کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2540537 1122596 2015 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cordycepin alleviates airway hyperreactivity in a murine model of asthma by attenuating the inflammatory process
ترجمه فارسی عنوان
کوردیپسین، کمخونی واکنش هوا را در یک مدل موش آسم کاهش می دهد با کاهش روند التهابی
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
چکیده انگلیسی


• Cordycepin could be considered as an adjuvant therapy for allergic asthma.
• Effect of cordycepin on asthma is attributed to mitigating airway inflammatory process.
• Cordycepin exhibits a protective effect on asthma by suppression of hyperresponsiveness and can be exploited therapeutically.

Cordycepin (Cor), which is a naturally occurring nucleoside derivative isolated from Cordyceps militaris, has been shown to exert excellent antiinflammatory activity in a murine model of acute lung injury. Thus, this study aimed to evaluate the antiasthmatic activity of Cor (10, 20, and 40 mg/kg) and to investigate the possible underlying molecular mechanisms. We found that Cor attenuated airway hyperresponsiveness, mucus hypersecretion, and ovalbumin (Ova)-specific immunoglobulin (Ig) E, and alleviated lung inflammation with decreased eosinophils and macrophages in the bronchoalveolar lavage (BAL) fluid. Notably, Cor reduced the upregulation of eotaxin, intercellular cell adhesion molecule-1 (ICAM-1), IL-4, IL-5, and IL-13 in the BAL fluid. Furthermore, Cor markedly blocked p38-MAPK and nuclear factor-kappaB (NF-κB) signalling pathway activation in the Ova-driven asthmatic mice. In conclusion, this study demonstrated that some of the antiasthmatic benefits of Cor attributable to diets and/or tonics may result from reductions in inflammatory processes and that these antiasthmatic properties involve the inhibition of Th2-type responses through the suppression of the p38-MAPK and NF-κB signalling pathways.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Immunopharmacology - Volume 26, Issue 2, June 2015, Pages 401–408
نویسندگان
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