کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2579996 1561592 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Protective effect of allyl methyl disulfide on acetaminophen-induced hepatotoxicity in mice
ترجمه فارسی عنوان
اثر محافظتی متيل دي سولفيد آلليل بر سميت کبدی ناشی از استامینوفن در موشها
کلمات کلیدی
آللییل متیل دی سولفید؛ استامینوفن؛ حفاظت از هپاتیت؛ آنتی اکسیدان
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


• AMDS reduced ALT, AST and LDH levels in acetaminophen-induced liver injury in mice.
• IL-6, TNF-α and CD45 expression induced by acetaminophen were attenuated by AMDS.
• AMDS depressed the elevated MDA and restored SOD, GSH-PX, GSH and GSH/GSSG levels.
• Histological liver injury induced by acetaminophen was alleviated by AMDS.

Multiple sulfur compounds of garlic have shown versatile medicinal activities in the prevention and treatment of various diseases. Allyl methyl disulfide (AMDS) was identified as one of the bioactive components in fresh garlic paste in our previous study. The purpose of this study was to investigate the hepatoprotective effect of AMDS against acetaminophen (APAP)-induced acute liver damage in mice. Results reveal that AMDS significantly alleviates APAP-induced elevation of alanine aminotransferase (ALT), aspartate aminotransferase (AST) and lactate dehydrogenase (LDH) levels in mice. Furthermore, AMDS significantly (p < 0.05) reduced the maleic dialdehyde (MDA) level in liver tissues and restored the activities of antioxidant enzymes SOD, GSH-PX and GSH towards normal levels. IL-6 and TNF-alpha (TNF-α) levels in the serum and liver were clearly increased by acetaminophen-damage (p < 0.05) and AMDS intake significantly suppressed acetaminophen-induced increase of the two cytokines (p < 0.05). The immunohistochemical and pathological analyses showed that AMDS could ameliorate the liver injury through the strong attenuation of the CD45 expression and HNE formation. All the results indicate that AMDS had the ability to protect hepatocytes from APAP-induced liver damage.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemico-Biological Interactions - Volume 249, 5 April 2016, Pages 71–77
نویسندگان
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