Murthy K K, Thibault G, Cantin M
Clinical Research Institute of Montreal, Quebec, Canada.
Biochem J. 1988 Mar 15;250(3):665-70. doi: 10.1042/bj2500665.
Atrial natriuretic factor-(Asn1-Tyr126)-peptide, the 13.6 kDa propeptide of atrial natriuretic factor (ANF), is stored in the secretory granules of atrial cardiocytes. ANF-(Ser99-Tyr126)-peptide, the 28-amino-acid species, is the circulating form of this hormone in the rat. As the site of maturation of the prohormone is still unknown, the present study was undertaken to understand the contribution of the circulation to the maturation process of pro-ANF. 125I-ANF-(Asn1-Tyr126)-peptide was incubated with whole rat blood, plasma or serum for different time intervals, and the products were analysed. There was minimal activation of the propeptide in either whole blood or plasma. Incubation with serum, however, resulted in the formation of an 11 kDa and a 3 kDa peptide which corresponded respectively to the N-terminal and C-terminal parts of the propeptide. These results suggest that hydrolysis of the propeptide in serum is brought about by enzymes that may be stimulated during coagulation but which may not play a major role in the activation of pro-ANF in the circulation. Plasma analysis at different time intervals after prohormone injection indicated a non-specific hydrolysis of the pro-ANF molecule. The disappearance rate curves, obtained with radiolabelled pro-ANF, suggested the presence of two components with half-lives of 2.1 +/- 0.4 min and 52.5 +/- 8.4 min respectively. A metabolic clearance rate of 1.49 +/- 0.22 ml/min and an initial distribution volume of 47.4 +/- 8 ml were calculated. These results indicate that the maturation of pro-ANF to its active circulating form takes place before it is released into the circulation.
心房利钠因子-(天冬酰胺1-酪氨酸126)-肽,即心房利钠因子(ANF)的13.6 kDa前体肽,储存于心房心肌细胞的分泌颗粒中。ANF-(丝氨酸99-酪氨酸126)-肽,这种28个氨基酸的物质,是该激素在大鼠体内的循环形式。由于激素原的成熟位点仍不清楚,因此进行了本研究以了解循环对前ANF成熟过程的作用。将125I-ANF-(天冬酰胺1-酪氨酸126)-肽与全血、血浆或血清孵育不同时间间隔,然后分析产物。全血或血浆中前体肽的激活作用极小。然而,与血清孵育导致形成了一个11 kDa和一个3 kDa的肽,它们分别对应于前体肽的N端和C端部分。这些结果表明,血清中前体肽的水解是由可能在凝血过程中被刺激的酶引起的,但这些酶可能在循环中前ANF的激活中不发挥主要作用。在前体激素注射后不同时间间隔的血浆分析表明前ANF分子存在非特异性水解。用放射性标记的前ANF获得的消失率曲线表明存在两个成分,其半衰期分别为2.1±0.4分钟和52.5±8.4分钟。计算出代谢清除率为1.49±0.22 ml/分钟,初始分布容积为47.4±8 ml。这些结果表明,前ANF在释放到循环之前就已成熟为其活性循环形式。