Sodium-Glucose Cotransporter Protein 2 Inhibitors: Novel Application for the Treatment of Obesity-Associated Hypertension.

inflammation metabolism neuro-humoral regulation obesity-associated hypertension sodium-glucose cotransporter protein 2 inhibitors

Journal

Diabetes, metabolic syndrome and obesity : targets and therapy
ISSN: 1178-7007
Titre abrégé: Diabetes Metab Syndr Obes
Pays: New Zealand
ID NLM: 101515585

Informations de publication

Date de publication:
2024
Historique:
received: 10 11 2023
accepted: 13 01 2024
medline: 31 1 2024
pubmed: 31 1 2024
entrez: 31 1 2024
Statut: epublish

Résumé

Obesity is becoming increasingly prevalent in China and worldwide and is closely related to the development of hypertension. The pathophysiology of obesity-associated hypertension is complex, including an overactive sympathetic nervous system (SNS), activation of the renin-angiotensin-aldosterone system (RAAS), insulin resistance, hyperleptinemia, renal dysfunction, inflammatory responses, and endothelial function, which complicates treatment. Sodium-glucose cotransporter protein 2 (SGLT-2) inhibitors, novel hypoglycemic agents, have been shown to reduce body weight and blood pressure and may serve as potential novel agents for the treatment of obesity-associated hypertension. This review discusses the beneficial mechanisms of SGLT-2 inhibitors for the treatment of obesity-associated hypertension. SGLT-2 inhibitors can inhibit SNS activity, reduce RAAS activation, ameliorate insulin resistance, reduce leptin secretion, improve renal function, and inhibit inflammatory responses. SGLT-2 inhibitors can, therefore, simultaneously target multiple mechanisms of obesity-associated hypertension and may serve as an effective treatment for obesity-associated hypertension.

Identifiants

pubmed: 38292009
doi: 10.2147/DMSO.S446904
pii: 446904
pmc: PMC10826576
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

407-415

Informations de copyright

© 2024 Hu et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

Auteurs

Yilan Hu (Y)

The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
Heart Center, Department of Cardiovascular Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, People's Republic of China.

Jiaqi Bao (J)

The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
Heart Center, Department of Cardiovascular Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, People's Republic of China.

Zhicheng Gao (Z)

The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
Heart Center, Department of Cardiovascular Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, People's Republic of China.

Lifang Ye (L)

Heart Center, Department of Cardiovascular Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, People's Republic of China.

Lihong Wang (L)

The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
Heart Center, Department of Cardiovascular Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, People's Republic of China.

Classifications MeSH