Short-term creatine supplementation changes protein metabolism signaling in hindlimb suspension

GN Marzuca-Nassr; MAS Fortes; L Guimarães-Ferreira; GM Murata; KF Vitzel; DAA Vasconcelos; RA Bassit; R Curi

doi:10.1590/1414-431X20198391

. 2019 Oct 7;52(10):e8391. doi: 10.1590/1414-431X20198391

Short-term creatine supplementation changes protein metabolism signaling in hindlimb suspension

GN Marzuca-Nassr ^1,², MAS Fortes ², L Guimarães-Ferreira ³, GM Murata ², KF Vitzel ^2,⁴, DAA Vasconcelos ², RA Bassit ⁵, R Curi ^2,⁶

PMCID: PMC6787955 PMID: 31596311

Abstract

The effect of a short-term creatine supplementation on hindlimb suspension (HS)-induced muscle atrophy was investigated. Creatine monohydrate (5 g/kg b.w. per day) or placebo, divided in 2 daily doses, was given by oral gavage for 5 days. Rats were maintained in HS with dietary supplementation concomitantly for 5 days. Body weight, soleus and EDL muscle masses, and cross-sectional areas (CSA) of the muscle fibers were measured. Signaling pathways associated with skeletal muscle mass regulation (FST, MSTN, FAK, IGF-1, MGF, Akt, mTOR, atrogin-1, and MuRF1 expressions, and Akt, S6, GSK3B, and 4EBP1 proteins) were evaluated in the muscles. Soleus muscle exhibited more atrophy than the EDL muscle due to HS. Creatine supplementation attenuated the decrease of wet weight and increased p-4EBP1 protein in the EDL muscle of HS rats. Also, creatine increased mTOR and atrogin-1 expressions in the same muscle and condition. In the absence of HS, creatine supplementation increased FAK and decreased MGF expressions in the EDL muscle. Creatine attenuated the increase in FST expression due to HS in the soleus muscle. MuRF1 expression increased in the soleus muscle due to creatine supplementation in HS animals whereas atrogin-1 expression increased still further in this group compared with untreated HS rats. In conclusion, short-term creatine supplementation changed protein metabolism signaling in soleus and EDL muscles. However, creatine supplementation only slightly attenuated the mass loss of both muscles and did not prevent the CSA reduction and muscle strength decrease induced by HS for 5 days.

Keywords: Creatine supplementation, Hindlimb suspension, Muscle disuse atrophy, Protein synthesis, Protein degradation

Introduction

Skeletal muscle disuse atrophy is characterized by a decrease in activity of protein synthesis and/or an increase in protein degradation pathways leading to a reduction of muscle mass and strength and in the cross-sectional area (CSA) of muscle fibers (1,2). Several strategies have been tested to attenuate muscle wasting such as electrical stimulation (3), physical exercise (4), and dietary supplementation; e.g., fish oil, leucine, isoleucine, valine, creatine, and L-carnitine (2,5,6). Creatine may act as an attenuating agent of skeletal muscle atrophy (6) and leads to an increase of physical exercise capacity (7). However, a consensus about the beneficial effects of creatine dietary supplementation in skeletal muscle atrophy is still lacking.

Creatine is a non-essential dietary nutrient and is present in meat and fish. Endogenous creatine synthesis occurs in the liver, kidney, and pancreas after a two-stage process using arginine and glycine as precursors. Skeletal muscle is the main site for creatine storage where creatine kinase converts it into phosphocreatine with the use of ATP (8–10). Creatine supplementation has been reported to act on skeletal muscle atrophy through an increase in strength, resistance to fatigue, intramuscular phosphocreatine content, and protein synthesis markers. Creatine supplementation decreases cytoplasmic Ca²⁺ levels, production of reactive oxygen species, contents of proinflammatory cytokines, satellite cell activation, and muscle cell apoptosis (11–13).

Creatine supplementation (250 mg/kg b.w. per day for 18 days) attenuated muscle mass loss in corticosteroid-induced muscle wasting in rats (14), and increased fat-free mass and strength in myopathies such as McArdle's disease, mitochondrial chronic progressive external ophthalmoplegia (CPEO), mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) in rodents (12,15). In mice, creatine supplementation (administered both in powder food (4.7%) and drinking water (1.4%) for 45 days) did not attenuate muscle atrophy after myotoxic injury (16) induced by dexamethasone treatment (17) or in a transgenic model of amyotrophic lateral sclerosis (18). In a condition of muscle atrophy induced by immobilization, creatine supplementation (5 g/kg b.w. per day for 14 days) attenuated muscle mass loss in rats (19). Creatine supplementation attenuated muscle mass loss in the upper-arm of young men (20) but had no effect in the leg muscles of human subjects after immobilization (21,22). Backx et al. (21) reported that, in healthy young men (mean of 23 years old) after muscle disuse atrophy caused by immobilization, creatine supplementation did not attenuate skeletal muscle loss and the decreased CSA of the quadriceps. These reports indicate the anti-atrophic effect of creatine is still controversial.

With the high incidence of chronic diseases and the increase in the aged population, there is an increased number of patients on short-term bed rest. The average hospitalization duration for adults is 5–7 days leading to a ∼0.6% loss of leg muscle mass per day (23). Taking this fact into consideration, the focus of this work was to evaluate the effects of a short-term creatine supplementation on muscle disuse. Due to the difficulty of developing bed-rest studies in humans, animal models were used. One of the most widely used experimental models to mimic the skeletal muscle loss induced by bed rest in humans is the hindlimb suspension (HS) in rodents.

We investigated the short-term effects of creatine supplementation on skeletal muscle signaling pathways involved in protein metabolism in rats with HS-induced atrophy. We hypothesized that short-term creatine supplementation would attenuate the skeletal muscle mass loss and muscle strength reduction by preventing the changes in protein metabolism signaling induced by short-term disuse.

Material and Methods

Animals

Eight-week-old male Wistar rats were obtained from the Animal Facility of the Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo. The animals were maintained under standard conditions of 12-h light/dark cycle at 23±2°C and food and water ad libitum (daily consumption was recorded). All experimental procedures were performed in accordance with the Guide for the Care and Use of Laboratory Animals (Institute of Laboratory Animal Resources, National Academy of Sciences, USA). Ethics Committee of the Institute of Biomedical Sciences, University of São Paulo, approved the experimental protocol and procedures of this study (No. 65/20/03).

Experimental study design

During the first three days of the experimental period, the animals were adapted to individual cages. Afterwards, the rats were divided into the following groups: control group (C, n=7); hindlimb suspension group (HS, n=8); creatine supplemented group (Cr, n=7); and creatine supplemented and hindlimb suspension group (Cr-HS, n=8). The animals received a daily oral supplementation of creatine monohydrate (Merck, Darmstadt, Germany) by gavage (5 g/kg b.w.), divided in 2 daily doses for 5 days. Eijnde et al. (24) reported that this dosage promotes an increase of 30 and 15% of free creatine and phosphocreatine, respectively, in the soleus muscle after 5 days of supplementation in rats. Similar responses were seen in humans with the dose commonly used, 20 g creatine monohydrate per day for 5 days (25,26). The same volume of water was given as placebo to the C and HS groups.

The HS is a well-established experimental model for induction of skeletal muscle atrophy as previously described (2,27). Animals were submitted to HS and dietary creatine supplementation concomitantly. Rats were then maintained in the HS and dietary supplementation with creatine or placebo for 5 days. After that, the animals were weighed and anesthetized using ketamine (90 mg/kg b.w.) and xylazine (10 mg/kg b.w.) by intraperitoneal administration. We removed the soleus and extensor digitorum longus (EDL) muscles of both limbs for histological and molecular analysis (western blotting and real-time polymerase chain reaction – RT-PCR) and euthanized the animals by exsanguination.

Analysis of muscle strength and fatigue resistance

An in vivo electrical stimulation protocol was used for determination of muscle contractile activity. For twitch force analysis, the stimulus consisted of 500-μs pulse at 1 Hz with adjusted voltage to produce maximum force. Electrical stimulus frequency was increased to 100 Hz to determine the tetanic force. Ten 1-s successive tetanic contractions at 100 Hz allowed the determination of fatigue resistance, with 10 s of recovery between them, by measuring the decrease in force production during the experimental protocol used. Maximal twitch and tetanic forces were recorded using the AqDados software (version 4.16, Lynx Tecnologia Eletronica Ltda., Brazil). Muscle strength and fatigue resistance were analyzed using the AqAnalysis software (version 4.16, Lynx Tecnologia Eletronica Ltda.). We used a similar procedure in previous studies (28).

Histological analysis

Serial sections were taken from the central portion of the soleus and EDL muscles according to Bodine and Baar (29). The slides were stained with hematoxylin and eosin (HE) for analysis of CSA of the soleus and EDL muscles fibers (150 fibers per muscle). Photographs were taken using an optical microscope (Nikon Eclipse E1000, Japan) attached to a digital camera (Nixon DXM 1200). The images were analyzed using the AxioVision program (version 4.8.1.0, Carl Zeiss Imaging Solutions, Germany). We used the same measurements in a previous study (2).

Analysis of Akt, S6, GSK3B, and 4EBP1 by western blot

The primary antibodies used were: p-protein kinase B (Akt) at Ser 473 (9271), Akt (9272), p-S6 at Ser 240/244 (5364), S6 (2217), p-GSK3B (glycogen synthase kinase3-beta) at Ser 9 (9323), GSK3B (9315), p-4EBP1 at Thr 37/46 (2855) and 4EBP1 (9644) from Cell Signaling Technology (USA). We used a similar procedure in previous studies (2,27,30).

Real-time polymerase chain reaction (RT-PCR)

Total RNA was extracted from skeletal muscles using RNeasy RNA isolation kit (Qiagen Inc, USA) according to the manufacturer's protocol and as used in our previous study (28). The following genes were evaluated: FST (follistatin); MSTN (myostatin); FAK (focal adhesion kinase); IGF-1 (insulin-like growth factor); MGF (mechano growth factor); Akt; mTOR (mammalian target of rapamycin); atrogin-1, and MuRF1. The primers sequences used in the experiments are displayed in Supplementary Table S1.

Statistical analysis

Statistical analysis was performed using the GraphPad Prism^® software (version 4.01; USA). Results are reported as means±SE and were analyzed by two-way analysis of variance (ANOVA) followed by the Bonferroni post-hoc test (for comparison between three or more groups). Outlier results were detected using the Grubbs' test of GraphPad Software (graphpad.com/quickcalcs/Grubbs1.cfm). The differences between groups were considered significant for P<0.05.

Results

Body weight, and soleus and EDL muscles masses

The HS group had lower body weight than the other groups after 5 days of experiment (Table 1). HS reduced wet (P<0.001) and dry (P<0.001) soleus muscle mass by 29–33% in the untreated (C) group. In the EDL muscle, the wet weight was significantly decreased by 16% (P<0.05) by HS, while the dry weight was decreased by 12% (P<0.05). Creatine supplementation had an effect on preventing muscle mass loss that was more notable in the EDL muscle, in the rats submitted to HS (Table 1).

Table 1. Body weight and muscle masses of soleus and extensor digitorum longus (EDL) muscles.

Measurements	Groups
	C	HS	Cr	Cr-HS
Body weight (g)
Day –3	201±2.3	201±4.6	200±4.6	207±3.3
Day 0	222±3.2	220±6.1	221±10.5	224±4.3
Day 5	251±4.0	216±3.3^b	251±9.0	206±11^c
Soleus muscle
Wet weight (mg/mm tibia length)	3.2±0.02	2.1±0.08^c	3.1±0.04	2.2±0.01^c
% loss due to HS in wet weight		33%		26%
Dry weight (mg/mm tibia length)	0.84±0.05	0.59±0.04^c	0.77±0.02	0.63±0.04^a
% loss due to HS in dry weight		29%		18%
EDL muscle
Wet weight (mg/mm tibia length)	3.8±0.08	3.2±0.01^a	3.3±0.02	3.0±0.02
% loss due to HS in wet weight		16%		9%
Dry weight (mg/mm tibia length)*	0.97±0.02	0.85±0.03	0.86±0.04	0.8±0.04
% loss due to HS in dry weight		12%		8%

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Data are reported as means±SE, n=7–8 animals. The results were compared using two-way ANOVA and Bonferroni post hoc test. ^aP<0.05; ^bP<0.01; ^cP<0.001: significant differences between hindlimb suspension groups and the respective controls (C vs HS or Cr vs Cr-HS). *P<0.05 for C and Cr groups vs C-HS and Cr-HS groups (main effects of HS), using two-way ANOVA only (no statistical differences using the Bonferroni post hoc test). C: control group; HS: hindlimb suspension group; Cr: creatine supplemented group; Cr-HS: creatine supplemented and hindlimb suspension group; EDL: extensor digitorum longus.

Analysis of strength and fatigue resistance in the soleus and EDL muscles

The absolute twitch force in the soleus and EDL muscles and the specific tetanic force in the EDL muscle were not changed as indicated by the inter-group analysis. However, HS decreased these parameters (P<0.05) compared with non-HS animals (Figure 1Aa and 2Aa). In the same way, the absolute tetanic forces in the soleus and EDL muscles were also significantly decreased by the hindlimb suspension (soleus muscle, Figure 1Ac: C vs HS, P<0.001 and Cr vs Cr-HS, P<0.01; EDL muscle, Figure 2Ac: C vs HS, P<0.05 and Cr vs Cr-HS, P<0.01). The specific twitch force and fatigue resistance did not change significantly in the soleus and EDL muscles due to either creatine supplementation or HS (Figure 1A and 2A).

Protein synthesis- and degradation-associated signaling in soleus and EDL muscles

The content of p-Akt and the p-Akt/Akt total ratio were reduced by 45%, due to HS in the soleus muscle of the placebo group (C vs HS, P<0.05) and were not significantly changed by creatine supplementation (Figure 1Ba and 1Bc). S6 and p-S6 protein contents were not altered by HS or supplementation (Figure 1Bd,e,f). Decreases of p-GSK3B content (C vs HS, 47%, P<0.05 and Cr vs Cr-HS, 64%, P<0.01) and of p-GSK3B/GSK3B total ratio (C vs HS, 48% reduction, P<0.05 and Cr vs Cr-HS, 61% reduction, P<0.05) were reported in the placebo and creatine groups due to HS (Figure 1Bg and 1Bi, respectively). The p-4EBP1 content was not significantly changed in the inter-group analysis. However, two-way ANOVA indicated that HS significantly increased 4EBP1 phosphorylation (34% and 20% in the placebo and creatine groups, respectively, P<0.05) (Figure 1Bj). Total 4EBP1 content was also significantly increased in both groups (C vs HS, 46%, P<0.001, and Cr vs Cr-HS, 23%, P<0.05) (Figure 1Bk).

In the EDL muscle, the contents of phosphorylated and total Akt and GSK3B proteins did not change after the HS or creatine supplementation (Figure 2B). The content of p-S6 and the p-S6/S6 ratio were not significantly changed in the inter-group analysis. However, HS decreased S6 phosphorylation in the placebo group (by 44%) whereas creatine supplementation increased p-S6 content during HS (by 76%) (P<0.05) (Figure 2Bd). For total S6 content, two-way ANOVA indicated a decrease in both groups due to HS (11% in the placebo group and 21% in the creatine group, P<0.05) (Figure 2Be). The p-4EBP1 content was significantly increased (61%, P<0.05) in the HS group treated with creatine (Figure 2Bj).

CSA of the soleus and EDL muscles fibers

The CSA of the soleus muscle fibers was markedly decreased due to HS in both groups compared to non-HS animals (C vs HS, P<0.01 and Cr vs Cr-HS, P<0.001) by 25-30% (Figure 3A). The CSA of the EDL muscle fibers did not change due to HS in both groups compared to non-HS (Figure 3B). Creatine supplementation did not alter muscle fiber CSA in both soleus and EDL muscles.

mRNA levels of FST, MSTN, FAK, IGF, MGF, Akt, mTOR, atrogin-1, and MuRF1 in soleus and EDL muscles

The expressions of MSTN, FAK, IGF-1, MGF, and Akt did not change in soleus muscle after the HS or with creatine supplementation (Supplementary Figure S1A). The expression of FST was increased due to HS in the C group (P<0.05) and creatine supplementation attenuated this change (Figure 4Aa). HS also resulted in an increased mTOR expression (P<0.01) (Figure 4Ab). The expression of atrogin-1 was increased after the HS period in both groups (P<0.001) and it was further increased in the Cr-HS compared with the C-HS group (P<0.01) (Figure 4Ac). The expression of MuRF1 was increased due to HS in the Cr group (Cr vs Cr-HS, P<0.01) (Figure 4Ad).

In the EDL muscle, the expressions of FST, IGF, Akt, and MuRF1 also did not change after the HS period or creatine supplementation (Supplementary Figure S1B). However, HS increased the expression of MSTN in EDL muscle both in the placebo and creatine groups (P<0.05) (Figure 4Ba). Regarding MGF expression, a reducing effect of creatine supplementation was observed (P<0.05) (Figure 4Bb). mTOR expression was increased due to HS in the Cr group (P<0.01) (Figure 4Bc); the expression of this gene in the Cr-HS group was higher than in C-HS rats (P<0.05). The expression of atrogin-1 increased after 5 days of HS in the Cr group (P<0.05) (Figure 4Bd). FAK expression increased in the creatine group compared with the placebo group (P<0.05) (Figure 4Be).

Discussion

We investigated the effects of short-term creatine supplementation on skeletal muscle mass and strength and signaling pathways associated with protein synthesis or degradation in rats submitted to HS-induced atrophy. Despite the attenuating effects on protein metabolism signaling changes induced by HS, creatine supplementation, started concomitantly with HS, slighted prevented the decrease in skeletal muscle mass but had no effect on muscle CSA and strength after five days of muscle disuse (main results observed in this study are in Figure 5). The mentioned findings may be associated to the length of the supplementation period, the intensity of the muscle disuse atrophy, or the dose of creatine. Although, in the current study, creatine and phosphocreatine contents were not measured in the target muscles, the supplementation protocol used was reported to increase creatine content in type I fiber-rich muscles such as the soleus. The already described switch of type I to type II fibers during HS (31) may affect creatine accumulation in soleus muscle.

The content of total creatine is dependent on the skeletal muscle fiber type. Type II fibers have higher levels of creatine and phosphocreatine. Rodent type IIa and IIb fibers contain ∼32 mM phosphocreatine and 7 mM creatine whereas type I fibers have ∼16 mM phosphocreatine and 7 mM creatine. The EDL, a type II fiber-rich muscle, has a higher K _m (160 µM) and higher V_max (100 nmol·h⁻¹·g⁻¹ wet weight) compared with the type I fiber-rich soleus muscle (K _m=73 µM and V_max=77 nmol·h⁻¹·g⁻¹ wet weight), as calculated using ¹⁴C-labelled creatine. Therefore, creatine uptake and accumulation is a muscle fiber type-dependent process (9,32). Based on the above, two different muscles were studied: soleus (predominantly type I/oxidative/slow fibers) and EDL (predominantly type II/glycolytic/fast fibers). More intense atrophy due to HS was found in the soleus muscle based on the percentage of decrease in muscle mass and muscle fibers CSA, as also previously reported (1,2).

To evaluate protein synthesis signaling (Akt-mTOR-S6), we analyzed the phosphorylation and activation of the key upstream enzyme Akt and the phosphorylation of the S6 protein as a downstream signaling of mTOR activation. The activation of this pathway contributes to an increase in skeletal muscle mass by stimulating protein synthesis. This pathway also inhibits the activation of MuRF1 and atrogin-1, associated with the activation of the ubiquitin-proteasome degradation pathway, and promotes an inhibition of phosphorylation of GSK3b and 4EBP1 that can act as repressors of protein translation (33). In the soleus muscle, HS reduced p-Akt content, which is one of the main activators of mTOR complex. HS did not change p-S6 protein but enhanced p-4EBP1 protein. The lowered phosphorylation (and inhibition) of GSK3B followed the lower activation of its upstream kinase Akt. Activation of GSK3B leads to inhibition of eukaryotic translation initiation factor 2 beta (eIF2β) and to suppression of protein translation. Degradation pathway may be enhanced as indicated by increased atrogin-1 mRNA expression. The lowered phosphorylation of Akt stops inhibiting FoXO protein and increases the atrogin-1 content, which is an activating factor of the ubiquitin-proteasome pathway (34). Even though FST is associated with muscle hypertrophy (by inhibiting myostatin), our findings agreed with another study that reported an increase of this marker at the beginning of the HS period (35). Creatine supplementation reduced FST and increased atrogin-1 expression during HS. Creatine supplementation had no marked hypertrophic effects in the soleus muscle. Conversely, it promoted an attenuation of the increase in FST expression and a greater increase in MuRF1 expression due to HS.

Based on these findings, creatine would not be expected to markedly attenuate soleus muscle atrophy under the experimental conditions investigated. Indeed, soleus muscle atrophy, evaluated by muscle mass and fiber size, was not significantly different between groups. The mentioned findings also contributed to the lack of significant creatine effect on preventing leg muscle strength decrease induced by HS.

The EDL muscle suffered less atrophy than the soleus due to HS, which is in accordance with previous studies (1,2,27). This was reflected in the molecular analysis as well, with few changes induced by HS, including the reduction of p-S6 protein content and increase of MSTN expression. Myostatin is a member of the transforming growth factor-beta (TGF-β) family that acts on muscle mass control (36). This factor activates ubiquitin ligases and proteasome proteolysis (37), inhibiting protein synthesis through the Akt-mTOR-S6 pathway (38). In opposition to the soleus, promising effects of creatine on reduction of EDL muscle mass loss were found; the supplementation increased FAK expression. We speculate that the increase in the expression of FAK could produce an increase in the activation of this marker. Fak, an enzyme involved in the mechanical signaling associated with skeletal muscle hypertrophy, has the ability to phosphorylate p70S6K1 in Tyr 397, independently of Akt and mTOR (39). In the same line, creatine supplementation reversed the S6 phosphorylation trend changes, which tended to decrease with HS but it was increased by concomitant creatine supplementation. These effects were not enough to counteract EDL mass loss induced by HS in the period studied but they may represent an advantage for muscle recovery after facing an atrophy-promoting condition. An increased expression of FAK may not be important during HS because there is no mechanical loading to elicit marked FAK expression. However, after the unloading or disuse condition, the increased FAK expression promoted by creatine supplementation could be beneficial to enhance muscle recovery after mechanical loading is re-established (as a “reload priming”). In fact, Hespel et al. (22) concluded that creatine supplementation improves muscle mass recovery during rehabilitation using resistance training after a period of 2 weeks of immobilization in young healthy volunteers.

Along with our study, other authors investigated the effects of creatine supplementation starting concomitantly with distinct atrophic models such as dexamethasone treatment (17) or immobilization (19,22). Hespel et al. (22) reported that creatine does not attenuate mass loss and does not change protein synthesis and degradation markers (Akt, FoxO3a, and MuRF1) in dexamethasone-induced muscle atrophy (17). Crassous et al. (16) described similar outcomes after injury in rats muscle regeneration. The mentioned observations may be due to the long duration of the supplementation period, the pre-loading protocol, or the different muscle atrophy model. In our study, the short-term supplementation and the HS protocol used may not have provided enough time for the alterations in creatine content to exert a more noticeable effect. Aoki et al. (19) reported that creatine supplementation starting seven days before immobilization attenuates skeletal muscle wasting in rats.

Backx et al. (21) reported that, in healthy young males, creatine supplementation (20 g per day) for five days before and during seven days of leg immobilization does not preserve or attenuate the muscle mass loss or strength decrease. We reported similar observation in the HS animal model used that mimics the human bed rest condition. Safdar et al. (40) supplemented healthy young subjects with creatine for 10 days (without exercise or dietary intervention) and reported an increase in protein synthesis through activation of FAK and subsequent activation of Akt downstream pathways, following the increase in EDL muscle FAK activation described.

Some limitations of the study have to be mentioned such as the short period of supplementation, a single dose of creatine used, determination of muscle creatine content, severe muscle mass loss induced by HS, and lack of some mRNA expression and protein content measurements. These limitations, however, do not jeopardize the reported findings.

In conclusion, short-term creatine supplementation (5 g/kg b.w. per day for 5 days) changed protein metabolism signaling in soleus and EDL muscles. However, creatine supplementation only slightly attenuated the mass loss of both muscles and did not prevent the CSA and muscle strength decrease induced by HS for 5 days.

Supplementary Material

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Acknowledgments

The authors are grateful to José Roberto Mendonça and Dr. Tatiana Carolina Alba-Loureiro for the excellent technical assistance. This research was carried out using financial support from the São Paulo State Research Foundation (FAPESP); National Council for Scientific and Technological Development (CNPq); Coordination for the Improvement of Higher Level/Education Personnel (CAPES); Universidad de La Frontera, Proyecto DI17-6002, Proyecto FONDECYT No 11180949, and Guggenheim Foundation. G.N.M.N. was the recipient of scholarships from Becas Chile (National Commission for Scientific and Technological Research – CONICYT, No: 72130103) and CAPES/PROEX. R.A.B. was the recipient of a scholarship from FAPESP (2013/17734-7). R.C. was the recipient of a scholarship from CNPq.

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[B17] 17.Nicastro H, Gualano B, de Moraes WM, de Salles Painelli V, da Luz CR, dos Santos Costa A, et al. Effects of creatine supplementation on muscle wasting and glucose homeostasis in rats treated with dexamethasone. Amino Acids. 2012;42:1695–1701. doi: 10.1007/s00726-011-0871-9. [DOI] [PubMed] [Google Scholar]

[B18] 18.Derave W, Van Den Bosch L, Lemmens G, Eijnde BO, Robberecht W, Hespel P. Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: effects of creatine treatment. Neurobiol Dis. 2003;13:264–272. doi: 10.1016/S0969-9961(03)00041-X. [DOI] [PubMed] [Google Scholar]

[B19] 19.Aoki MS, Lima WP, Miyabara EH, Gouveia CH, Moriscot AS. Deleteriuos effects of immobilization upon rat skeletal muscle: role of creatine supplementation. Clin Nutr. 2004;23:1176–1183. doi: 10.1016/j.clnu.2004.03.004. [DOI] [PubMed] [Google Scholar]

[B20] 20.Johnston AP, Burke DG, MacNeil LG, Candow DG. Effect of creatine supplementation during cast-induced immobilization on the preservation of muscle mass, strength, and endurance. J Strength Cond Res. 2009;23:116–120. doi: 10.1519/JSC.0b013e31818efbcc. [DOI] [PubMed] [Google Scholar]

[B21] 21.Backx EMP, Hangelbroek R, Snijders T, Verscheijden ML, Verdijk LB, de Groot LCPGM, et al. Creatine loading does not preserve muscle mass or strength during leg immobilization in healthy, young males: a randomized controlled trial. Sports Med. 2017;47:1661–1671. doi: 10.1007/s40279-016-0670-2. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B22] 22.Hespel P, Op't Eijnde B, Van Leemputte M, Urso B, Greenhaff PL, Labarque V, et al. Oral creatine supplementation facilitates the rehabilitation of disuse atrophy and alters the expression of muscle myogenic factors in humans. J Physiol. 2001;536:625–633. doi: 10.1111/j.1469-7793.2001.0625c.xd. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B23] 23.Dirks ML, Backx EM, Wall BT, Verdijk LB, van Loon LJ. May bed rest cause greater muscle loss than limb immobilization? Acta Physiol (Oxf) 2016;218:10–12. doi: 10.1111/apha.12699. [DOI] [PubMed] [Google Scholar]

[B24] 24.Eijnde BO, Richter EA, Henquin JC, Kiens B, Hespel P. Effect of creatine supplementation on creatine and glycogen content in rat skeletal muscle. Acta Physiol Scand. 2001;171:169–176. doi: 10.1046/j.1365-201x.2001.00786.x. [DOI] [PubMed] [Google Scholar]

[B25] 25.Casey A, Constantin-Teodosiu D, Howell S, Hultman E, Greenhaff PL. Creatine ingestion favorably affects performance and muscle metabolism during maximal exercise in humans. Am J Physiol. 1996;271:E31–E37. doi: 10.1152/ajpendo.1996.271.1.E31. [DOI] [PubMed] [Google Scholar]

[B26] 26.Greenhaff PL, Bodin K, Soderlund K, Hultman E. Effect of oral creatine supplementation on skeletal muscle phosphocreatine resynthesis. Am J Physiol. 1994;266:E725–E730. doi: 10.1152/ajpendo.1994.266.5.E725. [DOI] [PubMed] [Google Scholar]

[B27] 27.Marzuca-Nassr GN, Murata GM, Martins AR, Vitzel KF, Crisma AR, Torres RP, et al. Balanced diet-fed Fat-1 transgenic mice exhibit lower hindlimb suspension-induced soleus muscle atrophy. Nutrients. 2017;9:E1100. doi: 10.3390/nu9101100. pii: [DOI] [PMC free article] [PubMed] [Google Scholar]

[B28] 28.Fortes MA, Pinheiro CH, Guimaraes-Ferreira L, Vitzel KF, Vasconcelos DA, Curi R. Overload-induced skeletal muscle hypertrophy is not impaired in STZ-diabetic rats. Physiol Rep. 2015;3:e12457. doi: 10.14814/phy2.12457. pii: [DOI] [PMC free article] [PubMed] [Google Scholar]

[B29] 29.Bodine SC, Baar K. Analysis of skeletal muscle hypertrophy in models of increased loading. Methods Mol Biol. 2012;798:213–229. doi: 10.1007/978-1-61779-343-1. [DOI] [PubMed] [Google Scholar]

[B30] 30.Fortes MA, Marzuca-Nassr GN, Vitzel KF, da Justa Pinheiro CH, Newsholme P, Curi R. Housekeeping proteins: How useful are they in skeletal muscle diabetes studies and muscle hypertrophy models? Anal Biochem. 2016;504:38–40. doi: 10.1016/j.ab.2016.03.023. [DOI] [PubMed] [Google Scholar]

[B31] 31.Baldwin KM, Haddad F, Pandorf CE, Roy RR, Edgerton VR. Alterations in muscle mass and contractile phenotype in response to unloading models: role of transcriptional/pretranslational mechanisms. Front Physiol. 2013;4:284. doi: 10.3389/fphys.2013.00284. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B32] 32.Willott CA, Young ME, Leighton B, Kemp GJ, Boehm EA, Radda GK, et al. Creatine uptake in isolated soleus muscle: kinetics and dependence on sodium, but not on insulin. Acta Physiol Scand. 1999;166:99–104. doi: 10.1046/j.1365-201x.1999.00539.x. [DOI] [PubMed] [Google Scholar]

[B33] 33.Bonaldo P, Sandri M. Cellular and molecular mechanisms of muscle atrophy. Dis Model Mech. 2013;6:25–39. doi: 10.1242/dmm.010389. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B34] 34.Bodine SC, Baehr LM. Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1. Am J Physiol Endocrinol Metab. 2014;307:E469–E484. doi: 10.1152/ajpendo.00204.2014. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B35] 35.Stevenson EJ, Giresi PG, Koncarevic A, Kandarian SC. Global analysis of gene expression patterns during disuse atrophy in rat skeletal muscle. J Physiol. 2003;551:33–48. doi: 10.1113/jphysiol.2003.044701. [DOI] [PMC free article] [PubMed] [Google Scholar]

[B36] 36.McPherron AC, Lawler AM, Lee SJ. Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member. Nature. 1997;387:83–90. doi: 10.1038/387083a0. [DOI] [PubMed] [Google Scholar]

[B37] 37.Lokireddy S, McFarlane C, Ge X, Zhang H, Sze SK, Sharma M, et al. Myostatin induces degradation of sarcomeric proteins through a Smad3 signaling mechanism during skeletal muscle wasting. Mol Endocrinol. 2011;25:1936–1949. doi: 10.1210/me.2011-1124. [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]

[B38] 38.Trendelenburg AU, Meyer A, Rohner D, Boyle J, Hatakeyama S, Glass DJ. Myostatin reduces Akt/TORC1/p70S6K signaling, inhibiting myoblast differentiation and myotube size. Am J Physiol Cell Physiol. 2009;296:C1258–C1270. doi: 10.1152/ajpcell.00105.2009. [DOI] [PubMed] [Google Scholar]

[B39] 39.Klossner S, Durieux AC, Freyssenet D, Flueck M. Mechano-transduction to muscle protein synthesis is modulated by FAK. Eur J Appl Physiol. 2009;106:389–398. doi: 10.1007/s00421-009-1032-7. [DOI] [PubMed] [Google Scholar]

[B40] 40.Safdar A, Yardley NJ, Snow R, Melov S, Tarnopolsky MA. Global and targeted gene expression and protein content in skeletal muscle of young men following short-term creatine monohydrate supplementation. Physiol Genomics. 2008;32:219–228. doi: 10.1152/physiolgenomics.00157.2007. [DOI] [PubMed] [Google Scholar]

PERMALINK

Short-term creatine supplementation changes protein metabolism signaling in hindlimb suspension

GN Marzuca-Nassr

MAS Fortes

L Guimarães-Ferreira

GM Murata

KF Vitzel

DAA Vasconcelos

RA Bassit

R Curi

Abstract

Introduction