The potential role of atrial natriuretic peptide in the effects of Angiotensin-(1–7) in a chronic atrial tachycardia canine model. (26th February 2016)

• Record Type: Journal Article
• Authors: Zhao, Jun; Liu, Tiecheng; Liu, Enzhao; Li, Guangping; Qi, Lingshan; Li, Jian
• Is Part Of: Journal of the renin-angiotensin-aldosterone system. Volume 17:Number 1(2016:Mar.)
• Publication Date: 2016-02-26
• Subjects: Atrial fibrillation -- rapid atrial pacing -- Ang-(1–7) -- atrial natriuretic peptide; Renin-angiotensin system -- Periodicals; 616.132
• DOI: 10.1177/1470320315627409
• Languages: English
• ISSNs: 1470-3203

Abstract

Objective: The objective of this article is to investigate the possible role of atrial natriuretic peptide (ANP) in Angiotensin-(1–7) (Ang-(1–7)) signaling pathway on atrial electrical and structural remodeling in a chronic rapid atrial pacing canine model. Methods: Twenty-four dogs were randomly assigned to four groups: a sham group, paced control group, a paced + Ang-(1–7) group and a paced + Ang-(1–7) + A-71915 group. Atrial rapid pacing (ARP) at 600 bpm was maintained for 14 days except in the animals from the sham group. During the pacing, Ang-(1–7) (6 μgkg-1h-1) or Ang-(1–7) (6 μgkg-1h-1) + A-71915 (ANP receptor antagonist, 0.30 μgkg-1h-1) were given intravenously, respectively. After pacing, it was measured that electrophysiological parameters including atrial effective refractory periods (ERPs), inducibility and duration of atrial fibrillation (AF), I CaL and I Na changed, where I CaL refers to voltage-dependent L-type Ca 2+ current and I Na refers to cardiac sodium current. Then, the fibrosis and the expression of Cav1.2, I Nav 1.5α subunit, TGF-β1 and ANP in atria were assessed. Results: After ARP, compared with the sham group, the atrial ERPs at six sites in each dog were shortened with the increasing in inducibility and duration of AF in the paced control group. The density of I CaL, I Na and the expression of Cav1.2, I Nav 1.5α subunit mRNA were decreased. Atrial tissue from the paced dogs showed significant interstitial fibrosis. The expression of TGF-β1 and ANP in mRNA and protein levels were increased. Compared with the paced control group, the shortening of atrial ERPs, and the increasing of inducibility and duration of AF induced by ARP were alleviated by Ang-(1–7) treatment ( p < 0.05). The density of I CaL and I Na and the expression of Cav1.2 and I Nav 1.5α subunit mRNA were slightly decreased. Atrial tissue showed less interstitial fibrosis after Ang-(1–7) treatment. The increasing of ANP expression was improved by Ang-(1–7), while the increasing of TGF-β1 expression was alleviated by Ang-(1–7) ( p < 0.05). A-71915 treatment blocked the beneficial effects of Ang-(1–7) on the aforementioned electrophysiological parameters and atrial fibrosis. And A-71915 treatment blocked Ang-(1–7), improving the expression of TGF-β1 . Conclusion: Ang-(1–7) prevented atrial structural and electrical remodeling induced by ARP. Furthermore, Ang-(1–7) promoted ANP secretion, and ANP played a crucial role in the cardiac protection of the former.