کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8337904 | 1540970 | 2018 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Vitamin D3 supplementation decreases a unique circulating monocyte cholesterol pool in patients with type 2 diabetes
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کلمات کلیدی
PPARαp-PERKSR-A11,25-dihydroxy vitamin DoxLDLT2DMRCTABCCD36DBPSBPJnk1,25(OH)2D - 1،25 (OH) 2D25(OH)D - 25 (OH) D25-hydroxy vitamin D - 25 هیدروکسی ویتامین Dc-Jun N-terminal kinase - C-Jun N-terminal kinaseDiI - DIIGC/MS - GC / MSAtherosclerosis - آترواسکلروز(تصلب شریان)Randomized controlled trial - آزمایش تصادفی کنترل شدهcardiovascular disease - بیماری قلب و عروقیCHOP - تکه کردنstandard error of the mean - خطای استاندارد میانگینcluster of differentiation 36 - خوشه تمایز 36Type 2 diabetes mellitus - دیابت نوع دوCVD - رسوب دهی شیمیایی بخار endoplasmic reticulum - شبکه آندوپلاسمی Gas Chromatography Mass Spectrometry - طیف سنجی جرم کروماتوگرافی گازdiastolic blood pressure - فشار خون دیاستولیکsystolic blood pressure - فشار خون سیستولیکoxidized low density lipoprotein - لیپوپروتئین با چگالی کم اکسید شدهCholesterol metabolism - متابولیسم کلسترولSEM - مدل معادلات ساختاری / میکروسکوپ الکترونی روبشیMonocytes - مونوسیتهاFamilial hypercholesterolemia - هیپرکلسترولمی فامیلیinternational units - واحدهای بین المللیVitamin D - ویتامین دیATP binding cassette - کیت اتصال ATPPeroxisome proliferator-activated receptor gamma - گاما گیرنده گیرنده فعال پرولیفیزوم فعال
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
پیش نمایش صفحه اول مقاله
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چکیده انگلیسی
Cross-sectional studies indicate consistent associations between low 25(OH)D concentration and increased risk of cardiovascular disease (CVD), but results of randomized control trials (RCTs) are mixed. However, the majority of the RCTs do not focus on type 2 diabetics, potentially obscuring the effects of vitamin D in this population. In vitro 1,25(OH)2D3 downregulates macrophage cholesterol deposition, but the in vivo effects are unknown. To explore potential mechanisms of the effects of vitamin D on CVD risk in patients with type 2 diabetes, we isolated monocytes in a subset of 26 patients from our RCT of diabetics with baseline serum 25(OH)D <25Â ng/mL randomized to vitamin D3 4000 IU/day or placebo for 4 months. Upon enrollment, the mean 25(OH)D level was 17Â ng/mL, which increased to 36Â ng/mL after vitamin D and remained unchanged in the placebo group. Before randomization, groups demonstrated similar mean hemoglobin A1c and plasma lipids levels, none of which was significantly altered by vitamin D supplementation. Moreover, assessment of oxidized LDL uptake in monocytes cultured in the patient's own serum before vs. after treatment resulted in >50% reduction in the vitamin D group with no change in the placebo group. This was mediated through suppression of endoplasmic reticulum stress and scavenger receptor CD36 protein expression. The reduction in monocyte cholesterol uptake was reflected in a 19% decrease in total monocyte cholesterol content. Interestingly, cross-sectional analysis of circulating monocytes from vitamin D-deficient vs. sufficient diabetic patients revealed 8-fold higher cholesteryl ester content, confirming the capacity of these monocytes to uptake and carry cholesterol in the circulation. This study identifies a unique circulating cholesterol pool within monocytes that is modulated by vitamin D and has the potential to contribute to CVD in type 2 diabetes.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The Journal of Steroid Biochemistry and Molecular Biology - Volume 177, March 2018, Pages 187-192
Journal: The Journal of Steroid Biochemistry and Molecular Biology - Volume 177, March 2018, Pages 187-192
نویسندگان
Amy E. Riek, Jisu Oh, Isra Darwech, Veronica Worthy, Xiaobo Lin, Richard E. Jr., Rong M. Zhang, Carlos Bernal-Mizrachi,