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HIGH-AFFINITY NEUROPEPTIDE Y RECEPTOR ANTAGONISTS

机译:高效神经肽Y受体拮抗剂

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摘要

Neuropeptide Y (NPY) is one of the most abundant peptide transmitters in the mammalian brain. In the periphery it is costored and coreleased with norepinephrine from sympathetic nerve terminals. However, the physiological functions of this peptide remain unclear because of the absence of specific high-affinity receptor antagonists. Three potent NPY receptor antagonists were synthesized and tested for their biological activity in in vitro, ex vivo, and in vivo functional assays. We describe here the effects of these antagonists inhibiting specific radiolabeled NPY binding at Y1 and Y2 receptors and antagonizing the effects of NPY in human erythroleukmia cell intracellular calcium mobilization, perfusion pressure in the isolated rat kidney, and mean arterial blood pressure in anesthetized rats. [References: 24]
机译:神经肽Y(NPY)是哺乳动物大脑中最丰富的肽递质之一。在周围,它被分离并与交感神经末梢的去甲肾上腺素共释放。然而,由于缺乏特异性的高亲和力受体拮抗剂,该肽的生理功能仍不清楚。合成了三种有效的NPY受体拮抗剂,并在体外,离体和体内功能测定中测试了其生物学活性。我们在这里描述了这些拮抗剂抑制Y1和Y2受体上特异性放射性标记的NPY结合的作用,并拮抗NPY对人红细胞白血病细胞内钙动员,离体大鼠肾脏的灌注压和麻醉大鼠平均动脉血压的影响。 [参考:24]

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