Left-ventricular diastolic dysfunction may be prevented by chronic treatment with PPAR-α or -γ agonists in a type 2 diabetic animal model

Soo Kyung Kim, Zheng Shan Zhao, Yong Jik Lee, Kwang Eun Lee, Seok Min Kang, Donghoon Choi, Sung Kil Lim, Namsik Chung, Hyun Chul Lee, Bong Soo Cha

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

Objectives. The aim of this study was to determine whether the peroxisome proliferator-activated receptor (PPAR) ligands could prevent left-ventricular diastolic dysfunction (LVDD) in rats with advanced diabetes. In addition, this study examined whether the activity of malonyl-CoA decarboxylase (MCD), which is an enzyme related to the degradation of malonyl-CoA that is known to regulate the fatty acid metabolism, is changed by the diabetic state itself or by treatment with the PPAR ligands. Methods. Male Otsuka Long-Evans Tokushima Fatty (OLETF) rats, a model of type 2 diabetes, aged 28 weeks, were divided into 3 groups: the untreated, pioglitazone-treated (10 mg/kg/d), and fenofibrate-treated (150 mg/kg/d) groups. The rats were treated for 10 weeks. Male Long-Evans Tokushima Otsuka (LETO) rats were used as nondiabetic control. Doppler echocardiography and measurements of the MCD activity at the myocardium were performed. Results. At the age of 38 weeks, the OLETF rats treated with either pioglitazone or fenofibrate showed an improvement in the plasma glucose levels after glucose loading as well as an improvement in the fasting plasma insulin, triglyceride, and FFA levels compared to the untreated OLETF rats. The untreated OLETF rats showed a prolonged deceleration time of the E-wave (DTE) (74.3 ± 3.7 vs LETO, 56.3 ± 3.8 ms, P < 0.05) and a reduced ratio of the peak early diastolic velocity wave to the late diastolic wave (E/A ratio) (1.25 ± 0.06 vs LETO 1.54 ± 0.08, P < 0.05). Pioglitazone treatment in the OLETF rats improved the DTE (51.6 ± 1.7 ms, P < 0.05), and the fenofibrate treatment also improved the DTE (61.4 ± 4.3 ms, P < 0.05) and E/A ratio (1.57 ± 0.05, P < 0.05) compared to the untreated OLETF rats. The parameters related to the systolic function did not change among the groups at both pre- and post-treatments. The MCD activity of the myocardium was remarkably lower in the OLETF rats compared to the LETO rats (3.26 ± 0.38 vs 7.76 ± 0.84 nmol/min/mg protein, P < 0.05). The pioglitazone and fenofibrate treatments resulted in an increase in the MCD activity compared to that in the untreated rats (7.20 ± 0.74 and 8.33 ± 0.83 nmol/min/mg protein, P < 0.05, respectively). Conclusions. The PPAR-α or -γ agonists prevented LVDD in the advanced diabetic rat hearts, possibly through an improvement in the fatty acid metabolism in the myocardium or a correction of the hyperglycemia and/or hyperlipidemia.

Original languageEnglish
Pages (from-to)487-493
Number of pages7
JournalDiabetes/Metabolism Research and Reviews
Volume19
Issue number6
DOIs
Publication statusPublished - 2003 Nov

All Science Journal Classification (ASJC) codes

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Fingerprint Dive into the research topics of 'Left-ventricular diastolic dysfunction may be prevented by chronic treatment with PPAR-α or -γ agonists in a type 2 diabetic animal model'. Together they form a unique fingerprint.

  • Cite this