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Agmatine modulates calcium handling in cardiomyocytes of hibernating ground squirrels through calcium-sensing receptor signaling

机译:通过钙传感受体信号传导调节冬眠地松鼠心肌细胞的钙处理钙处理

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True hibernators are remarkable group of mammals whose hearts are resistant to such stressors as deep hypothermia, ischemia, arrhythmia. Capability of cardiac cells from hibernating species to effectively rule Ca2+ homeostasis during torpor is poorly studied. Better understanding of these mechanisms could allow to introduce new strategies for improvement the cardiac performance and may be useful for cardiovascular medicine. Here for the first time we have shown that the regulation of Ca2+ handling and thereby cardiomyocyte contractility by endogenous neurotransmitter agmatine occurs through the modulation of calcium-sensing receptor (CaSR). In isolated cardiocytes of hibernating ground squirrels generating stationary Ca2+ transients in the absence of actual myocellular excitation, low doses of this polyamine (up to 500 mu M) induce the G(beta gamma)-dependent activation of PI3-kinase with subsequent stimulation of Akt-kinase and nitric oxide (NO) production by endothelial NO-synthase (eNOS). NO production abolishes Ca2+ oscillations in virtue of the enhancement of Ca2+ reuptake by sarco (endo)plasmic Ca2+ ATPase (SERCA). Simultaneously, the activation of phospholipase A2 (PLA 2 ) and arachidonic-acid dependent Ca2+ entry occur providing replenishment of Ca2+ store. High concentrations of agmatine ( 2 mM) induce other CaSR-mediated pathways involving phospholipase C (PLC) pathway, the formation of inositoltriphosphate (IP3) and diacylglicerol (DAG) followed by induction of their targets: IP3 receptors and protein kinase C isoforms (PKC), respectively. Furthermore, it is also responsible for the stimulation of PLA(2) and elevation of intracellular calcium caused by arachidonic acid-regulated Ca2+-permeable (ARC) channels. Additionally, there is a potent store-operated Ca2+ entry (SOC) in cardiomyocyte. Negative (NPS 2143) and positive (R 568) allosteric modulators of CaSR recapitulate effects of low and high agmatine doses on Ca2+ handling and NO synthesis. These
机译:真正的冬眠者是一群非凡的哺乳动物,其心脏对这种压力源性耐受深度低温,缺血,心律失常。从冬眠物种中有效规则Ca2 +稳态的心脏细胞的能力很差。更好地理解这些机制可以允许引入改善心脏病的新策略,并且可能对心血管药物有用。在这里首次表明,通过调节钙传感受体(CasR),通过内源性神经递质刺激物的Ca2 +处理和由此心肌细胞收缩性的调节。在冬眠的地面鼠疫的孤立心细胞中产生固定式CA2 +瞬变的缺失在没有实际肌细胞激发的情况下,低剂量的这种多胺(高达500μm)诱导PI3-激酶的G(βγ) - 随后刺激Akt刺激-kinase和一氧化氮(NO)通过内皮无合成酶(ENOS)产生。由于Sarco(endo)素质Ca2 + ATP酶(Serca)的增强,因此不会产生CA2 +振荡的CA2 +振荡。同时,发挥磷脂酶A2(PLA 2)和花生酸依赖性CA2 +进入的激活,可提供CA2 +储存的补充。高浓度的毒素(& 2 mm)诱导涉及磷脂酶C(PLC)途径的其他CasR介导的途径,形成肌醇三磷酸(IP3)和二氨酰基丙烯醇(DAG),然后诱导其靶标:IP3受体和蛋白激酶C同种型(PKC)分别。此外,它还负责刺激PLA(2)和由花生酸调节的CA2 +可-E1METIBE(ARC)通道引起的细胞内钙的升高。另外,体内细胞中有强有力的商店操作的Ca2 +进入(SoC)。阴性(NPS 2143)和阳性(R 568)Casr的仿生调节剂的钙累积调节剂对Ca2 +处理和No合成的低和高茶草剂量的影响。这些

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