Oxidative stress indicators of rabbit breeds in Ibadan, Southwest Nigeria
- 77 Downloads
Within the rabbit population in Southwest of Nigeria, four breeds of rabbits consisting of Fauve de Bourgogne, Chinchilla, British Spot, and New Zealand White were evaluated for their oxidative status, as indices of physiological adaptation for optimal productivity. This investigation was carried out within July and August when least temperature-humidity index (THI) is observed in Ibadan, Southwest Nigeria. Thirty bucks per breed were housed individually and randomly allotted to experimental units. Blood samples were collected from all bucks and serum obtained using standard procedures. Serum oxidative stress indicators assay include total antioxidant capacity, lipid peroxidation, superoxide dismutase (SOD), catalase, and glutathione peroxidase activity was determined using standard procedures.
Results revealed that serum lipid peroxidation, total antioxidant activity, catalase, and glutathione peroxidase were not significantly (p > 0.05) affected by the breeds of rabbit. Fauve de Bourgogne, Chinchilla, and New Zealand White had statistically similar serum SOD activity and were significantly (p < 0.05) higher than serum SOD activity of British Spot rabbits. This shows that British Spot has the least superoxide anion scavenging ability across the breeds.
The breeds of rabbit assessed have similar oxidant generation capacity and antioxidant production, except British Spot that has the least superoxide scavenging which could increase oxidant accumulation within this breed of rabbit.
KeywordsAntioxidant production Physiology Pro-oxidant Rabbit breed Oxidants generation
Polyunsaturated fatty acids
Reactive oxygen species
Revolution per minute
Standard error of mean
Thiobarbituric acid reactive substances
The blood is easily and often influenced by the external environment including feeding practices, ambient temperature, type of shelter, and many other aspects of herd management since they are intimately related to metabolism (Marai and Habeeb 1998). Reactive oxygen species (ROS), the major culprits for causing oxidative stress, are constantly generated in vivo as an integral part of metabolism. ROS may cause oxidative stress when their level exceeds the threshold value. They trigger the progressive destruction of polyunsaturated fatty acids (PUFA), ultimately leading to membrane destruction (Kumar et al. 2011). The highly reactive hydroxyl radical is especially toxic because it can react with proteins, polysaccharides, nucleic acids, and polyunsaturated fatty acids and cause alteration of their structure and functions (Daniel et al. 2005). It is widely accepted that mitochondrial respiration is the primary source of reactive oxygen species (Turrens 2003), with 0.2 % of oxygen consumed converted into superoxide in the normal state (St. Pierre et al. 2002). Levels of ROS are determined by production and by the rate of ROS degradation and/or inactivation, an appropriate balance is important for maintaining cellular homeostasis (Jimoh 2016). Although low levels of ROS are essential in many biochemical processes, accumulation of ROS may damage biological macromolecules, i.e., lipids, proteins, carbohydrates, and DNA (Kumar et al. 2011). External factors such as heat, trauma, ultrasound, infections, radiations, toxins, etc., can lead to increase free radicals and other ROS and may lead to oxidative stress (Halliwell et al. 1992). Oxidative stress is considered to play a pivotal role in the pathogenesis of aging and several degenerative diseases, such as atherosclerosis, cardiovascular disease, type 2 diabetes and cancer (Storz 2005). The paucity of information exists on oxidative stress indicators of rabbits under climatic conditions of West Africa. It is important to document oxidative indicators in rabbit breeds in Nigeria, especially reports on thermal comfort conditions which could serve as the baseline for interpretations, diagnosis, and evaluating environmental contributions to oxidative stress in the tropics.
Materials and methods
The research was carried out at the rabbit unit of Teaching and Research Farm and Animal Physiology Laboratory, Department of Animal Science, both of the University of Ibadan, Ibadan, Nigeria. It is situated in the rainforest agro-ecological zone of Nigeria, between lat. 7° 27′ 18.74″ N and 7° 27′ 19.17″ N and long. 3° 53′ 13.98″ E and 3° 53′ 32.69″ E.
Experimental animals, design, and management
Four exotic breeds of rabbit consisting of Fauve de Bourgogne, Chinchilla, British Spot, and New Zealand White were used for the study. At the commencement of the trial, animals were confirmed to be of good health status, without abnormalities, and conform to the breed and/or age group categorization. Thirty bucks per breed were used, animals were housed individually, and allotted randomly into experimental units in a completely randomized design. The animals were fed 5 % of their body weight, with diets containing crude protein 17.05%, digestible energy 2592.06 Kcal/kg, crude fiber 10.02%, calcium 0.45%, and phosphorus 0.21%. Freshwater was available to the animals always. Other routines and periodic management practices necessary for rabbit production were carried out. This experiment was carried out when least Temperature Humidity Index is observed in the study area (within July and August), which depicts the highest thermal comfort in the study area (Jimoh and Ewuola 2018). Blood samples were collected from all bucks through the ear vein into plain sample bottles and were centrifuged at 3000 rpm for 15 min and supernatant separated as serum.Serum biochemical constituents were determined using spectrophotometric procedure; total protein, glucose, total cholesterol, sodium, chloride, phosphorus, magnesium, and potassium contents of the samples using commercial assay kits.
Serum oxidative stress indicators assay include total antioxidant capacity, lipid peroxidation, superoxide dismutase, catalase, and glutathione peroxidase activity.
Where CUA (mmol/L); concentration of uric acid.
K: absorbance of control (K1 − K0)
A: absorbance of the sample (A1 − A0).
UA: absorbance of uric acid solution (UA1 − UA0) (Koracevic et al. 2001)
The assay for lipid peroxidation; the reaction mixture in a total volume of 3.0 ml contained 1.0 ml serum and 1.0 ml of TCA (0.67%). All the test tubes were placed in a boiling water bath for a period of 45 min. The tubes were shifted to the ice bath and then centrifuged at 2500 rpm for 10 min. The amount of malondialdehyde (MDA) formed in each of the samples was assessed by measuring the optical density of the supernatant at 532 nm (Ohkawa et al. 1979).
Superoxide dismutase (SOD); 2.1 ml of 50 mM buffer, 0.02 ml of enzyme source, and 0.86 ml of distilled water. The reaction is initiated with 0.02 ml of 10 mM pyrogallol and change in absorbance monitored at 420 mm. One unit of SOD is defined as that amount of enzyme required to inhibit to auto-oxidation of pyrogallol by 50% in the standard assay system of 3 ml. The specific activity is expressed as unit/min/mg protein (Soon and Tan 2002).
Glutathione peroxidase activity; 0.5 ml of 0.4 M buffer, pH 7.0, 0.2 ml enzyme source, 0.2 ml of 2 mM GSH, and 0.1 ml of 0.2 mM H2O2 were added and incubated at room temperature for 10 min along with the control tube containing all reagents except enzyme source. The reaction arrested by adding 0.5 ml of 10 % TCA, centrifuged at 4000 rpm for 5 min, and the GSH content in 0.5 ml of supernatant was estimated. The activity expressed as microgram of GSH consumed/min/mg protein (Rotruck et al. 1973).
Catalase activity; the assay system contains 1.9 ml of 0.05 M buffer, pH 7.0, and 1.0 ml of 0.059 M H2O2. The reaction is initiated by addition of 0.1 ml enzyme source. The decrease in absorbance is monitored at 1 min interval for 5 min at 240 nm, and activity is expressed as nanomoles of H2O2 decomposed/min/mg protein (Beers and Sizer 1952).
Data obtained in this study was subjected to one-way analysis of variance of general linear procedure (SAS Institute Inc 2003), significant effects were detected with a confidence level of 95%, and New Duncan’s multiple range test of same software was used to separate means.
Serum biochemistry of four exotic breeds of rabbit
Fauve de Bourgogne
New Zealand White
Total Protein, g/L
The serum biochemical indices were assessed at least in Temperature Humidity Index which is indicative of thermal comfort. The obtained result showed that serum biochemical indices were not affected by breed differences, indicative of similar physiological status across the breeds. The animals had only one source of variation (breed), and the environmental conditions were indicative of thermal comfort in the study area. It can be suggested that the rabbit breeds have similarities in physiology under normal conditions.
The ranges of obtained values were in agreement with values reported by Ahemen et al. (2013), Odetola et al. (2012), and Ewuola et al. (2012), and were within the normal range of biochemical values as reported by Mitruka and Rawnsley (1977) and Duncan and Prasse (1986).
The decrease in plasma glucose could be due to the increase in glucose utilization to produce more energy for greater muscular expenditure required for high respiratory activity and/or the marked dilution of blood and body fluids as a whole caused by an increase in water consumption (Habeeb et al. 1992). Okab et al. (2008) reported that plasma total protein, globulins, total lipids, and cholesterol of New Zealand White rabbits were increased during the summer season and suggest that exposure of New Zealand rabbits to hot environmental conditions may have adverse physiological effects. Decrease in serum total proteins may be due to decrease in feed nitrogen intake which occurs under heat-stress conditions (Marai et al. 2007), decrease of protein synthesis as a result of the depression of anabolic hormonal secretion, and/or dilution of plasma proteins caused by the increase of the water consumed (El-Masry and Habeeb 1989). Total lipids and cholesterol were affected by the season and cholesterol were increased during the summer season in rabbit (Okab et al. 2008) and in dairy cattle (El-Masry and Marai 1991). They attributed these changes to variations in thyroidal activity at different seasons, as exposure to low environmental temperature stimulates the secretion of thyroxine. Thyroid hormones stimulate cholesterol synthesis as well as the hepatic mechanisms that remove cholesterol from the circulation. Cholesterol is the precursor in the biosynthesis of sex hormones. The decline in plasma cholesterol level may be because the rate of the later process exceeds that of the former, and the plasma cholesterol level drops before the metabolic rate rises (Guyton 1981). The decrease in Na+ and K+ are related to increases in loss of urinary Na+ and loss of skin K+ (Kumar et al. 2011). Enhanced heat dissipation during heat stress may also lead to electrolyte losses through sweat, saliva, polypnea, and urine. This may lead to falling in plasma Na+, K+, and Cl− concentration (Coppock et al. 1982). Scheneider et al. (1984) reported that heat stress in lactating dairy cows caused a significant loss of serum Na+ and K+. West (1999) also reported a similar fall in serum electrolyte concentration in dairy cows subjected to heat stress
British Spot rabbit had apparently highest values among the breeds; this suggests low antioxidant defense against free radical species metabolites, thus predisposing the animals to oxidative stress. Serum total antioxidant activity of the rabbits was not influenced significantly by breed differences. Similarly, British Spot had the highest value among the breeds for total antioxidant activity. This suggests that the lipid peroxidation in British Spot may be due to the deficit in certain free radical species metabolites scavenger (antioxidant) in the serum of the animals, but the other substrates elimination were high due to the activity of their systemic scavenger (antioxidant). Lipid peroxidation is a result of the combined effect of different free radicals and metabolites. The elimination of certain free radical/metabolites may not reduce the precipitation of the others that are active. Total antioxidant activity measures the combined activity of enzymatic and non-enzymatic antioxidants which act on specific substrates: superoxide dismutase (superoxide anion), catalase, and glutathione peroxidase (hydrogen peroxide). High total antioxidants activity could be due to the activity of one or more component antioxidants. Fauve de Bourgogne, Chinchilla, and New Zealand White had statistically similar serum SOD activity and were (p < 0.05) higher than British Spot rabbits. This confirms the earlier suggestions that British Spot has low superoxide dismutase anion (free radical species) scavenging ability, and the accumulations of the superoxide anion account for high-lipid peroxidation and subsequent oxidative stress in the animals. The catalase and glutathione peroxidase activity of British Spot was similar, though values were apparently (p > 0.05) lower than New Zealand White, but were (p > 0.05) higher than Chinchilla and Fauve de Bourgogne.
The body’s total antioxidant capacity serves to protect cells from excess production of ROS (Bloomer and Fisher-Wellman 2008; Brennan and Kantorow 2008). The reactive oxygen species contribute to an intensified synthesis of antioxidant enzymes in tissues and hence their elevated activity may be a manifestation of adaptation mechanisms in response to oxidative stress. A decreased activity of antioxidant enzymes or a decreased non-enzymatic antioxidant concentration may be caused by their intensified utilization in protection against oxidative tissue damage (Seven et al. 2001).
The great majority of the energy released under basal conditions is used by the cell for the maintenance of the Na+-K+ dependent ATP-ase activity. This increased the use of ATP associated with the intensification of oxygen consumption by the oxidative phosphorylation pathway that generates reactive oxygen species (Sies 1997).
The study reveals that the four breeds of rabbit have similar oxidative status. However, British Spot has low superoxide dismutase scavenging ability and could pose danger to lipid peroxidation at high metabolic or physiological conditions. This serves as reference values for oxidative status and interpretation of different condition for the rabbit breeds.
The authors are grateful to the management and staff of the Rabbitry Unit, Teaching and Research Farm, University of Ibadan, for their assistance in providing animals and housing for this work. Also, Dr. Ajayi Babajide Oluwaseun of Biochemistry Department, BOWEN University, Iwo, Osun State, Nigeria is appreciated for his technical assistance in oxidative status assay procedures and chemicals used.
This research did not receive any specific grant from any funding agency in the public, commercial or not-for-profit sector.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
OAJ designed, carried out the field work, and supervised the study, carried out the statistical analysis, and wrote the manuscript. The author read and approved the final manuscript.
Jimoh, Olatunji Abubakar Ph.D. (Registered Animal Scientist; Nigerian Institute of Animal Science)Lecturer and consultant,
Animal physiology and bioclimatology,
Department of Agricultural Technology, Federal Polytechnic Ado Ekiti, Ekiti State. Nigeria.
Ethics approval and consent to participate
The study was undertaken with approval from the institutional ethics committee for care and use of animal for research of the host institution.
Consent for publication
The author declares that he has no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- Ahemen T, Abu AH, Gbor V (2013) Haematological and serum biochemical parameters of rabbits fed varying dietary levels of water spinach Ipomoea aquatic leaf meal. Adv Appl Sci Res 42:370–373Google Scholar
- Duncan JR, Prasse KW (1986) Veterinary Laboratory Medicine, 2nd edn. Iowa State University Press, USA, p 2Google Scholar
- El-Masry KA, Habeeb AA (1989) Thyroid function in lactating Friesian cows and water buffaloes under winter and summer Egyptian conditions. Proceedings of 3rd Egyptian-British Conference on Animal, Fish and Poultry Production, Alexandria. Egypt 2:613–620Google Scholar
- Ewuola EO, Jimoh OA, Atuma OV, Soipe OD (2012) Haematological and serum biochemical response of growing rabbits fed graded levels of Moringa oleifera leaf meal. World Rabbit Science Association Proceedings 10th World Rabbit Congress – September 3–6, 2012– Sharm El- Sheikh –Egypt, pp 679–683Google Scholar
- Guyton AC (1981) Lipid metabolism. In: Textbook of Medical Physiology, 6th edn. W. B. Saunders Company, Philadelphia, pp 849–860Google Scholar
- Habeeb AA, Marai IFM, Kamal TH (1992) Heat stress in farm animals and the environment ed. C. J. C. Philips and D. Piggins. CAB International, Wallingford, pp 27–47Google Scholar
- Halliwell B, Gutteridge JMC, Cross CE (1992) Free radicals, antioxidants and human diseases: Where are we now? J Lab Clin Med 1196:598–620Google Scholar
- Jimoh OA (2016) Assessment of the oxidative stress markers and reproductive performance of four exotic breeds of rabbit in Ibadan. Ph.D. Thesis, University of Ibadan, Ibadan, Nigeria, pp 45–72Google Scholar
- Kumar S, Ajeet BVK, Meena K (2011) Review: Effect of heat stress in tropical livestock and different strategies for its amelioration. J Stress Physiol Biochem 7(1):45–54Google Scholar
- Marai IFM, Habeeb AA (1998) Adaptability of Bos taurous cattle under hot arid conditions. Ann Arid Zone 37(3):253–281Google Scholar
- Mitruka BM, Rawnsley HM (1977) Clinical Biochemical and Haematological Reference values in normal experimental animals. Masson Publishing, New York, pp 21–64Google Scholar
- Odetola MO, Ewuola EO, Adu AO (2012) Haematology, serum biochemistry and organ histopathology of rabbits fed graded levels of whole Kenaf seed meal. Int J Agric Res 72:86–92Google Scholar
- Okab AB, El-Banna SG, Koriem AA (2008) Influence of environmental temperatures on some physiological and biochemical parameters of New Zealand rabbit males. Slovak J Anim Sci 41(1):12–19Google Scholar
- SAS Institute Inc (2003) SAS/STAT User’s guide, version 8 for windows. SAS Inst. Inc, CaryGoogle Scholar
- Soon YY, Tan BKH (2002) Evaluation of the hypoglycemic and anti-oxidant activities of Morinda officinalis in streptozotocininduced diabetic rats. Singap Med J 43:77–85Google Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.