Volume 11 Supplement 1
Phosphatidic acid feeding increases muscle protein synthesis and select mTORC1 pathway signaling mediators in rodent skeletal muscle
© Mobley et al; licensee BioMed Central Ltd. 2014
Published: 1 December 2014
Human and cell culture studies have demonstrated that phosphatidic acid (PA) can increase muscle mass and anabolic signaling, respectively. However, no in vivo evidence to date has examined whether PA can increase intramuscular anabolic signaling in vivo. The purpose of this study was to examine – a) if PA feeding acutely increases post-prandial muscle protein synthesis (MPS) and anabolic signaling markers; and b) if PA can enhance the post-prandial anabolic effects of whey protein concentrate (WPC).
Male Wistar rats (~250 g) were fasted overnight (~18 h) and fed either: a) 1 ml water (n = 14), b) 28 mg PA (eq. to 1.5 g human dose; n = 8), c) 197 mg WPC (eq. to 10 g human dose; n = 8), or d) PA+WPC (n = 8). 2.5 h post-feeding rats were injected with 5.44 mg puromycin diHCl for MPS assessment via SUnSET and 3 hours post-feeding rats were euthanized and mixed gastrocnemius muscles were removed for immunoblotting analyses. The treatment of the animals in this study adhered to commonly accepted ethics guidelines.
Compared to water-fed rats, PA feeding caused an elevation in numerous Akt-mTOR markers and, in some instances, PA+WPC exhibted a greater increase in Akt-mTOR signaling markers (Erk1/2 Thr202/Tyr204, Bad Ser112, p70s6k Thr389). However, compared to water-fed rats, the PA, WPC, and PA+WPC groups exhibited greater MPS responses with no differences existing between conditions.
This is the first in vivo data demonstrating that PA feeding increases MPS. More post-prandial time course data with resistance exercise is needed to better elucidate how PA feeding affects muscle anabolism.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.