Article citationsMore>>
Volek, J.S., Volk, B.M., Gómez, A.L., Kunces, L.J., Kupchak, B.R., Freidenreich, D.J., Aristizabal, J.C., Saenz, C., Dunn-Lewis, C., Ballard, K.D., Quann, E.E., Kawiecki, D.L., Flanagan, S.D., Comstock, B.A., Fragala, M.S., Earp, J.E., Fernandez, M.L., Bruno, R.S., Ptolemy, A.S., Kellogg, M.D., Maresh, C.M. and Kraemer, W.J. (2013) Whey Protein Supplementation during Resistance Training Augments Lean Body Mass. Journal of the American College of Nutrition, 32, 122-135.
https://doi.org/10.1080/07315724.2013.793580
has been cited by the following article:
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TITLE:
Whey Protein Intake Modulates Lipid Metabolism by Transcriptionally Affecting PPARs and SREBP1c and Their Downstream Enzymes in Mice
AUTHORS:
Hajime Sasaki
KEYWORDS:
Whey Protein, Lipid Metabolism, PPARs, SREBP1c
JOURNAL NAME:
Food and Nutrition Sciences,
Vol.10 No.9,
September
3,
2019
ABSTRACT: Background: The effects of whey protein intake on the transcriptional expression of
genes related to lipid metabolism in mice were investigated herein. Methods: For 4 weeks, mice were fed AIN-93G composed of either casein or whey
protein as the protein source. Then the gastrocnemius muscle, liver, and
epididymal adipose tissue were excised. Expression levels of the transcription
factors, PPARα, PPARγ, and SREBP1c, and those of the enzymes modulated by these factors, HSL,
LPL, ACCα, and FAS, were measured by real-time PCR. The effects of whey protein
were compared to those of the case in control. Results: The mRNA expression of PPARα was enhanced in the gastrocnemius muscle, while that of PPARγ was increased in the liver and epididymal adipose tissue. The expression
of HSL and LPL was increased in the epididymal adipose tissue and gastrocnemius
muscle, respectively. The mRNA expression of SREBP1c was suppressed in all of
the three tissues. The expression of ACCα was suppressed in the gastrocnemius muscle and liver, while that of FAS
was suppressed in all of the three tissues. Conclusions: These results
indicate that whey protein intakes transcriptionally modulate PPARs and SREBP1c
directing lipid metabolism toward the enhancement of triglyceride breakdown and
suppression of fatty acid synthesis.
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