activity were studied in obese mice. Ovariectomised and sham operated mice were fed with high fat diet and low fat diet for 15 weeks. Furthermore, gemfibrozil (100 mg/kg) was orally with high fat and low fat diets to the ovariectomised and sham operated mice. Body weights significantly increased in ovariectomised mice compared to sham operated mice (P<0.001) while gemfibrozil supplementation prevented such increase. Steatosis was as well more pronounced in the livers of ovariectomised mice fed with high fat diet compared to sham operated mice. However, liver steatosis was not seen in gemfibrozil supplemented high fat diet fed mice. On the other hand gemfibrozil supplementation slightly increased the liver weights. High fat diet significa...
<p><b><u>Panel A</u>:</b> Effect of RLIP76 depletion by RLIP76 antisense on triglycerides level in R...
by Bezafibrate (BZ) could attenuate hepatic and white adipose tissue (WAT) abnormalities in male of...
We studied whether the peroxisomal proliferation, induction of 3-hydroxy-3-methyglutaryl-CoA reducta...
Gemfibrozil is a widely prescribed hypolipidemic agent in humans and a peroxisome proliferator and l...
While gemfibrozil and fenofibrate are prescribed for anti-dyslipidemia treatment, a rational basis f...
Peroxisome proliferator-activated receptor α (PPARα) is a therapeutic target for hyperli...
(A) BW of male mice from the BL background before (age 7–9 months) and after 60 days (age 9–11 month...
AIM: The aim of the present study was to evaluate whether activation of peroxisome proliferator-acti...
We have investigated if changes in hepatic lipid metabolism produced by old age are related to chang...
The effect of gemfibrozil, an analogue of clofibric acid, on the centrifugal behavior of peroxisomes...
We studied effects of PPARα agonists clofibric acid and gemfibrozil on cell growth and functions of ...
Peroxisome proliferator-activated receptors (PPAR) play an important role in the regulation of lipid...
<p>WT and CCR5<sup>-/-</sup> mice were infected with 5 cysts of <i>T. gondii</i> and treated with Ge...
Gemfibrozil is a fibric acid derivative used in the treatment of dyslipidemia. It activates peroxiso...
Obesity poses an increased risk of developing metabolic syndrome and closely associated nonalcoholic...
<p><b><u>Panel A</u>:</b> Effect of RLIP76 depletion by RLIP76 antisense on triglycerides level in R...
by Bezafibrate (BZ) could attenuate hepatic and white adipose tissue (WAT) abnormalities in male of...
We studied whether the peroxisomal proliferation, induction of 3-hydroxy-3-methyglutaryl-CoA reducta...
Gemfibrozil is a widely prescribed hypolipidemic agent in humans and a peroxisome proliferator and l...
While gemfibrozil and fenofibrate are prescribed for anti-dyslipidemia treatment, a rational basis f...
Peroxisome proliferator-activated receptor α (PPARα) is a therapeutic target for hyperli...
(A) BW of male mice from the BL background before (age 7–9 months) and after 60 days (age 9–11 month...
AIM: The aim of the present study was to evaluate whether activation of peroxisome proliferator-acti...
We have investigated if changes in hepatic lipid metabolism produced by old age are related to chang...
The effect of gemfibrozil, an analogue of clofibric acid, on the centrifugal behavior of peroxisomes...
We studied effects of PPARα agonists clofibric acid and gemfibrozil on cell growth and functions of ...
Peroxisome proliferator-activated receptors (PPAR) play an important role in the regulation of lipid...
<p>WT and CCR5<sup>-/-</sup> mice were infected with 5 cysts of <i>T. gondii</i> and treated with Ge...
Gemfibrozil is a fibric acid derivative used in the treatment of dyslipidemia. It activates peroxiso...
Obesity poses an increased risk of developing metabolic syndrome and closely associated nonalcoholic...
<p><b><u>Panel A</u>:</b> Effect of RLIP76 depletion by RLIP76 antisense on triglycerides level in R...
by Bezafibrate (BZ) could attenuate hepatic and white adipose tissue (WAT) abnormalities in male of...
We studied whether the peroxisomal proliferation, induction of 3-hydroxy-3-methyglutaryl-CoA reducta...