significantly greater in rings from preeclamptic than from normotensive patients whereas extracellular Ca-dependent contractions were comparably inhibited in both groups. Nifedipine, on the other hand, had little effect on the intracellular Ca-dependent contractions but significantly depressed extracellular Ca-dependent contractions. 5. Cicletanine-induced relaxation was uninfluenced by pretreatment with propranolol, ouabain, tetraethylammonium, procaine, indomethacin, cimetidine or tetrodotoxin but was antagonized by glibenclamide. 6. The results show that cicletanine inhibits contractile responses of human isolated inferior epigastric arteries by a mechanism unrelated to endothelial factors but associated with inhibition of calcium metabolism. An action of cicletanine on glibenclamide-sensitive K+ channels is also suggested. Cicletanine-induced inhibition was significantly greater in arteries from preclamptic patients.
机译:1.已在体外研究了水飞蓟素在正常血压的雌性女性和患有妊娠高血压(先兆子痫)的人类女性的上腹部下环的环制剂中的血管作用。 2. Cicletanine(10(-7)-10(-3)M)引起与10(-7)M去甲肾上腺素(NA)或60 mM K +预收缩的血管浓度依赖性舒张,但在前者中更有效。子痫前期患者环的松弛明显更大,并且不受内皮去除的影响。 3. Cicletanine可以剂量依赖性地减弱无钙培养基中对10(-5)M NA的细胞内Ca依赖性收缩反应以及随后的细胞外Ca依赖性收缩(在恢复外部Ca时)(10(血压正常和先兆子痫患者的动脉环中-5)M,3 x 10(-4)M)。 Cicletanine还松弛了25 mM K +预先收缩的环,但对80 mM K(+)引起的收缩无效。 4.子痫前期患者环中细胞内Ca依赖性收缩的抑制作用明显高于血压正常患者,而两组中细胞外Ca依赖性收缩的抑制作用均相当。另一方面,硝苯地平对细胞内钙依赖性收缩的影响很小,但显着抑制了细胞外钙依赖性收缩。 5.盐酸普萘洛尔,哇巴因,四乙铵,普鲁卡因,吲哚美辛,西咪替丁或河豚毒素预处理均未影响水杨酸诱导的舒张作用,但格列苯脲可拮抗。 6.结果表明,西乐他宁通过与内皮因子无关但与钙代谢抑制有关的机制抑制人孤立的上腹下动脉的收缩反应。还建议了西乐他宁对格列本脲敏感的K +通道的作用。子痫前期患者的动脉中Cicletanine诱导的抑制作用明显更大。

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