Scientific Study
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Products: Dried Cranberry
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The effect of cranberry consumption on lipid metabolism and inflammation in human apolipoprotein AI transgenic mice fed a high-fat and high-cholesterol diet.
Authors: Caceres, C., Kim, M. B., Bae, M., Pham, T. X., Lee, Y., Hu, S., ... & Lee, J. Y.
- Journals: Br J Nutr
- Pages:
- Year: 2020
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Lipid metabolism and inflammation contribute to cardiovascular disease development. This study investigated whether the consumption of cranberry (CR; Vaccinium macrocarpon) can alter high-density lipoprotein (HDL) metabolism and prevent inflammation in mice expressing human apolipoprotein A-I transgene (hApoAITg), which have similar HDL profiles to those of humans. Male hApoAITg mice were fed a modified American Institute of Nutrition-93M high-fat/high-cholesterol diet (16% fat, 0.25% cholesterol, w/w; n=15) or high-fat/high-cholesterol diet containing CR (5 % dried CR powder, w/w, n=16) for 8 weeks. There were no significant differences in body weight between the groups. Serum total cholesterol, non-HDL cholesterol and triglyceride concentrations were significantly lower in control than CR group with no significant differences in serum HDL-C and apoA-I. Mice fed CR showed significantly higher serum lecithin-cholesterol acyltransferase activity than the control. Liver weight and steatosis were not significantly different between the groups, but hepatic expression of genes involved in cholesterol metabolism was significantly lower in the CR group. In the epididymal white adipose tissue (eWAT), the CR group showed higher weights with decreased expression of genes for lipogenesis and fatty acid oxidation. The mRNA abundance of F4/80, a macrophage marker, and the numbers of crown-like structures were less in the CR group. In the soleus muscle, the CR group also demonstrated higher expression of genes for fatty acid β-oxidation and mitochondrial biogenesis than those of the control. In conclusion, although CR consumption elicited minor effects on HDL metabolism, it prevented obesity-induced inflammation in eWAT with concomitant alterations in soleus muscle energy metabolism.