نتایج جستجو برای: گیرنده فعال کننده تکثیر پروکسیزوم آلفا pparα
تعداد نتایج: 117534 فیلتر نتایج به سال:
Stress is a risk factor for several cardiovascular pathologies. PPARα holds a fundamental role in control of lipid homeostasis by directly regulating genes involved in fatty acid transport and oxidation. Importantly, PPARα agonists are effective in raising HDL-cholesterol and lowering triglycerides, properties that reduce the risk for cardiovascular diseases. This study investigated the role of...
مفصل زانو، محل شایعی جهت ایجاد استئوآرتریت بوده و علت احتمالی آن این است که این مفصل بیش از سایر مفاصل در معرض وارد شدن ضربه می باشد. استئوآرتریت اولیه هیچ علت خاصی ندارد اما استئوآرتریت ثانویه مربوط به مکانیک غیرطبیعی مفصل می باشد. استئوآرتریت درواقع یک واکنش فیزیولوژیک در مقابل نیروهای طولی و مکرر اعمال شده به مفصل می باشد. حس عمقی مفصل زانو از مجموع پیام های آوران از گیرنده های عضلات، تاندون...
پراکسیزوم ها از اجزاء دارای غشاء در داخل سلول ها هستند و یا به صورت اولیه و یا از پراکسیزوم های پیشین به وجود می آیند. بیوژنز پراکسیزوم را پروتئین های رمزگذاشته توسط ژن های pex (پراکسین ها)، ضمن مراحل بسته بندی غشاء، ورود پروتئین های ماتریکس و تکثیر پراکسیزوم، هدایت می کنند. pex3p، pex16p و pex19p در بیوژنز غشاء و pex11p در تکثیر پراکسیزوم نقش دارند. برای ورود پروتئین های ماتریکس، pex5p و pex7p...
Background: The peroxisome proliferator-activated receptor α (PPARα) plays an important role in the metabolism of lipoproteins and fatty acids, and seems to protect against the development of atherosclerosis. To evaluate the possible protective role of PPARα on cardiovascular function, the effect of the PPARα agonist, fenofibrate was assessed with respect to ischaemia/reperfusion injury and end...
Omega-3 fatty acids (FAs) have the potential to regulate gene expression via the peroxisome proliferator-activated receptor α (PPARα); therefore, genetic variations in this gene may impact its transcriptional activity on target genes. It is hypothesized that the transcriptional activity by wild-type L162-PPARα is enhanced to a greater extent than the mutated variant (V162-PPARα) in the presence...
Retinal vascular leakage, inflammation, and neovascularization (NV) are features of diabetic retinopathy (DR). Fenofibrate, a peroxisome proliferator-activated receptor α (PPARα) agonist, has shown robust protective effects against DR in type 2 diabetic patients, but its effects on DR in type 1 diabetes have not been reported. This study evaluated the efficacy of fenofibrate on DR in type 1 dia...
Peroxisome proliferator-activated receptor α (PPARα) belongs to the family of ligand-dependent nuclear transcription factors that regulate energy metabolism. Although there exists remarkable overlap in the activities of PPARα across species, studies utilizing exogenous PPARα ligands suggest species differences in binding, activation, and physiological effects. While unsaturated long-chain fatty...
Peroxisome proliferation activated receptor α (PPARα) is an important transcriptional regulator of lipid metabolism and is activated by high-fat diet (HFD) and fibrates in mammals. However, whether nutritional background affects PPARα activation and the hypolipidemic effects of PPARα ligands have not been investigated in fish. In the present two-phase study of Nile tilapia (Oreochromis niloticu...
To examine fatty acid accumulation and its toxic effects in cells, we analyzed skin fibroblasts from six patients with mitochondrial trifunctional protein deficiency, who had abnormalities in the second through fourth reactions in fatty acid β-oxidation system. We found free fatty acid accumulation, enhanced three acyl-CoA dehydrogenases, catalyzing the first reaction in the β-oxidation system ...
Dyslipidemia is a major risk factor for development of several obesity-related diseases. The peroxisome proliferator-activated receptor α (PPARα) is a ligand-activated transcription factor that regulates energy metabolism. Previously, we reported that 9-oxo-10,12-octadecadienoic acid (9-oxo-ODA) is presented in fresh tomato fruits and acts as a PPARα agonist. In addition to 9-oxo-ODA, we develo...
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