Literature DB >> 31942549

Further insights into cardiovascular outcomes in diabetic and non-diabetic states: inhibition of sodium-glucose co-transports.

Zhao Li1.   

Abstract

Cardiovascular diseases are the leading cause of morbidity and mortality in the world. Diabetes increase heart disease related to death by two- to four-fold. SGLT2 inhibitors are new antidiabetic agents. The growing evidence of cardiovascular benefit of SGLT2 inhibitors independent of their effects on glycemic control is especially intriguing. Several clinical trials have shown that sotagliflozin (SGLT1-1/2 inhibitor) decreases body weight and reduces blood pressure in adults with T2D. A phase 3 study designed to evaluate cardiovascular outcomes of sotagliflozin is currently ongoing. Many pre-clinical studies were conducted to investigate the potential mechanisms involved in cardiovascular benefits of SGLT1 or SGLT2 inhibition with or without diabetes. Although multiple mechanisms have been proposed, there are still not enough data to fully support the mechanisms of actions. This review aims to discuss the potential mechanisms involved in cardiovascular benefits of SGLT1 and SGLT2 inhibition in both diabetic and non-diabetic states.
Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved.

Entities:  

Keywords:  SGLT1; SGLT2; cardiovascular benefits; diabetic; non-diabetic

Year:  2019        PMID: 31942549      PMCID: PMC6946152          DOI: 10.1097/XCE.0000000000000178

Source DB:  PubMed          Journal:  Cardiovasc Endocrinol Metab        ISSN: 2574-0954


  25 in total

1.  Expression of Na+-D-glucose cotransporter SGLT2 in rodents is kidney-specific and exhibits sex and species differences.

Authors:  Ivan Sabolic; Ivana Vrhovac; Daniela Balen Eror; Maria Gerasimova; Michael Rose; Davorka Breljak; Marija Ljubojevic; Hrvoje Brzica; Anne Sebastiani; Serge C Thal; Christoph Sauvant; Helmut Kipp; Volker Vallon; Hermann Koepsell
Journal:  Am J Physiol Cell Physiol       Date:  2012-01-18       Impact factor: 4.249

2.  Effect of ipragliflozin, an SGLT2 inhibitor, on cardiac histopathological changes in a non-diabetic rat model of cardiomyopathy.

Authors:  Toshiyuki Takasu; Shoji Takakura
Journal:  Life Sci       Date:  2019-05-21       Impact factor: 5.037

3.  Dapagliflozin, a selective SGLT2 Inhibitor, attenuated cardiac fibrosis by regulating the macrophage polarization via STAT3 signaling in infarcted rat hearts.

Authors:  Tsung-Ming Lee; Nen-Chung Chang; Shinn-Zong Lin
Journal:  Free Radic Biol Med       Date:  2017-01-26       Impact factor: 7.376

4.  Empagliflozin Ameliorates Adverse Left Ventricular Remodeling in Nondiabetic Heart Failure by Enhancing Myocardial Energetics.

Authors:  Carlos G Santos-Gallego; Juan Antonio Requena-Ibanez; Rodolfo San Antonio; Kiyotake Ishikawa; Shin Watanabe; Belen Picatoste; Eduardo Flores; Alvaro Garcia-Ropero; Javier Sanz; Roger J Hajjar; Valentin Fuster; Juan J Badimon
Journal:  J Am Coll Cardiol       Date:  2019-04-23       Impact factor: 24.094

5.  Human cardiomyocytes express high level of Na+/glucose cotransporter 1 (SGLT1).

Authors:  Lubing Zhou; Ellen V Cryan; Michael R D'Andrea; Stanley Belkowski; Bruce R Conway; Keith T Demarest
Journal:  J Cell Biochem       Date:  2003-10-01       Impact factor: 4.429

6.  SGLT1 is a novel cardiac glucose transporter that is perturbed in disease states.

Authors:  Sanjay K Banerjee; Kenneth R McGaffin; Núria M Pastor-Soler; Ferhaan Ahmad
Journal:  Cardiovasc Res       Date:  2009-06-09       Impact factor: 10.787

7.  Effects of Sodium-Glucose Cotransporter 2 Inhibitors for the Treatment of Patients With Heart Failure: Proposal of a Novel Mechanism of Action.

Authors:  Milton Packer; Stefan D Anker; Javed Butler; Gerasimos Filippatos; Faiez Zannad
Journal:  JAMA Cardiol       Date:  2017-09-01       Impact factor: 14.676

Review 8.  [Roles of Sodium-Glucose Cotransporter 1 (SGLT1) in the Induction of Cardiac Remodeling].

Authors:  Masamichi Hirose; Naoko Matsushita; Nanae Ishida; Miho Ibi; Maki Saito
Journal:  Yakugaku Zasshi       Date:  2018       Impact factor: 0.302

9.  Cardiac sodium-dependent glucose cotransporter 1 is a novel mediator of ischaemia/reperfusion injury.

Authors:  Zhao Li; Vineet Agrawal; Mohun Ramratnam; Ravi K Sharma; Stephen D'Auria; Abigail Sincoular; Margurite Jakubiak; Meredith L Music; William J Kutschke; Xueyin N Huang; Lindsey Gifford; Ferhaan Ahmad
Journal:  Cardiovasc Res       Date:  2019-09-01       Impact factor: 10.787

10.  Angiotensin II-induced redox-sensitive SGLT1 and 2 expression promotes high glucose-induced endothelial cell senescence.

Authors:  Sonia Khemais-Benkhiat; Eugenia Belcastro; Noureddine Idris-Khodja; Sin-Hee Park; Lamia Amoura; Malak Abbas; Cyril Auger; Laurence Kessler; Eric Mayoux; Florence Toti; Valérie B Schini-Kerth
Journal:  J Cell Mol Med       Date:  2019-03-30       Impact factor: 5.310

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