Effects of dietary protein restriction on muscle fiber characteristics and mTORC1 pathway in the skeletal muscle of growing-finishing pigs
© The Author(s). 2016
Received: 30 December 2015
Accepted: 5 August 2016
Published: 22 August 2016
To investigate the effects of dietary crude protein (CP) restriction on muscle fiber characteristics and key regulators related to protein deposition in skeletal muscle, a total of 18 growing-finishing pigs (62.30 ± 0.88 kg) were allotted to 3 groups and fed with the recommended adequate protein (AP, 16 % CP) diet, moderately restricted protein (MP, 13 % CP) diet and low protein (LP, 10 % CP) diet, respectively. The skeletal muscle of different locations in pigs, including longissimus dorsi muscle (LDM), psoas major muscle (PMM) and biceps femoris muscle (BFM) were collected and analyzed.
Results showed that growing-finishing pigs fed the MP or AP diet improved (P < 0.01) the average daily gain and feed: gain ratio compared with those fed the LP diet, and the MP diet tended to increase (P = 0.09) the weight of LDM. Moreover, the ATP content and energy charge value were varied among muscle samples from different locations of pigs fed the reduced protein diets. We also observed that pigs fed the MP diet up-regulated (P < 0.05) muscular mRNA expression of all the selected key genes, except that myosin heavy chain (MyHC) IIb, MyHC IIx, while mRNA expression of ubiquitin ligases genes was not affected by dietary CP level. Additionally, the activation of mammalian target of rapamycin complex 1 (mTORC1) pathway was stimulated (P < 0.05) in skeletal muscle of the pigs fed the MP or AP diet compared with those fed the LP diet.
The results suggest that the pigs fed the MP diet could catch up to the growth performance and the LDM weight of the pigs fed the AP diet, and the underlying mechanism may be partly due to the alteration in energy status, modulation of muscle fiber characteristics and mTORC1 activation as well as its downstream effectors in skeletal muscle of different locations in growing-finishing pigs.
KeywordsDietary protein restriction Energy status Growing-finishing pigs mTORC1 Muscle fiber type
The skeletal muscle, which accounts for 20–50 % of total body mass, is the primary metabolic tissue, contributing up to 40 % of the resting metabolic rate [1, 2]. Meanwhile, it also acts as an endocrine organ, regulating the disposal of nutrient and energy consumption in the body by secreting myokines, such as interleukin (IL)-6 and IL-15 [3, 4]. Thus, development and maintenance of skeletal muscle are crucial for body health and life quality .
Mammalian target of rapamycin complex 1 (mTORC1) plays a key role in protein synthesis of skeletal muscle [6, 7], and constitutively consist of mTOR, regulatory associated protein of mTOR (Raptor), and mLST8/GβL [8, 9]. In brief, Raptor functions positively in mTORC1 pathway by acting as an adaptor to recruit substrates to mTOR [8, 9]. Additionally, mTORC1 promotes mRNA translation through multiple downstream effectors such as eukaryotic initiation factor (eIF) 4E-binding protein1 (4E-BP1) and p70S6 kinase (S6K1), resulting in protein synthesis . On the other hand, protein degradation in skeletal muscle is primarily mediated by activation of the ubiquitin (Ub)-proteasome pathway (UPP). There are two specific E3 ubiquitin ligases belonging to the UPP, muscle ring finger 1 (MuRF1) and muscle atrophy F-box (MAFbx), both are proposed to be central to the control of muscle proteolysis . Actually, protein deposition depends on the balance between the rates of protein synthesis and degradation.
It is well known that feeding-induced stimulation of protein deposition is most pronounced in skeletal muscle . Several studies reported that a high protein diet contributed to muscle mass raise [13–18]. However, over the past few years, some studies pointed out that a high protein diet failed to translate into muscle mass [19, 20], suggesting that a high protein intake may not necessarily lead to accumulation of muscle protein. In addition, numerous studies showed that chronic feeding of a low protein diet impaired activation of translation initiation, consequently reducing protein synthesis . Besides, maternal low protein diet during gestation and lactation could regulate myostatin pathway and protein synthesis in skeletal muscle of offspring at weaning stage . All the findings confirmed that a very important role for dietary protein level in modulating protein metabolism and muscle growth, but less is known about the mechanisms of protein deposition and myofiber development of the pigs influenced by a moderately restricted protein diet.
In general, skeletal muscle fiber types are distinguished according to the predominantly expressed isoform of myosin heavy chain (MyHC), which are referred to as type I, IIa, IIx and IIb [23–25]. Myofiber type proportions of longissimus dorsi muscle (LDM), psoas major muscle (PMM) and biceps femoris muscle (BFM) are varied due to their anatomical location (Additional file 1: Table S1) and thus they have different metabolic properties. Previous research conducted in the rats during periods of fasting observed that the degree of reduction in protein synthesis was not similar in various muscles [26, 27]. This led us to hypothesize that the expression levels for MyHC and muscle development regulators genes could specifically modulated in different muscle of pigs by protein-restricted diet. Therefore, the present study aimed to investigate the effects of restricted protein diet on growth performance, muscle fiber characteristics and protein expression of key molecules related to mTORC1 pathway in different locations of skeletal muscle of pigs.
All experimental procedures in the present study were reviewed and approved by the Animal Care and Use Committee of the Chinese Academy of Sciences.
Animals and diets
Ingredient composition and nutrient levels of the experimental diets (as-fed basis, %)
AP (16 % CP)
MP (13 % CP)
LP (10 % CP)
Ingredient composition, %
Nutrient levels, %
Met + Cys
Tissue sample collection
At the end of the trial, all the pigs were fasted overnight and sacrificed. Pigs were stunned by electrical shock (250 V, 0.5 A, for 5 to 6 s), exsanguinated, and eviscerated in a slaughterhouse. The head was removed, and the carcass was split longitudinally. Skeletal muscle tissue including LDM, PMM and BFM were dissected and weighted. Samples (about 2 × 1 × 1 cm) from LDM, PMM, and BFM were rapidly excised and immediately frozen in liquid nitrogen, then stored at -80 °C until analysis.
Measurement of ATP, ADP and AMP levels of skeletal muscle
Contents of ATP, ADP and AMP in skeletal muscle were determined according to previous publications with some modification . Tissue extracts (100 mg) were prepared from frozen LDM, PMM and BFM (within 1 wk after slaughter), using 1 mL 5 % perchloric acid, and the extracts were centrifuged at 13,000 × g for 8 min at 4 °C. The supernatants were neutralized with 2 mol/L KHCO3 and centrifuged again. The standards of ATP (FLAAS), ADP (A5285), AMP (01930) were purchased from Sigma (Sigma-Aldrich, MO, USA). High performance liquid chromatography (HPLC) was performed with a reverse-phase column (99603, C18, 5 μm, 250 × 4.6 mm, Dikma Technologies Inc.) and the column temperature was set at 25 °C. For measurements of metabolites, a mobile phase consisting of 215 mmol/L KH2PO4, 1.2 mmol/L tetrabutylammonium bisulfate, 1 % acetonitrile (pH 6.0) was used and the flow rate was maintained at 0.8 mL/min by a HPLC pump (600E; Waters, MA, USA). Eluted samples were detected at 260 nm with a dual λ absorbance detector (2478, Waters). Calibration curves were prepared by a six-point standard (0.2, 0.1, 0.05, 0.025, 0.0125 and 0.00625 mg/mL) of ATP, ADP and AMP in 0.6 mol/L perchloric acid, respectively. Total energy charge (EC) was calculated according to the equation: EC = (ATP + 0.5ADP)/(ATP + ADP + AMP).
RNA extraction and cDNA synthesis
Total RNA was isolated from LDM, PMM, and BFM samples using TRizol Reagent (Invitrogen-Life Technologies, CA, USA) [29, 30]. The integrity of RNA was evaluated by 1 % agarose gel electrophoresis. The concentration of the extracted RNA was checked by spectrophotometry using NanoDrop ND2000 (NanoDrop Technologies Inc., DE, USA), and purity of RNA was assessed by using the A260/A280 ratio, which ranged from 1.8–2.0. About 1.0 μg of total RNA was incubated with DNase I (Fermentas, WI, USA), and later used for reverse transcription using First-Strand cDNA Synthesis Kit according to the manufacturer’s protocol. The cDNA was synthesized with Oligo dT and superscript II reverse-transcriptase, and the cDNA were stored at -80 °C before further processing.
Quantitative real-time PCR
The Primers used for real-time PCR analysis
Primer sequences (5’→3’)
Product size, bp
Western blotting analysis
Western blot analysis was conducted according to the previous study . Briefly, about 30–50 μg of total protein extracted from muscle samples was separated by reducing SDS-PAGE electrophoresis. Western blots were incubated with primary antibodies rabbit anti- phospho (p)-mTOR (Ser2448, Cell Signaling Technology, USA), p-Raptor (Ser863, Santa Cruz Biotechnology, USA), p-4E-BP1 (Ser65, Cell Signaling Technology, USA) or p-S6K1 (Thr389, Cell Signaling Technology, USA) at a dilution of 1:1,000 after blocking with 5 % nonfat milk. The membranes were then rinsed in TBST and incubated with second antibody peroxidase-conjugated anti-goat or anti-rabbit IgG (Santa Cruz Biotechnology, Santa Cruz, CA) for 1 h at a dilution of 1:5,000. For examining the equal loading, mouse anti-β-actin (Santa Cruz Biotechnology, USA) diluted at 1:5,000 was used as internal control. Finally, the bands of the protein were visualized using a chemiluminescent reagent (Pierce, Rockford, USA) with a ChemiDoc XRS system (Bio-Rad, Philadelphia, PA, USA). We quantified the resultant signals using Alpha Imager 2200 software (Alpha Innotech Corporation, CA, USA) and normalized the data with inner control.
Data obtained from this study was analyzed by the One-way analysis of variance (ANOVA) using SAS 8.2 software (Cary, NC, USA) followed by a Duncan’s multiple comparison test. Differences between significant means were considered as statistically different at P < 0.05 and a trend toward significance at P < 0.10.
Growth performance and skeletal muscle mass weight
Growth performance and skeletal muscle mass weight of growing-finishing pigs fed the restricted protein diets1
AP (16 % CP)
MP (13 % CP)
LP (10 % CP)
Initial body weight, kg
Final body weight, kg
Average daily gain, g/d
Average daily feed intake, g/d
Longissimus dorsi muscle, g
Psoas major muscle, g
Biceps femoris muscle, g
Contents of ATP, ADP, AMP and EC value in skeletal muscle
Effect of the restricted protein diets on the content of ATP, ADP, AMP and EC value in the skeletal muscle of different locations of growing-finishing pigs1
AP (16 % CP)
MP (13 % CP)
LP (10 % CP)
Longissimus dorsi muscle
Psoas major muscle
Biceps femoris muscle
Gene mRNA expression of MyHC isoforms
Myokines, myogenic regulatory factors (MRFs) and E3 ubiquitin ligases associated genes mRNA expression
Protein expression of key molecules related to mTORC1 pathway
The present study showed that feeding the LP diet (10 % CP) to the growing-finishing pigs significantly retarded the growth performance even though the diet was supplemented with the limited amino acids. However, feeding the MP diet (13 % CP) restored the growth performance of pigs compared with those fed the LP diet. Furthermore, the MP diet improved the feed conversion efficiency of pigs to a level similar to that of AP diet (16 % CP), which is consistent with the previous studies that the growth response was unaffected in pigs fed the slightly low-protein diet [32–37]. In addition, a trend to significance was observed in the LDM weight of the MP-fed pigs relative to the other two groups. Overall, the results of the current study suggests that moderately restricted CP level in the diet would not negatively influence growth performance of the growing-finishing pigs, but an excessively reduced CP level in the diet could impair growth and development of the pigs.
The skeletal muscle, including LDM, PMM and BFM, is a highly heterogeneous tissue, mainly composed of myofiber types: oxidative (I and IIa), glycolytic (IIb) and intermediate (IIx) [38–40]. The tissues of LDM, PMM, BFM mainly contain the fiber type of IIb, whereas PMM contains higher oxidative type (I and IIa) than LDM or BFM, and for BFM, the proportion of type I fiber is higher than LDM, but for other fiber types the proportion is almost intermediate (Additional file 1: Table S1). The pigs fed the MP diet up-regulated mRNA expression of the oxidative isoform-MyHC IIa in the three types of skeletal muscle compared with those fed the LP- and/or AP diet, and the value of MyHC I in pigs fed the MP diet was higher than that of the LP-fed pigs in BFM only, whereas the mRNA levels of type IIb and IIx were unaffected by dietary CP level. Similar results have been reported previously that the proportion of oxidative isoforms was higher, while MyHC IIb was lower in the muscle of pigs fed the low CP diet than those fed the high CP diet [41–43]. Oxidative isoforms (I and IIa) fibers have a better aerobic ability  and a higher capacity to synthesize protein . Furthermore, several studies have found that fiber type composition produces important impacts on meat quality, for example, the increasing proportion of MyHC I fiber could be expected to improve tenderness of meat . Based on these, our findings indicate that feeding the MP diet to growing-finishing pigs might have a potential improvement of myofiber phenotype which is beneficial to meat quality.
Myofiber isoforms composition influences the biochemical and metabolic properties along with energy metabolism in the skeletal muscle of livestock animals and humans [47–49]. Thus we evaluated the energy status of LDM, PMM and BFM via determining the content of ATP, ADP, AMP and EC value. Interestingly, the values of those parameters were altered differently in various skeletal muscle locations of pigs fed the restricted protein diets. In specific, the highest ATP content and EC value were observed in LDM of the MP-fed pigs, PMM of the AP-fed pigs and BFM of the LP-fed pigs, respectively. Generally, low energy status induces AMP-activated protein kinase signaling pathway, the subsequent increase in the rate of myofiber degradation limits the fiber size and inhibits the mTORC1 pathway to facilitate the restoration of cellular energy status . It means that in order to maintain energy homeostasis, intracellular lower energy status could inhibit translational initiation and protein synthesis through down-regulating mTOR pathway . In another way, the energy status limitation has also linked to protein degradation via increasing the expression level of E3 ligases (MuRF1 and MAFbx) . Unexpectedly, in this study, restricted protein diet did not alter the mRNA abundance of MuRF1 and MAFbx in all three locations of the skeletal muscle.
Multiple data have indicated that the myogenic regulatory factors (MRFs) -MyoD and MyoG- relevant to muscle development and plasticity. The MyoD acts early in myogenesis to determine myogenic fate, while MyoG functions later in the differentiation of myoblasts into myotubes . Besides, MyoD is a potent activator of fast transcription in skeletal muscle, and it also directly acts on type II MyHC promoters and other fibre-type-specific promoters . Our results showed that the MP diet induced higher mRNA levels of MyoD and MyoG in BFM but not in LDM and PMM. It is likely that the increase of MyHC IIa responded to the MP diet was concomitant with the up-regulation of MRFs in the pigs. It is widely accepted that the expression level of myokine IL-6 is relatively high in the oxidative muscle fiber . Myokine IL-15, as a novel anabolic factor for skeletal muscle, is able to stimulate the accumulation of contractile proteins in the differentiated myocytes or muscle fibers , suggesting its critical role in muscle fiber development. In our experiment, the mRNA levels of IL-15 in the different locations of muscle tissue (LDM, PMM and BFM) were all markedly enhanced in pigs fed the MP diet compared to those fed the LP- and/or AP diet, indicating MP-fed pigs had a high capacity of protein deposition in the muscle tissue.
The activation of mTOR has been considered as nutrient and energy sensor of the cell and plays a prominent role in the regulation of protein synthesis [55–57]. The Raptor is a core component of mTORC1 primarily mediating cellular growth in response to anabolic stimuli. In the present study, we found that protein levels of p-mTOR were all up-regulated in the LDM, PMM and BFM of pigs fed the MP or AP diet compared with those fed the LP diet. Tendencies of the protein levels of p-Raptor and p-4E-BP1 were the same as that of p-mTOR in LDM, but in PMM there were no difference in the expression levels of the selected protein among treatments except for p-mTOR; in BFM, the protein level of p-4E-BP1 exerted the same tendency as p-mTOR, however, the values of p-Raptor and p-S6K1 were higher in AP-fed pigs than LP-fed pigs and intermediate in the MP-fed pigs. Collectively, the degree of mTOR pathway activation is not similar in skeletal muscle of different fiber type responding to the dietary protein level in the growing-finishing pigs. The current study is in agreement with a previous study which reported different sensitivity of various skeletal muscle fiber types in response to mTOR signaling molecules between plantaris and soleus . Based on the current results, we speculated that the MP diet-induced muscle mass weight increase in LDM is at least partially mediated through the activation of the mTORC1 signaling pathway.
In conclusion, our findings confirmed that the growing-finishing pigs chronically fed a moderately restricted protein diet (13 % CP) could catch up growth performance and LDM weight of the pigs offered the adequate protein level diet (16 % CP). It was partly attributed to the modulation of the fiber type characteristics and energy status, the up-regulated mRNA levels of myokines (IL-6, IL-15), MRFs (MyoD, MyoG), and the activation of mTORC1 pathway. These findings may provide new insight into the application of nutrition strategy in pig industry or even in human health.
ADFI, average daily feed intake; ADG, average daily gain; AP, adequate protein; BFM, biceps femoris muscle; CP, crude protein; eIF•4E-BP1, eukaryotic initiation factor 4E-binding protein1; IL-6, interleukin -6; LDM, longissimus dorsi muscle; LP, low protein; MAFbx, muscle atrophy F-box; MP, moderately restricted protein; MRFs, myogenic regulatory factors; mTORC1, mammalian target of rapamycin complex 1; MuRF1, muscle ring finger 1; MyHC, myosin heavy chain; PMM, psoas major muscle; S6K1, p70S6 kinase; UPP, ubiquitin proteasome pathway
This study was financially supported by the National Basic Research Program of China (2013CB127305), the Nature Science Foundation of Hunan Province (S2014J504I), the Major Project of Hunan Province (2015NK1002) and the National Science and Technology Ministry (2014BAD08B11).
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional file.
FNL, YLY and TJL conceived and designed the study. YHL and LW conducted the animal trial, analyzed and interpreted the data and wrote the paper. HKW, BT, KY and XFK revised the manuscript. YYL and YHD performed the chemical analyses. SC and FW assisted with tissue collection. All authors read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
- Matsakas A, Patel K. Skeletal muscle fibre plasticity in response to selected environmental and physiological stimuli. Histol Histopathol. 2009;24:611–29.PubMedGoogle Scholar
- Dickinson JM, Rasmussen BB. Amino acid transporters in the regulation of human skeletal muscle protein metabolism. Curr Opin Clin Nutr Metab Care. 2013;16:638–44.View ArticlePubMedPubMed CentralGoogle Scholar
- Pratesi A, Tarantini F, Bari MD. Skeletal muscle: an endocrine organ. Clin Cases Miner Bone Metab. 2013;10:11–4.PubMedPubMed CentralGoogle Scholar
- Li YH, Li FN, Lin BB, Kong XF, Tang YL, Yin YL. Myokine IL-15 regulates the crosstalk of co-cultured porcine skeletal muscle satellite cells and preadipocytes. Mol Biol Rep. 2014;41:7543–53.View ArticlePubMedGoogle Scholar
- Dideriksen K, Reitelseder S, Holm L. Influence of amino acids, dietary protein, and physical activity on muscle mass development in humans. Nutrients. 2013;5:852–76.View ArticlePubMedPubMed CentralGoogle Scholar
- Escobar J, Frank JW, Suryawan A, Nguyen HV, Kimball SR, Jefferson LS, et al. Physiological rise in plasma leucine stimulates muscle protein synthesis in neonatal pigs by enhancing translation initiation factor activation. Am J Physiol Endocrinol Metab. 2005;288:E914–21.Google Scholar
- Escobar J, Frank JW, Suryawan A, Nguyen HV, Davis TA. Amino acid availability and age affect the leucine stimulation of protein synthesis and eIF4F formation in muscle. Am J Physiol Endocrinol Metab. 2007;293:E1615–21.View ArticlePubMedPubMed CentralGoogle Scholar
- Bhaskar PT, Hay N. The two TORCs and Akt. Dev Cell. 2007;12:487–502.View ArticlePubMedGoogle Scholar
- Wullschleger S, Loewith R, Hall MN. TOR signaling in growth and metabolism. Cell. 2006;124:471–84.View ArticlePubMedGoogle Scholar
- Kimball SR, Jefferson LS. Control of translation initiation through integration of signals generated by hormones, nutrients, and exercise. J Biol Chem. 2010;285:29027–32.View ArticlePubMedPubMed CentralGoogle Scholar
- Mascher H, Tannerstedt J, Brink-Elfegoun T, Ekblom B, Gustafsson T, Blomstrand E. Repeated resistance exercise training induces different changes in mRNA expression of MAFbx and MuRF-1 in human skeletal muscle. Am J Physiol Endocrinol Metab. 2008;294:E43–51.View ArticlePubMedGoogle Scholar
- O'Connor PM, Kimball SR, Suryawan A, Bush JA, Nguyen HV, Jefferson LS, et al. Regulation of translation initiation by insulin and amino acids in skeletal muscle of neonatal pigs. Am J Physiol Endocrinol Metab. 2003;285:E40–53.Google Scholar
- Castaneda C, Charnley JM, Evans WJ, Crim MC. Elderly women accommodate to a low-protein diet with losses of body cell mass, muscle function, and immune response. Am J Clin Nutr. 1995;62:30–9.PubMedGoogle Scholar
- Zdanowicz MM, Slonim AE, Bilaniuk I, O'Connor MM, Moyse J, Teichberg S. High protein diet has beneficial effects in murine muscular dystrophy. J Nutr. 1995;125:1150–8.PubMedGoogle Scholar
- de Groot LC, van Staveren WA. Low-protein intakes and protein turnover in elderly women. Nutr Rev. 1996;54:58–60.View ArticlePubMedGoogle Scholar
- Evans WJ. Protein nutrition, exercise and aging. J Am Coll Nutr. 2004;23:601S–9S.View ArticlePubMedGoogle Scholar
- Morais JA, Chevalier S, Gougeon R. Protein turnover and requirements in the healthy and frail elderly. J Nutr Health Aging. 2006;10:272–83.PubMedGoogle Scholar
- Campbell WW. Synergistic use of higher-protein diets or nutritional supplements with resistance training to counter sarcopenia. Nutr Rev. 2007;65:416–22.View ArticlePubMedGoogle Scholar
- Tipton KD, Wolfe RR. Protein and amino acids for athletes. J Sports Sci. 2004;22:65–79.View ArticlePubMedGoogle Scholar
- Bray GA, Smith SR, de Jonge L, Xie H, Rood J, Martin CK, et al. Effect of dietary protein content on weight gain, energy expenditure, and body composition during overeating: a randomized controlled trial. JAMA. 2012;307:47–55.Google Scholar
- Deng D, Yao K, Chu WY, Li TJ, Huang RL, Yin YL, et al. Impaired translation initiation activation and reduced protein synthesis in weaned piglets fed a low-protein diet. J Nutr Biochem. 2009;20:544–52.Google Scholar
- Liu X, Pan S, Li X, Sun Q, Yang X, Zhao R. Maternal low-protein diet affects myostatin signaling and protein synthesis in skeletal muscle of offspring piglets at weaning stage. Eur J Nutr. 2015;54:971–9.View ArticlePubMedGoogle Scholar
- Mizunoya W, Iwamoto Y, Shirouchi B, Sato M, Komiya Y, Razin FR, et al. Dietary fat influences the expression of contractile and metabolic genes in rat skeletal muscle. PLoS One. 2013;8:e80152.Google Scholar
- Pette D, Staron RS. Myosin isoforms, muscle fiber types, and transitions. Microsc Res Tech. 2000;50:500–9.View ArticlePubMedGoogle Scholar
- Pette D, Staron RS. Myosin isoforms, muscle fiber types, and transitions. Microsc Res Tech. 2000;50(6):500–9.Google Scholar
- Preedy VR, Paska L, Sugden PH, Schofield PS, Sugden MC. The effects of surgical stress and short-term fasting on protein synthesis in vivo in diverse tissues of the mature rat. Biochem J. 1988;250:179–88.View ArticlePubMedPubMed CentralGoogle Scholar
- Davis TA, Fiorotto ML, Nguyen HV, Burrin DG, Reeds PJ. Response of muscle protein synthesis to fasting in suckling and weaned rats. Am J Physiol Regul Integr Comp Physiol. 1991;6:R1373–80.Google Scholar
- Goldman N, Chen M, Fujita T, Xu Q, Peng W, Liu W, et al. Adenosine A1 receptors mediate local anti-nociceptive effects of acupuncture. Nat Neurosci. 2010;13:883–8.Google Scholar
- Li YH, Li FN, Wu L, Liu YY, Wei HK, Li TJ, et al. Reduced dietary protein level influences the free amino acid and gene expression profiles of selected amino acid transceptors in skeletal muscle of growing pigs. J Anim Physiol Anim Nutr. 2016. doi:10.1111/jpn.12514.
- Li YH, Wei HK, Li FN, Chen S, Duan YH, Guo QP, et al. Supplementation of branched-chain amino acids in protein-restricted diets modulates the expression levels of amino acid transporters and energy metabolism associated regulators in the adipose tissue of growing pigs. Animal Nutrition. 2016. doi:10.1016/j.aninu.2016.01.003.
- Pfaffl MW. A new mathematical model for relative quantification in real-time RT–PCR. Nucleic Acids Res. 2001;29:e45.View ArticlePubMedPubMed CentralGoogle Scholar
- Sharda DP, Mahan DC, Wilson RF. Limiting Amino Acids in Low-Protein Corn-Soybean Meal Diets for Growing-Finishing Swine1,2. J Anim Sci. 1976;42(5):1175–81.Google Scholar
- Kerr BJ, McKeith FK, Easter RA. Effect on performance and carcass characteristics of nursery to finisher pigs fed reduced crude protein, amino acid-supplemented diets. J Anim Sci. 1995;73:433–40.View ArticlePubMedGoogle Scholar
- Le Bellego L, van Milgen J, Noblet J. Effect of high temperature and low-protein diets on the performance of growing-finishing pigs. J Anim Sci. 2002;80:691–701.View ArticlePubMedGoogle Scholar
- Edmonds MS, Baker DH. Effect of dietary protein and lysine fluctuations in the absence and presence of ractopamine on performance and carcass quality of late-finishing pigs. J Anim Sci. 2010;88:604–11.View ArticlePubMedGoogle Scholar
- Prandini A, Sigolo S, Morlacchini M, Grilli E, Fiorentini L. Microencapsulated lysine and low-protein diets: effects on performance, carcass characteristics and nitrogen excretion in heavy growing-finishing pigs. J Anim Sci. 2013;91:4226–34.View ArticlePubMedGoogle Scholar
- Tous N, Lizardo R, Vila B, Gispert M, Font IFM, Esteve-Garcia E. Effect of reducing dietary protein and lysine on growth performance, carcass characteristics, intramuscular fat, and fatty acid profile of finishing barrows. J Anim Sci. 2014;92:129–40.View ArticlePubMedGoogle Scholar
- Choi YM, Kim BC. Muscle fiber characteristics, myofibrillar protein isoforms, and meat quality. Livestock Science. 2009;122(2):105–18.Google Scholar
- Pette D, Staron RS. Transitions of muscle fiber phenotypic profiles. Histochem Cell Biol. 2001;115:359–72.PubMedGoogle Scholar
- Scheffler TL, Scheffler JM, Park S, Kasten SC, Wu Y, McMillan RP, et al. Fiber hypertrophy and increased oxidative capacity can occur simultaneously in pig glycolytic skeletal muscle. Am J Physiol Cell Physiol. 2014;306:C354–63.Google Scholar
- Karlsson A, Enfalt AC, Essen-Gustavsson B, Lundstrom K, Rydhmer L, Stern S. Muscle histochemical and biochemical properties in relation to meat quality during selection for increased lean tissue growth rate in pigs. J Anim Sci. 1993;71:930–8.PubMedGoogle Scholar
- Solomon MB, Caperna TJ, Mroz RJ, Steele NC. Influence of dietary protein and recombinant porcine somatotropin administration in young pigs: III. Muscle fiber morphology and shear force. J Anim Sci. 1994;72:615–21.PubMedGoogle Scholar
- Xiangyu Sun. Effeets of breeds and nutrient level on myofibre types and meat quality in pigs. Master Dissertation. 2009.Google Scholar
- Kim NK, Joh JH, Park HR, Kim OH, Park BY, Lee CS. Differential expression profiling of the proteomes and their mRNAs in porcine white and red skeletal muscles. Proteomics. 2004;4:3422–8.View ArticlePubMedGoogle Scholar
- Habets PE, Franco D, Ruijter JM, Sargeant AJ, Pereira JA, Moorman AF. RNA content differs in slow and fast muscle fibers: implications for interpretation of changes in muscle gene expression. J Histochem Cytochem. 1999;47:995–1004.View ArticlePubMedGoogle Scholar
- Maltin CA, Sinclair KD, Warriss PD, Grant CM, Porter AD, Delday MI, et al. The effects of age at slaughter, genotype and finishing system on the biochemical properties, muscle fibre type characteristics and eating quality of bull beef from suckled calves. Anim Sci. 1998;66:341–8.Google Scholar
- Bottinelli R, Reggiani C. Human skeletal muscle fibres: molecular and functional diversity. Prog Biophys Mol Biol. 2000;73:195–262.View ArticlePubMedGoogle Scholar
- Ryu YC, Kim BC. The relationship between muscle fiber characteristics, postmortem metabolic rate, and meat quality of pig longissimus dorsi muscle. Meat Sci. 2005;71:351–7.View ArticlePubMedGoogle Scholar
- Ryu YC, Kim BC. Comparison of histochemical characteristics in various pork groups categorized by postmortem metabolic rate and pork quality. J Anim Sci. 2006;84:894–901.View ArticlePubMedGoogle Scholar
- van Wessel T, de Haan A, van der Laarse WJ, Jaspers RT. The muscle fiber type-fiber size paradox: hypertrophy or oxidative metabolism? Eur J Appl Physiol. 2010;110:665–94.View ArticlePubMedPubMed CentralGoogle Scholar
- Bolster DR, Crozier SJ, Kimball SR, Jefferson LS. AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling. J Biol Chem. 2002;277:23977–80.View ArticlePubMedGoogle Scholar
- Krawiec BJ, Nystrom GJ, Frost RA, Jefferson LS, Lang CH. AMP-activated protein kinase agonists increase mRNA content of the muscle-specific ubiquitin ligases MAFbx and MuRF1 in C2C12 cells. Am J Physiol Endocrinol Metab. 2007;292:E1555–67.View ArticlePubMedGoogle Scholar
- Plomgaard P, Penkowa M, Pedersen BK. Fiber type specific expression of TNF-alpha, IL-6 and IL-18 in human skeletal muscles. Exerc Immunol Rev. 2005;11:53–63.PubMedGoogle Scholar
- Banzet S, Koulmann N, Simler N, Birot O, Sanchez H, Chapot R, et al. Fibre-type specificity of interleukin-6 gene transcription during muscle contraction in rat: association with calcineurin activity. J Physiol. 2005;566:839–47.Google Scholar
- Avruch J, Lin Y, Long X, Murthy S, Ortiz-Vega S. Recent advances in the regulation of the TOR pathway by insulin and nutrients. Curr Opin Clin Nutr Metab Care. 2005;8:67–72.View ArticlePubMedGoogle Scholar
- Avruch J, Long X, Ortiz-Vega S, Rapley J, Papageorgiou A, Dai N. Amino acid regulation of TOR complex 1. Am J Physiol Endocrinol Metab. 2009;296:E592–602.View ArticlePubMedGoogle Scholar
- Magnuson B, Ekim B, Fingar DC. Regulation and function of ribosomal protein S6 kinase (S6K) within mTOR signalling networks. Biochem J. 2012;441:1–21.View ArticlePubMedGoogle Scholar
- Baar K, Esser K. Phosphorylation of p70(S6k) correlates with increased skeletal muscle mass following resistance exercise. Am J Physiol. 1999;276:C120–7.PubMedGoogle Scholar