Ketogenic diet modulates cardiac metabolic dysregulation in streptozocin-induced diabetic rats

• Published in: The Journal of nutritional biochemistry Vol. 111; p. 109161
• Main Authors: Trang, Nguyen Ngoc, Lee, Ting-Wei, Kao, Yu-Hsun, Chao, Tze‐Fan, Lee, Ting-I, Chen, Yi-Jen
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2023
• Subjects: Adenosine Triphosphate - metabolism; Animals; diabetes mellitus; Diabetes Mellitus, Experimental - metabolism; Diabetic Cardiomyopathies - etiology; Diabetic Cardiomyopathies - metabolism; diabetic cardiomyopathy; Diet, Ketogenic; fatty acid metabolism; Fibrosis; Glucose - metabolism; inflammation; ketogenic diet; Ketone Bodies - adverse effects; Ketone Bodies - metabolism; Myocardium - metabolism; Myocytes, Cardiac; Rats; Streptozocin - adverse effects; DM; HR; diabetic cardiomyopathy; LVEDd; HDL-C; DBP; FBS; STZ; CD36; SGOT; EF; IL; BCAAs; BDH1; SUV; ND; ROS; SEM; FA; BHB; GAPDH; BWs; Bcl-2; AMPKα2; CPT-1β; HWs; LDL-C; FDG; diabetes mellitus; PERK; FS; p-eIF2α; ketogenic diet; inflammation; OXCT1; PDH; KD; SBP; ACC; GLUT; fatty acid metabolism; TC; ST2; TG; TNF-α; Bax; LVESd; ATP; HF; PET; SGPT; pAMPKα2
• ISSN: 0955-2863; 1873-4847
• DOI: 10.1016/j.jnutbio.2022.109161

The ketogenic diet (KD) might improve cardiac function in diabetic cardiomyopathy, but the mechanisms remain unclear. This study investigated the effects of KD on myocardial fatty acid (FA), glucose, and ketone metabolism in diabetic cardiomyopathy. Echocardiograms, biochemistry, and micro-positron emission tomography were performed to evaluate cardiac function and glucose uptake in control rats and streptozotocin-induced diabetes mellitus (DM) rats with normal diet (ND) or KD for 6 weeks. Histopathology, adenosine triphosphate measurement, and Western blot were performed in the ventricular myocytes to analyze fibrosis, FA, ketone body, and glucose utilization. The ND-fed DM rats exhibited impaired left ventricular systolic function and increased chamber dilatation, whereas control and KD-fed DM rats did not. The KD reduced myocardial fibrosis and apoptosis in the DM rats. Myocardial glucose uptake in the micro-positron emission tomography was similar between ND-fed DM rats and KD-fed DM rats and was substantially lower than the control rats. Compared with the control rats,  ND-fed DM rats had increased phosphorylation of acetyl CoA carboxylase and higher expressions of CD-36, carnitine palmitoyltransferase-1β, tumor necrosis factor-α, interleukin-1β, interleukin6, PERK, and e-IF2α as well as more myocardial fibrosis and apoptosis (assessed by Bcl-2, BAX, and caspase-3 expression); these increases were attenuated in the KD-fed DM rats. Moreover, ND-fed DM rats had significantly lower myocardial adenosine triphosphate, BHB, and OXCT1 levels than the control and KD-fed DM rats. The KD may improve the condition of diabetic cardiomyopathy by suppressing FA metabolism, increasing ketone utilization, and decreasing endoplasmic reticulum stress and inflammation.