机构地区:[1]Department of Pathophysiology, Medical College, Jinan University [2]Department of Developmental and Regenerative Biology, College of Life Science and Technology, Jinan University
出 处:《Journal of Reproduction and Contraception》2015年第2期67-72,共6页生殖与避孕(英文版)
基 金:supported by Science and Technology Planning Project of Guangzhou City,China(No.201300000114)
摘 要:Objective To investigate effects of clenbuterol (CLB) on the peroxisome proliferators- activated receptor γ (PPARγ) expression in adipose tissues of rats. Methods Twenty adult female Sprague-Dawley rats were randomly divided into 4 groups (5 rats per group). CLB solved in normal saline solution was given at the dose of 0 mg/kg body weight (bw) (group A, as the control), 0.4 mg/kg bw (group B, low-dose group), 2.0 mg/kg bw (group C, mid-dose group), and 18.5 mg/kg bw (group D, high-dose group)for 14 d by gavage consecutively, respectively. Methods of immunohistochemistry, quantitative Real-time PCR and Western blotting were performed to detect expression of PPARγ in the adipose tissue samples. Results PPARγ-positive immunostaining was strong in the controls and weak in the experimental groups. There was no difference on PPARγmRNA and protein between the low-dose group and the control (P〉0.05). With the increase of CLB doses, expression levels of PPARγmRNA and protein were significantly lower in mid- or high-dose group than those in the control (19〈0.01). Conclusions The PPARγ expression in adipose tissues of rats could be down-regulated after CLB exposure, and the decrease became more severe with the increasing doses.Objective To investigate effects of clenbuterol (CLB) on the peroxisome proliferators- activated receptor γ (PPARγ) expression in adipose tissues of rats. Methods Twenty adult female Sprague-Dawley rats were randomly divided into 4 groups (5 rats per group). CLB solved in normal saline solution was given at the dose of 0 mg/kg body weight (bw) (group A, as the control), 0.4 mg/kg bw (group B, low-dose group), 2.0 mg/kg bw (group C, mid-dose group), and 18.5 mg/kg bw (group D, high-dose group)for 14 d by gavage consecutively, respectively. Methods of immunohistochemistry, quantitative Real-time PCR and Western blotting were performed to detect expression of PPARγ in the adipose tissue samples. Results PPARγ-positive immunostaining was strong in the controls and weak in the experimental groups. There was no difference on PPARγmRNA and protein between the low-dose group and the control (P〉0.05). With the increase of CLB doses, expression levels of PPARγmRNA and protein were significantly lower in mid- or high-dose group than those in the control (19〈0.01). Conclusions The PPARγ expression in adipose tissues of rats could be down-regulated after CLB exposure, and the decrease became more severe with the increasing doses.
关 键 词:clenbuterol (CLB) peroxisome proliferators-activated receptor γ (PPARγ) adipose tissue rat
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