Apple Skin Extracts for Treating Cardiovascular Disease
Pharmaceutical and nutraceutical compositions and methods for treating cardiovascular disease, comprising apple skin extracts which can reduce cholesterol levels and inhibit low density lipoprotein (LDL) oxidation in a subject, are provided.
1 . A method for reducing the concentration of a serum lipid in a subject, comprising administering to the subject a composition comprising:
chlorogenic acid;
epicatechin;
quercetin-3-O-galactoside; and
quercetin-3-O-glucoside;
such that the concentration of the serum lipid is reduced in the subject when compared to the concentration of the serum lipid in a control group consuming an atherogenic diet.
2 . The method of claim 1 , wherein the composition comprises an apple peel extract.
3 . The method of claim 1 , wherein the composition inhibits oxidation of low density lipoprotein (LDL) in the subject.
4 . (canceled)
5 . The method of claim 1 , wherein reducing the concentration of a serum lipid comprises reducing the serum concentration of triglycerides, total cholesterol, non-high density lipoprotein-cholesterol (non-HDL-cholesterol), or any combination thereof.
6 . The method of claim 1 , wherein reducing the concentration of a serum lipid in the subject comprises reducing serum total cholesterol by at least about 12%, reducing serum non-HDL cholesterol by at least about 30%, or both.
7 . The method of claim 1 wherein administration of the composition increases the concentration of serum HDL cholesterol in the subject when compared to the concentration of serum HDL cholesterol in a control group consuming an atherogenic diet.
8 . A pharmaceutical or nutraceutical composition comprising:
chlorogenic acid;
epicatechin;
quercetin-3-O-galactoside; and
quercetin-3-O-glucoside.
9 . (canceled)
10 . The composition of claim 8 , wherein the composition is a functional food, a dietary supplement, or a food or beverage product.
11 - 15 . (canceled)
16 . The pharmaceutical or nutraceutical composition of claim 8 wherein in vitro administration of the composition inhibits at least 75% of Cu induced primary LDL oxidation products when the composition is administered at a concentration between about 0.5 and 10 mg/L.
17 . The pharmaceutical or nutraceutical composition of claim 8 wherein in vitro administration of the composition inhibits at least 75% of Cu induced secondary LDL oxidation products when the composition is administered at a concentration between about 0.5 and 5 mg/L.
18 . The pharmaceutical or nutraceutical composition of claim 8 wherein in vitro administration of the composition inhibits at least 40% of peroxyl radical-induced primary LDL oxidation products when the composition is administered at a concentration between about 5 and 10 mg/L.
19 . The pharmaceutical or nutraceutical composition of claim 8 wherein in vitro administration of the composition inhibits at least 75% of peroxyl radical-induced secondary LDL oxidation products when the composition is administered at a concentration between about 1 and 10 mg/L.
20 . The pharmaceutical or nutraceutical composition of claim 8 wherein the peroxyl radical-induced secondary LDL oxidation products are induced using 2,2′-azobis(2-methylpropionamidine)dihydrochloride (AAPH).