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Effects of natriuretic peptides on electrical conduction in the sinoatrial node and atrial myocardium of the heart

机译:利钠肽对心脏窦房结和心房心肌电传导的影响

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Natriuretic peptides, including B-type and C-type natriuretic peptide (BNP and CNP), are powerful regulators of the cardiovascular system; however, their electrophysiological effects in the heart, particularly in the sinoatrial node (SAN), are incompletely understood. We have used high-resolution optical mapping to measure the effects of BNP and CNP, and the roles of natriuretic peptide receptors (NPR-A, NPR-B and NPR-C), on electrical conduction within the SAN and atrial myocardium. In basal conditions BNP and CNP (50-500 nm) increased conduction velocity (CV) within the SAN by ~30% at the high dose and shifted the initial exit site superiorly. These effects sped conduction from the SAN to the surrounding atrial myocardium and were mediated by the NPR-A and NPR-B receptors. In the presence of isoproterenol (1 μm) the NPR-C receptor made a major contribution to the effects of BNP and CNP in the heart. In these conditions BNP, CNP and the NPR-C agonist cANF each decreased SAN CV and shifted the initial exit site inferiorly. The effects of cANF (30% reduction) were larger than BNP or CNP (~15% reduction), indicating that BNP and CNP activate multiple natriuretic peptide receptors. In support of this, the inhibitory effects of BNP were absent in NPR-C knockout mice, where BNP instead elicited a further increase (~25%) in CV. Measurements in externally paced atrial preparations demonstrate that the effects of natriuretic peptides on CV are partially independent of changes in cycle length. These data provide detailed novel insight into the complex effects of natriuretic peptides and their receptors on electrical conduction in the heart.
机译:利钠肽,包括B型和C型利钠肽(BNP和CNP),是心血管系统的强大调节剂。然而,它们在心脏,特别是在窦房结(SAN)中的电生理作用尚不完全清楚。我们已经使用高分辨率光学测绘来测量BNP和CNP的作用,以及利尿钠肽受体(NPR-A,NPR-B和NPR-C)对SAN和心房心肌内电传导的作用。在基础条件下,BNP和CNP(50-500 nm)在高剂量下可将SAN内的传导速度(CV)提高约30%,并更好地移动初始出口位置。这些作用加速了从SAN到周围心房心肌的传导,并由NPR-A和NPR-B受体介导。在存在异丙肾上腺素(1μm)的情况下,NPR-C受体对心脏中BNP和CNP的作用做出了重要贡献。在这些情况下,BNP,CNP和NPR-C激动剂cANF均会降低SAN CV并降低初始出口位点。 cANF(减少30%)的作用大于BNP或CNP(减少约15%),表明BNP和CNP激活多种利钠肽受体。为此,在NPR-C基因敲除小鼠中不存在BNP的抑制作用,而BNP引起CV进一步增加(〜25%)。对体外起搏的心房制剂进行的测量表明,利钠肽对CV的作用部分独立于周期长度的变化。这些数据为利钠肽及其受体对心脏电传导的复杂作用提供了详细的新颖见解。

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