Effects of exercise training on excitation–contraction coupling and related mRNA expression in hearts of Goto-Kakizaki type 2 diabetic rats

• Published in: Molecular and cellular biochemistry 2013-08, Vol.380 (1-2), p.83-96
• Main Authors: Salem, K. A., Qureshi, M. A., Sydorenko, V., Parekh, K., Jayaprakash, P., Iqbal, T., Singh, J., Oz, M., Adrian, T. E., Howarth, F. C.
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Biomedical and Life Sciences; Calcium; Calcium - metabolism; Calcium Channels, L-Type - metabolism; Calcium Channels, L-Type - physiology; Cardiology; Caveolin 3 - genetics; Cell Shape; Cells, Cultured; Connexin 43 - genetics; Diabetes; Diabetes Mellitus, Type 2 - genetics; Diabetes Mellitus, Type 2 - physiopathology; Exercise; Gene Expression; Heart; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - genetics; Intracellular Space; Life Sciences; Male; Medical Biochemistry; Membrane Potentials; Messenger RNA; Myocardial Contraction - physiology; Myocardium - metabolism; Myocytes, Cardiac - cytology; Myocytes, Cardiac - metabolism; Myocytes, Cardiac - physiology; Nerve Tissue Proteins - genetics; Oncology; Patch-Clamp Techniques; Physical Conditioning, Animal - physiology; Physical training; Potassium Channels, Tandem Pore Domain - genetics; Rats; Rats, Wistar; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; RNA, Messenger - metabolism; Rodents
• ISSN: 0300-8177; 1573-4919
• DOI: 10.1007/s11010-013-1662-2

Although, several novel forms of intervention aiming at newly identified therapeutic targets are currently being developed for diabetes mellitus (DM), it is well established that physical exercise continues to be one of the most valuable forms of non-pharmacological therapy. The aim of the study was to investigate the effects of exercise training on excitation–contraction coupling and related gene expression in the Goto-Kakizaki (GK) type 2 diabetic rat heart and whether exercise is able to reverse diabetes-induced changes in excitation–contraction coupling and gene expression. Experiments were performed in GK and control rats aged 10–11 months following 2–3 months of treadmill exercise training. Shortening, [Ca 2+ ] i and L-type Ca 2+ current were measured in ventricular myocytes with video edge detection, fluorescence photometry and whole cell patch clamp techniques, respectively. Expression of mRNA was assessed in ventricular muscle with real-time RT-PCR. Amplitude of shortening, Ca 2+ transients and L-type Ca 2+ current were not significantly altered in ventricular myocytes from GK sedentary compared to control sedentary rats or by exercise training. Expression of mRNA encoding Tpm2, Gja4, Atp1b1, Cacna1g, Cacnb2, Hcn2, Kcna3 and Kcne1 were up-regulated and Gja1, Kcnj2 and Kcnk3 were down-regulated in hearts of sedentary GK rats compared to sedentary controls. Gja1, Cav3 and Kcnk3 were up-regulated and Hcn2 was down-regulated in hearts of exercise trained GK compared to sedentary GK controls. Ventricular myocyte shortening and Ca 2+ transport were generally well preserved despite alterations in the profile of expression of mRNA encoding a variety of cardiac muscle proteins in the adult exercise trained GK diabetic rat heart.