Kocsis J F, McIlroy P J, Carsia R V
Department of Cell Biology, University of Medicine and Dentistry of New Jersey, School of Osteopathic Medicine, Stratford 08084, USA.
Gen Comp Endocrinol. 1995 Sep;99(3):364-72. doi: 10.1006/gcen.1995.1120.
The inhibitory action of atrial natriuretic peptides (ANPs) on mammalian aldosterone synthesis is well documented. In addition, other work indicates that ANP and an analogue of its second messenger, 8-Br-cGMP, inhibit aldosterone production by chicken adrenal steroidogenic cells. However, the interaction between angiotensin II (AII) and ANP in the regulation of avian aldosterone production is poorly understood because chicken adrenal steroidogenic cells, the commonly used in vitro avian model, are comparatively unresponsive to AII. By contrast, turkey (Meleagris gallopavo) adrenal steroidogenic cells are sensitive to AII. Thus, in the present study, the action of ANPs and related peptides and their interaction with other stimulators of aldosterone production were investigated using freshly isolated and briefly cultured turkey adrenal steroidogenic cells. Surprisingly, several ANPs [rat (r), human (h), chicken (c)], and rat brain natriuretic peptide (rBNP) were as efficacious as [Ile5]AII for stimulating aldosterone production (2 hr) in freshly isolated cell suspensions but were less potent than [Ile5]AII (ED50 of ANPs approximately 5-10 nM; [Ile5]AII ED50 approximately 0.1 nM). In addition, chicken ANP enhanced maximal aldosterone production induced by [Ile5]AII (1 nM), K+ (25 mM), and hACTH-(1-39) (ACTH) (1 nM): maximal enhancement of the action of these secretagogues was +49%, +137% and +15%, respectively (P < 0.05; n = 3). Furthermore, other ANPs and related peptides [rBNP and bovine aldosterone secretion inhibiting factor (bASIF)] enhanced maximal [Ile5]AII-induced aldosterone production: the order of maximal enhancement was rBNP (+180%) > hANP/rANP (+50%) > bASIF (+25%) (P < 0.05; n = 3).(ABSTRACT TRUNCATED AT 250 WORDS)
心房利钠肽(ANP)对哺乳动物醛固酮合成的抑制作用已有充分记录。此外,其他研究表明,ANP及其第二信使类似物8-溴-cGMP可抑制鸡肾上腺类固醇生成细胞的醛固酮产生。然而,由于常用的体外禽类模型鸡肾上腺类固醇生成细胞对血管紧张素II(AII)相对不敏感,因此对AII与ANP在禽类醛固酮产生调节中的相互作用了解甚少。相比之下,火鸡(吐绶鸡)肾上腺类固醇生成细胞对AII敏感。因此,在本研究中,使用新鲜分离并短期培养的火鸡肾上腺类固醇生成细胞,研究了ANP及其相关肽的作用以及它们与醛固酮产生的其他刺激物的相互作用。令人惊讶的是,几种ANP[大鼠(r)、人(h)、鸡(c)]和大鼠脑利钠肽(rBNP)在新鲜分离的细胞悬液中刺激醛固酮产生(2小时)的效果与[异亮氨酸5]AII相同,但效力低于[异亮氨酸5]AII(ANP的半数有效浓度约为5-10 nM;[异亮氨酸5]AII的半数有效浓度约为0.1 nM)。此外,鸡ANP增强了[异亮氨酸5]AII(1 nM)、钾离子(25 mM)和人促肾上腺皮质激素(1-39)(ACTH)(1 nM)诱导的最大醛固酮产生:这些促分泌剂作用的最大增强分别为+49%、+137%和+15%(P<0.05;n=3)。此外,其他ANP及其相关肽[rBNP和牛醛固酮分泌抑制因子(bASIF)]增强了最大[异亮氨酸5]AII诱导的醛固酮产生:最大增强顺序为rBNP(+180%)>人ANP/大鼠ANP(+50%)>bASIF(+25%)(P<0.05;n=3)。(摘要截断于250字)