| CPC A61K 31/202 (2013.01) [A61K 31/015 (2013.01); A61K 31/05 (2013.01); A61K 31/122 (2013.01); A61K 31/352 (2013.01); A61K 31/353 (2013.01); A61K 31/385 (2013.01); A61K 31/593 (2013.01); A61K 31/7048 (2013.01); A61K 36/53 (2013.01); A61K 45/06 (2013.01)] | 20 Claims |
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1. An oral formulation, comprising:
from 8 wt % to 48 wt % of polyunsaturated fatty acids including EPA and DHA,
additional polyunsaturated fatty acids including alpha lipoic acid (ALA),
from 0.1 wt % to 4 wt % stilbenoid including a member selected from the group consisting of resveratrol, vitisin A, pterostilbene, piceatannolin, astringin, piceid, and combinations thereof,
from 3 wt % to 15 wt % flavonoid including a member selected from the group consisting of flavonol, flavanone, anthocyanin, quercetin, and combinations thereof,
from 0.005 wt % to 2 wt % carotenoid,
from 0.1 wt % to 5 wt % D-limonene, and
from 100 IU to 2,000 IU vitamin D,
wherein the polyunsaturated fatty acids including EPA and DHA, the stilbenoid, the flavonoid, and the vitamin D are present in an amount and at a weight ratio that causes the oral formulation to induce a gene expression profile containing at least 20% of the genes in a gene expression profile of caloric restriction in a muscle tissue of a subject and protects skin cells against ultraviolet radiation when administered to the subject in a therapeutically effective amount, and
wherein the stilbenoid and the polyunsaturated fatty acids including EPA and DHA are present in the oral formulation at a weight ratio of from 1:50 to 1:20 of the stilbenoid to the polyunsaturated fatty acids including EPA and DHA.
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