نتایج جستجو برای: mafbx

تعداد نتایج: 254  

Journal: :PloS one 2015
Meng-Chuan Chen Yen-Lin Chen Chi-Feng Lee Chih-Huang Hung Tz-Chong Chou

Skeletal muscle atrophy, the most prominent phenotypic feature of cancer cachexia, is often observed in cancer patients undergoing chemotherapy. Magnolol (M) extracted from Magnolia officinalis exhibits several pharmacological effects including anti-inflammatory and anticancer activities. In this study, we investigated whether magnolol supplementation protects against the development of cachexi...

2017
Hyejin Lee Sang-Jin Lee Gyu-Un Bae Nam-In Baek Jae-Ha Ryu

Cachexia and sarcopenia are the main causes of muscle atrophy. These result in a reduction in the muscle fiber area, myo-protein content, and muscle strength, with various molecular modulators being involved. Although several reports have proposed potential therapeutic agents, no effective treatments have been found for muscle atrophy. We searched for myogenic modulators from medicinal plants t...

Journal: :Endocrinology 2006
Xiaonan Wang Zhaoyong Hu Junping Hu Jie Du William E Mitch

Conditions such as acidosis, uremia, and sepsis are characterized by insulin resistance and muscle wasting, but whether the insulin resistance associated with these disorders contributes to muscle atrophy is unclear. We examined this question in db/db mice with increased blood glucose despite high levels of plasma insulin. Compared with control littermate mice, the weights of different muscles ...

2012
Jing Xu Rongshan Li Biruh Workeneh Yanlan Dong Xiaonan Wang Zhaoyong Hu

Chronic kidney disease (CKD) accelerates muscle protein degradation by stimulating the ubiquitin proteasome system through activation of the E3 ligases, Atrogin-1/MAFbx and MuRF-1. Forkhead transcription factors (FoxOs) can control the expression of these E3 ligases, but the contribution of individual FoxOs to muscle wasting is unclear. To study this we created mice with a muscle-specific FoxO1...

Journal: :Frontiers in physiology 2015
Thomas K. Sin Benjamin Y. Yung Shea P. Yip Lawrence W. Chan Cesar S. Wong Eric W. Tam Parco M. Siu

Our current understanding on the molecular mechanisms by which sustained compression induces skeletal muscle injury is very limited. This study aimed to test the hypothesis that activation of SIRT1 by the natural antioxidant resveratrol could deactivate apoptotic and catabolic signaling in skeletal muscle exposed to moderate compression. Two cycles of 6-h constant pressure at 100 mmHg was appli...

Journal: :Journal of applied physiology 2012
Cécile Jamart Marc Francaux Guillaume Y Millet Louise Deldicque Delphine Frère Léonard Féasson

In this study, the coordinated activation of ubiquitin-proteasome pathway (UPP), autophagy-lysosomal pathway (ALP), and mitochondrial remodeling including mitophagy was assessed by measuring protein markers during ultra-endurance running exercise in human skeletal muscle. Eleven male, experienced ultra-endurance athletes ran for 24 h on a treadmill. Muscle biopsy samples were taken from the vas...

Journal: :Physiological genomics 2007
Yi-Wen Chen Chris M Gregory Mark T Scarborough Rongye Shi Glenn A Walter Krista Vandenborne

Disuse atrophy is a common clinical phenomenon that significantly impacts muscle function and activities of daily living. The purpose of this study was to implement genome-wide expression profiling to identify transcriptional pathways associated with muscle remodeling in a clinical model of disuse. Skeletal muscle biopsies were acquired from the medial gastrocnemius in patients with an ankle fr...

2012
Andrew R. Judge Scott K. Powers Leonardo F. Ferreira Marcas M. Bamman

in an increase in 20S and 26S proteasome activity under certain atrophy-inducing conditions. These new data suggest that the in vivo targets of MuRF1 may not be restricted to the thick filament proteins, and suggest possible roles in transcription and protein synthesis. Dr. Kandarian presented data on NF-kappaB signaling in skeletal muscle atrophy. The transcription factors p50 and Bcl-3 are re...

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