首页> 外文期刊>Research communications in molecular pathology and pharmacology >Effect of docosahexaenoic acid on intracellular calcium dynamics in vascular smooth muscle cells from normotensive and genetically hypertensive rats.
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Effect of docosahexaenoic acid on intracellular calcium dynamics in vascular smooth muscle cells from normotensive and genetically hypertensive rats.

机译:二十二碳六烯酸对正常血压和遗传性高血压大鼠血管平滑肌细胞内钙动态的影响。

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The effects of DHA treatment on intracellular Ca2+ dynamics in aortic smooth muscle cells isolated from young stroke-prone spontaneously hypertensive rats (SHRSP) and age-matched normotensive Wistar Kyoto rats (WKY) were investigated. The resting intracellular Ca2+ concentration ([Ca2+]i) before stimulation and the peak [Ca2+]i induced by 5-HT, angiotensin II and depolarizing concentration of KC1 were higher in SHRSP than in WKY. When added to the culture medium for 2 days, DHA at a concentration of 30 microM significantly suppressed the peak [Ca2+]i induced by these stimulants in aortic smooth muscle cells isolated from WKY, whereas smooth muscle cells of SHRSP were refractory to the suppression. DHA had no suppressive effect on the 5-HT-induced increase in the inositol triphosphate production. The present study indicates that DHA can suppress receptor-mediated Ca2+ influx, at least, through the voltage-dependent channel, in vascular smooth muscle cells. Since the intracellular Ca2+ plays an important role in regulating vascular tone, the suppressive effect of DHA on [Ca2+]i in vascular smooth muscle cells may be contributed to the beneficial properties of DHA on cardiovascular disorders. The precise mechanisms of action remain to be elucidated.
机译:研究了DHA处理对中风自发性年轻高血压大鼠(SHRSP)和年龄匹配的正常血压Wistar Kyoto大鼠(WKY)分离的主动脉平滑肌细胞内Ca2 +动力学的影响。 SHRSP中刺激前的静止细胞内Ca2 +浓度([Ca2 +] i)和5-HT,血管紧张素II和KC1的去极化浓度诱导的峰[Ca2 +] i高于WKY。当添加到培养基中2天时,浓度为30 microM的DHA在从WKY分离的主动脉平滑肌细胞中显着抑制了这些刺激物诱导的[Ca2 +] i峰,而SHRSP的平滑肌细胞则难以抑制这种抑制。 DHA对5-HT诱导的三磷酸肌醇产量增加没有抑制作用。本研究表明,DHA至少可以通过电压依赖性通道抑制血管平滑肌细胞中受体介导的Ca2 +内流。由于细胞内Ca2 +在调节血管紧张度中起重要作用,因此DHA对血管平滑肌细胞中[Ca2 +] i的抑制作用可能有助于DHA对心血管疾病的有益作用。确切的作用机制仍有待阐明。

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