Diabetes mellitus results in a diabetic cardiomyopathy (DC) with decreased cardiac contractile function and heart failure independent of vascular disease. Abnormal calcium (Ca) handling importantly contributes to DC with the sarcoplasmic reticulum (SR) CaATP'ase (SERCa2) being significantly decreased resulting in abnormal diastolic calcium flux.
In Aim I, we will determine if in transgenic (Tg) mice made diabetic (D)tetracycline (Tet) transactivator based conditional increases in SERCa2 activity have a positive or a negative Iongterm effect on contractile function and survival. Our result show that Tet based SERCa2 expression is feasible in DC hearts and has a positive contractile effect. We will also explore the effect of SERCa2 expression on the high energy phosphate status and positive or negative cardiac remodeling using Tg mice or viral vectors. Our results show that systolic Ca flux is abnormal and in Aim II, we will use conditional expression of putative ryanodine receptor (RyR2) interacting proteins: Sorcine, Homerlc and FKBP12.6 to influence systolic Ca handling. Our results show a positive effect of Sorcine, Homerlc, and FKBP12.6 expression on contractile function in DC hearts. We are interested in comparing the effects of SERCa2 vs.RyR2 interacting protein on the energetic status of the heart, remodeling and survival. In addition, D induced abnormalities in mitochondrial Ca handling, which we recently identified, will be explored.
In aim III, the contribution which O-linked glycosylation and hexosamine pathway activity makes to DC will be explored.Our result indicate that increased viral vector based expression of the O-GIcNAcase enzyme which removes N-acetyl glucosamine from proteins in myocytes from D hearts under in vivo conditions can improve Ca flux and contractile handling in spite of persistent hyperglycemia. These interesting results will be extended and specific proteins having altered O-glycosylation are identified. Novel insights and approaches to improve contractile function of the D heart in spite of persistent hyperglycemia will result from these investigations. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL066917-06
Application #
6922058
Study Section
Myocardial Ischemia and Metabolism Study Section (MIM)
Program Officer
Liang, Isabella Y
Project Start
2000-09-30
Project End
2008-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
6
Fiscal Year
2005
Total Cost
$385,208
Indirect Cost
Name
University of California San Diego
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Suarez, Jorge; Wang, Hong; Scott, Brian T et al. (2014) In vivo selective expression of thyroid hormone receptor ?1 in endothelial cells attenuates myocardial injury in experimental myocardial infarction in mice. Am J Physiol Regul Integr Comp Physiol 307:R340-6
Torres-Gonzalez, Moises; Gawlowski, Thomas; Kocalis, Heidi et al. (2014) Mitochondrial 8-oxoguanine glycosylase decreases mitochondrial fragmentation and improves mitochondrial function in H9C2 cells under oxidative stress conditions. Am J Physiol Cell Physiol 306:C221-9
Suarez, Jorge; McDonough, Patrick M; Scott, Brian T et al. (2013) Sorcin modulates mitochondrial Ca(2+) handling and reduces apoptosis in neonatal rat cardiac myocytes. Am J Physiol Cell Physiol 304:C248-56
Gawlowski, Thomas; Suarez, Jorge; Scott, Brian et al. (2012) Modulation of dynamin-related protein 1 (DRP1) function by increased O-linked-?-N-acetylglucosamine modification (O-GlcNAc) in cardiac myocytes. J Biol Chem 287:30024-34
Fricovsky, Eduardo S; Suarez, Jorge; Ihm, Sang-Hyun et al. (2012) Excess protein O-GlcNAcylation and the progression of diabetic cardiomyopathy. Am J Physiol Regul Integr Comp Physiol 303:R689-99
Makino, Ayako; Suarez, Jorge; Gawlowski, Thomas et al. (2011) Regulation of mitochondrial morphology and function by O-GlcNAcylation in neonatal cardiac myocytes. Am J Physiol Regul Integr Comp Physiol 300:R1296-302
Makino, A; Scott, B T; Dillmann, W H (2010) Mitochondrial fragmentation and superoxide anion production in coronary endothelial cells from a mouse model of type 1 diabetes. Diabetologia 53:1783-94
Hu, Yong; Suarez, Jorge; Fricovsky, Eduardo et al. (2009) Increased enzymatic O-GlcNAcylation of mitochondrial proteins impairs mitochondrial function in cardiac myocytes exposed to high glucose. J Biol Chem 284:547-55
Suarez, Jorge; Hu, Yong; Makino, Ayako et al. (2008) Alterations in mitochondrial function and cytosolic calcium induced by hyperglycemia are restored by mitochondrial transcription factor A in cardiomyocytes. Am J Physiol Cell Physiol 295:C1561-8
Makino, Ayako; Platoshyn, Oleksandr; Suarez, Jorge et al. (2008) Downregulation of connexin40 is associated with coronary endothelial cell dysfunction in streptozotocin-induced diabetic mice. Am J Physiol Cell Physiol 295:C221-30

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