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吲达帕胺与氢氯噻嗪对培养心肌细胞自发收缩的比较:对细胞外钙或钾变化的影响

Comparison of indapamide and hydrochlorothiazide on spontaneous contraction of cardiomyocytes in culture: the effect on alterations of extracellular calcium or potassium.

作者信息

Rabkin S W

机构信息

Faculty of Medicine, University of British Columbia, Vancouver, Canada.

出版信息

Gen Pharmacol. 1993 May;24(3):699-704. doi: 10.1016/0306-3623(93)90234-o.

Abstract
  1. The purpose of this study was to determine whether indapamide or hydrochlorothiazide had a direct action on the heart, specifically to determine whether either diuretic affected spontaneous contractile function of cardiomyocytes in culture or altered the response to increases in extracellular potassium or calcium. 2. Chick embryonic ventricular cells were cultured from 7-day-old chick embryo and myocardial cell aggregates were prepared. Spontaneous cardiac contractile frequency of ventricular myocyte aggregates was monitored. Indapamide [chloro-4-N-(methyl-2-indolinyl-1)-sulfamoyal-3-benzamide] over a concentration range of 10(-9)-10(-6) M did not alter cardiac contractile frequency. 3. Indapamide, in a dose dependent manner, significantly (P < 0.05) antagonized the effect of increases in extracellular potassium [K+]0 that produced a concentration dependent reduction in cardiac contractile frequency. In contrast, hydrochlorothiazide accentuated the effect of increased [K+]0 while hydrochlorothiazide did not alter spontaneous contractile frequency at the usual [K+]0 of 2.0 mM. 4. Indapamide produced a significant (P < 0.05) reduction in the effect of increases in extracellular calcium [Ca2+]0 on cardiac contractility while hydrochlorothiazide was associated with a slight accentuation of the effect of increased [Ca2+]0. Indapamide also slightly reduced the effect of the calcium agonist Bay K 8644, which increases intracellular calcium through voltage operated calcium channels. 5. These data indicate that diuretics modulate a cardiac response to changes in extracellular potassium and calcium. Indapamide antagonizes the effects of increases in extracellular potassium and calcium while hydrochlorothiazide has the opposite effect on the cardiac response to increases in [K+]0 or [Ca2+]0.
摘要
  1. 本研究的目的是确定吲达帕胺或氢氯噻嗪是否对心脏有直接作用,具体而言,是确定这两种利尿剂是否会影响培养的心肌细胞的自发收缩功能,或者改变对细胞外钾或钙增加的反应。2. 从7日龄鸡胚中培养鸡胚心室细胞,并制备心肌细胞聚集体。监测心室肌细胞聚集体的心脏自发收缩频率。浓度范围为10(-9)-10(-6) M的吲达帕胺[4-氯-N-(甲基-2-吲哚啉-1)-磺酰胺基-3-苯甲酰胺]未改变心脏收缩频率。3. 吲达帕胺以剂量依赖性方式显著(P<0.05)拮抗细胞外钾[K+]0增加所产生的作用,细胞外钾[K+]0增加会导致心脏收缩频率呈浓度依赖性降低。相比之下,氢氯噻嗪会加剧[K+]0增加的作用,而在通常的2.0 mM [K+]0水平下,氢氯噻嗪不会改变自发收缩频率。4. 吲达帕胺使细胞外钙[Ca2+]0增加对心脏收缩力的作用显著(P<0.05)降低,而氢氯噻嗪与[Ca2+]0增加的作用略有增强有关。吲达帕胺还略微降低了钙激动剂Bay K 8644的作用,Bay K 8644通过电压门控钙通道增加细胞内钙。5. 这些数据表明,利尿剂可调节心脏对细胞外钾和钙变化的反应。吲达帕胺拮抗细胞外钾和钙增加的作用,而氢氯噻嗪对心脏对[K+]0或[Ca2+]0增加的反应具有相反的作用。

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