Skip to main content

Mutations of Myocardial Mitochondrial DNA in Diabetic Patients

  • Chapter

Part of the book series: Developments in Cardiovascular Medicine ((DICM,volume 169))

Abstract

Mitochondrial DNA mutations in the myocardium have been reported in patients with idiopathic cardiomyopathy [1–3], and such mutations are thought to be one of several possible causes of cardiomyopathy. It has also been reported that these mutations can be acquired under the influence of free radicals and other factors with increasing age [4–6]. In the present study, myocardial mitochondrial DNA mutations were investigated using autopsy materials from diabetic patients as well as patients with other diseases, since diabetes mellitus is one of a number of diseases in which free radicals cause damage to various organs. The data presented in this article include some published previously [7] and additional new data.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   379.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Ozawa T, Tanaka M, Sugiyama S, Hattori K, Ito T, Ohno K, Takahashi A, Sato W, Takada G, Mayumi B, Yamamoto K, Adachi K, Koga Y, Toshima H. 1990. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy. Biochem Biophys Res Commun 170:830–836.

    Article  PubMed  CAS  Google Scholar 

  2. Ozawa T, Tanaka M, Sugiyama S, Ino H, Ohno K, Hattori K, Ohbayashi T, Ito T, Deguchi H, Kawamura K, Nakane Y, Hashiba K. 1991. Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson’s disease and mitochondrial encephalopathy. Biochem Biophys Res Commun 177:518–525.

    Article  PubMed  CAS  Google Scholar 

  3. Obayashi T, Hattori K, Sugiyama S, Tanaka M, Tanaka T, Itoyama S, Deguchi H, Kawamura K, Koga Y, Toshima H, Takeda N, Nagano M, Ito T, Ozawa T. 1992. Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy. Am Heart J 124:1263–1269.

    Article  PubMed  CAS  Google Scholar 

  4. Sugiyama S, Hattori K, Hayakawa M, Ozawa T. 1991. Quantitative analysis of age-associated accumulation of mitochondrial DNA with deletion in human hearts. Biochem Biophys Res Commun 180:894–899.

    Article  PubMed  CAS  Google Scholar 

  5. Hattori K, Tanaka M, Sugiyama S, Obayashi T, Ito T, Satake T, Hanaki Y, Asai J, Nagano M, Ozawa T. 1991. Age-dependent increase in deleted mitochondrial DNA in the human heart: Possible contributory factor to presbycardia. Am Heart J 121:1735–1742.

    Article  PubMed  CAS  Google Scholar 

  6. Hayakawa M, Sugiyama S, Hattori K, Takasawa M, Ozawa T. 1993. Age-associated damage in mitochondrial DNA in human hearts. Mol Cell Biochem 119:95–103.

    Article  PubMed  CAS  Google Scholar 

  7. Takeda N, Tanamura A, Iwai T, Nakamura I, Kato M, Ohkubo T, Noma K. 1993. Mitochondrial DNA deletion in human myocardium. Mol Cell Biochem 119:105–108.

    Article  PubMed  CAS  Google Scholar 

  8. Fein FS, Kornstein LB, Strobeck JE, Capasso JM, Sonneblick EH. 1980. Altered myocardial mechanics in diabetic rats. Circ Res 47:922–933.

    PubMed  CAS  Google Scholar 

  9. Takeda N, Nakamura I, Hatanaka T, Ohkubo T, Nagano M. 1988. Myocardial mechanical and myosin isoenzyme alterations in streptozotocin-diabetic rats. Jpn Heart J 29:455–463.

    Article  PubMed  CAS  Google Scholar 

  10. Takeda N, Ohkubo T, Tanamura A, Iwai T, Nakamura I, Hatanaka T, Nagano M. 1991. Myocardial mechanics and myosin isoenzymes in streptozotocin-induced diabetic rats. In: Nagano M, Dhalla NS, eds. The Diabetic Heart. New York: Raven Press 1991:291–299.

    Google Scholar 

  11. Savarese JJ, Berkowitz BA. 1979. Beta-adrenergic receptor decrease in diabetic rat hearts. Lief Sci 25:2075–2078.

    Article  CAS  Google Scholar 

  12. Heyliger CE, Pierce GN, Singal PK, Beamish RE, Dhalla NS. 1982. Cardiac alpha- and beta-adrenergic receptor alterations in diabetic cardiomyopathy. Basic Res Cardiol 77: 610–618.

    Article  PubMed  CAS  Google Scholar 

  13. Pierce GN, Dhalla NS. 1983. Sarcolemmal Na+-K+-ATPase activity in diabetic rat heart. Am J Physiol 245:C241–C247.

    PubMed  CAS  Google Scholar 

  14. Penpargkul S, Fein F, Sonnenblick EH, Scheuer J. 1981. Depressed cardiac sarcoplasmic reticular function from diabetic rats. J Mol Cell Cardiol 13:303–309.

    Article  PubMed  CAS  Google Scholar 

  15. Ganguly PK, Pierce GN, Dhalla KS, Dhalla NS. 1983. Defective sarcoplasmic reticular calcium transport in diabetic cardiomyopathy. Am J Physiol 244:E528–E535.

    PubMed  CAS  Google Scholar 

  16. Lopaschuk GD, Katz S, McNeill JH. 1983. The effect of alloxan- and streptozotocin-induced diabetes on calcium transport in rat cardiac sarcoplasmic reticulum. The possible involvement of long chain acylcarnitines. Can J Physiol Pharmacol 61:439–448.

    Article  PubMed  CAS  Google Scholar 

  17. Pierce GN, Dhalla NS. 1981. Cardiac myofibrillar ATPase activity in diabetic rats. J Mol Cell Cardiol 13:1063–1069.

    Article  PubMed  CAS  Google Scholar 

  18. Dillmann WH. 1980. Diabetes mellitus induces changes in cardiac myosin of the rat. Diabetes 29:579–582.

    PubMed  CAS  Google Scholar 

  19. Pavlakis S, Phillips PC, DiMauro S, DeVivo DC, Rowland LP. 1984. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Ann Neurol 16: 481–488.

    Article  PubMed  CAS  Google Scholar 

  20. Tanaka M, Ino H, Ohno K, Obayashi T, Ikebe S, Sano T, Ichiki T, Kobayashi M, Wada Y, Ozawa T. 1991. Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Biochem Biophys Res Commun 174:861–868.

    Article  PubMed  CAS  Google Scholar 

  21. Goto Y, Horai S, Matsuoka T, Koga Y, Nihei K, Kobayashi M, Nonaka I. 1992. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A correlative study of the clinical features and mitochondrial DNA mutation. Neurology 42:545–550.

    PubMed  CAS  Google Scholar 

  22. Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC. 1992. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nature Genet 1:11–15.

    Article  PubMed  CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1995 Kluwer Academic Publishers

About this chapter

Cite this chapter

Takeda, N., Tanamura, A., Iwai, T., Hayashi, Y., Nomura, S. (1995). Mutations of Myocardial Mitochondrial DNA in Diabetic Patients. In: Dhalla, N.S., Pierce, G.N., Panagia, V., Beamish, R.E. (eds) Heart Hypertrophy and Failure. Developments in Cardiovascular Medicine, vol 169. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-1237-6_5

Download citation

  • DOI: https://doi.org/10.1007/978-1-4613-1237-6_5

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4612-8526-7

  • Online ISBN: 978-1-4613-1237-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics