Marleau S, Nguyen T T, Du Souich P, Bellemare M, De Lean A, Ong H
Faculté de pharmacie, Université de Montréal, Québec, Canada.
Drug Metab Dispos. 1991 Jan-Feb;19(1):194-9.
The neutral endopeptidase 24.11 (NEP) has been shown to inactivate the atrial natriuretic factor (ANF) by opening the ring structure. To document the role of NEP in the metabolic fate of ANF in vivo, the effects of an infusion of thiorphan (25 micrograms/min/kg), a specific NEP inhibitor, on the kinetics and metabolism of endogenous ANF were studied in conscious rabbits. A bolus of [125I]ANF(99-126) was injected 50 min after the beginning of the infusion of thiorphan. Plasma samples containing the radioactive peptides were separated by reverse-phase HPLC. The parent compound could be separated from at least two other minor metabolites, corresponding to the elution position of [125I]ANF(99-105/106-126), the inactive ring-opened metabolite, and of [125I]ANF(103-126), an N-truncated analog. The generation of the N-truncated metabolite was increased by thiorphan. Thiorphan also induced an increase in plasma ANF (29%) that was closely associated with a 32% reduction in the systemic clearance of [125I]ANF(99-126), whereas no modification in the estimated secretion rate was detected. These results support a role for NEP in the regulation of endogenous ANF plasma levels. These results also suggest that specific inhibition of NEP may result in an increase in the apparent activity of alternative metabolic pathways.
中性内肽酶24.11(NEP)已被证明可通过打开环结构使心钠素(ANF)失活。为了证明NEP在体内ANF代谢命运中的作用,研究了特异性NEP抑制剂硫磷酰胺(25微克/分钟/千克)输注对清醒兔体内内源性ANF动力学和代谢的影响。在开始输注硫磷酰胺50分钟后,静脉注射一剂[125I]ANF(99 - 126)。含有放射性肽的血浆样品通过反相高效液相色谱法分离。母体化合物可与至少两种其他次要代谢物分离,这两种代谢物分别对应于[125I]ANF(99 - 105/106 - 126)(无活性的开环代谢物)和[125I]ANF(103 - 126)(N端截短类似物)的洗脱位置。硫磷酰胺使N端截短代谢物的生成增加。硫磷酰胺还导致血浆ANF增加(29%),这与[125I]ANF(99 - 126)的全身清除率降低32%密切相关,而未检测到估计分泌率有变化。这些结果支持NEP在调节内源性ANF血浆水平中的作用。这些结果还表明,特异性抑制NEP可能导致替代代谢途径的表观活性增加。