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Eplerenone inhibits the intracrine and extracellular actions of angiotensin II on the inward calcium current in the failing heart. On the presence of an intracrine renin angiotensin aldosterone system

机译:依普利农抑制血管紧张素II对衰竭心脏内向内钙电流的内分泌和细胞外作用。关于内分泌肾素血管紧张素醛固酮系统

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摘要

The influence of chronic administration of eplerenone on the intracrine as well as on the extracellular action of angiotensin II (Ang II) on L-type inward calcium current was investigated in the failing heart of cardiomyopathic hamsters (TO-2).For this, eplerenone (200 mg/kg/day) was administered orally to 2 month-old cardiomyopathic hamsters for a period of 3 months. Measurements of the peak inward calcium current (ICa) was performed in single cells under voltage clamp using the whole cell configuration.The results indicated that eplerenone suppressed the intracrine action of Ang II (10−8 M) on peak ICa density. Moreover, the intracellular dialysis of the peptide did not change the time course of ICa inactivation in animals treated chronically with eplerenone. The extracellular administration of Ang II (10−8 M) incremented the peak ICa density by only 20±8% (n=30) compared with 38±4% (n=35) (P<0.05) obtained in age-matched cardiomyopathic hamsters not exposed to eplerenone. Interestingly, the inhibitory of eplerenone (10− 7 M) on the intracrine action of Ang II was also found, in vitro, but required an incubation period of, at least, 24 h. The inhibitory action of eplerenone on the intracellular action of Ang II was partially reversed by exposing the eplerenone-treated cells to aldosterone (10 nM) for a period of 24 h what supports the view that: a) the mineralocorticoid receptor(MR) was involved in the modulation of the intracrine action of the peptide; b) the effect of eplerenone on the intracrine as well as on the extracellular action of Ang II was related ,in part, to a decreased expression of membrane-bound and intracellular AT1 receptors.In conclusion: a) eplerenone inhibits the intracrine action of Ang II on inward calcium current and reduces drastically the effect of extracellular Ang II on ICa; b) aldosterone is able to revert the effect of eplerenone; c) the mineralocorticoid receptor is an essential component of the intracrine renin angiotensin aldosterone system.
机译:在心肌病性仓鼠(TO-2)衰竭的心脏中,研究了长期服用依普利农对内分泌的影响以及血管紧张素II(Ang II)对L型内向钙电流的细胞外作用的影响。 (200 mg / kg /天)口服给予2个月大的心肌病仓鼠3个月。使用全电池配置在电压钳制下对单个细胞进行内向钙电流峰值的测量。结果表明,依普利农抑制了Ang II(10 -8 M)的内分泌作用ICa峰值密度。此外,在用依普利农长期治疗的动物中,该肽的细胞内透析没有改变ICa失活的时间过程。 Ang II(10 -8 M)的细胞外给药使峰值ICa密度仅增加20±8%(n = 30),而38±4%(n = 35)(P <0.05 )在未暴露于依普利农的年龄匹配的心肌病仓鼠中获得。有趣的是,在体外也发现依普利农(10 −7 M)对Ang II的内分泌作用具有抑制作用,但至少需要24 h的潜伏期。通过将依普利农处理的细胞暴露于醛固酮(10 nM)24小时,可以部分逆转依普利农对Ang II细胞内作用的抑制作用,这支持以下观点:a)涉及盐皮质激素受体(MR)在调节肽的内分泌作用中; b)依普利农对Ang II的内分泌和细胞外作用的影响部分与膜结合和细胞内AT1受体的表达降低有关。结论:a)依普利农抑制Ang的内分泌作用。 II对内向钙电流的影响,并大大降低细胞外Ang II对ICa的作用; b)醛固酮能够逆转依普利酮的作用; c)盐皮质激素受体是内分泌肾素血管紧张素醛固酮系统的重要组成部分。

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