Mammalian target of rapamycin signaling and ubiquitin-proteasome-related gene expression in skeletal muscle of dairy cows with high or normal body condition score around calving.
暂无分享,去创建一个
J. Adamski | C. Prehn | H. Sadri | H. Sauerwein | M. Ghaffari | K. Schuh | G. Dusel | C. Koch | D. Frieten | Jerzy Adamski | H. Sauerwein
[1] J. Loor,et al. Varying the ratio of Lys:Met while maintaining the ratios of Thr:Phe, Lys:Thr, Lys:His, and Lys:Val alters mammary cellular metabolites, mammalian target of rapamycin signaling, and gene transcription. , 2018, Journal of dairy science.
[2] M. Oikawa,et al. Effect of the periparturient period on blood free amino acid concentration in dairy cows/healthy cows , 2012 .
[3] D. Sabatini,et al. Ragulator-Rag Complex Targets mTORC1 to the Lysosomal Surface and Is Necessary for Its Activation by Amino Acids , 2010, Cell.
[4] K. Inoki,et al. Rags connect mTOR and autophagy , 2012, Small GTPases.
[5] J. Mcnamara,et al. Adaptations in body muscle and fat in transition dairy cattle fed differing amounts of protein and methionine hydroxy analog. , 2003, Journal of dairy science.
[6] Insulin signaling and skeletal muscle atrophy and autophagy in transition dairy cows either overfed energy or fed a controlled energy diet prepartum , 2016, Journal of Comparative Physiology B.
[7] J R Roche,et al. Invited review: Body condition score and its association with dairy cow productivity, health, and welfare. , 2009, Journal of dairy science.
[8] T. Rukkwamsuk,et al. Relationship between overfeeding and overconditioning in the dry period and the problems of high producing dairy cows during the postparturient period. , 1999, The Veterinary quarterly.
[9] B. Crossett,et al. Metabolic profiling of plasma amino acids shows that histidine increases following the consumption of pork , 2014, Diabetes, metabolic syndrome and obesity : targets and therapy.
[10] C. Lang,et al. Hormone, cytokine, and nutritional regulation of sepsis-induced increases in atrogin-1 and MuRF1 in skeletal muscle. , 2007, American journal of physiology. Endocrinology and metabolism.
[11] Y. Chilliard,et al. Effects of feeding intensity during the dry period. 2. Metabolic and hormonal responses. , 2003, Journal of dairy science.
[12] R. Bruckmaier,et al. Individual variability in physiological adaptation to metabolic stress during early lactation in dairy cows kept under equal conditions. , 2008, Journal of animal science.
[13] D. Casper,et al. Factors affecting body tissue mobilization in early lactation dairy cows. 2. Effect of dietary fat on mobilization of body fat and protein. , 1998, Journal of dairy science.
[14] S. Kersten,et al. Effects of prepartal body condition score and peripartal energy supply of dairy cows on postpartal lipolysis, energy balance and ketogenesis: an animal model to investigate subclinical ketosis , 2014, Journal of Dairy Research.
[15] H. Sadri,et al. Comparison of performance and metabolism from late pregnancy to early lactation in dairy cows with elevated v. normal body condition at dry-off. , 2019, Animal : an international journal of animal bioscience.
[16] S. Price,et al. Molecular signaling pathways regulating muscle proteolysis during atrophy , 2005, Current opinion in clinical nutrition and metabolic care.
[17] R. Loewith,et al. Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive , 2004, Nature Cell Biology.
[18] B. Kuhla,et al. Involvement of skeletal muscle protein, glycogen, and fat metabolism in the adaptation on early lactation of dairy cows. , 2011, Journal of proteome research.
[19] R. Erdman,et al. Factors affecting body tissue mobilization in early lactation dairy cows. 1. Effect of dietary protein on mobilization of body fat and protein. , 1997, Journal of dairy science.
[20] J. Wade Harper,et al. Ubiquitin-like protein activation by E1 enzymes: the apex for downstream signalling pathways , 2009, Nature Reviews Molecular Cell Biology.
[21] P. Stehle,et al. Appraisal of four pre-column derivatization methods for the high-performance liquid chromatographic determination of free amino acids in biological materials. , 1990, Journal of chromatography.
[22] G. Foxcroft,et al. Metabolic status and interval to first ovulation in postpartum dairy cows. , 1995, Journal of dairy science.
[23] T. Duffield,et al. Short communication: effects of monensin on 3-methylhistidine excretion in transition dairy cows. , 2000, Journal of dairy science.
[24] D. Nydam,et al. Dry period plane of energy: Effects on feed intake, energy balance, milk production, and composition in transition dairy cows. , 2015, Journal of dairy science.
[25] D J Glass,et al. Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy , 2001, Science.
[26] I. M. Sheldon,et al. Innate immunity and the sensing of infection, damage and danger in the female genital tract. , 2017, Journal of reproductive immunology.
[27] N. Lacetera,et al. Influence of body condition score on relationships between metabolic status and oxidative stress in periparturient dairy cows. , 2005, Journal of dairy science.
[28] B. Kuhla,et al. Increased anaplerosis, TCA cycling, and oxidative phosphorylation in the liver of dairy cows with intensive body fat mobilization during early lactation. , 2012, Journal of proteome research.
[29] P. Delafontaine,et al. IGF-1 prevents ANG II-induced skeletal muscle atrophy via Akt- and Foxo-dependent inhibition of the ubiquitin ligase atrogin-1 expression. , 2010, American journal of physiology. Heart and circulatory physiology.
[31] A. Ciechanover,et al. The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction. , 2002, Physiological reviews.
[32] Aaron Ciechanover,et al. Proteolysis: from the lysosome to ubiquitin and the proteasome , 2005, Nature Reviews Molecular Cell Biology.
[33] A. V. van Kessel,et al. Effects of peripartum propylene glycol supplementation on nitrogen metabolism, body composition, and gene expression for the major protein degradation pathways in skeletal muscle in dairy cows. , 2008, Journal of dairy science.
[34] D. Taillandier,et al. Regulation of ATP-ubiquitin-dependent proteolysis in muscle wasting. , 1994, Reproduction, nutrition, development.
[35] A. Goldberg,et al. Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules , 1994, Cell.
[36] H. Lapierre,et al. Peripartum performance and metabolism of dairy cows in response to prepartum energy and protein intake. , 2002, Journal of dairy science.
[37] J. Pires,et al. Effects of body condition score at calving on indicators of fat and protein mobilization of periparturient Holstein-Friesian cows. , 2013, Journal of dairy science.
[38] H. White. The Role of TCA Cycle Anaplerosis in Ketosis and Fatty Liver in Periparturient Dairy Cows , 2015, Animals : an open access journal from MDPI.
[39] R. Veerkamp,et al. Energy balance of dairy cattle in relation to milk production variables and fertility. , 2000, Journal of dairy science.
[40] J. Adamski,et al. Targeted Metabolomics of Dried Blood Spot Extracts , 2013, Chromatographia.
[41] C. Heuer,et al. Postpartum body condition score and results from the first test day milk as predictors of disease, fertility, yield, and culling in commercial dairy herds. , 1999, Journal of dairy science.
[42] C. I. Harris,et al. The urinary excretion of N-methyl histidine by cattle: validation as an index of muscle protein breakdown , 1981, British Journal of Nutrition.
[43] A. Suryawan,et al. Regulation of protein degradation pathways by amino acids and insulin in skeletal muscle of neonatal pigs , 2014, Journal of Animal Science and Biotechnology.
[44] R. Bruckmaier,et al. Mammalian target of rapamycin signaling and ubiquitin proteasome-related gene expression in 3 different skeletal muscles of colostrum- versus formula-fed calves. , 2017, Journal of dairy science.
[45] K. Pelin,et al. Identification of muscle specific ring finger proteins as potential regulators of the titin kinase domain. , 2001, Journal of molecular biology.
[46] S. A. Arriola Apelo,et al. Development of a model describing regulation of casein synthesis by the mammalian target of rapamycin (mTOR) signaling pathway in response to insulin, amino acids, and acetate. , 2016, Journal of dairy science.
[47] M. Hardy,et al. In vitro Methylation of Muscle Proteins , 1969, Nature.
[48] M. Houweling,et al. Protein and fat mobilization and associations with serum β-hydroxybutyrate concentrations in dairy cows. , 2012, Journal of dairy science.
[49] N. Kristensen,et al. Precursors for liver gluconeogenesis in periparturient dairy cows. , 2013, Animal : an international journal of animal bioscience.
[50] J. Adamski,et al. High-throughput extraction and quantification method for targeted metabolomics in murine tissues , 2017, Metabolomics.
[51] T. Overton,et al. Protein nutrition in late pregnancy, maternal protein reserves and lactation performance in dairy cows , 2000, Proceedings of the Nutrition Society.
[52] A. Lilienbaum. Relationship between the proteasomal system and autophagy. , 2017, International journal of biochemistry and molecular biology.
[53] C. Lang,et al. Effects of slow-release urea and rumen-protected methionine and histidine on mammalian target of rapamycin (mTOR) signaling and ubiquitin proteasome-related gene expression in skeletal muscle of dairy cows. , 2016, Journal of dairy science.
[54] S. Kalhan,et al. The Key Role of Anaplerosis and Cataplerosis for Citric Acid Cycle Function* , 2002, Journal of Biological Chemistry.
[55] A. Gomes,et al. Upregulation of proteasome activity in muscle RING finger 1‐null mice following denervation , 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[56] H. Sauerwein,et al. Bovine haptoglobin as an adipokine: serum concentrations and tissue expression in dairy cows receiving a conjugated linoleic acids supplement throughout lactation. , 2012, Veterinary immunology and immunopathology.
[57] A. Russell,et al. The role and regulation of MAFbx/atrogin-1 and MuRF1 in skeletal muscle atrophy , 2011, Pflügers Archiv - European Journal of Physiology.
[58] G. Mortier,et al. qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data , 2007, Genome Biology.
[59] S. Gygi,et al. During muscle atrophy, thick, but not thin, filament components are degraded by MuRF1-dependent ubiquitylation , 2009, The Journal of cell biology.
[60] Thomas B Farver,et al. A Body Condition Scoring Chart for Holstein Dairy Cows , 1989 .
[61] D. Nandi,et al. The ubiquitin-proteasome system , 2006, Journal of Biosciences.
[62] E. Roets,et al. Variations in the concentrations of free amino acids in the plasma of the dairy cow at parturition , 1972, Journal of Dairy Research.
[63] T. Ziv,et al. The E2 Ubiquitin-conjugating Enzymes Direct Polyubiquitination to Preferred Lysines , 2010, The Journal of Biological Chemistry.
[64] M. D. Armstrong,et al. 3-methylhistidine, a component of actin. , 1967, Biochemical and biophysical research communications.
[65] J. Drackley,et al. ADSA Foundation Scholar Award. Biology of dairy cows during the transition period: the final frontier? , 1999, Journal of dairy science.
[66] V. Beneš,et al. The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. , 2009, Clinical chemistry.
[67] J. Bakker,et al. Free amino acids in plasma and muscle of high yielding dairy cows in early lactation. , 1995, Journal of dairy science.