PO Uadia1 , KO Orumwensodia1, GE Arainru2, EO Agwubike2, CBN Akpata1
1Department of Biochemistry; 2Department of Human Kinetics and Sports Science, University of Benin, Benin City, Nigeria; 2Department of Human Kinetics and Sports Science, University of Benin, Benin City, Nigeria;For correspondence:- PO Uadia Email: psouadia@uniben.edu Tel:+2348055783197
Received: 6 May 2015 Accepted: 4 January 2016 Published: 28 February 2016
Citation: Uadia P, Orumwensodia K, Arainru G, Agwubike E, Akpata C. Effect of physical and flexibility exercise on plasma levels of some liver enzymes and biomolecules of young Nigerian adults. Trop J Pharm Res 2016; 15(2):421-425 doi: 10.4314/tjpr.v15i2.28
© 2016 The authors.
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Introduction
Exercise is defined as bodily movement produced by the contraction of skeletal muscle that substantially increases energy expenditure [1]. Thompson et al [2], also defined exercise or physical activity as any bodily movement produced by skeletal muscles that results in energy usage beyond resting energy expenditure. From these definitions, it is clear that physical activity exerts the body muscles and involves the expenditure of energy in form of ATP. Depending on the overall effect physical exercise has on the body, it is grouped into three types; aerobic (endurance), anaerobic (resistant) and flexibility exercise [1,3-5]. The immense benefits from exercising include enhanced mood, self-esteem and improved physical appearance. Also, exercise helps in the reduction of several diseases such as cancers, cardiovascular diseases, non-insulin dependent diabetes (type II diabetes), osteoporosis and ultimately reduction in premature mortality [6]. Again, exercise aids cardiovascular and respiratory functions, slows the loss of muscular strength thereby enhancing muscle tone, increases bone mass, slows the process of aging, aids digestion and bowel function, promotes sound sleep and prevents depression [6]. These benefits would depend on the type, intensity, duration and frequency of exercise programme, and the characteristics of the individual at baseline [7]. However, the benefits of exercising are transient and reversible [8].
Hence, in a bid to perform maximally and ensure survival, the body tends to adjust to strain imposed on it by stress such as physical exercise, thus, affecting the body's anatomical, physiological as well as its metabolic state [9]. Nonetheless, some forms of exercise and particularly strenuous exercise are also accompanied by some deleterious effects. In this context, muscle damage post exercise leads to substantial increase in myocellular protein levels in the blood [10,11]. It has been shown that prolonged physical exercise results in transient elevations of biochemical markers of muscular damage such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatine kinase (CK), and lactate dehydrogenase (LDH) [12]. Therefore and in agreement with Bray [13], the benefits from exercising is maximized when exercises are directed at meeting the individual's needs and capacity.
The objective of this study was to evaluate the effect of physical and flexibility exercise on plasma levels of some liver enzymes and other biomolecules in apparently healthy young Nigerian adults.
Methods
Subjects
Sixteen (16) young Nigerian adult students who were apparently healthy and not on any exercise regimen were used for this study. They included eleven (11) males, aged 25.40 ± 1.09 years and five (5) females, aged 22.83 ± 0.83 years. Participants were instructed to maintain their daily dietary habits for the duration of the research period and avoid taking medications such as pain relievers.
Exercise program
The study was carried out four (4) times a week (Monday, Wednesday, Friday and Saturday), between the hours of 5:30 and 7:30 am, for a period of six (6) weeks. Each participant covered a total distance of 56,500 m. The exercise regimen which was mainly aerobic began with jogging of varied but specified distances and immediately followed by various flexibility exercises (calisthenics, which included; sit ups, neck rotations (left-right, back-forward), arm and waist rotations (left-right, back-forward), press-up, Limbs stretches, imaginary cycling-with the back lying on the floor, etc.).
Blood sampling and analysis
Pre-exercise (24 h before exercise) and post exercise (24 h after exercise) intravenous blood samples were obtained from the participants (at a sitting position) in the morning after a 12-h fast. About 10 ml blood sample was collected into heparinized bottles before and after the exercise. Samples were immediately placed in an ice bath and centrifuged at 2500 rpm for 10 min. Aliquots of the resulting plasma were stored at -80 °C until analyzed. All enzyme assays were done using the Selectra ProS auto analyzer (Elitech Group, France) and reagent kits were procured from Elitech clinical systems (Elitech Group, France). Albumin, total protein and bilirubin were determined spectrophotometrically as described by Randox reagent kit, (Randox, UK).
The measurement of serum albumin was based on its quantitative binding to the indicator 3, 3’, 5, 5’- tetrabromo –n cresol sulphonephthalein (bromocresol green, BCG). Albumin –BCG complex absorbs maximally at 578 nm, the absorbance being directly proportional to the concentration of albumin in the sample. Total protein was estimated by the Biuret method, wherein, cupric ions in an alkaline medium interact with protein peptide bonds resulting in the formation of a coloured complex which is read spectrophotometrically at 546 nm. Direct (conjugated) bilirubin reacts with diazotized sulphanilic acid in alkaline medium to form a blue colored complex. Total bilirubin is determined in the presence of caffeine, which releases albumin bound bilirubin, by the reaction with diazotized sulphanilic acid. Both absorbance are read at 578 nm. While, indirect bilirubin is the difference between total and direct bilirubin.
Statistical analysis
All statistical analyses were carried out using Microsoft Excel (Windows 8.0). Descriptive statistics are presented as mean and standard error of mean. Comparison of continuous variables was done using Student paired t-test. P ˂ 0.05 was considered statistically significant.
Results
Enzyme profile
The results of the effect of six (6) weeks physical and flexibility exercise on plasma levels of liver enzymes' activity of male and female participants are presented in Tables 1 and 2 below.
shows that only AST and LDH values showed significant (p ˂ 0.05) increase post-exercise. However, there was a non-significant (p ˃ 0.05) decrease in the values of ALT, ALP and GGT post-exercise.
indicate that ALT, AST and GGT increased post-exercise, but the increase was only significant for AST post-exercise; ALP and LDH values decreased though not significantly (p ˃ 0.05) post-exercise. However, all values were within the reference range.
Biochemical profile
The effect of six (6) weeks physical and flexibility exercise on plasma levels of some biochemical parameters of both sexes, was tested and shown in Tables 3 and 4 below.
There was an insignificant (p ˃ 0.05) decrease in the bilirubin values post-exercise as seen from . However, a significant (p ˂ 0.05) decrease in the post-exercise results for total protein and albumin was also observed.
From the results presented in , there was no significant (p ˃ 0.05) difference in the results of all female participants. Although, there was a general decrease in post-exercise values.
Discussion
The efficacy of physical exercise in health management and disease control has been suggested for the sustenance of healthy living. This study provides some scientific data to support this concept. The results obtained from this study indicate that physical exercise could be of immense benefit to an individual's health. Alanine aminotransferase (ALT) which is predominantly found in the liver, but with smaller amounts in the kidneys, heart, muscles, pancreas, and used as an indicator for liver injury, showed a decrease in the post-exercise values as against the pre-exercise values, although this decrease was not statistically significant (p ˃ 0.05). This suggests that the pattern, intensity and duration of the exercise regimen did not cause damage to the liver which is the major source of ALT. This is in agreement with Davries et al [14]. A similar result was reported by Sreenivasa et al [15], after subjecting patients with non-alcoholic steatohepatitis to exercise, while Nuri et al [16], reported a significant decrease in serum ALT values in postmenopausal women with breast cancer who were subjected to a fifteen week exercise regimen.
AST is not as specific an indicator of liver damage as ALT because of its multi-organ distribution. Therefore, stressors such as physical exercise could impact negatively on the heart and skeletal muscles, thus leading to the release of AST into the bloodstream, which eventually leads to increase in serum AST levels [17]. This was the trend noticed when the post-exercise results of AST for both male and female participants were considered. The results presented in Tables 1 and 2, showed a significant (p ˂ 0.05) increase in AST values after the six weeks physical and flexibility exercise. The sources of the AST are likely from injured muscle and probably heart tissues, which are major sources of AST rather than the liver. Also, due to this multiple organ distribution of ALP, increased serum activity may be caused by a wide variety of disorders involving several organs. Findings from this study showed that there was no significant change (p ˃ 0.05) in the pre- and post-exercise values of both male and female participants. This result, in conjunction with those of ALT and AST indicates a healthy liver function post-exercise.
The LDH test is used to detect tissue damage and as an aid in the diagnosis of heart attack and liver disease [18]. Although, the post-exercise results for male participants showed a significant increase over the pre-exercise results, there was a decrease in the post exercise result when compared with the pre-exercise results for female participants, however, this decrease was not statistically significant. The increase in LDH levels for the male participants may be due to increased damage to muscle cells following the exercise regimen, which may not have occurred in the women.
The post-exercise GGT (gamma-glutamyl transferase) results obtained for male participants showed a non-significant (p > 0.05) decrease. Meanwhile, there was an insignificant increase in the post-exercise value for female participations. These results are in agreement with the GGT values reported by Statland et al [19] and Ayca et al [20]. Thus, agreeing with earlier results obtained for ALT, AST, ALP and LDH, indicating a healthy liver post-exercise.
The result for total protein concentration (Tables 3 and 4) showed that there was a decrease in the post-exercise value of both male and female participants when compared with their pre-exercise values. However, while the decrease in the male participants was statistically significant, the decrease in the female participants was not statistically significant. A plausible reason for this decrease in total protein value has been suggested [21-23], to be due to increased demand of glucogenic amino acids for the generation of energy leading to increased degradation of proteins. A similar result was obtained for plasma albumin. Bilirubin, which is a yellowish coloured product of hemoglobin degradation is a marker for hepatobiliary injury, especially cholestasis [24]. Also, in acute human hepatic injury, total bilirubin can be a better indicator of disease severity compared to ALT [25]. Bilirubin may also be increased due to non-hepatic causes such as hemolysis. Therefore, the non-significant changes observed in all bilirubin values (i.e., total, direct and indirect bilirubin), which were within normal physiological range, could be due to the fact that the exercise regimen did not cause liver injury.
Conclusion
The results obtained indicates that a 6-week physical and flexibility exercise programme did not cause any adverse change in liver and serum parameters as they remained within reference range.
Declarations
Acknowledgement
References
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