نتایج جستجو برای: pparα genotypes

تعداد نتایج: 57885  

2012
Wei Chen Yanping Xia Xuelan Zhao Hao Wang Wenjie Chen Maohua Yu Yiming Li Hongying Ye Yu Zhang

BACKGROUND Obesity-related diabetes mellitus leads to increased myocardial uptake and oxidation of fatty acids, resulting in a form of cardiac dysfunction referred to as lipotoxic cardiomyopathy. We have shown previously that Astragalus polysaccharides (APS) administration was sufficient to improve the systemic metabolic disorder and cardiac dysfunction in diabetic models. METHODOLOGY/PRINCIP...

2012
Robert Ringseis Gaiping Wen Klaus Eder

Recent studies in rodents convincingly demonstrated that PPARα is a key regulator of genes involved in carnitine homeostasis, which serves as a reasonable explanation for the phenomenon that energy deprivation and fibrate treatment, both of which cause activation of hepatic PPARα, causes a strong increase of hepatic carnitine concentration in rats. The present paper aimed to comprehensively ana...

Journal: :Molecular pharmacology 2010
Hyun Woo Jeong Joo-Won Lee Woo Sik Kim Sung Sik Choe Hyun Jung Shin Gha Young Lee Dongkyu Shin Jun Hee Lee Eun Bok Choi Hyun Kyu Lee Gyu Hwan Yon Bongjun Cho Hye Ryung Kim Sung Hee Choi Young Sun Chung Seung Bum Park Heekyoung Chung Seonggu Ro Jae Bum Kim

Activation of peroxisome proliferator-activated receptors (PPARs) have been implicated in the treatment of metabolic disorders with different mechanisms; PPARα agonists promote fatty acid oxidation and reduce hyperlipidemia, whereas PPARγ agonists regulate lipid redistribution from visceral fat to subcutaneous fat and enhance insulin sensitivity. To achieve combined benefits from activated PPAR...

2016
Ya-Yuan Chang Hui-Min Su Szu-Han Chen Wen-Tsong Hsieh Jong-Ho Chyuan Pei-Min Chao

We previously reported that bitter melon seed oil (BMSO) was an effective anti-steatosis and antiobesity agent. Since the major fatty acid α-eleostearic acid (α-ESA) in BMSO is a peroxisome proliferator-activated receptor α (PPARα) activator, the objective was to investigate the role of PPARα in BMSO-modulated lipid disorders and α-ESA metabolism. C57BL/6J wild (WD) and PPARα knockout (KO) mice...

2015
Hua Alexander Mach Diane Bielenberg

Background: Current targeted therapies in pancreatic cancer have been ineffective. The tumor stroma, including intraand peri-tumoral inflammation and fibrosis, is increasingly implicated in pancreatic cancer. Pancreatic cancer is characterized by a highly fibrotic tumor environment resulting in stromal resistance to chemotherapy. Peroxisome proliferator-activated receptor-alpha (PPARα), a ligan...

اشراقیان, محمد رضا , امینی, محسن, حسینی, سعید , رحمانی, مظاهر , عبدی, خسرو , محبوب, سلطان علی, مهدی پور, پروین, پیشوا, حمیده,

Background and Aim: The normal plasma fatty acid (FA) composition changes in hypertriglyceridemic obese and overweight indiuviduals. The objective of this study was to determine the plasma fatty acid composition in hypertriglyceridemic obese or overweight subjects with different FABP2 genotypes. Methods and Materials: Forty-six hypertriglyceridemic subjects (33 men and 13 women, 25-60 years old...

2017
Rosalba Florio Laura De Lellis Viviana di Giacomo Maria Carmela Di Marcantonio Loredana Cristiano Mariangela Basile Fabio Verginelli Delfina Verzilli Alessandra Ammazzalorso Sampath Chandra Prasad Amelia Cataldi Mario Sanna Annamaria Cimini Renato Mariani-Costantini Gabriella Mincione Alessandro Cama

Head and neck paragangliomas (HNPGLs) are rare tumors that may cause important morbidity, because of their tendency to infiltrate the skull base. At present, surgery is the only therapeutic option, but radical removal may be difficult or impossible. Thus, effective targets and molecules for HNPGL treatment need to be identified. However, the lack of cellular models for this rare tumor hampers t...

Journal: :Biochimie 2011
Marco Fidaleo Ségolène Arnauld Marie-Claude Clémencet Grégory Chevillard Marie-Charlotte Royer Melina De Bruycker Ronald J A Wanders Anne Athias Joseph Gresti Pierre Clouet Pascal Degrace Sander Kersten Marc Espeel Norbert Latruffe Valérie Nicolas-Francès Stéphane Mandard

Peroxisomal 3-ketoacyl-CoA thiolase B (Thb) catalyzes the final step in the peroxisomal β-oxidation of straight-chain acyl-CoAs and is under the transcription control of the nuclear hormone receptor PPARα. PPARα binds to and is activated by the synthetic compound Wy14,643 (Wy). Here, we show that the magnitude of Wy-mediated induction of peroxisomal β-oxidation of radiolabeled (1-(14)C) palmita...

2015
Maria Thomas Stefan Winter Britta Klumpp Miia Turpeinen Kathrin Klein Matthias Schwab Ulrich M. Zanger

The cytochrome P450, CYP2C8, metabolizes more than 60 clinically used drugs as well as endogenous substances including retinoic acid and arachidonic acid. However, predictive factors for interindividual variability in the efficacy and toxicity of CYP2C8 drug substrates are essentially lacking. Recently we demonstrated that peroxisome proliferator-activated receptor alpha (PPARα), a nuclear rece...

2014
Inmaculada Moreno-Santos Francisco Javier Pavón Miguel Romero-Cuevas Antonia Serrano Carolina Cano Margarita Suardíaz Juan Decara Juan Suarez Fernando Rodríguez de Fonseca Manuel Macías-González

To further understand the pharmacological properties of N-oleoylethanolamine (OEA), a naturally occurring lipid that activates peroxisome proliferator-activated receptor alpha (PPARα), we designed sulfamoyl analogs based on its structure. Among the compounds tested, N-octadecyl-N'-propylsulfamide (CC7) was selected for functional comparison with OEA. The performed studies include the following ...

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