A dipeptidyl peptidase-IV inhibitor improves diastolic dysfunction in Dahl salt-sensitive rats

• Published in: Journal of molecular and cellular cardiology 2019-04, Vol.129, p.257-265
• Main Authors: Nakajima, Yuri, Ito, Shin, Asakura, Masanori, Min, Kyung-Duk, Fu, Hai Ying, Imazu, Miki, Hitsumoto, Tatsuro, Takahama, Hiroko, Shindo, Kazuhiro, Fukuda, Hiroki, Yamazaki, Satoru, Asanuma, Hiroshi, Kitakaze, Masafumi
• Format: Article
• Language: English
• Subjects: Cardiac fibrosis; Left ventricular diastolic dysfunction; Left ventricular diastolic pressure–volume relationship; Renal dysfunction; Renin–angiotensin–aldosterone system
• ISSN: 0022-2828; 1095-8584
• DOI: 10.1016/j.yjmcc.2019.03.009

To date, there is no established treatment for heart failure with preserved ejection fraction (HFpEF). Dipeptidyl peptidase-IV (DPP-IV) inhibitors reportedly have improved not only diabetes mellitus but also heart failure with systolic dysfunction in experimental models. We investigated the effects of a DPP-IV inhibitor on HFpEF in rats. Dahl salt-sensitive rats were fed either high-salt (high-salt diet (HSD): 8% NaCl) or low-salt diets (0.3% NaCl) from 6.5 weeks of age. They were then treated with or without a DPP-IV inhibitor, vildagliptin (10 mg/kg/day, orally), from 11 weeks of age for 9 weeks and analyzed at the age of 20 weeks. HSD rats mimicked the pathophysiology of HFpEF. There were no differences in heart rate, blood pressure, left ventricular (LV) systolic function, or the extent of LV hypertrophy between HSD rats with or without vildagliptin. However, vildagliptin decreased LV end-diastolic pressure, the most reliable hemodynamic parameter of HFpEF in HSD rats. Vildagliptin also decreased the LV distensibility index, a sensitive marker of LV diastolic function in HSD rats. Vildagliptin decreased the expression of collagen genes in HSD hearts and attenuated LV interstitial fibrosis (HSD with vehicle and vildagliptin, 2.9% vs. 1.9%; P