Evolution of potential biomarkers of acute muscle injury after physical exercise

Abstract

Skeletal muscle injury is a frequent event and diagnosis using the classical blood markers sometimes produces unsatisfactory results. Therefore, objective of the study was to detect new biomarkers in plasma, saliva and urine in response to acute muscle damage induced by physical exercise. A cross-sectional study was conducted with 27 American football players. Before the physical exercises (T0), 60 minutes (T1) and 24 hours (T2) after physical exercise, was determined the clinical, biochemical and molecular parameters, including ADA, TBARS, leukocytes, lymphocytes and comet assay. The serum ADA was significantly higher in T1 and T2, in the urine there was a significant increase in T1, in the saliva there was no significant differences. There was an increase in serum TBARS in T2, saliva and urine in T1. The leukocytes increased in T1 and decreased in T2. Through the comet assay was observed significant DNA damage in T1 and T2. Serum and urinary ADA activity, serum, urinary and salivary TBARS are robust and promising biomarkers of acute muscle injury and that the comet assay allows a quick and effective evaluation of DNA lesions induced by physical exercise and could be used to monitor athletes avoiding injuries that are more serious.

Keywords:
Biomarkers/serum; Biomarkers/saliva; Biomarkers/urine; Exercise; Athletes; Athletic injuries; Adenosine deaminase/analysis; DNA

INTRODUCTION

Every high-performance sport demands more and more from its athletes because the competitions and training put the athlete’s body under constant physiological and psychological stress, often because they happen in a short time, not allowing the musculature to regenerate (^{Wilcock, Cronin, Hing, 2006}). This stress can progress from a benign initial phase to a subclinical injury, which will impair performance and cause wear and tear on the athlete, contributing to the withdrawal of competitions (^{Lazarim et al., 2009}).

Intense physical activity requires a greater energy demand with a consequent increase in the release of AMP, ADP and intra and extracellular ATP to aid in the control of processes such as platelet aggregation, vascular tone control, neurotransmission, membrane permeability, cardiac function and muscle contraction associated with the exercise. (Broberg, ^Sahlin, 1989; ^{Erlinge, Burnstock, 2008}).

Thus, ectonucleotidase enzymes expressed on the surface of several cells, hydrolyze these nucleotides then controlling their levels. This enzymatic complex includes the enzymes E-NTPDase (ectonucleoside triphosphate diphosphohydrolase), E-NPP (ectonucleotide pyrophosphatase/phosphodiesterase), E-5′-nucleotidase and adenosine deaminase (ADA) (^{Fürstenau et al., 2006}). Adenosine can be directly inactivated on the cell surface through the sequential actions of ADA, which catalyzes the irreversible deamination of adenosine and leads to inosine (^{Blackburn, Kellems, 2005}).

In addition, a probable cause of fatigue, muscle damage and inflammation is the occurrence of ruptures of fragile sarcomeres when high forces are applied and are not absorbed and, as a result of interruption of sarcomeres, due to heavy/prolonged physical exercise, may occur release of enzymes that are present in the cytoplasm of muscle cells by lesioning the ultrastructure of the fibers and development of an important inflammatory response. (^{Evans, Meredith, Cannon, 1986}; ^{Córdova Martínez, Alvarez-Mon, 1999}).

Even ADA being found in small amounts in muscle tissue, it can temporarily increase its serum concentrations as a result of muscle injuries because it is widely distributed in cells of the immune system that participate in the processes of degeneration and regeneration of muscle and surrounding connective tissue after muscle damage (^{Livi, 1999}; ^{Tidball, 2005}; ^{Wassmansdorf, 2012}).

ADA is a potent inflammatory biomarker that can be determined in both blood and biological fluids as it is widely distributed in human tissues and is associated primarily with CD4 + T lymphocyte proliferation and performs tight control of extracellular adenosine concentrations (^{Chielle et al., 2015}; ^{Livi, 1999}; ^{Zavialov et al., 2010}).

Moreover, with increased oxygen consumption (O₂) due to the practice of intense physical exercises, acute or chronic oxidative lesions may occur in the cells due to the production of reactive oxygen species (ROS) and consequent lipoperoxidation (^{He et al., 2016}). As biomarker of oxidative stress, more specifically lipid peroxidation of the cell membrane, are the substances that react with thiobarbituric acid (TBARS), increasing the levels of this product indicates the existence of oxidative stress in the cells, increasing the risk of cellular rupture and contributing to muscle injury (^{Alleman et al., 2014}).

The responses to the tissue damage may increase in hours and days due to the worsening of the oxidative stress and the infiltration of cells of the immune system that will go to the site of the injury to clean the cellular debris, increasing the inflammatory process (^{Baroni et al., 2010}; ^{Chevion et al., 2003}; ^{Souza Jr., Pereira, 2008}). Therefore, the search for an early diagnosis of muscle injuries and methods that provide quick results has been an increasing practice in high-performance professional modalities, since the current biochemical monitoring is relatively non-specific and involves some physical and psychological discomfort. The objective of this study was to evaluate TBARS and serum ADA and in other no invasive biological samples such as saliva and urine, as well as evidence that biomarkers of DNA damage may be useful in predicting the onset of overtraining which is a condition of fatigue and drop in physical performance that occurs after intense training and competitions

MATERIAL E METHODS

Participants

This essay included 27 male athletes from an American football team from the city of São Miguel do Oeste - SC. The sampling process was performed for convenience and all athletes signed the Free and Informed Consent Form. The Committee of Ethics and research with human beings of the University of the West of Santa Catarina approved the study under the protocol number 1.629.054. For the composition of the samples, inclusion, and exclusion criteria were adopted according to the organization chart 1.

Experimental procedures

The athletes were submitted to a questionnaire prior to performing physical activity, where information was collected regarding age, weight, height, time of physical activity and systolic and diastolic blood pressure. Athletes’ blood pressure was measured before and after physical activity using a manual sphygmomanometer and a Premium brand stethoscope (Accumed-Glicomed, RJ, Brazil). The height of the athletes was measured in centimeters (cm), in a wall stadiometer, Professional ES2020 Sanny® (American Medical do Brasil Ltda, SP, Brazil), and the weight was verified in kilograms (kg), in G-techC scale, model Glass 180, platform type (Accumed-Glicomed, RJ, Brazil).

In order to perform the physical training, the athletes were instructed to stay a 3-day period of rest. The group of athletes was submitted to training protocol, as shown in Table I and all training was supervised by the researchers. Further details of the experimental protocol and training program are described in ^{Uchida et al. (2006}), ^{Hartman et al. (2007}), ^{Hasani-Ranjbar et al. (2012}). The performance of the athletes was controlled. These exercises were chosen because they require a great muscular capacity for development. During the exercises, the athletes did not rest, and recovery was active. The air temperature during testing was 21 °C and relative humidity amounted to 62 %, through the Matsuri Temperature and Humidity Meter (Biogênese Comércio de Artigos Médicos Ltda, PR, Brazil).

TABLE I
Training protocol

Warning-up
Exercice	Sequence
Stationary bicycle	2 minutes
Training
Exercice	Sequence
Step	3 sets of 20 repetitions
Arm bending bosu	3 sets of 20 repetitions
Forward and curl whit dumble (10 kg)	3 sets of 20 repetitions
Development with bars and dumbbells (10 kg)	3 sets of 20 repetitions
Triceps French with washer (15 kg)	3 sets of 20 repetitions
Swing with kettlebell (12 kg)	3 sets of 20 repetitions
Burpee	3 sets of 20 repetitions
Isometric squat	3 sets of 20 repetitions
Medicine ball throw (5 kg)	3 sets of 20 repetitions
Bench triceps	3 sets of 20 repetitions
Speed running	5 minutes

• This sequence of exercises was repeated for 60 minutes.

Samples of blood, saliva, and urine were collected three times: 60 minutes before starting the exercises with the athlete rested (T0), 60 minutes after the physical exercise battery (T1) and 24 hours after the physical exercise battery (T2). All athletes were assessed before and after a single physical exercise session. The blood samples were collected by venipuncture and placed in collection tubes with anticoagulant EDTA and tube without anticoagulant and with separator gel that was left at room temperature for 20 minutes and then centrifuged for 10 minutes at 4000 rpm to obtain the serum.

For saliva collection, athletes were instructed to rinse the mouth with water 3 times; subsequently, a Salivette® was supplied, which consists of a conical container with an absorbent filter. Participants were instructed to remove the filter and place it in the mouth for a period of 3 minutes as recommended by the manufacturer (Salivette Tubes Sarstedt, Nümbrecht, Germany). Afterward, the filter was relocated to the centrifuge container. The samples were frozen at -20 °C, as recommended by ^{Sereg et al. (2011}) until analysis moment.

The urine was collected in a sterile vial, approximately 50 mL. The athletes were instructed to discard the first urine stream and collect midstream directly into the bottle provided. The samples were centrifuged to remove cells, bacteria and crystals, and the supernatant used for laboratory analysis.

In serum, saliva and urine samples, ADA activity was determined by the commercial kit (Ebram Laboratory of Products LTDA® - São Paulo, Brazil), based on the enzymatic deamination of adenosine in inosine by a kinetic form in BIO2000 equipment (BIOPLUS®- São Paulo, Brazil). The values were expressed in U/L. The leukocytes and lymphocytes were analyzed and counted by fluorescence flow cytometry on XS-800i equipment (Sysmex-Roche Diagnostic USA). Lipid Peroxidation was estimated by the measurement of Thiobarbituric Acid Reactive Substances (TBARS) according to the method established by ^{Lapenna et al. (2001}). The reaction product was measured spectrophotometrically at 532 nm and the results were expressed in nmol/L. The evaluation of induced damage to the genetic material was performed by comet assay technique in peripheral lymphocytes as described by ^{Singh et al. (1998}).

Data were expressed as mean ± standard deviation. The Kolmogorov-Smirnov test was used to examine the distribution of variables. Data comparisons were performed by one-way analysis of variance (one-way ANOVA), followed by Tukey`s test (parametric variables) or Kruskal-Wallis`s test followed by Dunn’s test (nonparametric variables). The value of p<0.05 was considered statistically significant. Data were analyzed using Statistica 6.0® software (StatSoft, Tulsa, USA).

RESULTS

The study population consisted of 27 male volunteers with an average age of 22.5±4.2 years old, average weight of 81.9±13.8 kg, average height of 1.79±0.6 meters and physical activity time with an average of 4.0±2.6 years. The volunteers’ blood pressure did not present a significant difference during the three moments (T0, T1 and T2) as shown in Table II.

TABLE II
Basic characteristics of the study population

		T0	T1	T2
N	27
Gender	Male
Age (yaers)	22.5±4.2
Activity time (yaers)	4.0±2.6
Weight (kg)	81.9±13.8
Height (m)	1.79±0.6
Systolic BP (mmHg)		127±11	120±9	123±13
Diastolica BP (mmHg)		79±10	76±8	76±9

• Data were expressed as mean and standard deviation. T0: before the exercises were performed; T1: 60 minutes after physical exercises; T2: 24 hours after physical exercises; BP: Blood Pressure.

There was a significant increase in serum ADA activity in T1 (p<0.0001) and T2 (p<0.05) when compared to T0, followed by a significant decrease in T2 when compared to T1 (p<0.0001). There were no significant changes in ADA activity in saliva. In urine, it was observed a significant increase in ADA activity in T1 (p<0.0001) when compared to T0, followed by a significant decrease in T2 when compared to T1 (p<0.0001) (Figure 1A, B, C). The Table III show a significant increase of total leukocytes in T1 when compared to T0 and a significant decrease in T2 when compared to T1. There was also a significant increase in the amount of lymphocytes in T1 and T2 compared to T0. There was a significant increase in serum TBARS 24 hours after physical exercise (p<0.05). In urine and saliva, it was observed significant increases in T1 when compared to T0, while in urine there was a decrease in T2, salivary TBARS remained significantly increased in T2 when compared to T0 (p<0.0001). Through the comet assay we observed a significant increase of DNA damage in T1 and T2 when compared to T0 (p<0.001), evidencing in these times a greater number of lymphocytes with a tail of Grade 3 and 4 (Figure 2A, B).

TABLE III
Quantification of leukocytes, lymphocytes and TBARS in the studied times

Time (hours)
	T0	T1	T2
Leukocytes (mm3)	8044±1536	9596±1708a	7481±1398b
Lymphocytes (mm3)	2275±159	3399±237a	2817±180b
TBARS in serum (mmol/L)	309±118	397±257*	419±259c
TBARS in urine (mmol/L)	13.6±7.3	80.1±14.3a	35.5±10.7d
TBARS in saliva (mmol/L)	19.4±11.7	26.6±18.0a	34.3±21.6ab

• Data are expressed as means ± SD or median. The data were processed by analysis of variance (One-Way - ANOVA), followed by the Tukey test or Kruskal-Wallis test, followed by the Dunn test. T0: before the exercises are performed; T1: 60 minutes after physical exercises; T2: 24 hours after physical exercises. ^a p<0.001 when compared to T0. ^b p<0.01 when compared to T1. ^c p<0.05 when compared to T0. ^d p<0.0001 when compared to T1.

DISCUSSIONS

Intense physical activity requires a greater energy demand with a consequent increase in the release of AMP, ADP and intra and extracellular ATP to aid in the control of numerous processes (^{Broberg, Sahlin, 1989}; ^{Erlinge, Burnstock, 2008}). ATP and other nucleotides and nucleosides are found in all organ systems where they produce effects both by intracellular and extracellular mechanisms. Intracellular ATP is primarily utilized to drive energy-requiring processes such as active transport, cell motility, and biosynthesis, whereas extracellular ATP is considered a powerful signaling molecule (^{Yegutkin, 2008}). Clear signalling roles for ATP and other nucleotides (ADP, UTP, UDP) have been established in several tissues, including potent neurotransmission in the central nervous system, muscle contractility (^{Ralevic, Burnstock, 1998}; Burnstock, 2007), blood flow distribution and oxygen delivery (^{Gonzalez-Alonso, Olsen, Saltin, 2002}; ^{Sprague, Stephenson, Ellsworth, 2007}); immune responses and control of leukocyte trafficking between the blood and tissues (^{Bours et al., 2006}; ^{Salmi, Jalkanen, 2005}).

The result of ATP/ADP breakdown via sequential ectonucleotidase reactions is the release of adenosine. Measurements of extracellular adenosine levels (by using enzyme-coupled chemiluminescent or electrochemical methods) demonstrated direct hypoxia-induced releases of micromolar concentrations of this nucleoside from the rat hippocampal slices and cultured rat cortical astrocytes (^{Martin et al. 2007}).

Thus, enzymes expressed in the cytoplasm and on the surface of muscle cells increase their activity to degrade adenosine (^{Fürstenau et al., 2006}). One of the main enzymes that perform this process is ADA, an enzyme that degrades adenosian in iosine (Fürstenau et al., 2006). ADA is also an inflammatory enzyme involved in the maturation of cells of the immune system (^{Chielle et al., 2015}; ^{Ferreira et al., 2007}; ^{Livi, 1999}). The intense physical effort can stimulate a greater production of ATP with subsequent degradation and increase of adenosine, as well as, there is a greater intensity in the inflammatory process which are related to the number of lesions induced by exhaustive physical exercises. In this sense, the results of this study suggest that the increased activity of serum and urinary ADA could be indirect markers of changes in muscle tissue since this enzyme would be concomitantly increased due to the increase of adenosine, its substrate, as well as the inflammatory process installed.

The results showed a significant increase in serum and urinary ADA 60 minutes after intense physical activity, decreasing significantly after 24 hours (Figure 1A and 1C) when compared with the same individuals rested. Associated with this, an increase in the total count of leukocytes and lymphocytes was observed in Table III, which also increased significantly after 60 minutes of intense physical exercise, decreasing after 24 hours. It is believed that a serious increase in serum and urinary ADA in athletes with high loads of physical training should be an important indicator of muscle changes, such as exhaustion.

FIGURE 1
Adenosine deaminase activity. (A) Serum ADA activity; (B) ADA activity in saliva; (C) ADA activity in urine. Data are expressed as means ± SD or median. The data were processed by analysis of variance (One-Way - ANOVA), followed by the Tukey test or Kruskal-Wallis test, followed by the Dunn test. T0: before the exercises are performed; T1: 60 minutes after physical exercises; T2: 24 hours after physical exercises. ^a p<0.0001 when compared to T0. ^b p<0.05 when compared to T0. ^c p<0.0001 when compared to T1.

Taking the important anti-inflammatory role for adenosine into account, an abundant expression of ecto-ADA in the tissues may provide an efficient mean for scavenging cell-surrounding adenosine with subsequent sustained activation of dendritic cells and T-lymphocytes during inflammation, even despite the general state of immune suppression (^{Desrosiers et al, 2007}). In addition, lymphoid ecto-ADA, in association with CD26, has been proposed to have a catalytic-independent function as a co-stimulatory molecule during T cell antigen receptor-CD3 complex engagement (^{Martin et al., 1995}), and during the immunological synapse formation (^{Pacheco et al., 2005}), thus promoting an augmented T cell activation and production of proinflammatory cytokines. Compared to lymphocytes, vascular endothelium displays relatively low ecto-ADA activity, however endothelial cell-surface expressions of ADA and its counter-ligand CD26 can be coordinately up-regulated in areas of ongoing inflammation and diminished oxygen supply (^{Van Linden, Eltzschig, 2007}).

It is emphasized that during physical exercises microtraumas and ruptures of the contractile structures and the components of the skeletal muscle cytoskeleton occur, which result in a moderate inflammatory response and release of intracellular proteins into the blood, whose objective is the healing process, recovery and physiological adaptation of the athlete (^{Nóbrega, 2005}; ^{Santos et al., 2004}). However, this recovery is not achieved by individuals undergoing intense and prolonged physical exercises, exhaustive and very frequent training (^{Rogero, Mendes, Tirapegui, 2005}), compromising the tissue regeneration process, which results in a greater frequency of injuries and a decrease in athlete performance (^{Tidball, 2005}).

Also the energy demand during physical activity generates an increase in the oxygen supply (O₂) to the tissues and stimulates the oxidative metabolism, favoring the formation of free radicals (^{Ji, 2002}; ^{Wyatt, Donaldson, Brown, 2013}), which are related to the processes of lipid peroxidation, DNA damage and protein oxidation (^{Finaud, Lac, Filare, 2006}). In this study, a significant increase in serum, urinary and salivary TBARS levels was observed (Table III), evidencing an oxidative exacerbation proportionally related to the increase in O₂ demand and to the inflammatory process, favoring muscular lesions and the appearance of diseases (^{Ye et al., 2016}). Also, a significant increase in the comet assay (Figure 2) was observed 60 minutes and 24 hours after intense physical exercise. The comet assay is a reproducible and sensitive electrophoretic technique to detect the presence of single-strand breaks (SSB) of DNA, lesions at alkaline and SSB sensitive sites at sites of incomplete excision repair in mammalian cells in vitro and in vivo. Through this technique, it is possible to evaluate DNA damage and repair in proliferating and non-proliferating cells at the individual level (^{Hartmann et al., 2003}).

FIGURE 2
Quantification of DNA damage through the comet assay (A). Photomicrography of comet assays on lymphocytes (B). The data were processed by analysis of variance (One-Way - ANOVA), followed by the Tukey test or Kruskal-Wallis test, followed by the Dunn test. T0: before the exercises are performed; T1: 60 minutes after physical exercises; T2: 24 hours after physical exercises. In A, B, C, D and E, class 0, 1, 2, 3, and 4 comets respectively. The tail size of the comet is proportional to the damage to the genetic material. ^a p<0.0001 when compared to T0

As shown, ADA activity and serum and urine TBARS levels were significantly higher 60 minutes after intense physical exercise, decreasing 24 hours later, accompanied by a significant increase in leukocytes, lymphocytes and the comet test runoff, showing that these biomarkers could be routinely used to monitor acute muscle injuries and could indicate muscle depletion, oxidative stress and DNA damage in athletes after intense physical exercise, thus helping to prevent cumulative injuries that impair athletes’ performance. Some limitations of this study should be recognized as: i the cross-sectional design of the study prevents a demonstrated etiological association between markers, a longitudinal follow-up study is more appropriate for this type of research; ii the study does not address the lifestyle, ethnicity, genetics of volunteers; iii it was not possible to determine the levels of adenosine before and after intense physical exercises.

Nevertheless, this study allowed us to analyze the cellular biochemical alterations that occur in the lesions of the locomotor system in the intense physical exercises, besides highlighting the use of important biological samples, such as saliva and urine, for the biomarkers search of muscular lesions. The results presented here demonstrate that saliva and especially urine can be used for this research and are as accurate as blood to monitor the athlete, standing out with advantages because the collection does not present any discomfort, besides being practical and easy, the samples do not coagulate, in addition to having good stability.

Based on this, these biomarkers could be dosed in non-invasive samples and at different times, especially serum and urinary ADA activity, serum TBARS, urinary and salivary biomarkers which in the future could be used indirectly to evaluate acute muscle injuries, as well as the comet test would allow a rapid and effective evaluation of exercise-induced DNA lesions and could be used to evaluate and monitor athletes in exhaustive training, avoiding more serious injuries.

Acknowledgments

The work had the financial support of the Article 170 - Constitution of the State of Santa Catarina. The authors wish to thank all the volunteers who participated and the University of Western Santa Catarina (UNOESC), SC, Brazil, for their support in this study.

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• Conflict Of Interest

  None

Publication Dates

• Publication in this collection
  28 Oct 2019
• Date of issue
  2019

History

• Received
  29 Sept 2017
• Accepted
  02 May 2018