Advances in Biological Chemistry
Vol.04 No.06(2014), Article ID:50824,6 pages
10.4236/abc.2014.46046

Consideration of Blood Serum Biochemical Parameters of Yellow Fin Sea Bream (Acantopagrus latus Houttuyn, 1782) and Orange-Spotted Grouper (Epinephelus coioides Hamilton, 1822)

Paria Akbary

Fisheries Group, Department of Marine Sciences, Chabahar Maritime University, Chabahar, Iran

Email: paria.akbary@gmail.com

Copyright © 2014 by author and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY).

http://creativecommons.org/licenses/by/4.0/

Received 12 August 2014; revised 28 September 2014; accepted 15 October 2014

ABSTRACT

Serum biochemical parameters are important aspects in the management of endangered species. The values of these parameters can be used for confirming the maturity and for monitoring any changes in the quality of waters and related soils. The aim of this research was to determine the reference values of biochemical factors in Acantopagrus latus and Epinephelus coioides. Blood samples were collected from captured fish from coastal waters of Chabahar (Ramin waterfront). Serum levels of glucose, Blood Urea Nitrogen (BUN), cholesterol (CHO), triglyceride, total protein, albumin, calcium (Ca2+), phosphorus (P), sodium (Na+), bilirubin and potassium (K+) were measured. The results showed that the levels of albumin and bilirubin in E. coioides were significantly higher than A. latus and there were significant differences in all of the serum values (except P and glucose) between A. latus and E. coioides (P < 0.05). It can be concluded that the values of blood biochemical parameters may be affected by physiological factors such as the species of fish.

Keywords:

Serum, Acantopagrus latus, Epinephelus coioides, Electrolyte, Non Electrolyte

1. Introduction

As the aquaculture industry expands, there is an increasing need for improved diagnostic methods. There are few tools available to diagnose and monitor diseases on fishes. The analysis of blood indices has proven to be a valuable approach for analysing the health status of aquatic animals as these indices provide reliable information on metabolic disorders, deficiencies and chronic stress status before they are present in a clinical setting [1] . Exogenous factors, such as management [2] , diseases [3] and stress [4] , always induce major changes in blood composition. For example, significant fluctuations were detected in the concentrations of cortisol, glucose, cholesterol and other basic components in response to handling and hypoxic stress [2] [5] [6] .

One of the difficulties in assessing the state of health of natural fish population has been the paucity of reliable references of the normal condition. In pursuit to this goal, many fish physiologists have turned to studies of hematology. Blood serum biochemical data are used routinely in health care of humans and domestic animals. Blood biochemical evaluations are also gradually becoming a routine practice for determining health status in fish [7] - [9] , and only a few normal values for small number biochemical parameters have been established for some teleosts [10] .

Yellow fin sea bream (Acantopagrus latus Houttuyn, 1782) and Orange-spotted grouper (Epinephelus coioides Hamilton, 1822) are protandrous and protogeny hermaphroditic from family percidae and serranidae respectively and being distributed off southern Japan, southeastern China, Taiwan, southeastern Asia, Persian Gulf and Australia and in the Indian Ocean to southeastern Africa [11] - [14] . They are considered to be two of the most commercially important marine fish in Iran, due to their consumer preference and are newly successful cultured in the coastal area of Iran.

These economically important fish are under threat because of their continuous exposure to toxic chemical- rich industrial effluents that are discharged into the Pacific Gulf and illegal fishing practices. There is an urgent need to revive them through processes of conservation, management and mariculture, so knowledge of the blood serum biochemical factors in order to detect the health of fish is a basic prerequisite for successful management.

This present study would form a baseline data for assessment of health status of A. latus and E. coioides as well as reference point for future comparative study effects of different endogenous and exogenous factors on blood biochemical of these two fish species.

2. Materials and Methods

2.1. Experiment Design

A. latus and E. coioides fishes were captured by set net, 20 - 30 m deep on the sea bottom, from coastal waters of Chabahar (Ramin waterfront) in February 2013. In this study totally 20 fish (n = 10 A. latus (1.101 ± 23.78 g); n = 10 E. coioides (1.250 ± 34.5 g)) captured. Blood samples collected from each individual and body weight was measured.

2.2. Blood Collection

Blood sampling was performed immediately after fish were captured. Samples were collected from behind the anal fin using a 5 ml 22 no, plastic syringe. The blood samples about 2.5 ml were placed into vacutaineers tubes.

2.3. Biochemical Analyses

Biochemical analyses were conducted at state Sadaf Medical Laboratory (Chabahar, Iran). Blood samples were centrifuged at 3000 rpm for 10 min and extracted serum samples were stored at −20˚C prior to further analysis. A suite of Biochemical analyses for parameters, such as glucose, cholesterol, triglyceride, total protein, blood urea nitrogen, bilirubin, albumin, Ca2+, phosphorus were carried out using an automated analyzer (Auto Analyzer Hitachi 917, Japan ), with a Pars Azmoon kit (Co, Pars Azmoon, Tehran, Iran). Na+ and K+ were assessed by flame photometer (PFP 7, UK) [15] .

2.4. Statistical Analysis

All statistical analyses were performed using the computer program SPSS ver16.0 (SPSS, Chicago, IL). Significant differences of parameters between two fish species were determined with independent t-test. The correlation coefficients between parameters were calculated by Pearson correlation coefficients. Liner regressions were used to determine the relationship between serum biochemical parameters showing significant differences significant parameters are reported as means ± standard deviation.

3. Results

Table 1 shows the mean and standard deviation values for each blood biochemical parameters in A. latus and E. coioides. The results showed that that the serum levels of albumin and bilirubin in E. coioides were significantly higher than A. latus and there were significant differences in all of the serum values (except P and glucose) between A. latus and E. coioides (P < 0.05).

Table 2 and Table 3 show correlation coefficient of blood serum biochemical parameters of A. latus and E. coioides respectively. Significant positive correlation of glucose on Ca2+ (r = 0.695, P < 0.05), protein on Ca2+ (r = 0.704, P < 0.05) and CHO on P (r = 0.860, P < 0.01) in A. latus and protein on BUN (r = 0.721, P < 0.05) and Ca2+ and K+ (0.840, P < 0.01) in E. coioides were observed. There were significant negative correlations of CHO on Ca2+ (r = −0.641, P < 0.05) and BUN on Ca2+ (r = −0.695, P < 0.05) in A. latus and P on Ca2+ (r = −0.735, P < 0.05) in E. coioides.

Significant negative and positive regressions of parameters in both A. latus and E. coioides have been shown in Table 4.

Table 1. Changes of blood serum biochemical parameters (Means ± SD) of Acantopagrus latus and Epinephelus coioides.

The differences between two species were tested by using independent t-test. Different letters of each row indicate a significant difference (P < 0.05).

Table 2. Correlation of blood serum biochemical parameters in Acantopagrus latus.

Correlation coefficient of serum cholesterol was determined by spearman and the other parameters was determined pearson. *Correlation is significant at the 0.05. **Correlation is significant at the 0.01 level.

Table 3. Correlation of blood serum biochemical parameters in Epinephelus coioides.

Correlation coefficient of serum cholesterol was determined by spearman and the other parameters was determined pearson. *Correlation is significant at the 0.05. **Correlation is significant at the 0.01 level.

Table 4. Regression equations between significant parameters in both Acantopagrus latus and Epinephelus coioides.

4. Discussion

The wild populations of A. latus and E. coioides have almost collapsed in recent years to intensive fishing and water pollution, prompting the development of aquaculture facilities for the commercial culture of these species [11] - [14] . A rearing system for the maximization of fish productivity is the aim of fishery management programmers, and an evaluation of the physiological status of the fish during rearing is necessary to achieve this. Serum biochemical data are of immense importance in monitoring the health status of aquatic organisms, especially in fisheries management programs [7] - [9] .

The serum levels of different biochemical values in A. latus and E. coioides were as follows: Na+ (328.50 ± 32.03, 271.90 ± 27.88), K+ (2.12 ± 0.42, 3.43 ± 0.39), Ca2+ (19.80 ± 2.97, 16.80 ± 2.34), P (2.35 ± 0.40, 2.40 ± 0.57) (mmol/l) and CHO (257.30 ± 35.51, 137.30 ± 42.11), triglyceride (102.02 ± 11.82, 68.10 ± 15.34), BUN (3.82 ± 0.55, 2.66 ± 0.45), bilirubin (0.24 ± 0.04, 0.44 ± 0.13), glucose (44.25 ± 16.18, 43.70 ± 10.11) (mg/dl), protein (4.31 ± 0.32, 3.92 ± 0.36) and albumin (0.15 ± 0.03, 0.36 ± 0.05) (g/dl) respectively (as shown Table 1). The results showed that the serum levels of albumin and bilirubin in E. coioides were significantly higher than A. latus and there were significant differences in all of the serum values (except P and glucose) between A. latus and E. coioides (P < 0.05). It can be concluded that perhaps further confounding these values are variables such as age, sex, dietary state and stress all of which may alter blood values [16] [17] .

Electrolyte (Na+, K+, Ca2+ and P) levels indicate the operation of a variety of homeostatic mechanisms in the body [18] . In this study, both in A. latus and E. coioides Na+ levels were higher than the values in Scorpaena porcus (195.07 ± 1.70 mmol/l) [17] , Scophthalmus aquosus (157 ± 0.3 - 186 ± 0.4 mmol/l) [19] and Salmo salar (137 ± 1.1 - 196 ± 18.6 mmol/l) [20] but were lower than those of Rutilus frissi (387.1 ± 11.5 - 420.7 ± 7.1 mmol/l) [21] . K+ levels were lower than the values in Scophthalmus aquosus (4.10 ± 0.18 - 5.48 ± 0.15 mmol/l) [19] and Rutilus frissi (37.9 ± 7.4 - 39.9 ± 10.6 mmol/l) [21] but were higher than those of Salmo salar (1.3 ± 0.4 - 4.5 ± 0.1 mmol/l) [20] . At the same time, the densities of K+ were similar to those reported in Scorpaena porcus (3.81 ± 0.18 mmol/l) [17] . Ca2+ activities were higher than values reported in Scorpaena porcus (3.66 ± 0.07 mmol/l) [17] , Salmo salar (3.3 ± 0.1 - 4.7 ± 1.4 mmol/l) [22] and Scophthalmus aquosus (3.49 ± 0.11 - 4.43 ± 0.10 mmol/l) [19] but were similar to those reported in Rutilus frissi (15.9 ± 1.5 - 21.6 ± 1 mmol/l) [21] . P values were lower than those from Scorpaena porcus (15.12 ± 0.26 mmol/l) [17] and Rutilus frissi (19.2 ± 1 - 28.9 ± 2.8 mmol/l) [21] .

The levels of glucose and cortisol are considered to be specific indicators of sympathetic activation during stress conditions [6] [21] . This study showed that there were significant differences in all of the serum values (except P and glucose) between A. latus and E. coioides (P < 0.05). Glucose levels were lower than those reported in Rutilus frissi (83.8 ± 11.3 - 209.8 ± 23.2 mg/dl) [21] . In the present study, the albumin and bilirubin levels from E. coioides were significantly higher than A. latus. Albumin, BUN, Triglyceride and CHO levels were lower than those reported in Rutilus frissi [21] but bilirubin and protein levels were similar to Rutilus frissi [21] . The ranges of serum biochemistry vary from species to species and can be influenced by many biotic and abiotic factors such as water temperature, seasonal pattern, food, age and sex of the fish [23] . The increased plasma protein concentration can be caused by structural liver alternations that reduce aminotransferase activity, with concurrent reduction in deamination capacity [24] . Hrubec et al. [24] stated that protein level in striped bass increased with age.

Hill [25] reported that cholesterol concentrations increase as the fish size increased. A high blood urea concentration recorded in M. cephalus is likely to be a sign of stress associated with the increase in the cortisol level [26] .

In this study, significant positive correlation of glucose on Ca2+ (r = 0.695, P < 0.05), protein on Ca2+ (r = 0.704, P < 0.05) and CHO on P (r = 0.860, P < 0.01) in A. latus and protein on BUN (r = 0.721, P < 0.05) and Ca2+ and K+ (0.840, P < 0.01) in E. coioides were observed. There were significant negative correlations of CHO on Ca2+ (r = −0.641, P < 0.05) and BUN on Ca2+ (r = −0.695, P < 0.05) in A. latus and P on Ca2+ (r = −0.735, P < 0.05) in E. coioides. Also significant positive correlation of CHO on P was observed in Rutilus frissi [21] .

5. Conclusion

In conclusion, variations between blood biochemical parameters among fish species depend on the sampling technique, analyses methods, age, habitat and diet [16] [17] .

Finally, the results showed that the levels of albumin and bilirubin in E. coioides were significantly higher than A. latus and there were significant differences in all of the serum values (except P and glucose) between A. latus and E. coioides. It can be concluded that the values of blood biochemical parameters may be affected by physiological factors such as the species of fish. Also, the results of present study may also be helpful in obtaining standard values of blood parameters. Furthermore, examining blood parameters may allow us understand biological and ecological characteristics of these species.

Acknowledgements

We gratefully acknowledge the members of Sadaf Medical Laboratory in Chabahar, Iran for measuring of blood serum biochemical parameters.

References

  1. Bahmani, M., Kazemi, R. and Donskaya, P. (2001) A Comparative Study of Some Hematological Features in Young Reared Sturgeons (Acipenser persicus and Huso huso). Fish Physiology and Biochemistry, 24, 135-140. http://dx.doi.org/10.1023/A:1011911019155
  2. Svobodova, Z., Vykusova, B., Modra, H., Jarkovsky, J. and Smutna, M. (2006) Haematological and Biochemical Profile of Harvest Size Carp during Harvest and Post-Harvest Storage. Aquaculture Research, 37, 959-965. http://dx.doi.org/10.1111/j.1365-2109.2006.01511.x
  3. Chen, Y.E., Jin, S. and Wang, G.L. (2005) Study on Blood Physiological and Biochemical Indices of Vibrio alginilyticus Disease of Lateolabrax japonicas. Journal of Oceanography Taiwan Strait, 24, 104-108.
  4. Cnaani, A., Tinman, S., Avidar, Y., Ron, M. and Hulata, G. (2004) Comparative Study of Biochemical Parameters in Response to Stress in O.aureus, O. mossambicus and Two Strains of O. niloticus. Aquaculture Research, 35, 1434- 1440. http://dx.doi.org/10.1111/j.1365-2109.2004.01167.x
  5. Kubokawa, K., Watanabe, T., Yoshioka, M. and Iwata, M. (1999) Effects of Acute Stress on Plasma Cortisol, Sex Steroid Hormone and Glucose Levels in Male and Female Sockeye Salmon during the Breeding Season. Aquaculture, 172, 335-349. http://dx.doi.org/10.1016/S0044-8486(98)00504-3
  6. Skjervold, P.O., Fjaera, S.O., Ostby, P.B. and Einen, O. (2001) Live-Chilling and Crowding Stress before Slaughter of Atlantic Salmon (Salmo salar). Aquaculture, 192, 265-280. http://dx.doi.org/10.1016/S0044-8486(00)00447-6
  7. Ranzani-Paiva, M.J.T., Rodrigues, E.L., Veiga, M.L., Eiras, A.C. and Campos, B.E.S. (2003) Differential Leukocytes Counts in “Dourado” Salminus maxillous Valenciennes, 1840, from the Mogi-Guacu River, Pirassiununga, SP. Brazilian Journal of Biology, 63, 517-525. http://dx.doi.org/10.1590/S1519-69842003000300018
  8. Coz-Rakovac, R., Strunjak-Perovic, I., Hacmanjek, M., Topic, P.N., Lipej, Z. and Sostaric, B. (2005) Blood Chemistry and Histological Properties of Wild and Cultured Sea Bass (Dicentrarchus labrax) in the North Adriatic Sea. Veterinary Research Communication, 29, 677-687. http://dx.doi.org/10.1007/s11259-005-3684-z
  9. Tavares-Dias, M. and Moraes, F.R. (2007) Haematological and Biochemical Reference Intervals for Farmed Channel Catfish. Journal of Fish Biology, 71, 383-388. http://dx.doi.org/10.1111/j.1095-8649.2007.01494.x
  10. Zhou, X., Li, M., Abbas, K. and Wang, W. (2009) Comparison of Haematology and Serum Biochemistry of Cultured and Wild Dojo Loach Misgurnus anguillicaudatus. Fish Physiology and Biochemistry, 35, 435-441. http://dx.doi.org/10.1007/s10695-008-9268-4
  11. Abbassi, F., Oryan, S. and Matinfar, A. (2007) Reversal Sex Change in the Protogynous Fish Epinephelus coioides in the Persian Gulf Water. Journal of Biology, 2, 121-127.
  12. Hedayati, A., Safahieh, A., Savar, A. and Ghofleh Marammaz, I.J. (2010) Detection of Mercury Chloride Acute Toxicity in Yellowfin Sea Bream (Acanthopagrus latus). World Journal of Fish and Marine Sciences, 2, 86-92.
  13. Savari, A., Hedayati, A., Safahieh, A.R. and Movahedinia, A. (2010) Changes in Some Serum Biochemical Values of Yellowfin Sea Bream (Acanthopagrus latus) in Mahshahr Creeks (Persian Gulf). Global Veterinaria, 5, 233-238.
  14. Iwatsuki, Y. (2013) Review of the Acanthopagrus latus Complex (Perciformes: Sparidae) with Descriptions of Three New Species from the Indo-West Pacific Ocean. Journal of Fish Biology, 83, 64-95. http://dx.doi.org/10.1111/jfb.12151
  15. Burtis, C.A. and Ashwood, E.R. (1994) Tietz Textbook of Clinical Chemistry. 2th Edition, W.B. Sunders Company, Philadelphia.
  16. Harikrishnan, R., Nisha Rani, M. and Balasundaram, C. (2003) Hematological and Biochemical Parameter in Common Carp (Cyprinus carpio) Following Herbal Treatment for Aeromonas hydrophila Infection. Aquaculture, 221, 41-50. http://dx.doi.org/10.1016/S0044-8486(03)00023-1
  17. Celik, E.S. (2004) Blood Chemistry (Electrolytes, Lipoproteins and Enzymes) Values of Black Scorpion Fish (Scorpanea procus Linneaus 1758) in the Dardanelles, Turkey. Journal of Biological Sciences, 4, 716-719. http://dx.doi.org/10.3923/jbs.2004.716.719
  18. Clarke, F. (1998) A Review of the Scientific Justifications for Maintaining Cetaceans in Captivity. A Report for the Whale and Dolphin Conservation Society (WDCS), Frances Clark, Bath, UK.
  19. Dawson, M.A. (1990) Blood Chemistry of the Windowpane Flounder Scophthalmus aquasus in Long Island Sound Geographical, Seasonal and Experimental Variations. Fishery Bulletin, 88, 429-437.
  20. Bergheim, A., Kroglund, F., Vatne, D.F. and Rosseland, B.O. (1990) Blood Plasma Parameters in Farmed Atlantic Salmon (Salmo salar L.) Transferred to Sea Cages at Age Eight to Ten Months. Aquaculture, 84, 159-165. http://dx.doi.org/10.1016/0044-8486(90)90345-N
  21. Makhlough, M., Shahsavani, D. and Kazerani, H.R. (2012) Blood Serum Electrolyte and Non-Electrolyte Parameters in Breeding Rutilus frisii Kutum Kammensky. Journal of Veterinary Reaserch, 67, 53-58.
  22. Jawad, L., Al-Mukhtar, M.A. and Ahmed, H.K. (2004) The Relationship between Haematocrit and Some Biological Parameters of the Indian Shad, Tenualosa ilisha (Family Clupidae). Animal Biodiversity Conservation, 27, 478-483.
  23. Kavadias, S., Castritsi-Catharios, J. and Dessypris, A. (2004) Annual Cycles of Growth Rate, Feeding Rate, Food Conversion, Plasma Glucose and Plasma Lipids in the Population of European Sea Bass (Dicentrarchus labrax L.) Farmed in Floating Marine Cages. Journal of Applied Ichthyology, 19, 29-34. http://dx.doi.org/10.1046/j.1439-0426.2003.00346.x
  24. Hrubec, T.C., Smith, S.A. and Robertson, J.J. (2001) Age-Related Changes in Hematology and Plasma Chemistry Values of Hybrid Striped Bass (Morone chrysops × Morone saxatilis). Veterinary Clinical Pathology, 30, 8-15. http://dx.doi.org/10.1111/j.1939-165X.2001.tb00249.x
  25. Hill, S. (1982) A Literature Review of the Blood Chemistry of Rainbow Trout, Salmo gairdneri Rich. Journal of Fish Biology, 20, 535-569. http://dx.doi.org/10.1111/j.1095-8649.1982.tb03954.x
  26. Borges, A., Siqueira, D.R., Jurinitz, D.F., Zanini, R., do Amaral, F., Wasswemann, G.F., et al. (2007) Biochemical Composition of Seminal Plasma and Annual Variations in Semen Characteristics of Jundia Rhamdia quelen (Quoy and Gaimard, Pimelodidae). Fish Physiology and Biochemistry, 31, 45-53. http://dx.doi.org/10.1007/s10695-005-4742-8