首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >Upregulation of the kappa opioidergic system in left ventricular rat myocardium in response to volume overload Adaptive changes of the cardiac kappa opioid system in heart failure
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Upregulation of the kappa opioidergic system in left ventricular rat myocardium in response to volume overload Adaptive changes of the cardiac kappa opioid system in heart failure

机译:容量超负荷导致左心室大鼠心肌Kappa视蛋白系统的上调心脏衰竭中心脏Kappa阿片系统的适应性变化

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Opioids have long been known for their analgesic effects and are therefore widely used in anesthesia and intensive care medicine. However, in the last decade research has focused on the opioidergic influence on cardiovascular function. This project thus aimed to detect the precise cellular localization of kappa opioid receptors (KOR) in left ventricular cardiomyocytes and to investigate putative changes in KOR and its endogenous ligand precursor peptide prodynorphin (PDYN) in response to heart failure. After IRB approval, heart failure was induced using a modified infrarenal aortocaval fistula (ACF) in male Wistar rats. All rats of the control and ACF group were characterized by their morphometrics and hemodynamics. In addition, the existence and localization as well as adaptive changes of KOR and PDYN were investigated using radioligand binding, double immunofluorescence confocal analysis, RT-PCR and Western blot. Similar to the brain and spinal cord, [H-3]U-69593 KOR selective binding sites were detected the left ventricle (LV). KOR colocalized with Ca(v)1.2 of the outer plasma membrane and invaginated T-tubules and intracellular with the ryanodine receptor of the sarcoplasmatic reticulum. Interestingly, KOR could also be detected in mitochondria of rat LV cardiomyocytes. As a consequence of heart failure, KOR and PDYN were up-regulated on the mRNA and protein level in the LV. These findings suggest that the cardiac kappa opioidergic system might modulate rat cardiomyocyte function during heart failure. (C) 2015 Elsevier Ltd. All rights reserved.
机译:阿片类药物因其镇痛作用而久负盛名,因此被广泛用于麻醉和重症监护医学。然而,在过去的十年中,研究集中在对心血管功能的视皮醇功能的影响上。因此,该项目旨在检测左心室心肌细胞中κ阿片受体(KOR)的精确细胞定位,并研究心衰中KOR及其内源性配体前体肽前强啡肽(PDYN)的假定变化。 IRB批准后,使用改良的肾下主动脉瓣瘘(ACF)在雄性Wistar大鼠中诱发心力衰竭。对照组和ACF组的所有大鼠均通过形态学和血流动力学进行表征。此外,使用放射性配体结合,双重免疫荧光共聚焦分析,RT-PCR和蛋白质印迹研究了KOR和PDYN的存在和定位以及适应性变化。与脑和脊髓相似,在左心室(LV)中检测到[H-3] U-69593 KOR选择性结合位点。 KOR与外部质膜的Ca(v)1.2共定位,并侵入T管,并在细胞内与肌浆网的ryanodine受体共存。有趣的是,还可以在大鼠LV心肌细胞的线粒体中检测到KOR。心力衰竭的结果是,KOR和PDYN在LV的mRNA和蛋白水平上调。这些发现表明,在心脏衰竭期间,心脏κ视蛋白能系统可能调节大鼠心肌细胞的功能。 (C)2015 Elsevier Ltd.保留所有权利。

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