Evaluation of hematological parameters, oxidative stress, Iron and unsaturated Iron binding capacity levels in Kangal shepherd dogs, before and after orchiectomy

  • Ibrahım Yurdakul Sivas Cumhuriyet University, Faculty of Veterinary Medicine, Department of Surgery. Sivas, Türkiye
  • Barıs Atalay Uslu Sivas Cumhuriyet University, Faculty of Veterinary Medicine, Department of Reproduction and Artificial Insemination. Sivas, Türkiye
Keywords: Antioxidant, Kangal shepherd dog, iron, oxidative stress, hematology

Abstract

Gonadectomy is a widely used method in reproductive health management, and behavior disorder therapies of domestic animals. Anemia and its development, one of the complications of surgical castration, which has been done so much recently in shelter dogs and dogs kept at home, has been investigated in male Kangal shepherd dogs. In castrated male Kangal shepherd dogs was to investigate the relationship between gonadectomy and oxidant and antioxidant levels, Iron (Fe) concentrations, unsaturated iron binding capacity (UIBC) and some blood parameters (RBC, HGB, HCT, MCV, RDW, MCHC). Blood samples were taken from 20 adult Kangal dogs brought to a clinic before castration (Day 0) and on the 1st, 3rd and 7th days. Some biochemical analyzes and blood parameters were evaluated in the blood samples taken. For this purpose, serum total oxidant–antioxidant capacity (TAC–TOC), Iron (Fe) concentrations, unsaturated iron binding capacity (UIBC) and some blood parameters (RBC, HGB, HCT, MCV, RDW, MCHC) were examined. In this study, it was evaluated the relationship between gonadectomy and oxidant–antioxidant capacity and Fe metabolism at some serum parameters in male dogs. After the orchidectomy operation, a remarkable decrease in clinical and statistical blood parameters was observed. As a result of this study, in the analysis of blood parameters, a severe picture of anemia was observed. It was determined an important role in erythropoiesis, with orchidectomy. The statistical difference in blood parameters (P<0.05) was indicative of this.

Downloads

Download data is not yet available.

References

Kustritz R. Effects of surgical sterilization on canine and feline health and society. Reprod. Dom. Anim. [Internet]. 2012; 47: 214–222. doi: https://doi.org/mb56

Lund EM, Armstrong PJ, Kirk CA, Klausner JS. Prevalence and risk factors for obesity in adult dogs from private US veterinary practices. Intern. J. Appl. Res. Vet. Med. 2006; 4(2):177–186

Plotnikov E, Korotkova E, Voronova, Sazhina N, Petrova E, Artamonov A, Chernayavskaya L, Dorozhko E. Comparative investigation of antioxidant activity of human serum blood by amperometric, voltammetric, and chemiluminescent methods. Arch. Med. Sci. [Internet]. 2016; 12(5):1071–1076. doi: https://doi.org/mb57

Singer JW, Samuels AI, Adamson JW. Steroids and hematopoiesis. I. The effect of steroids on in vitro erythroid colony growth: Structure/ activity relationships. J.Cell. Physiol. [Internet]. 1976; 88(2):127. doi: https://doi.org/dnmrc6

Schiavone S, Jaquet V, Trabace L, Krause KH. Severe life stress and oxidative stress in the brain: from animal models to human pathology. Antioxid. Redox Signal. [Internet]. 2013; 18(12):1475–1490. doi: https://doi.org/gffm5g

Fonseca R, Rajkumar SV, White WL, Tefferi A, Hoagland HC. Anemia after orchiectomy. Ame. J. Hematol. [Internet]. 1998; 59(3):230–233. doi: https://doi.org/fg5srt

Silva E, Schumacher J, Passler T. Castration of dogs using local anesthesia after sedating with xylazine and subanesthetic doses of ketamine. Front. Vet. Sci. [Internet]. 2020; 6:1–7. doi: https://doi.org/mb58

Handelman GJ, Levin NW. Red cell survival: relevance and mechanism involved. J. Renal Nutr. [Internet]. 2010; 20(5):84−88. doi: https://doi.org/cqp355

Lucchi L, Bergamini S, Iannone A, Perrone S, Stipo L, Olmeda F, Caruso F, Tomasi A, Albertazzi A. Erythrocyte susceptibility to oxidative stress in chronic renal failure patients under different substitutive treatments. Artific. Organs. [Internet]. 2005; 29(1)67–72. doi: https://doi.org/br2hnh

Gabrielsen JS. Iron and testosterone: interplay and clinical implications. Curr. Sex. Health Reports. [Internet]. 2017; 9:5–11. doi: https://doi.org/mb59

Alonso‐Alvarez C, Bertrand S, Faivre B, Chastel O, Sorci G. Testosterone and oxidative stress: the oxidation handicap hypothesis. Proceed. the Royal Soc. Biol. Sci. [Internet]. 2007; 274(1611):819‐825. doi: https://doi.org/d5g4rw

Buchanan KL, Evans MR, Goldsmith AR, Bryant DM, Rowe LV. Testosterone influences basal metabolic rate in male house sparrows: a new cost of dominance signaling? Proceed. the Royal Soc. Biol. Sci. [Internet]. 2001; 268(1474):1337–1344. doi: https://doi.org/d9dnbs

Hayden SJ, Albert TJ, Watkins TR, Swenson ER. Anemia in critical illness, Insights into etiology, consequences, and management. Ame. J. Resp. Crit. Care Med. [Internet]. 2012; 185(10):1049–1057. doi: https://doi.org/fzbt9j

Martinez C, Mooney CT, Shiel RE, Tang PK, Mooney L, O’neill EJ. Evaluation of red blood cell distribution width in dogs with various illnesses. Can. Vet. J. 2019; 60(9): 964–971. Cited in: PubMed; PMID 31523082.

Dainiak N. The role of androgens in the treatment of anemia of chronic renal failure. Semin. Nephrol. 1985; 5(2):147–154. Cited in: PubMed; PMID 3843789.

Anup R, Balasubramanian KA. Surgical stress and the gastrointestinal tract. J. Surgical Res. [Internet]. 2000; 92(2):291–300. doi: https://doi.org/bp2dwq

Lee JY, Kim MC. Comparison of oxidative stress status in dogs undergoing laparoscopic and open ovariectomy. The J. Vet. Med. Sci. [Internet]. 2014; 76(2):273–276. doi: https://doi.org/f5x3wv

Mahalingam A, Kumar N, Maiti SK, Sharma AK, Dimri U, Kataria M. Laparoscopic sterilization vs. open method sterilization in dogs: a comparison of two techniques. Turkish J. Vet. Anim. Sci. [Internet]. 2009; 33(5):427–436. doi: https://doi.org/ksrj

Sanchez–Medal L. The hemopoietic action of androstanes. Prog. Hematol. 1971; 7: 111–136. Cited in: PubMed; PMID 4950580.

Rasheed N, Ahmad A, Al–Sheeha M, Alghasham A, Palit G. Neuroprotective and anti–stress effect of A68930 in acute and chronic unpredictable stress model in rats. Neurosci. Lett. [Internet]. 2011; 504:151–155. doi: https://doi.org/10.1016/j.neulet.2011.09.021

Sorce S, Krause KH. NOX enzymes in the central nervous system: from signaling to disease. Antioxid. Redox Signal. [Internet]. 2009; 11(10):2481–2504. doi: https://doi.org/bqtgqv

Chainy GBN, Samantaray S, Samanta L. Testosterone– induced changes in testicular antioxidant system. Androl. [Internet]. 1997; 29(6):343–349. doi: https://doi.org/bj8vgk

Aydilek N, Aksakal M, Karakilçik AZ. Effects of testosterone and vitamin E on the antioxidant system in rabbit testis. Androl. [Internet]. 2004; 36(5):277–281. doi: https://doi.org/b5nhb3

Bokov AF, Ko D, Richardson A. The effect of gonadectomy and estradiol on sensitivity to oxidative stress. Endocr. Res. [Internet]. 2009; 34(1–2):43–58. doi: https://doi.org/b8gjrj

Shahidi NT. Androgens and erythropoiesis. The New England J. Med. [Internet]. 1973; 289:72–80. doi: https://doi.org/cw93s5

Juca TG, Pencina KM, Ganz T, Thomas G, Travison TG, Kantoff PW, Nguyen PL, Taplin ME, Kibel AS. Mechanisms responsible for reduced erythropoiesis during androgendeprivation therapy in men with prostate cancer. Ame. J. Physiol. Endocrinol. Metab. 2018; 315(6):E1185–E1193. doi: https://doi.org/mb6d

Al–Sharefi A, Mohammed A, Abdalaziz A. Jayasena CN. Androgens and anemia: Current Trends and Future Prospects. Frontiers in Endocrinol 2019; 10:754. doi: https://doi.org/mb6f

Published
2024-01-13
How to Cite
1.
Yurdakul I, Uslu BA. Evaluation of hematological parameters, oxidative stress, Iron and unsaturated Iron binding capacity levels in Kangal shepherd dogs, before and after orchiectomy. Rev. Cient. FCV-LUZ [Internet]. 2024Jan.13 [cited 2024Dec.2];34(1):6. Available from: https://produccioncientificaluz.org/index.php/cientifica/article/view/41474
Section
Veterinary Medicine