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Doğal Olarak Kilo Alan veya Obezite Gelişen Kedilerde Lipid Profili, Oksidatif Stres ve Tiyol-Disülfür Düzeyleri Arasındaki İlişkiler

Yıl 2024, Cilt: 19 Sayı: 3, 148 - 154, 29.12.2024
https://doi.org/10.17094/vetsci.1499578

Öz

Bu çalışmada, doğal olarak fazla kilo almış olan veya obezitenin geliştiği kedilerde sistemik inflamasyonun, oksidatif stresin ve lipid profilinin değerlendirilmesi amaçlandı. Çalışmada, vücut kondisyon skoru (BCS) >8 olan on obez kedi (obezite geliştiren grup), BCS skoru >6 olan on fazla kilolu kedi (fazla kilolu grup) ve BCS skoru 4-5 olan on ideal kilolu kedi (kontrol grubu) incelendi. Aşırı kilo almış olan ve obezitenin geliştiği kedilerde, serum AST (P < ,001), albumin (P = ,002) ve toplam protein (TP) (P < ,001) düzeylerinin kontrol grubundaki kedilerde tanımlanan değerlerden anlamlı derecede yüksek olduğu belirlendi. Ayrıca, obezitenin geliştiği, kedilerde kan serumu yüksek yoğunluklu lipoprotein (HDL) (P = ,009) ve trigliserit (TG) (P < ,001) düzeyleri kontrol grubundaki kedilerde belirtilen değerlerden anlamlı derecede yüksek bulundu. Obezitenin geliştiği kedilerde, serum prokalsitonin (PCT), paraoksonaz-1 (PON-1), toplam tiyol, doğal tiyol ve MDA düzeylerinin aşırı kilolu kedilere göre anlamlı derecede yüksek olduğu saptandı (P < ,001). Sonuç olarak veteriner hekimlerin klinik değerlendirmelerinde, doğal olarak fazla kilo almış olan veya obezitenin geliştiği kedilerde, karaciğer fonksiyonları ve lipid metabolizması ile ilgili olan ve sistemik inflamasyon ve oksidatif stresi gösteren parametrelerdeki anlamlı düzeydeki değişiklikleri dikkate almalarının yararlı olacağı kanısına varıldı.

Etik Beyan

Etik onay Ankara Üniversitesi Hayvan Deneyleri Yerel Etik Kurulu'ndan (2022-22-197) alındı.

Destekleyen Kurum

Türkiye Bilimsel ve Teknolojik Araştırma Kurumu (TÜBİTAK)

Proje Numarası

1919B012214043

Kaynakça

  • 1. Montoya M, Morrison JA, Arrignon F, Spofford N, Charles H, Hours M-A and Biourge V. Life expectancy tables for dogs and cats derived from clinical data. Front Vet Sci. 2023;21(10):1082102.
  • 2. Laurence C, Paragon BM, Lemuet B, Benet JJ, Blanchard G. Prevalence and risk factors of obesity in an urban population of healthy cats. J Feline Med Surg. 2009;11(2): 135-140.
  • 3. Wallis N, Raffan E. The genetic basis of obesity and related metabolic diseases in humans and companion animals. Genes. 2020;11(11):1378.
  • 4. Biourge V, Nelson RW, Feldman EC, Willits NH, Morris JG, Rogers QR. Effect of weight gain and subsequent weightloss on glucose tolerance and insulin response in healthy cats. J Vet Intern Med. 1997;11(2):86-91.
  • 5. Scarlett JM, Donoghue S. Associations between body condition and disease in cats. J Am Vet Med Assoc. 1998;212(11):1725-1731.
  • 6. Martins TO, Ramos RC, Possidonio G, et al. Feline obesity causes hematological and biochemical changes and oxidative stress – a pilot study. Vet Res Commun. 2023;47(1):167-177.
  • 7. Matur E, Özcan M, Ekiz EE, et al. Use of serum procalcitonin (PCT) level and PCT mRNA expression as a potential clinical biomarker in cats with bacterial and viral infections. J Feline Med Surg. 2022;24(12):595-602.
  • 8. Rossi G. Acute phase proteins in cats: Diagnostic and prognostic role, future directions, and analytical challenges. Vet Clin Pathol. 2023;52(Suppl 1):37-49.
  • 9. Marek G. Decreases in paraoxonase-1 activities promote a pro-inflammatory effect of lipids peroxidation products in non-smoking and smoking patients with acute pancreatitis. Int J Med Sci. 2018;15(14):1619-1630.
  • 10. Gonzalez-Arostegui LG, Munoz-Prieto A, Garcia-Lopez G. Ceron JJ, Tvarijonaviciute A, Rubio, CP. Changes in biomarkers of the redox status in whole blood and red blood cell lysates in canine hypothyroidism. Vet Res Commun. 2024;48(4):2185-2192.
  • 11. Mehdi M, Rizvi SI. Human plasma paraoxonase 1 (PON1) arylesterase activity during aging: correlation with susceptibility of LDL oxidation. Arch Med Res. 2012;43(6): 438-443.
  • 12. Novak F, Vavrova L, Kodydkova J, et al. Decreased paraoxonase activity in critically ill patients with sepsis. Clin Exp Med. 2010;10(1):21-25.
  • 13. Laflamme D. Development and validation of a body condition score system for cats: a clinical tool. Feline Pract. 1997;25(5-6):13-18.
  • 14. Draper HH, Hadley H. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990;186:421-431.
  • 15. Eckerson HW, Wyte CM, La Du BN. The human serum paraoxonase/arylesterase polymorphism. Am J Hum Genet. 1983;35(6):1126-1138.
  • 16. Erel O, Neselioglu SA. Novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47(18):326-332.
  • 17. Courcier EA, O’Higgins R, Mellor DJ, Yam PS. Prevalence and risk factors for feline obesity in a first opinion practice in Glasglow, Scotland. J Feline Med Surg. 2010;12(10):746-753.
  • 18. Shoveller AK, Di Gennaro J, Lanman C, Spangler D. Trained vs untrained evaluator assessment of body condition score as a predictor of percent body fat in adult cats. J Feline Med Surg. 2014;16(12):957-965.
  • 19. Kawasumi K, Iwazaki E, Okada Y, Arai T. Effectiveness of feline body mass index (fBMI) as new diagnostic tool for obesity. Jpn J Vet Res. 2016;64(1):51-56.
  • 20. Fujiwara M, Mori N, Sato T, et al. Changes in fatty acid composition in tissue and serum of obese cats fed a high fat diet. BMC Vet Res. 2015;13(11):200.
  • 21. Okada Y, Ueno H, Mizorogi T, Ohara K, Kawasumi K, Arai T. Diagnostic Criteria for Obesity Disease in Cats. Front Vet Sci. 2019;27(6):284.
  • 22. De Freitas VD, Castilho AR, da Conceiçao LAV, et al. Metabolic evaluation in overweight and obese cats and association with blood pressure. Cienc Rural. 2018;48(1): e20170217.
  • 23. Bauer JE. Comparative lipid and lipoprotein metabolism. Vet Clin Pathol. 1996;25(2): 49-56.
  • 24. Hoenig M, Wilkins C, Holson JC, Ferguson DC. Effects of obesity on lipid profiles in neutered male and female cats. Am J Vet Res. 2003;64(3):99-303.
  • 25. Kotani K, Watanabe J, Miura K, Gugliucci A. Paraoxonase 1 and non-alcoholic fatty liver disease: A meta-analysis. Molecules. 2021;26(8):2323.
  • 26. Swiatkiewicz I, Wroblewski M, Nuszkiewicz J, Sutkowy P, Wroblewska J, Wozniak A. The role of oxidative stress enhanced by adiposity in cardiometabolic diseases. Int J Mol Sci. 2023;24(7):6382.
  • 27. Dağ T, Şahinduran Ş. Measurement of paraoxonase and telomerase enzymes and HDL (high density lipoprotein) values and research of their possible relationships with each other in bloodserum of obese cats. MAE Vet Fak Derg. 2021;6(3):104-108.
  • 28. Tvarijonaviciute A, Ceron JJ, Holden SL, Morris PJ, Biourge V, German AJ. Effects of weight loss in obese cats on biochemical analytes related to inflammation and glucose homeostasis. Domes Anim Endocrinol. 2012;42(3):129-141.
  • 29. Tursun S, Gülerman HF, Gazyağcı S, Şahin Y, Erel Ö, Neşelioğlu S. Investigation of Thiol/Disulfide balance in obese rats with non-alcoholic fatty liver disease. Pediatr Gastroenterol Hepatol Nutr. 2021;24(5):443-454.
  • 30. Giannuzzi D, Mota LFM, Pegolo S, et al. Prediction of detailed blood metabolic profile using milk infrared spectra and machine learning methods in dairy cattle. J Dairy Sci. 2023;106(5):3321-3344.
  • 31. Mengen E, Uçaktürk SA, Kocaay P, Kaymaz O, Neşelioğlu S, Erel O. The significance of Thiol/Disulfide homeostasis and ischemia-modified albumin levels in assessing oxidative stress in obese children and adolescents. J Clin Res Pediatr Endocrinol. 2020;12(1):45-54.
  • 32. Nemet D, Barkan S, Epstein Y, Friedland O, Kowen G, Eliakim A. Short- and long-term beneficial effects of a combined dietary-behavioral- physical activity intervention for the treatment of childhood obesity. Pediatrics. 2005;115(4):e443-449.
  • 33. Zaldivar F, McMurray RG, Nemet D, Galassetti P, Mills PJ, Cooper DM. Body fat and circulating leukocytes in children. Int J Obes (Lond). 2006;30(6):906-911.
  • 34. Radakovich LB, Truelove MP, Pannone SC, Oliver CS, Santangelo KS. Clinically healthy overweight and obese dogs differ from lean controls in select CBC and serum biochemistry values. Vet Clin Pathol. 2017;46(2):221-226.
  • 35. Tanner AE, Martin J, Saker, KE. Oxidative stress and inflammatory state induced by obesity in the healthy feline. J Anim Physiol Anim Nutr (Berl). 2007;91:163-166.

The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats

Yıl 2024, Cilt: 19 Sayı: 3, 148 - 154, 29.12.2024
https://doi.org/10.17094/vetsci.1499578

Öz

This study aimed to evaluate systemic inflammation, oxidative stress and lipid profile in cats that had either naturally gained excess weight or had developed obesity. The following groups were examined in the study: ten obese cats with a body condition score of (BCS) >8 (the obesity group), ten overweight cats with a BCS score of >6 (the overweight group) and ten ideal weight cats with a BCS score of 4-5 (the control group). In the cats that had either gained too much weight or had become obese, the serum AST (P < .001), albumin (P = .002) and total protein (TP) (P < .001) levels were found to be significantly higher than the values determined in the control group cats. Furthermore, blood serum high-density lipoprotein (HDL) (P = .009) and triglyceride (TG) (P < .001) levels in cats that had developed obesity were found to be significantly higher than the values defined in the control group cats. In the obese cats, serum procalcitonin (PCT), paraoxonase-1 (PON-1), total thiol, native thiol and MDA levels were found to be significantly higher than in overweight cats (P < .001). As a result, it was concluded that it would be useful for veterinarians to consider significant changes in parameters related to liver function and lipid metabolism, as well as to emphasize systemic inflammation and oxidative stress in their clinical evaluations in cats that had either naturally gained excess weight or had developed obesity.

Etik Beyan

Ethical approval was obtained from Ankara University’s Animal Experiments Local Ethics Committee (2022-22-197).

Destekleyen Kurum

Scientific and Technological Research Council of Türkiye (TÜBİTAK)

Proje Numarası

1919B012214043

Kaynakça

  • 1. Montoya M, Morrison JA, Arrignon F, Spofford N, Charles H, Hours M-A and Biourge V. Life expectancy tables for dogs and cats derived from clinical data. Front Vet Sci. 2023;21(10):1082102.
  • 2. Laurence C, Paragon BM, Lemuet B, Benet JJ, Blanchard G. Prevalence and risk factors of obesity in an urban population of healthy cats. J Feline Med Surg. 2009;11(2): 135-140.
  • 3. Wallis N, Raffan E. The genetic basis of obesity and related metabolic diseases in humans and companion animals. Genes. 2020;11(11):1378.
  • 4. Biourge V, Nelson RW, Feldman EC, Willits NH, Morris JG, Rogers QR. Effect of weight gain and subsequent weightloss on glucose tolerance and insulin response in healthy cats. J Vet Intern Med. 1997;11(2):86-91.
  • 5. Scarlett JM, Donoghue S. Associations between body condition and disease in cats. J Am Vet Med Assoc. 1998;212(11):1725-1731.
  • 6. Martins TO, Ramos RC, Possidonio G, et al. Feline obesity causes hematological and biochemical changes and oxidative stress – a pilot study. Vet Res Commun. 2023;47(1):167-177.
  • 7. Matur E, Özcan M, Ekiz EE, et al. Use of serum procalcitonin (PCT) level and PCT mRNA expression as a potential clinical biomarker in cats with bacterial and viral infections. J Feline Med Surg. 2022;24(12):595-602.
  • 8. Rossi G. Acute phase proteins in cats: Diagnostic and prognostic role, future directions, and analytical challenges. Vet Clin Pathol. 2023;52(Suppl 1):37-49.
  • 9. Marek G. Decreases in paraoxonase-1 activities promote a pro-inflammatory effect of lipids peroxidation products in non-smoking and smoking patients with acute pancreatitis. Int J Med Sci. 2018;15(14):1619-1630.
  • 10. Gonzalez-Arostegui LG, Munoz-Prieto A, Garcia-Lopez G. Ceron JJ, Tvarijonaviciute A, Rubio, CP. Changes in biomarkers of the redox status in whole blood and red blood cell lysates in canine hypothyroidism. Vet Res Commun. 2024;48(4):2185-2192.
  • 11. Mehdi M, Rizvi SI. Human plasma paraoxonase 1 (PON1) arylesterase activity during aging: correlation with susceptibility of LDL oxidation. Arch Med Res. 2012;43(6): 438-443.
  • 12. Novak F, Vavrova L, Kodydkova J, et al. Decreased paraoxonase activity in critically ill patients with sepsis. Clin Exp Med. 2010;10(1):21-25.
  • 13. Laflamme D. Development and validation of a body condition score system for cats: a clinical tool. Feline Pract. 1997;25(5-6):13-18.
  • 14. Draper HH, Hadley H. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990;186:421-431.
  • 15. Eckerson HW, Wyte CM, La Du BN. The human serum paraoxonase/arylesterase polymorphism. Am J Hum Genet. 1983;35(6):1126-1138.
  • 16. Erel O, Neselioglu SA. Novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47(18):326-332.
  • 17. Courcier EA, O’Higgins R, Mellor DJ, Yam PS. Prevalence and risk factors for feline obesity in a first opinion practice in Glasglow, Scotland. J Feline Med Surg. 2010;12(10):746-753.
  • 18. Shoveller AK, Di Gennaro J, Lanman C, Spangler D. Trained vs untrained evaluator assessment of body condition score as a predictor of percent body fat in adult cats. J Feline Med Surg. 2014;16(12):957-965.
  • 19. Kawasumi K, Iwazaki E, Okada Y, Arai T. Effectiveness of feline body mass index (fBMI) as new diagnostic tool for obesity. Jpn J Vet Res. 2016;64(1):51-56.
  • 20. Fujiwara M, Mori N, Sato T, et al. Changes in fatty acid composition in tissue and serum of obese cats fed a high fat diet. BMC Vet Res. 2015;13(11):200.
  • 21. Okada Y, Ueno H, Mizorogi T, Ohara K, Kawasumi K, Arai T. Diagnostic Criteria for Obesity Disease in Cats. Front Vet Sci. 2019;27(6):284.
  • 22. De Freitas VD, Castilho AR, da Conceiçao LAV, et al. Metabolic evaluation in overweight and obese cats and association with blood pressure. Cienc Rural. 2018;48(1): e20170217.
  • 23. Bauer JE. Comparative lipid and lipoprotein metabolism. Vet Clin Pathol. 1996;25(2): 49-56.
  • 24. Hoenig M, Wilkins C, Holson JC, Ferguson DC. Effects of obesity on lipid profiles in neutered male and female cats. Am J Vet Res. 2003;64(3):99-303.
  • 25. Kotani K, Watanabe J, Miura K, Gugliucci A. Paraoxonase 1 and non-alcoholic fatty liver disease: A meta-analysis. Molecules. 2021;26(8):2323.
  • 26. Swiatkiewicz I, Wroblewski M, Nuszkiewicz J, Sutkowy P, Wroblewska J, Wozniak A. The role of oxidative stress enhanced by adiposity in cardiometabolic diseases. Int J Mol Sci. 2023;24(7):6382.
  • 27. Dağ T, Şahinduran Ş. Measurement of paraoxonase and telomerase enzymes and HDL (high density lipoprotein) values and research of their possible relationships with each other in bloodserum of obese cats. MAE Vet Fak Derg. 2021;6(3):104-108.
  • 28. Tvarijonaviciute A, Ceron JJ, Holden SL, Morris PJ, Biourge V, German AJ. Effects of weight loss in obese cats on biochemical analytes related to inflammation and glucose homeostasis. Domes Anim Endocrinol. 2012;42(3):129-141.
  • 29. Tursun S, Gülerman HF, Gazyağcı S, Şahin Y, Erel Ö, Neşelioğlu S. Investigation of Thiol/Disulfide balance in obese rats with non-alcoholic fatty liver disease. Pediatr Gastroenterol Hepatol Nutr. 2021;24(5):443-454.
  • 30. Giannuzzi D, Mota LFM, Pegolo S, et al. Prediction of detailed blood metabolic profile using milk infrared spectra and machine learning methods in dairy cattle. J Dairy Sci. 2023;106(5):3321-3344.
  • 31. Mengen E, Uçaktürk SA, Kocaay P, Kaymaz O, Neşelioğlu S, Erel O. The significance of Thiol/Disulfide homeostasis and ischemia-modified albumin levels in assessing oxidative stress in obese children and adolescents. J Clin Res Pediatr Endocrinol. 2020;12(1):45-54.
  • 32. Nemet D, Barkan S, Epstein Y, Friedland O, Kowen G, Eliakim A. Short- and long-term beneficial effects of a combined dietary-behavioral- physical activity intervention for the treatment of childhood obesity. Pediatrics. 2005;115(4):e443-449.
  • 33. Zaldivar F, McMurray RG, Nemet D, Galassetti P, Mills PJ, Cooper DM. Body fat and circulating leukocytes in children. Int J Obes (Lond). 2006;30(6):906-911.
  • 34. Radakovich LB, Truelove MP, Pannone SC, Oliver CS, Santangelo KS. Clinically healthy overweight and obese dogs differ from lean controls in select CBC and serum biochemistry values. Vet Clin Pathol. 2017;46(2):221-226.
  • 35. Tanner AE, Martin J, Saker, KE. Oxidative stress and inflammatory state induced by obesity in the healthy feline. J Anim Physiol Anim Nutr (Berl). 2007;91:163-166.
Toplam 35 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Veteriner Biyokimya
Bölüm Araştırma Makaleleri
Yazarlar

Efe Kurtdede 0000-0001-8436-3332

Nisa Taşkın 0009-0008-4344-146X

Emre Salih İspir 0000-0003-4216-5287

Erman Gülendağ 0000-0002-3335-7247

Proje Numarası 1919B012214043
Yayımlanma Tarihi 29 Aralık 2024
Gönderilme Tarihi 11 Haziran 2024
Kabul Tarihi 12 Eylül 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 19 Sayı: 3

Kaynak Göster

APA Kurtdede, E., Taşkın, N., İspir, E. S., Gülendağ, E. (2024). The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats. Veterinary Sciences and Practices, 19(3), 148-154. https://doi.org/10.17094/vetsci.1499578
AMA Kurtdede E, Taşkın N, İspir ES, Gülendağ E. The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats. Veterinary Sciences and Practices. Aralık 2024;19(3):148-154. doi:10.17094/vetsci.1499578
Chicago Kurtdede, Efe, Nisa Taşkın, Emre Salih İspir, ve Erman Gülendağ. “The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats”. Veterinary Sciences and Practices 19, sy. 3 (Aralık 2024): 148-54. https://doi.org/10.17094/vetsci.1499578.
EndNote Kurtdede E, Taşkın N, İspir ES, Gülendağ E (01 Aralık 2024) The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats. Veterinary Sciences and Practices 19 3 148–154.
IEEE E. Kurtdede, N. Taşkın, E. S. İspir, ve E. Gülendağ, “The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats”, Veterinary Sciences and Practices, c. 19, sy. 3, ss. 148–154, 2024, doi: 10.17094/vetsci.1499578.
ISNAD Kurtdede, Efe vd. “The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats”. Veterinary Sciences and Practices 19/3 (Aralık 2024), 148-154. https://doi.org/10.17094/vetsci.1499578.
JAMA Kurtdede E, Taşkın N, İspir ES, Gülendağ E. The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats. Veterinary Sciences and Practices. 2024;19:148–154.
MLA Kurtdede, Efe vd. “The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats”. Veterinary Sciences and Practices, c. 19, sy. 3, 2024, ss. 148-54, doi:10.17094/vetsci.1499578.
Vancouver Kurtdede E, Taşkın N, İspir ES, Gülendağ E. The Relationship Between Lipid Profile, Oxidative Stress, and Thiol-Disulfide Levels in Healthy, Naturally Overweight and Obese Cats. Veterinary Sciences and Practices. 2024;19(3):148-54.

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