Abstract
Di-α-tocopherone, a recently characterized metabolite of α-tocopherol isolated from animal tissues, was tested for biological activity with respect to resorption-gestation in Vit. E-deficient rats, nutritional muscular dystrophy in rabbits and hereditary muscular dystrophy in mice. The results indicate that this metabolite has less than 5% of the Vit. E activity of α-tocopherol and that it possesses no therapeutic value in treatment of the congenital myopathy. Its probable role in metabolism is that of a terminal oxidation product rather than an active form of Vit. E.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 242-245 |
| Number of pages | 4 |
| Journal | Proceedings of the Society for Experimental Biology and Medicine |
| Volume | 113 |
| Issue number | 1 |
| DOIs | |
| State | Published - May 1963 |
Bibliographical note
Funding Information:Supported by a grant from National Science Foundation.