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人类心房利钠因子的血小板结合位点。钠摄入的特征及影响

Platelet binding sites for atrial natriuretic factor in humans. Characterization and effects of sodium intake.

作者信息

Schiffrin E L, Deslongchamps M, Thibault G

出版信息

Hypertension. 1986 Jun;8(6 Pt 2):II6-10. doi: 10.1161/01.hyp.8.6_pt_2.ii6.

Abstract

Platelets bear receptors for vasoactive peptides such as angiotensin II and vasopressin. The presence of binding sites for another vasoactive peptide, atrial natriuretic factor, was therefore investigated in human platelets. 125I-labeled synthetic atrial natriuretic factor bound specifically to human platelets. Steady-state and kinetic experiments demonstrated the existence of one class of high-affinity low-capacity binding sites for atrial natriuretic factor in platelets with a dissociation constant of 30 pM. The order of potency of atrial natriuretic factor fragments showed that the structural requirements of the high-affinity binding site detected were similar to those of receptors for atrial natriuretic factor in rat blood vessels and adrenal zona glomerulosa. To study the regulation of these binding sites by sodium, normal young men were subjected successively in random order to a low-sodium (40 mmol per day) and high-sodium (300 mmol per day) diet for 4 days. Binding of atrial natriuretic factor to platelets was higher with the low-sodium diet (10.3 +/- 1.0 sites per cell) than with the high-sodium diet (7.1 +/- 0.7 sites per cell). In conclusion, human platelets bear binding sites for atrial natriuretic factor, the density of which may be modulated by sodium intake. The platelet is a useful model for investigating atrial natriuretic factor receptors in different physiopathological conditions in humans.

摘要

血小板带有血管活性肽如血管紧张素II和血管加压素的受体。因此,研究人员对人血小板中另一种血管活性肽——心房利钠因子的结合位点进行了研究。125I标记的合成心房利钠因子与人血小板特异性结合。稳态和动力学实验证明,血小板中存在一类心房利钠因子的高亲和力低容量结合位点,解离常数为30 pM。心房利钠因子片段的效价顺序表明,所检测到的高亲和力结合位点的结构要求与大鼠血管和肾上腺球状带中心房利钠因子受体的结构要求相似。为了研究钠对这些结合位点的调节作用,正常年轻男性被随机依次接受低钠(每天40 mmol)和高钠(每天300 mmol)饮食4天。低钠饮食时心房利钠因子与血小板的结合率(每细胞10.3±1.0个位点)高于高钠饮食(每细胞7.1±0.7个位点)。总之,人血小板带有心房利钠因子的结合位点,其密度可能受钠摄入量的调节。血小板是研究人类不同生理病理条件下心房利钠因子受体的有用模型。

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