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Erratum: Untargeted muscle tissue metabolites profiling in young, adult, and old rats supplemented with tocotrienol-rich fraction
Siti Liyana Saud Gany1
Jen Kit Tan1
Kok Yong Chin2
Nur Haleeda Hakimi1
Nazirah Ab Rani1
Nurhazirah Ihsan3
Suzana Makpol1*- 1Department of Biochemistry, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Kuala Lumpur, Malaysia
- 2Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Kuala Lumpur, Malaysia
- 3Menara Sime Darby Oasis Corporate Park, Petaling Jaya, Malaysia
The greatest significant influence on human life span and health is inevitable ageing. One of the distinguishing characteristics of ageing is the gradual decrease of muscle mass and physical function. There has been growing evidence that tocotrienol can guard against age-associated chronic diseases and metabolic disorders. This study aimed to elucidate the effects of tocotrienol-rich fraction (TRF) on muscle metabolomes and metabolic pathways in ageing Sprague Dawley (SD) rats. Three months, 9 months, and 21 months old male SD rats were divided into control and treated groups with 10 rats per group. Rats in control and treated groups were given 60 mg/kg body weight/day of palm olein and 60 mg/kg body weight/day of TRF, respectively, via oral gavage for 3 months. Muscle performance was assessed at 0 and 3 months of treatment by measuring muscle strength and function. Our results showed that TRF treatment caused a significant increase in the swimming time of the young rats. Comparison in the control groups showed that metabolites involved in lipid metabolisms such as L-palmitoyl carnitine and decanoyl carnitine were increased in ageing. In contrast, several metabolites, such as 3-phosphoglyceric acid, aspartic acid and aspartyl phenylalanine were decreased. These findings indicated that muscle metabolomes involved in lipid metabolism were upregulated in aged rats. In contrast, the metabolites involved in energy and amino acid metabolism were significantly downregulated. Comparison in the TRF-supplemented groups showed an upregulation of metabolites involved in energy and amino acid metabolism. Metabolites such as N6-methyl adenosine, spermine, phenylalanine, tryptophan, aspartic acid, histidine, and N-acetyl neuraminic acid were up-regulated, indicating promotion of amino acid synthesis and muscle regeneration. Energy metabolism was also improved in adult and old rats with TRF supplementation as indicated by the upregulation of nicotinamide adenine dinucleotide and glycerol 3-phosphate compared to the control group. In conclusion, the mechanism underlying the changes in skeletal muscle mass and functions in ageing was related to carbohydrate, lipid and amino acid metabolism. Tocotrienol supplementation showed beneficial effects in alleviating energy and amino acid synthesis that may promote the regeneration and renewal of skeletal muscle in ageing rats.
1 Introduction
The greatest significant influence on human life span and health is inevitable ageing. Most individuals on earth are middle-aged or older, and in high-income nations, the proportion of those over 60 is increasing faster than that of any other age group (Beard et al., 2016). The number of Americans 65 years old and above was anticipated to be around 43.1 million in 2012, and by the year 2050, it is expected to increase to 83.7 million (Ortman et al., 2014). By 2050, 1.6 billion people over 65 are expected to live on the planet (Roberts et al., 2018). This demographic transformation is one of the most significant socio-economic issues of the current decade because ageing is linked to several comorbidities that lead to fast-rising health care expenses (Gasior et al., 2012). One of the distinguishing characteristics of ageing is the gradual decrease of muscle mass and physical function, often known as sarcopenia (Roubenoff, 2000). Sarcopenia typically begins in the fifth decade of life (Miljkovic et al., 2015; Cruz-Jentoft et al., 2010; Clark and Manini, 2012). It can affect mobility and increase the risk of falling, thus increasing the cost of healthcare and hospitalisation, which increases the economic burden within the society (Chung et al., 2018). Since sarcopenia is now recognised as a significant clinical phenomenon, interdisciplinary efforts are being made to recognise, comprehend, prevent and treat this disorder (Cooper et al., 2013; Jean-Yves Reginster, 2016).
Insight into the molecular mechanisms that cause ageing has advanced remarkably. Sarcopenia may result from various age-related molecular and cellular damage, also known as the hallmarks or pillars of ageing. These include loss of proteostasis, dysregulated nutrient sensing, stem cell exhaustion/dysfunction, cellular senescence, genomic instability, mitochondrial dysfunction and epigenetic alterations (López-Otín et al., 2013) (Kennedy et al., 2014). One of the most significant roles of skeletal muscle is its exceptional ability to produce force and power. Strength, or the maximum capacity of skeletal muscle to generate force, is a function of the muscle’s cross-sectional area and the nervous system’s ability to activate the corresponding motor fully. According to cross-sectional research, older adults strongly correlate muscle size and maximum strength. However, a more nuanced association has been found in studies that tracked changes in muscle strength and mass over time (Goodpaster et al., 2006) (Lauretani et al., 2003).
The simultaneous decrease of skeletal muscle mass and strength with age affects independence and quality of life by reducing locomotor performance and jeopardising metabolic health. This is shown in the solid epidemiological links between sarcopenia and dynapenia, risk of non-communicable diseases (such as diabetes, chronic obstructive pulmonary disease and cancer), and ensuing morbidity and mortality (Nichols et al., 2019; Newman et al., 2006). Developing methods for stratification, identifying targets for treatment, and triaging those in need of early intervention could all be accomplished by identifying molecular signals linked to muscle ageing (Sood et al., 2015; Xia et al., 2013).
In recent years, utilising omics technologies (such as transcriptomics, proteomics and metabolomics) has allowed researchers to better understand the underlying causes of various illness states and create biomarkers for either diagnosis or prognosis (Bhattacharya et al., 2014; Zierer et al., 2015). For instance, metabolomic methods have already provided insight into alterations in the muscle metabolome with ageing. A recent study by Fazelzadeh and others into age-related changes in muscle metabolome revealed that metabolites linked to mitochondrial function, fibre type and tissue turnover varied between age groups (Fazelzadeh et al., 2016). It is anticipated that local levels of metabolites will reflect the age-related changes in gene expression levels in muscle. According to a recent animal study, age impacts muscle glucose and fatty acid metabolism (Houtkooper et al., 2011). In another study, it was found that ageing causes changes in lipid and glucose metabolism that are specific to certain muscle groups and are consistent with mitochondrial dysfunction (Garvey et al., 2014).
Intriguingly, baseline levels of metabolites from the tricarboxylic acid cycle were reported to be lower in healthy older adults than in younger people in muscle biopsies. These differences were accompanied by lower concentrations of ATP, ADP, branched-chain amino acids, and acylcarnitine in older, healthy subjects, suggesting impaired mitochondrial function or a lower number of mitochondria in the older subjects’ muscle, which in turn may be a result of the older subjects’ lower habitual physical activity (Fazelzadeh et al., 2016). Biochemical features of mammals’ skeletal muscle have been shown to change in the course of ageing, mainly within the energy metabolism system (Ermini 1976). This study looks into untargeted metabolomics whereby all the low molecular weight compounds or metabolites that are present and participate in biochemical reactions at a particular time are captured and quantified (Horgan and Kenny 2011). Utilising a metabolomic-based approach could provide insight into the overall molecular mechanisms of disease progressions and how a therapeutic agent works at a metabolic level.
The metabolic basis of sarcopenia is not very much known, and there have been no reports on how tocotrienol can affect the metabolic profiling of skeletal muscle in ageing and sarcopenia. Sarcopenia has been shown to decrease metabolic activities in mitochondria, muscle, kidney, and methylation compared with the declined metabolic activities for antioxidation in frailty (Kameda et al., 2020). There has been growing evidence that tocotrienol, which is a vitamin E isomer, can prevent the onset of age-related chronic illnesses and metabolic disturbances, like obesity (Zhao et al., 2016; Fukui 2019; Pang and Chin 2019), cardiovascular disease (Ramanathan et al., 2018), type-2 diabetes mellitus (Chung et al., 2020; Mahjabeen et al., 2021), arthritis (Haleagrahara et al., 2014; Radhakrishnan et al., 2014; Chin et al., 2019), osteoporosis (Shen et al., 2017) and sarcopenia (Khor et al., 2014; Khor et al., 2016; Chung et al., 2018; Lim et al., 2019).
Vitamin E comprises two subgroups: tocopherols and tocotrienols (Schneider 2005). It has been established that tocotrienols have superior anti-inflammatory and antioxidant activities compared to α-tocopherols (Peh et al., 2016). Palm oil is the most abundant source of tocotrienols, referred to as tocotrienol-rich fraction (TRF). Using palm oil as a lipid carrier appears to enhance the bioavailability and solubility of the treatment, improving the permeability and effectiveness of medications, stabilising the emulsification of formulation between emulsifier and surfactant, and extending the shelf life of the therapeutic agent. Palm oil has demonstrated beneficial behaviour in giving variety in medicine design, shape and delivery (Goon et al., 2019). The long-chain triglycerides in palm oil are enzymatically processed before being taken up by enterocytes and absorbed into the bloodstream (Goon et al., 2019).
The skeletal muscle ageing process is typically accompanied by impaired muscle metabolism, including mitochondrial dysfunction and insulin resistance (Distefano and Goodpaster, 2017). However, strategies to slow ageing have mostly failed to achieve their desired response. As a result, the current study aimed to identify any potential impacts of TRF on several metabolic pathways in the ageing Sprague Dawley rat’s muscle tissue.
2 Materials and methods
2.1 Animal model
Three months old, 9 months old and 21 months old male Sprague Dawley (SD) rats were purchased from Laboratory Animal Resources Unit (LARU), University Kebangsaan Malaysia. They were separated into three groups of young (3 months old), adult (9 months old) and old (21 months old). Rats in each group were further divided into subgroups of control and treated groups with 10 rats per group. After a week of acclimatisation, rats were housed one per cage and provided food and water ad libitum. Rats in control and treated groups were given 60 mg/kg body weight/day of refined, bleached, and deodorised (RBD) palm olein (Sime-Darby Plantation Berhad) and 60 mg/kg body weight/day of tocotrienol-rich fraction (TRF) (Sime-Darby Plantation Berhad) via oral gavage for 3 months respectively. Muscle function tests were performed at 0 months before the start of the TRF administration and after 3 months of TRF administration. Blood samples were also taken via retro-orbital sinus at 0 months, 1.5 and 3 months of TRF administration. After 3 months of the TRF administration, the rats were sacrificed, and organs were harvested, including the gastrocnemius and soleus muscle from both hind legs. They were snap frozen and stored at −80°C until further analyses. The University Kebangsaan Malaysia ethical committee approved all animal protocols used in this study with approval number BIOK/FP/2020/SUZANA/25-MAR/1099-MAR-2020-DEC.2022.
2.2 Vitamin E preparation
TRF (Golden Tri™ E 70) and RBD palm olein were a gift from Sime Darby Plantation Berhad. TRF consists of 24% α-tocopherol, 27% α-tocotrienol, 4% β-tocotrienol, 32% γ-tocotrienol and 14% δ-tocotrienol in every Gram of TRF. RBD palm olein consist of 0.054% free fatty acids, 0.043% moisture and impurities, 0.45% peroxide values and 64.71% iodine value. 60 mg/kg body weight of TRF was administered to the rats in the treated group over 3 months. TRF mixture was prepared every week in a dark room by adding 2.4 g of TRF into 40 ml of RBD palm olein in a falcon tube and vortexed until thoroughly mixed. The falcon tube was wrapped with aluminium foil to protect it from sunlight and kept at 4°C.
2.3 Muscle function tests
2.3.1 Weight-loaded performance swim test
Experimental rats were loaded with the weight of 3% body weight at the base of the tail and forced to swim in the water of 22 ± 1°C temperature and 30 cm depth. The time from when the rats were put in the water to the point at which rats failed to return to the water surface within 10 s was recorded as exhaustion time.
2.3.2 Grid-hang test
The rat was placed onto the cage lid. The rat was allowed to accommodate to the environment for 3–5 s before the lid was turned over slowly and held at least 30 cm over a rat cage containing 5–7 cm soft bedding. The cage lid hang time (seconds) is defined as the amount of time it takes the rat to fall from the inverted lid. The hang time was measured from the time the lid was inverted to the time that the rat fell off the lid (determined visually and measured using a stopwatch). The procedure was repeated three times with a rest interval between hang attempts of 2–3 min. The “Holding Impulse” which is associated with the hanging test is equivalent to the hang time multiplied by the body weight (gm sec or Newtons sec; with a conversion factor—9.806 × 10–3 N/gm).
2.4 Euthanization of animals
On day 90 of the study, all rats were fasted for the night before being sacrificed for necropsy analysis. The combination of ketamine, xylazine and zoletil-50 (tiletamine and zolazepam) known as KTX agents was utilised as the anaesthetic in this study. The lower right quadrant of the abdomen was chosen for intraperitoneal injection of the KTX agents because of their speed, effectiveness, and lack of discomfort. Each rat received 0.1 ml/250 g of body weight KTX. The rats were then left for about 30 min to allow the KTX agents to give their sedative effects. This was observed by clinical indicators which include confusion and loss of consciousness, depression of respiration or rapid, irregular breathing, steadily declining heart rate and blood pressure, as well as urine and defecation. The rats were afterwards euthanised by decapitation using a decapitator from Modiezhan Sdn. Bhd, Kuala Lumpur, Malaysia.
2.5 Collection of organs
The sacrificed rats’ internal organs, including the brain, heart, lungs, liver, spleen, kidneys, gastrocnemius muscle and soleus muscle were dissected. The weight of the organs was taken as promptly as possible to prevent drying, and they were examined in relation to the body weight of the animals after being washed with 90% normal saline to remove any adhering tissue. The organs were then kept frozen in a -80°C freezer.
2.6 Tissue sample preparation
Gastrocnemius muscle was thawed, and 1 g of tissue was dissected. Samples were cut into smaller pieces using scissors and transferred to a 15 ml tube. 1 ml of mass spec water was added into the tube and the samples were sonicated in ice. Samples were kept homogenated at -80°C until ready to be used.
2.7 Metabolomic analysis by UHPLC-MS/MS
A muscle tissue sample was thawed and placed in a glass tube filled with one ul Avanti (internal standard), 800 ul 100% methanol (MeOH) and subsequently vortexed. Then, 1.6 ml 100% Dicromethane (DCM) was added using a glass pipette and incubated in a vortex at room temperature for 1 hour at 300 rpm. After that, 600 ul of distilled water was added to form two layers. The sample was then vortexed for 1,000 × g for 10 min at room temperature. Then 1.0 ml lower phase (organic/lipid) was collected in a new glass tube and dried at 1,000 rpm at room temperature in a centrifuge vacuum. Then 1.0 ml upper phase (aqueous/polar/metabolomic) was collected and dried. The dried extracts were kept at −80°C. When the samples were ready to run, it was reconstituted with 100 ul isopropanol:MeOH (1:1) and 100 ul was transferred through a filter to vials using syringe and syringe filters. For the quality control (QC) sample, 5 uL of all samples were mixed from each vial into a tube, spun down, and 100 ul were transferred into a vial and capped (Goon et al., 2021). The vials were randomly placed into the Liquid Chromatography-Mass Spectrometry and run for 3 days. Untargeted metabolomics analysis was performed using the UHPLC system (Dionex Ultimate 3,000; Thermo specific) and Orbitrap-MS (Q Exactive HF, Thermo Scientific).
2.8 Statistical analysis
Metabolomic profiles were compared among groups using MetaboAnalyst 5.0 software. Principal component analysis (PCA) was used to perform multivariate data analysis. Data sets were then scaled and processed to minimise technical variability between individual samples before extracting pertinent biological information (van den Berg et al., 2006). T-tests and fold-change analysis were conducted (Xia and Wishart 2016). A p-value of 0.05 was regarded as statistically significant.
3 Result
3.1 Measurement of exhaustion time via weight-loaded performance swim test
The exhaustion time was significantly decreased at 3 months in adult control rats (AC) and old control rats (OC) as compared to young control rats (YC) (Figure 1A). Treatment with TRF significantly increased the exhaustion time at 3 months of young treated rats (YT) as compared to YC. No significant change was observed in the adult and old treated groups after 3 months of TRF treatment.
FIGURE 1
FIGURE 1. (A) Weight-loaded performance swim test. (B). Hang time. (C) Holding Impulse. Data are presented as mean ± SD. *p < 0.05, significantly different compared to control, ap < 0.05, significantly different compared to young control rats; bp < 0.05, significantly different compared to young treated rats; cp < 0.05, significantly different compared to adult control rats. Data was analysed using one way ANOVA with a post hoc LSD.
As for the grid hang test, we did not obtain any significant differences between the control and treated groups of rats.
3.2 Measurement of hang time and holding impulse
Results showed a significant decrease in the hang time of adult and old control rats compared to young control rats after 3 months. However, no significant change was observed in the hang time and holding impulse after 3 months of TRF treatment (Figure 1B,C).
3.3 Differential metabolomic analysis between control and treated groups
Principle component analysis (PCA) of young control rats (YC) against adult control rats (AC) generated a 39.6% variation in AC when compared to YC in the positive mode, whereby the PC1 score was 24.5%, and PC2 score was 15.1% (Supplementary Figure S1A). The PCA score plot for negative mode described a variation of 42.3% with 27.1% of PC1 and 15.2% of PC2 (Supplementary Figure S1B). PCA score plot showed good separation in positive mode but slight overlapping in negative mode.
PCA of YC against old control rats (OC) generated 52.4% variation in OC compared to YC in the positive mode whereby the PC1 score was 39% and PC2 score was13.4% (Supplementary Figure S1C). The PCA score plot for negative mode described a variation of 56.2% with 42.9% of PC1 and 13.3% of PC2 (Supplementary Figure S1D). PCA score plot showed good separation in both positive and negative modes.
PCA of AC against OC generated 53.3% variation in OC compared to AC in the positive mode, whereby the PC1 score was 38.7%, and the PC2 score was 14.6% (Supplementary Figure S1E). The PCA score plot for negative mode described a variation of 59.8% with 45.4% of PC1 and 14.4% of PC2 (Supplementary Figure S1F). PCA score plot showed good separation in both positive and negative modes.
PCA of YC against young treated (YT) generated a 35.7% variation in YT compared to YC in the positive mode, whereby the PC1 score was 20.7%, and the PC2 score was 15% (Supplementary Figure 2A). The PCA score plot for negative mode described a variation of 43.7% with 24.8% of PC1 and 18.9% of PC2 (Supplementary Figure 2B). PCA score plot showed overlapping in both positive and negative modes.
PCA of AC against adult treated (AT) showed 39.1% variation in AT compared to AC in the positive mode whereby PCI score was 22.3%, and PC2 score was 16.8% (Supplementary Figure 2C). The PCA score plot for negative mode described a variation of 45.3% with 27.5% of PC1 and 17.8% of PC2 (Supplementary Figure 2D). PCA score plot showed overlapping in both positive and negative modes.
PCA of OC against old treated (OT) showed 54% variation in OT compared to OC in the positive mode whereby PC1 score was 40.8%, and PC2 score was 13.2% (Supplementary Figure 2E). The PCA score plot for negative mode described a variation of 54.9% with 35.3% of PC1 and 19.6% of PC2 (Supplementary Figure 2F). PCA score plot showed overlapping in both positive and negative modes.
3.4 Metabolites profiling and regulation in control and treated groups of rats
Control groups were compared between young, adult and old groups to study the effect of age on the expression of metabolites. A comparison between YC and AC generated 19 identified metabolites from 81 metabolic features (Table 1). L-Palmitoyl carnitine was the most up-regulated metabolite in AC, followed by decanoyl carnitine and glycerol 3-phosphate. In contrast, 3-phosphoglyceric acid was the most down-regulated metabolite followed by several other metabolites such as phosphoenol pyruvic acid, aspartyl phenylalanine and nicotinamide adenine dinucleotide. A comparison between YC and OC generated a total of 53 identified metabolites from 81 metabolic features (Table 2). Decanoyl carnitine was the most up-regulated metabolite in OC followed by L-palmitoyl carnitine. In contrast, the majority of the metabolites in OC were downregulated such as aspartyl phenylalanine (the most down-regulated metabolite) followed by amino acids such as arginine, aspartic acid, glutamic acid, histidine, leucine/isoleucine, lysine, phenylalanine, tryptophan, tyrosine and valine. A comparison between AC and OC generated 53 identified metabolites from 81 metabolic features (Table 3). Glycerol 3-phosphate was the most up-regulated metabolite in OC followed by mannose 6-phosphate/fructose 1-phosphate/fructose 6-phosphate/glucose 6-phosphate and 3-phosphoglyceric acid. In contrast, most of the metabolites in OC were downregulated with leucyl-glycine being the most down-regulated metabolite followed by other amino acids.
TABLE 1
TABLE 1. List of significant metabolites in AC against YC.
TABLE 2
TABLE 2. List of metabolites in OC against YC.
TABLE 3
TABLE 3. List of metabolites in AC vs. OC.
Profiled metabolites identified in the control groups were compared based on fold-change. Based on these comparisons, carnitine was the major metabolite group involved in all three control groups. Decanoyl carnitine was found to be up-regulated by 4.69-fold in AC against YC (Table 1), 25.93-fold in OC against YC (Table 2) and 5.53-fold in OC against AC (Table 3). Besides that, L-palmitoyl carnitine was up-regulated by 10.74-fold in AC against YC (Table 1) and 13.87-fold in OC against YC (Table 2). Glycerol 3-phosphate was another major metabolite that was found to be up-regulated in all three control groups, with an increase of 7.30-fold in AC against YC (Table 1) and 4.85-fold in OC against YC (Table 2) and 35.38-fold in OC against AC (Table 3). Mannose 6-phosphate/Fructose 1-phosphate/beta-D-Fructose-6-phosphate/Glucose 1-phosphate was found to be up-regulated in both OC against YC (Table 2) (3.83-fold) and OC against AC (Table 3) (11.41-fold).
In contrast, phosphoenolpyruvate (PEP) metabolite showed an 18.07-fold decrease in AC against YC (Table 1). Another major metabolite group that was found to be involved in all three groups is glycerate, which includes glyceric acid and 3-phosphoglyceric acid. Glyceric acid was found to be down-regulated by 2.41-fold in AC against YC (Table 1), 8.24-fold in OC against YC (Table 2) and 3.42-fold in OC against AC (Table 3). 3-Phosphoglyceric acid was down-regulated by 40.86-fold in AC against YC (Table 1) and 3.69-fold in OC against YC (Table 2). However, it was up-regulated by 11.06-fold in OC against AC (Table 3).
Treatment groups were compared based on fold change against untreated control groups of young, adult and old rats. A total of 81 metabolic features were identified. Comparisons between YC and YT groups identified seven significant metabolites (Table 4). Decanoyl carnitine and L-palmitoyl carnitine showed an up-regulation of 2.81-fold and 7.41-fold, respectively in TRF-treated rats. Aspartyl phenylalanine and nicotinamide adenine dinucleotide (NAD+) were down-regulated by 3.37-fold and 2.27-fold, respectively. A comparison between AC and AT groups identified 16 significant metabolites (Table 5). NAD + showed the highest up-regulation (7.79-fold) while citric acid showed the most down-regulation (17.30-fold). Spermine was up-regulated by 3.56-fold and aspartic acid by 1.26-fold. A comparison between OC and OT groups identified 11 significant metabolites (Table 6). Nine of the 11 metabolites showed up-regulation, with aspartic acid being the most up-regulated by 8.98-fold, followed by N6-Me-Adenosine (4.54-fold), phenylalanine (2.13-fold), tryptophan (2.07-fold) and histidine (1.84-fold). Only carnitine and L-acetyl carnitine showed down-regulation by 1.15-fold and 1.19-fold, respectively.
TABLE 4
TABLE 4. List of metabolites in YT against YC.
TABLE 5
TABLE 5. List of metabolites in AT against AC.
TABLE 6
TABLE 6. List of metabolites in OT against OC.
3.5 Biochemical pathways analysis of muscle metabolomes in control and treated groups of rats
Pathway analysis was performed using MetaboAnalyst on the muscle metabolomes expression during ageing. A comparison of profiled metabolites between AC and YC generated 21 biochemical pathways (Figure 2). The significant pathways involved were primarily fructose and mannose metabolism, glycolysis/gluconeogenesis, amino sugar and nucleotide sugar metabolism, glycerolipid metabolism, TCA cycle, pentose phosphate pathway and glyoxylate and dicarboxylate metabolism (Supplementary Table S1). Pathways were identified as significant with a p-value <0.05 and an impactor of >1.0. Metabolites profiled in OC compared to YC generated 39 biochemical pathways (Figure 3). The significant pathways involved were primarily histidine metabolism; pentose phosphate pathway; beta-alanine metabolism; phenylalanine, tyrosine and tryptophan biosynthesis; arginine biosynthesis; glutathione metabolism; purine metabolism; pentose and glucuronate interconversions; fructose and mannose metabolism; and arginine and proline metabolism (Supplementary Table S2). Comparison of profiled metabolites in OC and AC generated 39 biochemical pathways (Figure 4). The significant pathways involved were primarily histidine metabolism, pentose phosphate pathway; arginine biosynthesis; phenylalanine, tyrosine and tryptophan biosynthesis; D-glutamine and D-glutamate metabolism and fructose and mannose metabolism (Supplementary Table S3).
FIGURE 2
FIGURE 2. Biochemical pathway analysis of metabolites profiled for YC vs. AC.
FIGURE 3
FIGURE 3. Biochemical pathway analysis of metabolites profiled for YC vs. OC.
FIGURE 4
FIGURE 4. Biochemical pathway analysis of metabolites profiled for AC vs. OC. a: Fructose and mannose metabolism.
The effect of TRF treatment on the metabolic pathway was determined by comparing the muscle metabolomes expression in the TRF-treated group with the untreated control group. A comparison of the profiled metabolites in the TRF-treated group against the control group of the young rats generated three metabolites (Figure 5) whereby nicotinate and nicotinamide metabolism was the significant biochemical pathway (Supplementary Table S4). In the adult group, a comparison between the profiled metabolites of AT against AC, generated a total of 21 biochemical pathways (Figure 6), with the significant pathways involved primarily being fructose and mannose metabolism; alanine, aspartate and glutamate metabolism; amino sugar and nucleotide sugar metabolism; and nicotinate and nicotinamide metabolism (Supplementary Table S5). In the old group, a comparison between profiled metabolites of OT against OC, generated 12 biochemical pathways (Figure 7). The significant pathways involved were histidine metabolism and phenylalanine, tyrosine and tryptophan biosynthesis (Supplementary Table S6).
FIGURE 5
FIGURE 5. Biochemical pathway analysis of metabolites profiled for YC vs. YT.
FIGURE 6
FIGURE 6. Biochemical pathway analysis of metabolites profiled for AC vs. AT.
FIGURE 7
FIGURE 7. Biochemical pathway analysis of metabolites profiled for OC vs. OT.
4 Discussion
Sustaining the health of one’s muscles requires a sufficient intake of vitamin E. In a previous study using animal models, severe tocopherol deficiency has been observed to impair muscle performance even though vitamin E deficiency is rarely reported in humans (Nier et al., 2006; Rafique et al., 2004). Decrease in muscle mass and function in sarcopenia has been reported to be correlated with low vitamin E levels, as shown by the physical performance test. Invecchiare in Chianti study reported that the level of vitamin E daily intake positively correlates with knee extension strength and total the physical performance (Cesari et al., 2004) indicating the requirement of vitamin E in maintaining muscle strength and function.
In this study, physical performance was observed by conducting the weight-loaded performance swim test and the grid hang test. The results of our study showed that muscle strength was reduced with ageing. Treatment with TRF for 3 months however, increased the exhaustion time in weight-loaded performance swim test of young rats eventhough no similar effects were observed in adult and old rats treated with TRF. This might occur because the young TRF-treated rats have more significant muscle regeneration potential than the adult or old TRF-treated rats. The ability of muscles to regenerate relied entirely on the renewal of satellite cells, which eventually declined with age (Dumont et al., 2015). It has been previously reported that ageing causes the number of satellite cells to decrease (Miljkovic et al., 2015). According to a study by Khor et al., 2016, senescent myoblasts have low proliferative capacities, which showed downregulation of myogenic differentiation genes but increased expression of oxidative damage-associated genes. This study may explain the reduced ability of adults and old TRF-treated rats to regenerate muscle in this study.
This study also demonstrated that supplementation of TRF to young, adult and old rats for 3 months could reduce the levels of DNA damage indicating the capacity of TRF to reduce damaged DNA due to excessive ROS generation. This finding was in line with a previous study which reported that tocotrienols are rich vitamin E derivatives that aid in preventing DNA damage brought on by ageing (Chin et al., 2019; Georgousopoulou et al., 2017; Pathak et al., 2021; Taridi et al., 2014). A previous randomised clinical trial involving middle-aged and older adults supplemented with tocotrienol for 6 months showed a significant reduction in DNA damage by 3 months, which is a benefit that persisted through the 6 months of the study (Chin et al., 2019).
In this study, the effect of TRF supplementation on young, adult and old Sprague Dawley rats and its molecular mechanism was elucidated using an untargeted metabolomic approach. The animal model used in this study has been reported to be appropriate for studying sarcopenia (Shavlakadze and Grounds, 2006) (Chai et al., 2011; Schiaffino and Mammucari, 2011; Pötsch et al., 2014; Kob et al., 2015; Tarantini et al., 2019). Aged rat models are the most natural ageing model and have morbidities and mechanisms reasonably similar to those found in humans with sarcopenia (Baek et al., 2020). Rats grow quickly and at around 6 weeks old, they are sexually mature, and after five or 6 months, they are socially mature. An adult animal’s month is roughly similar to 2.5 years in a human (Andreollo et al., 2012). The decline in physical activity that occurs with ageing causes metabolic changes and worsens metabolic abnormalities (Pataky et al., 2021).
In this study, the metabolites profile of the control groups was compared to provide insight into the metabolites regulated by ageing. Distinctive characteristics of ageing skeletal muscle metabolomes were summarised in Figure 8. Our results showed the reduction of alanine, phenylalanine, tyrosine and glycine as well as the branched-chain amino acids (BCAAs)—isoleucine, leucine and valine in the old control group indicating an imbalance between protein synthesis and breakdown during ageing. Interestingly, none of these amino acid alterations was present in the young or adult groups, indicating that ageing affects dysregulated amino acid metabolism. A biomarker of muscle protein degradation, 3-methylhistidine, was noticeably downregulated in the muscle tissue of the elderly control group. This metabolite is not recycled but quantitatively excreted in the urine and has been proposed as an index of muscle protein turnover.
FIGURE 8
FIGURE 8. Muscle metabolomes changes in ageing rats. Metabolite concentrations in muscle specimens are depicted graphically and subjected to quantitative analysis. Box and whiskers plots with 95% confidence intervals are presented for quantified amino acids. Analysis was performed using one-way Anova with Tukey’s post hoc analysis. *p < 0.05.
One of the most striking metabolite changes with age is in the level of biochemical markers of glucose metabolism. Levels of glycolytic intermediates decreased significantly in the muscle of adults and old rats. 3-Phosphoglycerate and phosphoenol pyruvate were each detected with decreased fold change in the adult and old control groups besides downregulation of nicotinamide adenine dinucleotide (NAD), a co-enzyme central to metabolism. Glycolysis is the primary pathway of glucose metabolism for energy production (Xiang et al., 2021). A decrease in glycolytic intermediate means that there is an impairment in energy production. It is often believed that ageing causes glucose intolerance, and skeletal muscle is the primary site of glucose uptake (Kohrt and Holloszy, 1995). Previous research reported that resting skeletal muscle glycogen stores were 60% lower in old than young individuals (Meredith et al., 1989). This suggests an age-related impairment in the glycogen synthase pathways (Consitt et al., 2019). Other studies have reported that skeletal muscle glycogen synthase activity is diminished in older adults compared to younger individuals (Pehleman et al., 2005; Poulsen et al., 2005; Biensø et al., 2015).
Carnitine is an amino acid derivative that functions as a transporter of long-chain fatty acids from the cytosol to the mitochondrial matrix for fatty acid β-oxidation (Gnoni et al., 2020). Acylcarnitine is a metabolite of fatty acid transportation whereby fatty acyl CoA will be released from acylcarnitine for fatty acid oxidation. Decanoyl carnitine and L-palmitoyl carnitine are medium-chain acylcarnitine, an intermediate of fatty acid β-oxidation by-products (Ramos-Roman et al., 2012). It is also a marker for incomplete fatty acid oxidation (Mai et al., 2013), and acylcarnitine accumulation is a marker for mitochondrial dysfunction (Al-Bakheit et al., 2016). This study shows an increase in decanoyl carnitine and L-palmitoyl carnitine levels in ageing rats, which is in line with recent reports that suggest the rise of acylcarnitine levels may be caused by the impairment of lipid oxidation or a natural response to an excess lipid supply (Ramos-Roman et al., 2012). It is known that lipid oxidation indeed decreases in elderly individuals (Calles-Escandón and Poehlman, 1997).
Phosphoenolpyruvate is an intermediate for both glycolysis and gluconeogenesis. It can be converted to pyruvate by pyruvate kinase to produce energy (Hamasaki et al., 1978). Recent studies have reported that the ageing of C. elegans is highlighted by a progressive decline in cytosolic phosphoenolpyruvate carboxykinase, which is the enzyme responsible for converting pyruvate to phosphoenolpyruvate in gluconeogenesis (Yuan et al., 2016). This study shows a decrease in phosphoenolpyruvate in the adult control compared to the young control group indicating inefficient glycolysis and gluconeogenesis. Thus, changes in phosphoenolpyruvate with age are likely involved in energy metabolism that acutely affects the physiology of ageing organisms, thus impacting the ageing process (Feng et al., 2016).
In this study, TRF supplemented group was compared with the RBD palm olein supplemented group as a control to provide insight into the different metabolites being regulated by TRF supplementation in young (3 months old), adult (9 months old) and old (21 months old) rats. The RBD palm olein was used in this study as it is the carrier for TRF. It is the liquid form of palm oil that is edible and is commonly used for cooking, which is easily accessible. TRF used in this study was extracted from the Malaysian palm tree Elaeis guineensis. Palm-based TRF is easily accessible and has been studied for its therapeutic properties, mainly in Malaysia. On the other hand, the Westerns are more inclined toward annatto oil or rice bran oil-based TRF. What differs between these oils is the amount of vitamin E homologs in them. Annatto and rice bran oil-based TRF encompasses a higher concentration of δ-tocotrienol and a lower amount of tocopherol (Frega et al., 1998; Burdeos et al., 2012; Allen et al., 2017). Contrarily, palm oil is one of the most abundant natural sources of tocotrienols, which contains up to 800 mg/kg weight of the α- and γ-tocotrienol isotypes in crude palm oil (also known as tocotrienol-rich fraction). In palm oil, vitamin E is distributed as 30% tocopherols and 70% tocotrienols (Sen et al., 2010). Therefore, utilising palm-based TRF in this study may produce robust knowledge in the metabolomic analysis as both tocotrienol and tocopherol would affect multiple genes and metabolic pathways (Pang and Chin, 2019).
Rats supplemented with TRF for 3 months showed an increase in spermine in the adult treated group. The same metabolite was downregulated in the adult control rats when compared to young control group. Spermine, which is oxidised by spermine oxidase, is an essential regulator of muscle gene expressions and fibre size. Studies have shown that a repressed level of spermine leads to muscle atrophy (Ceci et al., 2017). The decrease in spermine with ageing observed in this study was counter-regulated by TRF as shown by the increase of spermine with TRF treatment indicating that supplementation of TRF can reverse the repression of spermine due to ageing. Another metabolite that was found to be upregulated with TRF treatment in adult rats was nicotinamide adenine dinucleotide (NAD). Previous research has reported a decline in NAD+ concentrations with ageing in a tissue-specific manner (Braidy et al., 2011; Massudi et al., 2012). NAD+ is a coenzyme that facilitates redox reactions in all living cells mainly for energy production (Obrador et al., 2021). The upregulation of NAD+ in this study after 3 months of TRF supplementation in the adult treated group coincides with the TRF antioxidant properties that may have reversed the ageing-decline of NAD+ and promoted energy production.
Another metabolite highly downregulated with TRF treatment in the adult group was citric acid, which shows a 17.30-fold downregulation in the treated group compared to the control group. Citric acid is an intermediate of the tricarboxylic acid (TCA) cycle (Baldwin and Krebs 1981), which is involved in a metabolic pathway converting carbohydrates, proteins and fats into carbon dioxide and water to produce energy. Evidence demonstrates that energy production progressively decreases with age, mainly due to the decline in mitochondrial function (Bratic and Trifunovic 2010). A decrease in the level of citric acid shows usage of the metabolite in the TCA cycle, which in this study is shown in the TRF-treated group. Thus, showing that TRF supplementation reverses the age-associated decrease in energy production.
In this study, glycerol 3-phosphate was highly upregulated with ageing. Glycerol 3-phosphate is produced from the phosphorylation of glycerol by a glycerol kinase. The source of glycerol can be from the breakdown of triacylglycerol or triglycerides via lipolysis. Glycerol 3-phosphate is converted to dihydroxyacetone phosphate (DHAP), an intermediate of glycolysis and gluconeogenesis by glycerol 3-phosphate dehydrogenase (mGDPH) utilising NAD+ via a reversible reaction. Studies have shown that loss of mGDPH attenuates muscle regeneration, while overexpression of it ameliorated dystrophic pathology in mice (Liu et al., 2018). Muscle regeneration decreases with age as ageing causes satellite cells to malfunction, influencing their regenerative and self-renewal capacities (Sousa-Victor et al., 2014). Other studies have also shown how age reduces glycerol 3-phosphate (Nemutlu et al., 2015). The findings of this study showed that there was an accumulation of glycerol 3-phosphate in old rats which was alleviated by TRF treatment. This agrees with a previous study, which reported that TRF increases the proliferation capacity of senescent myoblasts, thus increasing muscle regeneration (Khor et al., 2016). The accumulation of glycerol 3-phosphate was linked with increased NAD+, because less NAD+ is converted to NADH due to less conversion of glycerol 3-phosphate to DHAP. In this study, an upregulation of NAD+ was seen after 3 months of TRF supplementation in the adult group.
As for the muscle metabolomes expression in the old group of rats, several metabolites particularly the amino acids were downregulated. TRF treatment however, increased the expression of aspartic acid, phenylalanine, tryptophan and histidine besides upregulating N6-Me-adenosine, cytidine, xanthine, indoleacrylic acid and N-acetylneuraminic acid in old rats. Aspartic acid is important in glutamate flux through the TCA cycle and glutamate transamination (Birsoy et al., 2015). A previous study showed that aspartic acid levels decreased in old age (Lo et al., 2020) which was similar to the findings of this current study. However, with TRF treatment, the aspartic acid level was upregulated by 8.98-fold in old group of rats. This shows that TRF supplementation reverses the age-declining cause of aspartic acid involvement in biochemical pathways of TCA cycle activity (Lancha et al., 2009).
The metabolites profiled also detected an upregulation of N6-Me-Adenosine. Researchers in Bonn, Germany, have reported that adenosine, a metabolite and signaling molecule, can enhance muscle function and brown fat during ageing and obesity. N6-methyladenosine is a methylation product which occurs in the N6-position of adenosine, the most prevalent internal modification of eukaryotic mRNA. Many reports have suggested that N6-methyladenosine modulates gene expression, which regulates cellular processes, including cell self-renewal, differentiation, invasion and apoptosis (He et al., 2019). Recent studies have shown that N6-methyladenosine plays an essential function in skeletal muscle development by regulating myoblast proliferation and differentiation during myogenesis and is the key to biological processes and regulatory pathways during skeletal muscle development (Zhang et al., 2020). N6-methyladenosine can accurately regulate stem cell differentiation and reprogram it during stem cell development by modulating the gene expression involved in the corresponding processes (Wang et al., 2019). Similar to the function of glycerol 3-phosphate, which plays a role in muscle regeneration, our results showed that N6-methyl adenosine was downregulated in old rats when compared to the young and adult control groups. However, after 3 months of TRF supplementation, the concentration of N6-methyl adenosine has increased in both adult and old groups of rats, showing that TRF supplementation might be involved in facilitating the muscle regeneration process. Significant metabolic changes between the control and treated group were summarised in Figure 9.
FIGURE 9
FIGURE 9. Significant metabolic changes after tocotrienol-rich fraction treatment.
The muscle performance finding from this study was limited as there were logistic issues due to the Covid-19 pandemic and the lack of proper software to observe the behaviour of the rats during the muscle performance tests. Therefore, further study is needed to explain the effect of TRF on muscle performance. However, the molecular analysis of the mechanism of TRF in reducing the level of oxidative stress in muscle supported by the modulation of the metabolic pathways observed in the present study strengthens the properties of TRF as a potential agent to prevent age-related muscle degeneration and sarcopenia.
5 Conclusion
Our data indicate that TRF improves muscular function, and delays muscle degeneration due to ageing in Sprague Dawley rats. Our findings also showed the principal variations in muscle metabolomes due to ageing as shown in the old and young groups of rats which were related to tissue turnover, fibre size and mitochondrial function. The effect of tocotrienol-rich fraction on reducing several metabolites such as glycerol 3-phosphate and upregulating several amino acids and N6-Me-adenosine are likely to ameliorate muscle regeneration and cell self-renewal in the old group of rats. The mechanisms underlying the modulation in skeletal muscle metabolomes expression following TRF supplementation positively impact the potential treatment of sarcopenia in aged rats.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The animal study was reviewed and approved by the Universiti Kebangsaan Malaysia Animal Ethical Committee.
Author contributions
SM designed the study and supervised the project. SS, NA, and NH performed the experiments and prepared the figures. SM and JT provided experimental technical assistance and commented on the results. SS, JT, and SM wrote the paper. All authors contributed to the article and approved the submitted version.
Funding
This study was financially supported by the Universiti Kebangsaan Malaysia Grant DIP/2019/030.
Conflict of interest
Author NI was employed by the company Sime Darby Plantation Berhad.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmolb.2022.1008908/full#supplementary-material
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Keywords: tocotrienol, sarcopenia, untargeted metabolites, skeletal muscle, ageing
Citation: Saud Gany SL, Tan JK, Chin KY, Hakimi NH, Ab Rani N, Ihsan N and Makpol S (2022) Untargeted muscle tissue metabolites profiling in young, adult, and old rats supplemented with tocotrienol-rich fraction. Front. Mol. Biosci. 9:1008908. doi: 10.3389/fmolb.2022.1008908
Received: 01 August 2022; Accepted: 15 September 2022;
Published: 14 October 2022.
Edited by:
Xiaoyang Su, Rutgers, The State University of New Jersey, United StatesReviewed by:
Zhaoyue Zhang, The Rockefeller University, United StatesLin Wang, Chinese Academy of Medical Sciences and Peking Union Medical College, China
Copyright © 2022 Saud Gany, Tan, Chin, Hakimi, Ab Rani, Ihsan and Makpol. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Suzana Makpol, suzanamakpol@ppukm.ukm.edu.my