Helin K, Tikkanen I, Hohenthal U, Fyhrquist F
Minerva Institute for Medical Research, Helsinki, Finland.
Eur J Pharmacol. 1994 Oct 24;264(2):135-41. doi: 10.1016/0014-2999(94)00450-1.
Synthesis of angiotensin-converting enzyme is induced during its chronic inhibition. Like angiotensin-converting enzyme, neutral endopeptidase (EC 3.4.24.11) is a plasma membrane peptidase. We studied changes of the two enzymes in lung, kidney and serum in a coronary ligation model of experimental congestive heart failure, and during chronic inhibition of the enzymes. Coronary-ligated rats (n = 19) and sham-operated controls (n = 18) were given SCH 34826 [(S)-N-[N-[1-[[(2,2-dimethyl-1,3-dioxolan-4-yl) methoxy]carbonyl]-2-phenylethyl]-L-phenylalanine]-beta-alanine], a specific neutral endopeptidase inhibitor (n = 13), captopril (n = 12), or vehicle (n = 12) for 4 days, and exsanguinated. Pulmonary angiotensin-converting enzyme was induced both by captopril (52% compared to vehicle) and by SCH 34826 (21%). Serum angiotensin-converting enzyme was induced by captopril (44%). Neutral endopeptidase was induced in lung by captopril (73%), and in kidney by SCH 38426 (32%). Compared to controls, the relative heart weight of rats with heart failure was increased by 29%, and the plasma level of atrial natriuretic peptide elevated by 74%, but enzyme activities were not different. We conclude that, in the rat, separate inhibition of either angiotensin-converting enzyme or neutral endopeptidase induces both enzymes, and that the induction varies in different tissues. Alterations in the substrates of the two enzymes, e.g. in bradykinin, might cause these changes.
血管紧张素转换酶在其长期受抑制期间会被诱导合成。与血管紧张素转换酶一样,中性内肽酶(EC 3.4.24.11)也是一种质膜肽酶。我们在实验性充血性心力衰竭的冠状动脉结扎模型中以及在这些酶的长期抑制过程中,研究了肺、肾和血清中这两种酶的变化。给冠状动脉结扎的大鼠(n = 19)和假手术对照组(n = 18)给予SCH 34826 [(S)-N-[N-[1-[[(2,2-二甲基-1,3-二氧戊环-4-基)甲氧基]羰基]-2-苯乙基]-L-苯丙氨酸]-β-丙氨酸],一种特异性中性内肽酶抑制剂(n = 13)、卡托普利(n = 12)或赋形剂(n = 12),持续4天,然后放血处死。卡托普利(与赋形剂相比增加52%)和SCH 34826(增加21%)均可诱导肺血管紧张素转换酶。卡托普利可诱导血清血管紧张素转换酶(增加44%)。卡托普利可诱导肺中性内肽酶(增加73%),SCH 38426可诱导肾中性内肽酶(增加32%)。与对照组相比,心力衰竭大鼠的相对心脏重量增加了29%,心房利钠肽的血浆水平升高了74%,但酶活性并无差异。我们得出结论,在大鼠中,单独抑制血管紧张素转换酶或中性内肽酶均可诱导这两种酶,且诱导作用在不同组织中有所不同。这两种酶底物的改变,例如缓激肽的改变,可能导致了这些变化。