Okayama Igakkai Zasshi (Journal of Okayama Medical Association)
Online ISSN : 1882-4528
Print ISSN : 0030-1558
Studies on Coenzyme Q Contents in Serum Lipoproteins
Part II. Changes in the Concentrations of Coenzyme Q9 and α-tocopherol in Rats with Isoproterenol Induced Myocardial Necrosis
Nobuhito MINAMI
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1984 Volume 96 Issue 1-2 Pages 171-179

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Abstract

Myocardial necrosis was induced experimentally by the method of Rona, and coenzyme Q9 and α-tocopherol concentrations were measured in the serum and lipoprotein fractions. There was no significant change in the serum coenzyme Q9 concentrations after isoproterenol administration. In contrast, the serum α-tocopherol levels decreased 6h and 12h after the administration, and the α-tocopherol-cholesterol ratio decreased within 12h. In control subjects, most of coenzyme Q9 was distributed in the VLDL and LDL fractions, while most of α-tocopherol was present in the HDL fraction. The coenzyme Q9 levels decreased 6h, 12h and 24h after isoproterenol administration in VLDL, and the lowest level was at 12h. On the other hand, the coenzyme Q9 level elevated within 12h in the LDL fraction. The α-tocopherol level decreased rapidly in the VLDL fraction, reaching a minimum within 6h, and showed an increase at 12h in the LDL fraction. There was no significant change in the HDL fraction. The coenzyme Q9-cholesterol ratio increased within 12h in the LDL fraction and within 6h in the HDL fraction. The α-tocopherol-cholesterol ratio decreased within 6h in the VLDL and HDL fractions, while there was no significant change in the LDL fraction. The coenzyme Q9-α-tocopherol ratio increased within 6h in the VLDL and HDL fractions and within 12h in the serum and LDL fraction. These results indicate that the metabolism of coenzyme Q9 is different from that of α-tocopherol in lipoproteins. It is concluded that coenzyme Q is mainly transported from VLDL (and chylomicron) to LDL at the onset of acute vascular accidents, for the lipase activity is stimulated by hormones, and then coenzyme Q is carried from LDL and HDL to mitochondria rich organs through the LDL receptor or other routes.

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