کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2580265 1561611 2015 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Lycopene protects against acute zearalenone-induced oxidative, endocrine, inflammatory and reproductive damages in male mice
ترجمه فارسی عنوان
لیکوپن در مقابل آسیب های اکسیداتیو، غدد درون ریز، التهابی و تولید مثل ناشی از حاد زئیرالنون در موش های نر محافظت می کند
کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


• Lycopene was able to prevent ZEA-induced damage in testes of mice.
• Lycopene protects against the decrease in GST, GPx and GR activities induced by ZEA.
• Lycopene prevents the decrease of δ-ALA-D activity caused by ZEA in the testes.
• ZEA induced modification of antioxidant and inflammatory status.
• ZEA increase interleukins 1β, 2, 6, 10, tumor necrosis factor-α and bilirubin levels.

Male mice received lycopene for 10 days before a single oral administration of zearalenone (ZEA). After 48 h testes and blood were collected. Mice treated with lycopene/ZEA exhibited amelioration of the hematological changes. Lycopene prevented the reduction in the number and motility of spermatozoa and testosterone levels, indicating a protective effect in the testicular damage induced by ZEA. Lycopene was also effective in protecting against the decrease in glutathione-S-transferase, glutathione peroxidase, glutathione reductase and δ-aminolevulinic acid dehydratase activities caused by ZEA in the testes. Exposure of animals to ZEA induced modification of antioxidant and inflammatory status with increase of reduced glutathione (GSH) levels and increase of the oxidized glutathione, interleukins 1β, 2, 6, 10, tumor necrosis factor-α and bilirubin levels. Lycopene prevented ZEA-induced changes in GSH levels and inhibited the processes of inflammation, reducing the damage induced by ZEA. Altogether, our results indicate that lycopene was able to prevent ZEA-induced damage in the mice.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemico-Biological Interactions - Volume 230, 25 March 2015, Pages 50–57
نویسندگان
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