نتایج جستجو برای: pgc1α 1

تعداد نتایج: 2752853  

2017
Louisa Dowal Pooja Parameswaran Sarah Phat Syamala Akella Ishita Deb Majumdar Jyoti Ranjan Chahan Shah Saie Mogre Kalyani Guntur Khampaseuth Thapa Stephane Gesta Vivek K Vishnudas Niven R Narain Rangaprasad Sarangarajan

Obesity is marked by chronic, low-grade inflammation. Here, we examined whether intrinsic differences between white and brown adipocytes influence the inflammatory status of macrophages. White and brown adipocytes were characterized by transcriptional regulation of UCP-1, PGC1α, PGC1β, and CIDEA and their level of IL-6 secretion. The inflammatory profile of PMA-differentiated U937 and THP-1 mac...

2017
Liming Yu Bing Gong Weixun Duan Chongxi Fan Jian Zhang Zhi Li Xiaodong Xue Yinli Xu Dandan Meng Buying Li Meng Zhang Bin Zhang Zhenxiao Jin Shiqiang Yu Yang Yang Huishan Wang

Enhancing mitochondrial biogenesis and reducing mitochondrial oxidative stress have emerged as crucial therapeutic strategies to ameliorate diabetic myocardial ischemia/reperfusion (MI/R) injury. Melatonin has been reported to be a safe and potent cardioprotective agent. However, its role on mitochondrial biogenesis or reactive oxygen species (ROS) production in type 1 diabetic myocardium and t...

2016
Satoshi Miyamoto Cheng-Chih Hsu Gregory Hamm Manjula Darshi Maggie Diamond-Stanic Anne-Emilie Declèves Larkin Slater Subramaniam Pennathur Jonathan Stauber Pieter C. Dorrestein Kumar Sharma

AMP-activated protein kinase (AMPK) is suppressed in diabetes and may be due to a high ATP/AMP ratio, however the quantitation of nucleotides in vivo has been extremely difficult. Via matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) to localize renal nucleotides we found that the diabetic kidney had a significant increase in glomerular ATP/AMP ratio. Untargeted ...

2017
Fintan Geoghegan Robert J. Buckland Eric T. Rogers Karima Khalifa Emma B. O’Connor Mary F. Rooney Parviz Behnam-Motlagh Torbjörn K. Nilsson Kjell Grankvist Richard K. Porter

Acquired cisplatin resistance is a common feature of tumours following cancer treatment with cisplatin and also of non-small cell lung cancer (H1299) and mesothelioma (P31) cell lines exposed to cisplatin. To elucidate the cellular basis of acquired cisplatin resistance, a comprehensive bioenergetic analysis was undertaken. We demonstrate that cellular oxygen consumption was significantly decre...

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