15-Title: Assessment of enzymatic leucocytic stress response in Rathi cattle from Rajasthan during varying ambiences

15-Title: Assessment of enzymatic leucocytic stress response in Rathi cattle from Rajasthan during varying ambiences

Authors: Ashish Joshi, Nalini Kataria, Shesh Asopa and AK Kataria

Source: Ruminant Science (2022)-11(1):67-72.

How to cite this manuscript: Joshi Ashish, Kataria Nalini, Asopa Shesh and Kataria AK (2022). Assessment of enzymatic leucocytic stress response in Rathi cattle from Rajasthan during varying ambiences. Ruminant Science 11(1):67-72.

Abstract

For the present study, blood samples were collected from 1200 apparently healthy Rathi female calves, heifers and cows aged two weeks to 12 years old during moderate (300), extreme hot (300), extreme cold (300) and rainy ambiences (300) from private dairies located in and around Bikaner district, Rajasthan. Assessment of cellular stress responses was carried out by determining enzymatic biomarkers of oxidative stress viz catalase and SOD in leucocytes. The overall mean values of leucocytic catalase and SOD were significantly (p0.05) lower during extreme cold, hot and rainy ambiences as compared to moderate mean overall value. The overall mean values of catalase and SOD in cows were maximum and of calves were minimum significantly (p0.05) in all the ambiences. In calves, pre-ruminant revealed maximum leucocytic catalase and SOD values while in the heifer’s category, post-pubertal had significantly (p0.05) higher values of leucocytic catalase and SOD in comparison to pre-pubertal in each ambience. In the cow’s category, among group A animals, pregnant dry and in group B animals, multipara had significantly (p0.05) higher values of leucocytic catalase and SOD in each ambience. In all the physiological states of Rathi cattle, maximum per cent variations were observed in rainy ambience. It can be concluded that among all the physiological states, cows showed maximum enzymatic stress response in leucocytes during the rainy ambience.

References

Anonymous (2016). Manual of Antioxidants in Leucocytes. EdS: N Kataria, A Joshi and AK Kataria. Department of Veterinary Physiology, College of Veterinary and Animal Science, Bikaner, Rajasthan. pp 2-10.

Bhavsar Tanvi D, Arora Sunil, Maan Ruchi and Kataria Nalini (2020). Study of physiological effects of oxidative stress in buffalo calves from arid tracts. Ruminant Science 9(1):91-94.

Dalvi SH, Panchal PB, Ambade RB, Dighe DG and Deshmukh RD (2021). Serum electrolytes levels during short journey transportation stress in adult goats. Ruminant Science 10(2):359-362.

Duncan DB (1955). Multiple range and multiple F tests. Biomet 11:1-42.

Gautam N, Das S, Mahapatra SK, Chakraborty SP, Kundu PK and Roy S (2010). Age-associated oxidative damage in lymphocytes. Oxidative Medicine and Cellular Longevity 3(4):275-282.

Goth L (1991). A simple method for determination of serum catalase activity and revision of reference range.  Clinica Chimica  Acta 196:143-152.

Jain NC (1986). In: Schalm’s Veterinary Haematology. 4th  Edn, Lea and Febiger, Philadelphia. pp 2-198.

Joshi A and Kataria N (2018). Alterations in serum 5’ nucleotidase activity of Rathi female calves, heifers and cows from arid tracts during extreme ambiences. Acta Biomedica Scientia 5(2):43-50.

Kataria N and Kataria AK (2008). Activity of ornithine carbamoyltransferase in the serum of Rathi cattle. Indian cow 5(17):12-15.

Kataria N and Kataria AK (2013). Ambience-associated variations in serum biomarkers of oxidative stress in donkey of arid tracts in India. Egyptian Journal of Biology 15:44-47.

Kataria N, Kataria AK and Maan R (2010). Evaluation of oxidative stress due to hot environmental condition in healthy Marwari goats from arid tract in India. Philippine Journal of Veterinary and Animal Sciences 36(2):175-184.

Kidson C (1962). Variations in catalase activity in human leukocytes. Blood 19(1):82-88.

Kliger E, Kristal B, Shapiro G, Chezar J and Sela S (2017). Primed polymorphonuclear leukocytes from hemodialysis patients enhance monocyte transendothelial migration. American Journal of Physiology-Heart and Circulatory Physiology 313(5):H974-H987.

Maan R and Kataria N (2020). Assessment of fluid status of female Murrah buffaloes from arid tracts of Rajasthan during extreme ambiences. European Journal of Pharmaceutical and Medical Research 7(9):434-439.

Mili Bhabesh, Das Gunjan, Gogoi Amrit, Laltlankimi, Chutia Tukheswar, Devi Rajkumari Mandakini and Chaudhary JK (2021). Comparative hemato-biochemical profile of Assam hill goats and black Bengal goats in subtropical climatic condition of Nagaland. Ruminant Science 10(2):353-357.

Noblet PB and Cuttst JH (1967).  Separation of blood leukocytes by ficoll gradient. Canadian Veterinary Journal 8(5):110-111.

Ogata M, Mizugaki J, Taketa K and Takahara S (1977). Activities of catalase in leucocytes and glucose-6-phosphate dehydrogenase in erythrocytes of hypocatalasemia and acatalasemia.  Tohoku Journal of Experimental Medicine 122(1):93-97.

Sheikh Amir Amin, Mahapatra PS, Devi Jonali, Nabi Burhan and Sofi Omer Mohi Udin (2021). Ameliorative effect of cold drinking water in summer stressed crossbred cattle. Ruminant Science 10(2):347-352.

Singh Alok and Verma Diwakar (2021). Appraisal of serum metabolites and assorted immune oxidative parameters during transition period in goats of central India. Ruminant Science 10(1):49-56.

Singh Archita and Kataria Nalini (2020). Effect of extreme environmental temperature on plasma mono amine oxidase, bicarbonate level and urine bicarbonate level in non-descript goat of Indian arid tract. Ruminant Science 9(2):341-344.

Winterbourn C, Hawkin R, Brian M and Carell R (1975). The estimation .of red cell superoxide dismutase Activity.  Journal of Laboratory and Clinical Medicine 85:337-340.