Yu Lamei, Yuan Kuichang, Phuong Hoang Thi Ai, Park Byung Mun, Kim Suhn Hee
Department of Physiology, Research Institute for Endocrine Sciences Chonbuk National University Medical School, Jeonju, Republic of Korea.
Department of Internal Medicine, Yanbian University, China.
Peptides. 2016 Dec;86:33-41. doi: 10.1016/j.peptides.2016.09.009. Epub 2016 Sep 20.
Angiotensin-(1-5) [Ang-(1-5)], which is a metabolite of Angiotensin-(1-7) [Ang-(1-7)] catalyzed by angiotensin-converting enzyme (ACE), is a pentapeptide of the renin-angiotensin system (RAS). It has been reported that Ang-(1-7) and Ang-(1-9) stimulate the secretion of atrial natriuretic peptide (ANP) via Mas receptor (Mas R) and Ang II type 2 receptor (ATR), respectively. However, it still remains unknown whether Ang-(1-5) has a similar function to Ang-(1-7). We investigated the effect of Ang-(1-5) on ANP secretion and to define its signaling pathway using isolated perfused beating rat atria. Ang-(1-5) (0.3, 3, 10μM) stimulated high pacing frequency-induced ANP secretion in a dose-dependent manner. Ang-(1-5)-induced ANP secretion (3μM) was attenuated by the pretreatment with an antagonist of Mas R (A-779) but not by an antagonist of ATR (losartan) or ATR (PD123,319). An inhibitor for phosphatidylinositol 3-kinase (PI3K; wortmannin), protein kinase B (Akt; API-2), or nitric oxide synthase (NOS; L-NAME) also attenuated the augmentation of ANP secretion induced by Ang-(1-5). Ang-(1-5)-induced ANP secretion was markedly attenuated in isoproterenol-treated hypertrophied atria. The secretagogue effect of Ang-(1-5) on ANP secretion was similar to those induced by Ang-(1-9) and Ang-(1-7). These results suggest that Ang-(1-5) is an active mediator of renin-angiotensin system to stimulate ANP secretion via Mas R and PI3K-Akt-NOS pathway.
血管紧张素 -(1 - 5)[Ang -(1 - 5)]是血管紧张素 -(1 - 7)[Ang -(1 - 7)]经血管紧张素转换酶(ACE)催化后的代谢产物,是肾素 - 血管紧张素系统(RAS)的一种五肽。据报道,Ang -(1 - 7)和Ang -(1 - 9)分别通过Mas受体(Mas R)和血管紧张素II 2型受体(ATR)刺激心房利钠肽(ANP)的分泌。然而,Ang -(1 - 5)是否具有与Ang -(1 - 7)类似的功能仍不清楚。我们使用离体灌注搏动大鼠心房研究了Ang -(1 - 5)对ANP分泌的影响,并确定其信号通路。Ang -(1 - 5)(0.3、3、10μM)以剂量依赖性方式刺激高起搏频率诱导的ANP分泌。用Mas R拮抗剂(A - 779)预处理可减弱Ang -(1 - 5)诱导的ANP分泌(3μM),但用ATR拮抗剂(氯沙坦)或ATR(PD123,319)预处理则无此作用。磷脂酰肌醇3 - 激酶(PI3K;渥曼青霉素)、蛋白激酶B(Akt;API - 2)或一氧化氮合酶(NOS;L - 硝基精氨酸甲酯)的抑制剂也减弱了Ang -(1 - 5)诱导的ANP分泌增加。在异丙肾上腺素处理的肥大心房中,Ang -(1 - 5)诱导的ANP分泌明显减弱。Ang -(1 - 5)对ANP分泌的促分泌作用与Ang -(1 - 9)和Ang -(1 - 7)诱导的作用相似。这些结果表明,Ang -(1 - 5)是肾素 - 血管紧张素系统的一种活性介质,可通过Mas R和PI3K - Akt - NOS途径刺激ANP分泌。