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Cardiac role of frog ANF: negative inotropism and binding sites in Rana esculenta.

机译:青蛙的心脏作用AND:负性肌力和食肉蛙的结合位点。

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摘要

To elucidate the role of atrial natriuretic peptides (NPs) in the amphibian heart, the myotropic effects and the cardiac distribution of frog atrial natriuretic factor (fANF) have been studied in Rana esculenta. Spontaneously, beating in vitro isolated working heart preparations were treated with increased concentrations (10(-11)-10(-8) M) of fANF-(1-24). The peptide at 10(-9) and 10(-8) M significantly reduced heart rate (HR) and, on the electrically paced preparations, decreased cardiac output (CO), stroke volume (SV) and work. Such negative inotropism was abolished by pretreatment with the pertussis toxin or by blocking the particulate guanylate cyclase (GC) with anantin while it was independent both from the functional impairment of the endocardium-endothelium by Triton X-100 and the inhibition of the soluble guanylate cyclase by 1 H-(1,2,4,) oxadiazolo-(4,3-a) quinoxalin-1-one (ODQ). By autoradiography, two classes of high and low affinity NPs binding sites were detected in the ventricular endocardium and myocardium and in the bulbus arteriosus. The analysis of displacement binding data using the radioligand [125I]-rat atrial natriuretic peptide [125I-rANP-(1-28)], its cold counterpart and the fANF-(1-24) showed that in the ventricular myocardium, the low affinity NPs sites bound both the heterologous and the homologous ligands at a concentration close to that responsible for the negative inotropism and chronotropism.
机译:为了阐明心钠素在两栖动物心脏中的作用,在蛙蛙中研究了青蛙心钠素的促肌力作用和心脏分布。自发地,用增加浓度的(10(-11)-10(-8)M)fANF-(1-24)处理体外跳动的离体工作心脏制剂。在10(-9)和10(-8)M时,该肽可显着降低心率(HR),而在电起搏的制剂中,其心输出量(CO),中风量(SV)和工作量则降低。通过用百日咳毒素预处理或用antantin阻断颗粒鸟苷酸环化酶(GC)可以消除这种负性肌力作用,而它既不受Triton X-100对心内膜内皮功能的损害,又不受可溶性鸟苷酸环化酶的抑制1 H-(1,2,4,)oxadiazolo-(4,3-a)quinoxalin-1-one(ODQ)。通过放射自显影,在心室心内膜和心肌以及动脉球囊中检测到两类高亲和力和低亲和力的NPs结合位点。使用放射性配体[125I]-大鼠心钠素[125I-rANP-(1-28)],其冷对应物和fANF-(1-24)对置换结合数据进行分析,结果显示在心室心肌中,低亲和力的NP位点以接近负负性变力和变时性的浓度结合异源和同源配体。

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