کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8337105 | 1540656 | 2014 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Polyphenol-rich blackcurrant extract prevents inflammation in diet-induced obese mice
ترجمه فارسی عنوان
عصاره سیاه و سفید غنی از پلی فنول جلوگیری از التهاب در موش های چاق مبتلا به رژیم غذایی
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کلمات کلیدی
TNFαPPARγ coactivator 1αribosomal protein large P0NAFLDUCPstearoyl CoA desaturase 1SCD-1RPLP0acyl-CoA oxidase 1TBK1IRFCD68TFAMDIOCLSIKKADIPOQNF-κBLPSSREBP-1cFASPGC-1αPPARadiponectin - آدیپونکتینAnthocyanins - آنتوسیانین fatty acid synthase - اسید چرب سنتازinflammation - التهاب( توروم) Blackcurrant - انگور سیاهinterleukin - اینترلوکینBCE - بانک مرکزی اروپاcardiovascular disease - بیماری قلب و عروقیNonalcoholic fatty liver disease - بیماری کبدی چربی غیر الکلیtumor necrosis factor α - تومور نکروز عامل αTANK-binding kinase 1 - تین کیناز 1Cluster of differentiation 68 - خوشه تمایز 68CVD - رسوب دهی شیمیایی بخار Crown-like structures - ساختارهای تاج مانندinterferon regulatory factor - عامل تنظیمی اینترفرونmitochondrial transcription factor A - عامل رونویسی میتوکندری Anuclear factor-κB - فاکتور هسته ای κBlipopolysaccharide - لیپوپلی ساکاریدObesity - مرض چاقیMacrophage infiltration - نفوذ مکروفاژUncoupling protein - پروتئین جدا کردنsterol regulatory element-binding protein 1c - پروتئین وابسته به استرول تنظیم کننده پروتئین 1cdiet-induced obesity - چاقی ناشی از رژیم غذاییPeroxisome proliferator activated receptor - گیرنده فعال فعال پروکسیوم
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
چکیده انگلیسی
Obesity is closely associated with chronic, low-grade inflammation. We investigated if polyphenol-rich blackcurrant extract (BCE) can prevent inflammation in vivo. Male C57BL/6J mice were fed a modified AIN-93M control diet containing high fat/high cholesterol (16% fat, 0.25% cholesterol by weight) or the control diet supplemented with 0.1% BCE (wt/wt) for 12 weeks. In BCE-fed mice, the percentage of body weight and adipocyte size of the epididymal fat were significantly lower than those of control mice. There were fewer crown-like structures (CLS) with concomitant decreases in F4/80, cluster of differentiation 68 and inhibitor of nuclear factor κB kinase ε (IKKε) mRNA in the epididymal adipose of BCE-fed mice. F4/80 and IKKε mRNA levels were positively correlated with CLS number. In the skeletal muscle of mice fed with BCE, mRNA expression of genes involved in energy expenditure and mitochondrial biogenesis, including PPARα, PPARδ, UCP-2, UCP-3 and mitochondrial transcription factor A, were significantly increased. When splenocytes from BCE-fed mice were stimulated by lipopolysaccharides, tumor necrosis factor α and interleukin-1β mRNA were significantly lower than control splenocytes. Together, the results suggest that BCE supplementation decreases obesity-induced inflammation in adipose tissue and splenocytes, at least in part, by modulating energy metabolism in skeletal muscle.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The Journal of Nutritional Biochemistry - Volume 25, Issue 10, October 2014, Pages 1019-1025
Journal: The Journal of Nutritional Biochemistry - Volume 25, Issue 10, October 2014, Pages 1019-1025
نویسندگان
Tyler Benn, Bohkyung Kim, Young-Ki Park, Casey J. Wegner, Ellen Harness, Tae-Gyu Nam, Dae-Ok Kim, Jong Suk Lee, Ji-Young Lee,