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Summary

Changes in metabolism of lipidperoxides was observed in rats in which myocardial infarction was induced by isoproterenol. The mortality rate in isoproterenol treated animals were high (35% to 40%). Histopathological examination of the heart tissues showed extensive confluent necrosis of the myocardium with interfascicular spaces of edema. Degeneration of muscle fibers resulting in disintegration of sarcoplasm and nuclear fragmentation. Confluent lesions were observed in the apex and papillary muscles with focal lesions in other areas of the ventricle. Biochemical studies showed that there was an increase in the levels of lipidperoxide, free fatty acids, glutathione, taurine and decrease in activity of superoxide dismutase and catalase, during experimental myocardial infarction. The effect of administration of Vitamin A, Vitamin C, Vitamin E, and a fatty acid transmembrane transport molecule carnitine on the severity of myocardial infarction was also studied in rats. Judging from the mortality and histopathological studies, it was observed that the order of protection offered to the myocardium from experimental myocardial infarction is as follows — carnitine, Vitamin A, Vitamin C and Vitamin E offered the least protection.

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References

  • Burton, K.P. (1984) Fed. Proc. 43, 294–297i

    Google Scholar 

  • Cheesman, H.K., Collins, M., Proudfoot, K., Slater, T.F., Buron, W.G., Webb, A.C. and Ingold, K.U. (1986) Biochem. J. 235, 507–514.

    Google Scholar 

  • Chubb, J. and Huxtable, R.J. (1978) Eur. J. Pharmacol. 48. 357–367.

    Article  Google Scholar 

  • DiLuzio, N.R. (1973) Fed. Proc. 32, 1875–1881.

    Google Scholar 

  • Dolora, P. Ledda, F., Mugelli, A., Mantelli, L., Zilletti, Franconi, F & Giotti, A. (1978) in Taurin and neurological disorders (Barbean, A & Nuxlabb TJ Eds.) Raven Press, 151. Dormandy, J.A.,

    Google Scholar 

  • Hoare, E., Khattab, A.H., Arrowsmith, D.E., and Dormandy, T.L. (1973). Br. Med. J. 4, 581–583.

    Article  Google Scholar 

  • Goldstein, B.D. and Balchum, O.J. (1967) Proc. Soc. Exp. Biol. Med. 126, 356–358.

    Google Scholar 

  • Gudbjarnason, S., Emillson, A. and Gudmundsdottir, A. (1983). In: Arterial Pollution (H. Peeters, G.A. Gresham and R. Paoletti Eds.) Pleenum Publishing Co. 115–124.

    Google Scholar 

  • Itaya, K. (1977) J. Lipid. Res. 18, 663–665.

    Google Scholar 

  • Kakkar, P., Das, B. and Viswanafh-, P.N. (1984) Ind. J. Biochem. Biophys. 21, 130–132.

    Google Scholar 

  • Kumari, S.S. and Menon, V.P. (1987). Ind. J. Exp. Biol. 25, 419–423.

    Google Scholar 

  • Kumari, S.S. and Menon, V.P. (1988) J. Biosci. 13, 257–262.

    Article  Google Scholar 

  • Lenninger, A.L. and Schneider, M. (1959) J. Biophys. Biochem. Cytol. 5, 109–116.

    Article  Google Scholar 

  • Machlay, A.C. and Chance, B. (1954) In: Methods of Biochemical analysis (D. Glick Ed.) Interscience, New York. 1, 357–424.

    Google Scholar 

  • Meerson, F.Z. (1980) Basic Res. Cardiol. 75, 479–500.

    Article  Google Scholar 

  • Myers, L.S. (1973) Fed. Proc. 32, 1882–1894.

    Google Scholar 

  • Neely, J.R. and Morgan, H.E. (1974) Ann. Rev. Physiol. 36, 413–459.

    Article  Google Scholar 

  • Nichans Jr., W.G. and Sammuelsson, B. (1968) Eur. J. Biochem. 6, 126–130.

    Article  Google Scholar 

  • Opie, L.H. (1969) Amer. Heart J. 77, 100–122

    Article  Google Scholar 

  • Parker Jr., C.J. (1980) Anal. Biochem. 108, 303–305.

    Article  Google Scholar 

  • Patterson, I.W. and Lazarow, A. (1955) In: Methods of Biochemical analysis (D. Glick Ed.) Interscience, New York. 2, 259–278.

    Chapter  Google Scholar 

  • Takenchu, N., Tanaka, F., Katayama, Y., Matsumiya, K., and Yamamura, Y. (1976) Exp. Gerontol. 11, 179–185.

    Article  Google Scholar 

  • Thomas, H.A., Mueller, P.K., and Lyaman, R.L. (1968) Science 159, 532–537.

    Article  Google Scholar 

  • Wittmer, J. T., Idell Wenger, J.A., Rovetto, M. J., and Neely, J.R. (1978) J. Biol. Chem. 253. 4305–4309.

    Google Scholar 

  • Xia, Y., Hill, K.E. and Burk, R.F. (1985) J. Nutr. 115, 733–742.

    Google Scholar 

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© 1992 Birkhäuser Verlag, Basel/Switzerland

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Menon, V.P., Kumari, S.S., Jayadeep, A., Kumar, J.S.S., Mathew, S., Kurup, P.A. (1992). Effect of Different Antioxidants in Experimental Myocardial Infarction. In: Ong, A.S.H., Packer, L. (eds) Lipid-Soluble Antioxidants: Biochemistry and Clinical Applications. Molecular and Cell Biology Updates. Birkhäuser Basel. https://doi.org/10.1007/978-3-0348-7432-8_37

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  • DOI: https://doi.org/10.1007/978-3-0348-7432-8_37

  • Publisher Name: Birkhäuser Basel

  • Print ISBN: 978-3-0348-7434-2

  • Online ISBN: 978-3-0348-7432-8

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