کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10737076 | 1046337 | 2005 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Different response of senescent female Sprague-Dawley rats to gemfibrozil and rosiglitazone administration
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
سالمندی
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چکیده انگلیسی
Eighteen-month-old Sprague-Dawley rats present age-related alterations in lipid and glucose metabolism and are resistant to the effect of PPARα-activating hypolipidemic drugs, such as gemfibrozil. We tested if these animals were responsive to the administration of rosiglitazone, an insulin-sensitizer acting on PPARγ. We determined in 18-month-old female Sprague-Dawley rats treated for 21 days with a daily dose of 3 mg gemfibrozil/kg or 3 mg rosiglitazone/kg: (i) plasma concentrations of total cholesterol (TC), triglycerides (TG), nonesterified fatty acids (NEFA), glucose, insulin and leptin, (ii) hepatic concentrations of TG, NEFA and cholesteryl esters (CE), and (iii) the liver expression and binding activity of peroxisome proliferator-activated receptor α (PPARα), and several of its target genes, hepatic nuclear factor-4 (HNF-4), and liver X receptor α (LXRα). Although gemfibrozil induced mild effects on hepatic PPARα, HNF-4, and LXRα, only rosiglitazone significantly reduced plasma TG (59%), glucose (19%), insulin (61%), and leptin (66%), and liver TG (43%), CE (49%), and NEFA (27%). These changes were associated to an increased body weight gain and a decrease in visceral fat (8.7-fold and 37% vs. control females, respectively). The beneficial effect of rosiglitazone treatment in 18-month-old female rats could be related to a direct effect on white adipose tissue.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Gerontology - Volume 40, Issue 7, July 2005, Pages 588-598
Journal: Experimental Gerontology - Volume 40, Issue 7, July 2005, Pages 588-598
نویسندگان
Elena Sanguino, Núria Roglans, Marta Alegret, Rosa M. Sánchez, Manuel Vázquez-Carrera, Juan C. Laguna,