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Shortening and intracellular Ca 2+ in ventricular myocytes and expression of genes encoding cardiac muscle proteins in early onset type 2 diabetic Goto–Kakizaki rats
Author(s) -
Salem K. A.,
Adrian T. E.,
Qureshi M. A.,
Parekh K.,
Oz M.,
Howarth F. C.
Publication year - 2012
Publication title -
experimental physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 101
eISSN - 1469-445X
pISSN - 0958-0670
DOI - 10.1113/expphysiol.2012.066639
Subject(s) - medicine , ventricle , endocrinology , myocyte , myh6 , cardiac muscle , cardiology , biology , myosin , microbiology and biotechnology , myosin light chain kinase , myh7
There has been a spectacular rise in the global prevalence of type 2 diabetes mellitus. Cardiovascular complications are the major cause of morbidity and mortality in diabetic patients. Contractile dysfunction, associated with disturbances in excitation–contraction coupling, has been widely demonstrated in the diabetic heart. The aim of this study was to investigate the pattern of cardiac muscle genes that are involved in the process of excitation–contraction coupling in the hearts of early onset (8–10 weeks of age) type 2 diabetic Goto–Kakizaki (GK) rats. Gene expression was assessed in ventricular muscle with real‐time RT‐PCR; shortening and intracellular Ca 2+ were measured in ventricular myocytes with video edge detection and fluorescence photometry, respectively. The general characteristics of the GK rats included elevated fasting and non‐fasting blood glucose and blood glucose at 120 min following a glucose challenge. Expression of genes encoding cardiac muscle proteins ( Myh6/7 , Mybpc3 , Myl1/3 , Actc1 , Tnni3 , Tnn2 , Tpm1/2/4 and Dbi ) and intercellular proteins ( Gja1/4/5/7 , Dsp and Cav1/3 ) were unaltered in GK ventricle compared with control ventricle. The expression of genes encoding some membrane pumps and exchange proteins was unaltered ( Atp1a1/2 , Atp1b1 and Slc8a1 ), whilst others were either upregulated ( Atp1a3 , relative expression 2.61 ± 0.69 versus 0.84 ± 0.23) or downregulated ( Slc9a1 , 0.62 ± 0.07 versus 1.08 ± 0.08) in GK ventricle compared with control ventricle. The expression of genes encoding some calcium ( Cacna1c/1g , Cacna2d1/2d2 and Cacnb1/b2 ), sodium ( Scn5a ) and potassium channels ( Kcna3/5 , Kcnj3/5/8/11/12 , Kchip2 , Kcnab1 , Kcnb1 , Kcnd1/2/3 , Kcne1/4 , Kcnq1 , Kcng2 , Kcnh2 , Kcnk3 and Kcnn2 ) were unaltered, whilst others were either upregulated ( Cacna1h , 0.95 ± 0.16 versus 0.47 ± 0.09; Scn1b , 1.84 ± 0.16 versus 1.11 ± 0.11; and Hcn2 , 1.55 ± 0.15 versus 1.03 ± 0.08) or downregulated ( Hcn4 , 0.16 ± 0.03 versus 0.37 ± 0.08; Kcna2 , 0.35 ± 0.03 versus 0.80 ± 0.11; Kcna4 , 0.79 ± 0.25 versus 1.90 ± 0.26; and Kcnj2 , 0.52 ± 0.07 versus 0.78 ± 0.08) in GK ventricle compared with control ventricle. The amplitude of ventricular myocyte shortening and the intracellular Ca 2+ transient were unaltered; however, the time‐to‐peak shortening was prolonged and time‐to‐half decay of the Ca 2+ transient was shortened in GK myocytes compared with control myocytes. The results of this study demonstrate changes in expression of genes encoding various excitation–contraction coupling proteins that are associated with disturbances in myocyte shortening and intracellular Ca 2+ transport.