Liver and skeletal muscle ceramides in alloxan-induced diabetes

Cover Page

Cite item

Full Text

Abstract

Aim. To study of liver and sceletal muscle ceramides in alloxan-induced diabetes at different periods after alloxan exposure. Methods. Repeated experiments were performed on white male rats. Diabetes was modeled by alloxan hydrochloride solution intraperitoneal injection. The disease development was monitored using clinical and laboratory parameters. Ceramides in tissues were determined in intact animals (control), at the 10, 20, 30, 45 and 60 day after the alloxan injection. Ceramides level in the plates was determined by thin layer chromatography using the external standard. Results. In intact animals, ceramides level in liver was twice as high as in muscle. At all terms after alloxan injection, ceramide level was significantly higher compared to controls, and was in muscle compared to liver, with similar change pattern. Up to the 20th day, a significant increase of ceramide level was observed compared to control (eightfold in liver and sevenfold in muscle). By 30th day, a partial recovery was registered, followed by subsequent increase of ceramide level. This indicates the influence of compensation mechanisms in the early stages of the experiment with further decompensation on late stages. Conclusion. In alloxan-induced type 1 diabetes, ceramide level in insulin-dependent tissues depends on the term after the alloxan injection; the findings are of great importance for the research of secondary insulin resistance, as well as other diabetes-associated pathological conditions, exact mechanisms.

About the authors

M R Bagautdinov

Izhevsk State Medical Academy, Izhevsk, Russia; Republican Clinical Hospital for Mental Diseases, Izhevsk, Russia

Email: vesalii@mail.ru

References

  1. Алеева Г.Н., Киясов А.П., Миннебаев М.М. Динамика β- и α-клеточных популяций поджелудочной железы и содержания глюкозы в крови крыс при аллоксановом диабете // Бюл. эксперим. биол. и мед. - 2002. - №2. - С. 151-153.
  2. Бочаров Е.Ф., Шестенко О.П. Экспериментальные модели сахарного диабета // Вопр. вирусол. - 1986. - Т. 31, №4. - C. 393-400.
  3. Хиггинс Д.А. Разделение и анализ липидных компонентов мембран. Биологические мембраны: методы / Под ред. Дж.Б. Финдлей. - М.: Медицина, 1990. - С. 151-195.
  4. Adams J.M., Pratipanawatr T., Berria R. et al. Ceramide content is increased in skeletal muscle from obese insulin-resistant humans // Diabetes. - 2004. - Vol. 53. - P. 25-31.
  5. Aerts J.M., Ottenhoff R., Powlson A.S. et al. Pharmacological inhibition of glucosylceramide synthase enhances insulin sensitivity // Diabetes. - 2007. - Vol. 56, N 5. - P. 1341-1349.
  6. Folch J., Less M., Sloan-Stanley G.N. A simple method for isolation and purification of total lipid from animal tissues // J. Biol. Chem. - 1957. - Vol. 226, N 2. - P. 497-499.
  7. Gorska M., Dobrzyn A., Zendzian-Piotrowska M., Gorski J. Effect of streptozotocin-diabetes on the functioning of the sphingomyelin signaling pathway in skeletal muscle of the rat // Horm. Metab. Res. - 2004. - Vol. 36. - P. 14-21.
  8. Langeveld M., Aerts J.M. Glycosphingolipids and insulin resistance // Prog. Lipid. Res. - 2009. - Vol. 48, N 3-4. - P. 196-205.
  9. Straczkowski M., Kowalska I., Nikolajik A. et al. Relationship between insulin sensitivity and sphingomyelin signaling pathway in human skeletal muscle // Diabetes. - 2004. - Vol. 53. - P. 1215-1221.
  10. Summers S.A. Ceramides in insulin resistance and lipotoxicity // Prog. Lipid. Res. - 2006. - Vol. 45, N 1. - P. 42-72.
  11. Tong M., de la Monte S.M. Mechanisms of ceramide-mediated neurodegeneration // J. Alzheimers. Dis. - 2009. - Vol. 16, N 4. - P. 705-714.
  12. Uruska A., Araszkiewicz A. Insulin resistance in patients with type 1 diabetes // Pediatr. Endocrinol. Diabetes Metab. - 2009. - Vol. 15, N 2. - Р. 19-23.
  13. Yang G., Badeanlou L., Bielawski J. et al. Central role of ceramide biosynthesis in body weight regulation, energy metabolism and the metabolic syndrome // Am. J. Physiol. Endocrinol. Metab. - 2009. - Vol. 12. - Р. 211-224.

© 2014 Bagautdinov M.R.

Creative Commons License

This work is licensed
under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.





This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies