کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2540347 1559760 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Betulin attenuates lung and liver injuries in sepsis
ترجمه فارسی عنوان
بتینین موجب آسیب ریه و کبد در سپسیس می شود
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
چکیده انگلیسی


• Betulin significantly increases the survival rate of CLP-induced septic rats.
• Betulin attenuates lung and liver injuries in CLP-induced septic rats.
• The anti-inflammatory effect contributes to the organ protection of betulin.
• Betulin inhibits the NF-κB and MAPK signaling pathway in septic rats.

Sepsis is a complex condition with unacceptable mortality. Betulin is a natural extract with multiple bioactivities. This study aims to evaluate the potential effects of betulin on lung and liver injury in sepsis. Cecal ligation and puncture was used to establish the rat model of sepsis. A single dose of 4 mg/kg or 8 mg/kg betulin was injected intraperitoneally immediately after the model establishment. The survival rate was recorded every 12 h for 96 h. The organ injury was examined using hematoxylin and eosin staining and serum biochemical test. The levels of proinflammatory cytokines and high mobility group box 1 in the serum were measured using ELISA. Western blotting was used to detect the expression of proteins in NF-κB and MAPK signaling pathways. Betulin treatment significantly improved the survival rate of septic rats, and attenuated lung and liver injury in sepsis, including the reduction of lung wet/dry weight ratio and activities of alanine aminotransferase and aspartate aminotransferase in the serum. In addition, levels of tumor necrosis factor-α, interleukin-1β, interleukin-6 and high mobility group box 1 in the serum were also lowered by betulin treatment. Moreover, sepsis-induced activation of the NF-κB and MAPK signaling pathway was inhibited by betulin as well. Our findings demonstrate the protective effect of betulin in lung and liver injury in sepsis. This protection may be mediated by its anti-inflammatory and NF-κB and MAPK inhibitory effects.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Immunopharmacology - Volume 30, January 2016, Pages 50–56
نویسندگان
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