| Literature DB >> 32819717 |
Hidekazu Shirai1, Emiko Sato1, Akiyo Sekimoto1, Taeko Uchida1, Yuji Oe2, Sadayoshi Ito2, Hiroshi Sato3, Nobuyuki Takahashi4.
Abstract
We have previously demonstrated that manipulation of the renin angiotensin system (RAS) has large effects on digestive efficiency. However, the effects of aldosterone on body weight, adiposity, and glucose absorption in the intestine remains unknown. We here demonstrated that lack of aldosterone synthase (ASKO) in mice did not affect adiposity. In contrast, mice administered with aldosterone were resistant to diet-induced obesity. This is due to gastrointestinal loss of dietary glucose. As expected, ASKO mice had increased glucose absorption, whereas mice administered with aldosterone had reduced glucose absorption in the small intestine. Furthermore, the level of protein expression of sodium glucose transporter 1 (SGLT1) in the mucosa of the jejunum was higher in ASKO mice, and lower in mice administered with aldosterone than control mice. Our findings indicate that aldosterone plays an important role on SGLT-1-mediated glucose absorption in the small intestine.Entities:
Keywords: Adiposity; Aldosterone; Glucose absorption; Sodium glucose transporter 1
Year: 2020 PMID: 32819717 DOI: 10.1016/j.bbrc.2020.07.119
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575