Atarashi K, Franco-Saenz R, Mulrow P J, Snajdar R M, Rapp J P
J Hypertens Suppl. 1984 Dec;2(3):S293-5.
Extracts of rat atrial muscle lowered basal aldosterone release from rat adrenal glomerulosa cell suspensions, and partially inhibited the stimulation of aldosterone release by adrenocorticotropic hormone (ACTH) and angiotensin II. Atriopeptin I, an atrial peptide with natriuretic, diuretic and smooth muscle relaxant activities, significantly decreased basal aldosterone release at 1 pM concentrations. Also, atriopeptin I decreased the sensitivity of the glomerulosa cells to adrenocorticotropin and angiotensin II. These data suggest that peptides contained in mammalian atria affect sodium excretion not only by a direct effect on the kidney, but also indirectly through inhibition of aldosterone production.
大鼠心房肌提取物可降低大鼠肾上腺球状带细胞悬液中基础醛固酮的释放,并部分抑制促肾上腺皮质激素(ACTH)和血管紧张素II对醛固酮释放的刺激作用。心房肽I是一种具有利钠、利尿和平滑肌舒张活性的心房肽,在浓度为1 pM时可显著降低基础醛固酮的释放。此外,心房肽I还降低了球状带细胞对促肾上腺皮质激素和血管紧张素II的敏感性。这些数据表明,哺乳动物心房中所含的肽类不仅通过对肾脏的直接作用影响钠排泄,还通过抑制醛固酮的产生间接发挥作用。