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Abstract

Twenty eight male Sprague Dawley rats (aged 3 months) were used in the study. The animals were given feed and water as ad libitum. Sprague dawley rats were randomly divided into 4 groups as 7 rats in each group. Except for the control one, aflatoxin B1 (7.5 μg / 200 g), resvera- trol (60 mg / kg) was administered to rats of 3 other groups. At the end of the 16th day, blood, semen and tissue specimens were taken by decapitation under ether anesthesia. When we evaluate the spermatological parameters, it is understood that resveratrol has a statistically significant difference in terms of sperm motility and viability (membrane integrity) compared to the control group and aflatoxin B1 administration groups, indicating a protective effect on spermatological parameters. In terms of pathological parameters - histopathological examination - in the control and resveratrol groups, seminiferous tubules were observed to be in normal structure. In the group treated with aflatoxin, the regular structure of the spermatogenic cells deteriorated and the seminiferous tubules became necrotic and degenerative. In the group treated with Afb1 + res, the decreasing of necrotic and degenerative changes were determined compared with in the group treated with aflatoxin. As immunohistochemical examination, cleaved caspase 3 expression was found to be very low in the control and resveratrol groups. Cleaved caspase 3 expression was severely exacerbated in seminiferous tubules in aflatoxin group but cleaved caspase 3 expression level decreased in Afb1 + res. In the biochemical direction, resveratrol has been shown to inhibit the adverse effects of aflatoxin on antioxidant levels and to show a protective effect. For this purpose, the use of resveratrol with antioxidant activity was investi- gated in preventing or ameliorating damage to aflatoxin B1. It has been concluded that resveratrol effectively prevent the aflatoxin-induced testicular damage and lipid peroxidation. It has also been shown that resveratrol has protective effects on sperm motility and viability.

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Authors and Affiliations

A.D. Omur
B. Yildirim
Y.S. Saglam
S. Comakli
M. Ozkaraca
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Abstract

The present study aimed to investigate the contamination of poultry feed with aflatoxin B1 and zearalenone at laying hen farms in Tehran suburbs. The poultry feed was selected from five laying hen farms. A total of 60 poultry feed samples were collected from each farm during four consecutive seasons, from spring to winter of 2021. High-performance liquid chromatography was used to determine the amount of aflatoxin B1 and zearalenone. The mean aflatoxin B1 and zearalenone concentrations in various seasons showed significant differences (p<0.01). The highest reported aflatoxin concentration was in winter, with a mean concentration of 1366.53±77.85 ng/kg. The lowest concentrations were reported in autumn and summer, indicating a significant difference (p<0.01). The highest concentration of zearalenone was reported in summer, with a mean concentration of 150.72±10.35 μg/kg. The lowest concentration was reported in winter, with a mean concentration of 22.87±10.35 μg/kg, indicating a statistically significant difference (p<0.01). Overall, the concentrations of aflatoxin B1 and zearalenone toxins significantly differed in various poultry farms. The poultry farm D had the highest aflatoxin contamination with a mean concentration of 648.08±59.89 ng/kg. Poultry farms A, B, and C had the highest zearalenone concentrations with mean concentrations of 125.17±20.61, 96.04±20.61, and 99.49±20.61 μg/kg, respectively. Autumn was the only season showing significant differences regarding zearalenone toxin concentration in poultry farms.
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Bibliography

1. Assumaidaee AA, Ali NM, Ahmed SW (2020) Zearalenone Mycotoxicosis: Pathophysiology and Immunotoxicity. Iraq J Vet Med 44: 29-38.
2. Ayofemi Olalekan Adeyeye S (2020) Aflatoxigenic fungi and mycotoxins in food: a review. Crit Rev Food Sci Nutr 60: 709-21.
3. Battilani P, Toscano P, Van der Fels-Klerx HJ, Moretti A, Camardo Leggieri M, Brera C (2016) Aflatoxin B1 contamination in maize in Europe increases due to climate change. Sci Rep 6: 24328.
4. Chang H, Kim W, Park J-H, Kim D, Kim CR, Chung S, Lee C (2017) The occurrence of zearalenone in South Korean feedstuffs be-tween 2009 and 2016. Toxins 9: 223.
5. Choudhary AK, Kumari P (2010) Management of mycotoxin contamination in preharvest and postharvest crops: present status and future prospects. J Phytol 2: 37-52.
6. Cinar A, Onbaşı E (2019) Mycotoxins: The hidden danger in foods. Mycotoxins food Saf 1-21.
7. Ersali A, Grigoran K, Baho-Aldini F, Ghasemi R, Ersali M (2008) Transition of Aflatoxin from Feedstuff to Animal Milk and Pasteur-ized Milk in Shiraz City and Suburbs (South Iran). Iran J Toxicol 2: 3-3.
8. FAO (2004) Food and Agriculture Organization of the United nations (FAO). Vitamin and mineral requirements in human nutrition, 246-278. https://www.fao.org/3/y2809e/y2809e.pdf.
9. Filazi A, Yurdakok-Dikmen B, Kuzukiran O, Sireli UT (2017) Mycotoxins in poultry. Poult Sci J 2017: 73-92.
10. Furian AF, Fighera MR, Royes LFF, Oliveira MS (2022) Recent advances in assessing the effects of mycotoxins using animal models. Curr Opin Food Sci 47: 100874.
11. Gruber-Dorninger C, Jenkins T, Schatzmayr G (2019) Global mycotoxin occurrence in feed: A ten-year survey. Toxins 11: 375.
12. Haque MA, Wang Y, Shen Z, Li X, Saleemi MK, He C (2020) Mycotoxin contamination and control strategy in human, domestic animal and poultry: A review. Microb Pathog 142: 104095.
13. Hassan YI, Zhou T, Bullerman LB (2016) Sourdough lactic acid bacteria as antifungal and mycotoxin-controlling agents. J Food Sci Technol Int 22: 79-90.
14. Hussain Z, Khan MZ, Saleemi MK, Khan A, Rafique S (2016) Clinicopathological effects of prolonged intoxication of aflatoxin B1 in broiler chicken. J Pak Vet J 36: 477- 81.
15. Iran Standard and Industrial Research Institute (2019) National Standard Committee for Feed and Agricultural Products, Animal Feed – Sampling No 7570.
16. Kajuna F, Temba B, Mosha R (2013) Surveillance of aflatoxin B1 contamination in chicken commercial feeds in Morogoro, Tanzania. Livest Res Rur Dev 25: 51.
17. Lalah JO, Omwoma S, Orony D (2019) Aflatoxin B1: Chemistry, environmental and diet sources and potential exposure in human in Kenya. In: Long X (ed) Aflatoxin B1 Occurrence, Detection and Toxicological Effects. IntechOpen, London, pp 1-33.
18. Magan N, Aldred D (2007) Post-harvest control strategies: minimizing mycotoxins in the food chain. Int J Food Microbiol 119: 131-139.
19. Mayahi M, Razi JM, Salamat N (2007) Isolation of Aspergillus spp and determination of aflatoxin level in fish meal, maize and soya meal. Chamran Univ J 17: 95-105.
20. Mohammadi S, Ghahremani E, Dehestaniathar S, Zandi S, Zakariai A, Mohammadi M, Karimi Z (2021) Determination of aflatoxin B1 concentration in poultry feed in the poultry farms of Sanandaj using ELISA method. Sci J Kurd Univ Med Sci 25: 49-56.
21. Mohsen AH, Mohsen IH, Risan MH (2022) Aflatoxins and its effect on human and animals: Article Review. World Bull Pub Health 10: 6-24.
22. Monge MP, Magnoli CE, Chiacchiera SM (2012) Survey of Aspergillus and Fusarium species and their mycotoxins in raw materials and poultry feeds from Córdoba, Argentina. Mycotoxin Res 28: 111-122.
23. National Standard of Iran (2009) determination of zearalenone by high performance liquid chromatography method and purification by immunoaffinity column – test method No 12257. http://www.isiri.org.
24. National Standard of Iran (2003) Measurement of Group B and G Aflatoxins by High Performance Liquid Chromatography and Purifi-cation with Immunoaffinity Column – Test Method No 6872. http://www.isiri.org.
25. Negash D (2018) A review of aflatoxin: occurrence, prevention, and gaps in both food and feed safety. Appl Microb Res 1: 35-43.
26. Nemati Z, Janmohammadi H, Taghizadeh A, Nejad HM, Mogaddam G, Arzanlou M (2014) Occurrence of aflatoxins in poultry feed and feed ingredients from northwestern Iran. Eur J Zool Res 3: 56-60.
27. Omotayo OP, Omotayo AO, Mwanza M, Babalola OO (2019) Prevalence of Mycotoxins and Their Consequences on Human Health. Toxicol Res 35: 1-7.
28. Rahimi E, Kargar A, Zamani F (2008) Assessment of aflatoxin B1 levels in animal feed of dairy farms in Chaharmahal & Bakhtiari. Vet Res Biol 79: 66-71.
29. Ropejko K, Twarużek M (2021) Zearalenone and its metabolites – general overview, occurrence, and toxicity. Tox 13: 35.
30. Shi J, He J, Lin J, Sun X, Sun F, Ou C, Jiang C (2016) Distinct response of the hepatic transcriptome to Aflatoxin B1 induced hepato-cellular carcinogenesis and resistance in rats. J Sci Rep 6: 34628.
31. Tahir NI, Hussain S, Javed M, Rehman H, Shahzady TG, Parveen B, Ali KG (2018) Nature of aflatoxins: Their extraction, analysis, and control. J Food Saf 38: e12561.
32. Waśkiewicz A, Goliński, P (2015) Mycotoxins in cereals and cereal products. In: Rios C (ed) Occurrence, toxicity and prevention. oc-currence, toxicology, and management strategies. Nova Science Publisher, New York, pp 55-97.
33. Xu R, Kiarie EG, Yiannikouris A, Sun L, Karrow NA (2022) Nutritional impact of mycotoxins in food animal production and strategies for mitigation. J Anim Sci Biotechnol 13: 69.
34. Yiannikouris A, Jouany J (2002) Mycotoxins in feeds and their fate in animals: a review. Anim Res 51: 81-99.
35. Zain ME (2011) Impact of mycotoxins on humans and animals. J Saudi Chem Soc 15: 129-144.
36. Zinedine A, Soriano JM, Molto JC, Manes J (2007) Review on the toxicity, occurrence, metabolism, detoxification, regulations and in-take of zearalenone: an oestrogenic mycotoxin. Food Chem Toxicol 45: 1-18.

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Authors and Affiliations

A. Sohrabi
1
M.H. Movassaghghazani
2
J. Shayegh
3
A.R. Karamibonari
3
F. Tajedini
4

  1. Faculty of Veterinary Medicine, Shabestar Branch, Islamic Azad University, Shabestar, Iran
  2. Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, Shabestar Branch, Islamic Azad University, Shabestar, Iran
  3. Department of Pathobiology, Faculty of Veterinary Medicine, Shabestar Branch, Islamic Azad University, Shabestar, Iran
  4. Department of Basic Sciences, Faculty of Veterinary Medicine, Karaj Branch, Islamic Azad University, Karaj, Iran
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Abstract

This study aimed to determine the effects of dexamethasone and minocycline alone and combined treatment with N-acetylcysteine (NAC) and vitamin E on serum coenzyme Q10 (CoQ10) and matrix metalloproteinase-9 (MMP-9) levels in rats administered aflatoxin B1 (AFB1). The study was carried out on 66 male Wistar rats. Following the intraperitoneal (IP) administration of AFB1 at dose of 2 mg/kg, minocycline (45 and 90 mg/kg, IP) and dexamethasone (5 and 20 mg/kg, IP) were administered alone and combined with NAC (200 mg/kg, IP) and vitamin E (600 mg/kg, IP). CoQ10 and MMP-9 levels were analyzed using the HPLC-UV method and a commercial kit by ELISA, respectively. AFB1 increased MMP-9 level and decreased CoQ10 level compared to the control group. After dexamethasone and minocycline administration, there is no increase in CoQ10 level, which is caused by AFB1. However, dexamethasone and minocycline combined with NAC+vitamin E caused significant increases in CoQ10 levels. Dexamethasone and minocycline alone and combined with NAC+vitamin E decreased MMP-9 levels compared to the single AFB1 treated group. The use of MMPs inhibitors and oxidative stress-reducing agents is anticipated to be beneficial in the poisoning with AFB1.
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Authors and Affiliations

B. Tras
1
H. Eser Faki
1
Z. Ozdemir Kutahya
2
E. Bahcivan
3
B. Dik
1
K. Uney
1

  1. Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Selcuk, Alaeddin Keykubat Campus, New Istanbul Road. No:371, Konya, 42130, Turkey
  2. Department of Pharmacology and Toxicology, Faculty of Ceyhan Veterinary Medicine, University of Cukurova, Fatih Sultan Mehmet District, Inonu Boulevard, No: 242, Adana, 01330, Turkey
  3. Department of Medical Pharmacology, Faculty of Medicine, University of Amasya, Akbilek District. Dominion Street, National Sovereignty Campus, No:4/3, 05100, Turkey

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