Mycotoxin binders potential on histological of ovary mice exposed by zearalenone

Aim: This study was conducted to examine the potential of mycotoxin binder in ceasing zearalenone (ZEN) effect on mice reproduction. ZEN mycotoxin can induce reactive oxygen species that may cause damage and cell death. ZEN is estrogenic so that it may affect the reproductive organs failure. Mate...

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Main Authors: Abdul Samik, Erma Safitri
Format: Article
Language:English
Published: Veterinary World 2017-03-01
Series:Veterinary World
Subjects:
Online Access:http://www.veterinaryworld.org/Vol.10/March-2017/14.pdf
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author Abdul Samik
Erma Safitri
author_facet Abdul Samik
Erma Safitri
author_sort Abdul Samik
collection DOAJ
description Aim: This study was conducted to examine the potential of mycotoxin binder in ceasing zearalenone (ZEN) effect on mice reproduction. ZEN mycotoxin can induce reactive oxygen species that may cause damage and cell death. ZEN is estrogenic so that it may affect the reproductive organs failure. Materials and Methods: Mycotoxin binder administration to female mice exposed to ZEN was aimed to count the number of primary follicles, secondary follicles, tertiary follicles, de Graaf's follicles, and the corpus luteum (CL). Negative control group (C) was not exposed to ZEN and without the administration of mycotoxin binders, while positive control group (C+) was exposed to 0.1 mg/mouse/day ZEN and without the provision of mycotoxin binders. Treatment groups (T1, T2, T3) were exposed to 0.1 mg/mouse/day ZEN and mycotoxin binders 0.5; 1; 2 mg/BW/day. Results: ZEN and mycotoxin binders administration was conducted for 10 days. The number of primary follicles, secondary, tertiary, de Graaf's follicles and CL in negative control (C-) was 14.2±1.36, 11.2±0.28, 6.5±0.53, 7.5±0.74, and 2.3±0.35. The number in positive control (C+) group was as follows 7.1±0.12, 3.7±1.17, 3.8±1.21, 1.5±0.62, and 2.3±0.34. Results in treatment 1 (T1) were as follows 6.2±0.16, 5.2±0.16, 3.6±0.16, 2.6±0.19, and 2.6±0.10; in treatment 2 (T2) 7.8±0.28, 5.8±0.53, 3.7±0.26, 2.7±0.26, and 2.5±0.10; and in treatment 3 (T3) 8.4±0.34, 8.4±0.34, 4.6±0.34, 4.5±1.01, and 3.4±0.23. Conclusion: The number of follicles and CL more in line with increasing doses of mycotoxin binders. Required more than 2 mg/mouse/day mycotoxin binders to inhibit the effects of ZEN so that its can maintain the number of primary follicle, secondary follicle, tertiary follicle, the de Graaf's follicle, and the number of CL in the ovary of ZEN-exposed female mice (Mus musculus).
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spelling doaj.art-fa6b6d0e8bee48eab9f8592f3da8508c2022-12-21T22:08:31ZengVeterinary WorldVeterinary World0972-89882231-09162017-03-0110335335710.14202/vetworld.2017.353-357Mycotoxin binders potential on histological of ovary mice exposed by zearalenoneAbdul Samik0Erma Safitri1Department of Veterinary Reproduction, Faculty of Veterinary Medicine, Universitas Airlangga, Indonesia.Department of Veterinary Reproduction, Faculty of Veterinary Medicine, Universitas Airlangga, Indonesia; Stem Cells Research Division of Institute Tropical Disease, Universitas Airlangga, Indonesia.Aim: This study was conducted to examine the potential of mycotoxin binder in ceasing zearalenone (ZEN) effect on mice reproduction. ZEN mycotoxin can induce reactive oxygen species that may cause damage and cell death. ZEN is estrogenic so that it may affect the reproductive organs failure. Materials and Methods: Mycotoxin binder administration to female mice exposed to ZEN was aimed to count the number of primary follicles, secondary follicles, tertiary follicles, de Graaf's follicles, and the corpus luteum (CL). Negative control group (C) was not exposed to ZEN and without the administration of mycotoxin binders, while positive control group (C+) was exposed to 0.1 mg/mouse/day ZEN and without the provision of mycotoxin binders. Treatment groups (T1, T2, T3) were exposed to 0.1 mg/mouse/day ZEN and mycotoxin binders 0.5; 1; 2 mg/BW/day. Results: ZEN and mycotoxin binders administration was conducted for 10 days. The number of primary follicles, secondary, tertiary, de Graaf's follicles and CL in negative control (C-) was 14.2±1.36, 11.2±0.28, 6.5±0.53, 7.5±0.74, and 2.3±0.35. The number in positive control (C+) group was as follows 7.1±0.12, 3.7±1.17, 3.8±1.21, 1.5±0.62, and 2.3±0.34. Results in treatment 1 (T1) were as follows 6.2±0.16, 5.2±0.16, 3.6±0.16, 2.6±0.19, and 2.6±0.10; in treatment 2 (T2) 7.8±0.28, 5.8±0.53, 3.7±0.26, 2.7±0.26, and 2.5±0.10; and in treatment 3 (T3) 8.4±0.34, 8.4±0.34, 4.6±0.34, 4.5±1.01, and 3.4±0.23. Conclusion: The number of follicles and CL more in line with increasing doses of mycotoxin binders. Required more than 2 mg/mouse/day mycotoxin binders to inhibit the effects of ZEN so that its can maintain the number of primary follicle, secondary follicle, tertiary follicle, the de Graaf's follicle, and the number of CL in the ovary of ZEN-exposed female mice (Mus musculus).http://www.veterinaryworld.org/Vol.10/March-2017/14.pdfcorpus luteumfolliclesmycotoxin binderszearalenone
spellingShingle Abdul Samik
Erma Safitri
Mycotoxin binders potential on histological of ovary mice exposed by zearalenone
Veterinary World
corpus luteum
follicles
mycotoxin binders
zearalenone
title Mycotoxin binders potential on histological of ovary mice exposed by zearalenone
title_full Mycotoxin binders potential on histological of ovary mice exposed by zearalenone
title_fullStr Mycotoxin binders potential on histological of ovary mice exposed by zearalenone
title_full_unstemmed Mycotoxin binders potential on histological of ovary mice exposed by zearalenone
title_short Mycotoxin binders potential on histological of ovary mice exposed by zearalenone
title_sort mycotoxin binders potential on histological of ovary mice exposed by zearalenone
topic corpus luteum
follicles
mycotoxin binders
zearalenone
url http://www.veterinaryworld.org/Vol.10/March-2017/14.pdf
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AT ermasafitri mycotoxinbinderspotentialonhistologicalofovarymiceexposedbyzearalenone