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The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1990 Sep;86(3):777–784. doi: 10.1172/JCI114774

Alterations in phospholipid N-methylation of cardiac subcellular membranes due to experimentally induced diabetes in rats.

V Panagia 1, Y Taira 1, P K Ganguly 1, S Tung 1, N S Dhalla 1
PMCID: PMC296792  PMID: 2144301

Abstract

Phosphatidylethanolamine N-methylation was examined in cardiac subcellular membranes after inducing chronic experimental diabetes in rats (65 mg streptozotocin/kg, i.v.). The incorporation of radiolabeled methyl groups from S-adenosyl-L-methionine in diabetic sarcolemma was significantly depressed at all three catalytic sites (I, II, and III) of the methyltransferase system. An increase in methyl group incorporation was evident at site I without any changes at sites II and III in diabetic sarcoplasmic reticulum and mitochondria. Similar changes were also seen for the individual N-methylated lipids (monomethyl-, dimethylphosphatidylethanolamine, and phosphatidylcholine) specifically formed at each catalytic site in all cardiac membranes from diabetic animals. These alterations in N-methylation were reversible by a 14-d insulin therapy to the diabetic animals. In the presence of 10 microM ATP and 0.1 microM Ca2+, N-methylation was maximally activated at site I in both control and diabetic sarcolemma and sarcoplasmic reticulum, but not in mitochondria. Incubation of cardiac membranes with of S-adenosyl-L-methionine showed that Ca2(+)-stimulated ATPase activities in both sarcolemma and sarcoplasmic reticulum were augmented; however, the activation of diabetic sarcolemma was lesser and that of diabetic sarcoplasmic reticulum was greater in comparison with the control preparations. These results identify alterations in phosphatidylethanolamine N-methylation in subcellular membranes from diabetic heart, and it is suggested that these defects may be crucial in the development of cardiac dysfunction in chronic diabetes.

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Selected References

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  1. Alemany S., Varela I., Harper J. F., Mato J. M. Calmodulin regulation of phospholipid and fatty acid methylation by rat liver microsomes. J Biol Chem. 1982 Aug 25;257(16):9249–9251. [PubMed] [Google Scholar]
  2. Barbee R. W., Shepherd R. E., Burns A. H. T3 treatment does not prevent myocardial dysfunction in chronically diabetic rats. Am J Physiol. 1988 Feb;254(2 Pt 2):H265–H273. doi: 10.1152/ajpheart.1988.254.2.H265. [DOI] [PubMed] [Google Scholar]
  3. Chen V., Ianuzzo C. D., Fong B. C., Spitzer J. J. The effects of acute and chronic diabetes on myocardial metabolism in rats. Diabetes. 1984 Nov;33(11):1078–1084. doi: 10.2337/diab.33.11.1078. [DOI] [PubMed] [Google Scholar]
  4. Dhalla N. S., Pierce G. N., Panagia V., Singal P. K., Beamish R. E. Calcium movements in relation to heart function. Basic Res Cardiol. 1982 Mar-Apr;77(2):117–139. doi: 10.1007/BF01908167. [DOI] [PubMed] [Google Scholar]
  5. Ganguly P. K., Dhalla K. S., Innes I. R., Beamish R. E., Dhalla N. S. Altered norepinephrine turnover and metabolism in diabetic cardiomyopathy. Circ Res. 1986 Dec;59(6):684–693. doi: 10.1161/01.res.59.6.684. [DOI] [PubMed] [Google Scholar]
  6. Ganguly P. K., Panagia V., Okumura K., Dhalla N. S. Activation of Ca2+-stimulated ATPase by phospholipid N-methylation in cardiac sarcoplasmic reticulum. Biochem Biophys Res Commun. 1985 Jul 16;130(1):472–478. doi: 10.1016/0006-291x(85)90441-3. [DOI] [PubMed] [Google Scholar]
  7. Ganguly P. K., Pierce G. N., Dhalla K. S., Dhalla N. S. Defective sarcoplasmic reticular calcium transport in diabetic cardiomyopathy. Am J Physiol. 1983 Jun;244(6):E528–E535. doi: 10.1152/ajpendo.1983.244.6.E528. [DOI] [PubMed] [Google Scholar]
  8. Ganguly P. K., Rice K. M., Panagia V., Dhalla N. S. Sarcolemmal phosphatidylethanolamine N-methylation in diabetic cardiomyopathy. Circ Res. 1984 Oct;55(4):504–512. doi: 10.1161/01.res.55.4.504. [DOI] [PubMed] [Google Scholar]
  9. Harigaya S., Schwartz A. Rate of calcium binding and uptake in normal animal and failing human cardiac muscle. Membrane vesicles (relaxing system) and mitochondria. Circ Res. 1969 Dec;25(6):781–794. doi: 10.1161/01.res.25.6.781. [DOI] [PubMed] [Google Scholar]
  10. Heyliger C. E., Rodrigues B., McNeill J. H. Effect of choline and methionine treatment on cardiac dysfunction of diabetic rats. Diabetes. 1986 Oct;35(10):1152–1157. doi: 10.2337/diab.35.10.1152. [DOI] [PubMed] [Google Scholar]
  11. Lamers J. M., Hartog J. M., Verdouw P. D., Hülsmann W. C. Dietary fatty acids and myocardial function. Basic Res Cardiol. 1987;82 (Suppl 1):209–221. doi: 10.1007/978-3-662-08390-1_25. [DOI] [PubMed] [Google Scholar]
  12. Makino N., Dhalla K. S., Elimban V., Dhalla N. S. Sarcolemmal Ca2+ transport in streptozotocin-induced diabetic cardiomyopathy in rats. Am J Physiol. 1987 Aug;253(2 Pt 1):E202–E207. doi: 10.1152/ajpendo.1987.253.2.E202. [DOI] [PubMed] [Google Scholar]
  13. Malhotra A., Penpargkul S., Fein F. S., Sonnenblick E. H., Scheuer J. The effect of streptozotocin-induced diabetes in rats on cardiac contractile proteins. Circ Res. 1981 Dec;49(6):1243–1250. doi: 10.1161/01.res.49.6.1243. [DOI] [PubMed] [Google Scholar]
  14. Okumura K., Panagia V., Beamish R. E., Dhalla N. S. Biphasic changes in the sarcolemmal phosphatidylethanolamine N-methylation activity in catecholamine-induced cardiomyopathy. J Mol Cell Cardiol. 1987 Apr;19(4):357–366. doi: 10.1016/s0022-2828(87)80581-3. [DOI] [PubMed] [Google Scholar]
  15. Panagia V., Ganguly P. K., Dhalla N. S. Characterization of heart sarcolemmal phospholipid methylation. Biochim Biophys Acta. 1984 Mar 7;792(3):245–253. doi: 10.1016/0005-2760(84)90192-9. [DOI] [PubMed] [Google Scholar]
  16. Panagia V., Ganguly P. K., Okumura K., Dhalla N. S. Subcellular localization of phosphatidylethanolamine N-methylation activity in rat heart. J Mol Cell Cardiol. 1985 Dec;17(12):1151–1159. doi: 10.1016/s0022-2828(85)80111-5. [DOI] [PubMed] [Google Scholar]
  17. Panagia V., Lamers J. M., Singal P. K., Dhalla N. S. Ca2+- and Mg2+-dependent ATPase activities in the deoxycholate-treated rat heart sarcolemma. Int J Biochem. 1982;14(5):387–397. doi: 10.1016/0020-711x(82)90024-6. [DOI] [PubMed] [Google Scholar]
  18. Panagia V., Makino N., Ganguly P. K., Dhalla N. S. Inhibition of Na+-Ca2+ exchange in heart sarcolemmal vesicles by phosphatidylethanolamine N-methylation. Eur J Biochem. 1987 Aug 3;166(3):597–603. doi: 10.1111/j.1432-1033.1987.tb13555.x. [DOI] [PubMed] [Google Scholar]
  19. Panagia V., Okumura K., Makino N., Dhalla N. S. Stimulation of Ca2+-pump in rat heart sarcolemma by phosphatidylethanolamine N-methylation. Biochim Biophys Acta. 1986 Apr 14;856(2):383–387. doi: 10.1016/0005-2736(86)90049-0. [DOI] [PubMed] [Google Scholar]
  20. Panagia V., Okumura K., Shah K. R., Dhalla N. S. Modification of sarcolemmal phosphatidylethanolamine N-methylation during heart hypertrophy. Am J Physiol. 1987 Jul;253(1 Pt 2):H8–15. doi: 10.1152/ajpheart.1987.253.1.H8. [DOI] [PubMed] [Google Scholar]
  21. Penpargkul S., Schaible T., Yipintsoi T., Scheuer J. The effect of diabetes on performance and metabolism of rat hearts. Circ Res. 1980 Dec;47(6):911–921. doi: 10.1161/01.res.47.6.911. [DOI] [PubMed] [Google Scholar]
  22. Pierce G. N., Kutryk M. J., Dhalla N. S. Alterations in Ca2+ binding by and composition of the cardiac sarcolemmal membrane in chronic diabetes. Proc Natl Acad Sci U S A. 1983 Sep;80(17):5412–5416. doi: 10.1073/pnas.80.17.5412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Pitts B. J. Stoichiometry of sodium-calcium exchange in cardiac sarcolemmal vesicles. Coupling to the sodium pump. J Biol Chem. 1979 Jul 25;254(14):6232–6235. [PubMed] [Google Scholar]
  24. Prasad C., Edwards R. M. Increased phospholipid methylation in the myocardium of alcoholic rats. Biochem Biophys Res Commun. 1983 Mar 16;111(2):710–716. doi: 10.1016/0006-291x(83)90363-7. [DOI] [PubMed] [Google Scholar]
  25. Seager M. J., Singal P. K., Orchard R., Pierce G. N., Dhalla N. S. Cardiac cell damage: a primary myocardial disease in streptozotocin-induced chronic diabetes. Br J Exp Pathol. 1984 Oct;65(5):613–623. [PMC free article] [PubMed] [Google Scholar]
  26. Taira Y., Ganguly P. K., Panagia V., Dhalla N. S. Increased SR phospholipid N-methylation in skeletal muscle of diabetic rats. Am J Physiol. 1988 Sep;255(3 Pt 1):E347–E352. doi: 10.1152/ajpendo.1988.255.3.E347. [DOI] [PubMed] [Google Scholar]
  27. Vance D. E., Ridgway N. D. The methylation of phosphatidylethanolamine. Prog Lipid Res. 1988;27(1):61–79. doi: 10.1016/0163-7827(88)90005-7. [DOI] [PubMed] [Google Scholar]

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