keyword
MENU ▼
Read by QxMD icon Read
search

(Muscle protein breakdown) OR (Muscle protein degradation) OR (Muscle Atrophy)

keyword
https://www.readbyqxmd.com/read/30103010/integrated-analysis-of-mrna-and-mirna-expression-profiles-reveals-muscle-growth-differences-between-adult-female-and-male-chinese-concave-eared-frogs-odorrana-tormota
#1
Yilin Shu, Jinquan Xia, Qiang Yu, Gang Wang, Jihui Zhang, Jun He, Huan Wang, Ling Zhang, Hailong Wu
The Chinese concave-eared torrent frog (Odorrana tormota) is the first known non-mammalian vertebrate that can communicate using ultrasound. In this species, females are approximately four times as large as males, in which the female growth rate is obviously higher than that of male. Until now, the molecular mechanisms underlying muscle growth development differences between male and female frogs have not been reported. Here, we integrated mRNA and miRNA expression profiles to reveal growth differences in the hindlimb muscles of 2-year-old frogs...
August 10, 2018: Gene
https://www.readbyqxmd.com/read/30101916/a-case-of-neurolymphomatosis-in-the-cauda-equina-diagnosed-by-an-open-biopsy
#2
Ryo Sasaki, Yasuyuki Ohta, Yuto Yamada, Koh Tadokoro, Yoshiaki Takahashi, Kota Sato, Jingwei Shang, Mami Takemoto, Nozomi Hishikawa, Toru Yamashita, Takao Yasuhara, Isao Date, Shuntaro Ikegawa, Nobuharu Fujii, Koji Abe
Neurolymphomatosis is a rare form of extranodal malignant lymphoma defined as the infiltration of malignant lymphocytes into the central or peripheral nerve. We herein report a case of neurolymphomatosis in the cauda equina diagnosed by an open surgical biopsy. He presented with muscle weakness, atrophy, numbness and hypoesthesia in the bilateral lower extremities with the accumulation of 18 fluoro-2-deoxyglucose (FDG) in the bilateral cauda equina. Cerebrospinal fluid (CSF) cytology (three times) and flow cytometry (two times) and biopsies of the left sural nerve, bone marrow, paranasal sinus and left testis were all negative for malignancy, so finally we performed a surgical open biopsy of the cauda equina by laminectomy and diagnosed him with diffuse large B-cell lymphoma (DLBCL) in the cauda equina...
August 10, 2018: Internal Medicine
https://www.readbyqxmd.com/read/30097998/-the-application-of-stable-isotope-tracers-to-study-human-musculoskeletal-protein-turnover-a-tale-of-bag-filling-and-bag-enlargement
#3
D Joe Millward, Ken Smith
The nutritional regulation of protein and amino acid balance in human skeletal muscle carried out by the authors with Mike Rennie is reviewed in the context of a simple physiological model for the regulation of the maintenance and growth of skeletal muscle, the "Bag Theory." Beginning in London in the late 1970s the work has involved the use of stable isotopes to probe muscle protein synthesis and breakdown with two basic experimental models, primed-dose continuous tracer infusions combined with muscle biopsies and arterio-venous (A-V) studies across a limb, most often the leg, allowing both protein synthesis and breakdown as well as net balance to be measured...
August 11, 2018: Journal of Physiology
https://www.readbyqxmd.com/read/30096535/copper-or-and-arsenic-induces-autophagy-by-oxidative-stress-related-pi3k-akt-mtor-pathways-and-cascaded-mitochondrial-fission-in-chicken-skeletal-muscle
#4
Yu Wang, Hongjing Zhao, Yizhi Shao, Juanjuan Liu, Jinglun Li, Liyang Luo, Mingwei Xing
Autophagy is an ubiquitin proteasome system for degradation of intracellular damaged proteins and organelles. Both as environmental pollutants, flourishing data show arsenic (As) and copper (Cu) as robust oxidative stress inducers. Whether this kind of damage correlates with autophagy through the phosphoinositide-3-kinase/protein kinase b/mammalian target of rapamycin (PI3K/AKT/mTOR) pathway still remains elusive. A 12-week exposures of Cu or/and As to chicken time-dependently displayed significant element residue in the pectoralis...
August 4, 2018: Journal of Inorganic Biochemistry
https://www.readbyqxmd.com/read/30092791/counteracting-roles-of-mhci-and-cd8-t-cells-in-the-peripheral-and-central-nervous-system-of-als-sod1-g93a-mice
#5
Giovanni Nardo, Maria Chiara Trolese, Mattia Verderio, Alessandro Mariani, Massimiliano de Paola, Nilo Riva, Giorgia Dina, Nicolò Panini, Eugenio Erba, Angelo Quattrini, Caterina Bendotti
BACKGROUND: The major histocompatibility complex I (MHCI) is a key molecule for the interaction of mononucleated cells with CD8+ T lymphocytes. We previously showed that MHCI is upregulated in the spinal cord microglia and motor axons of transgenic SOD1G93A mice. METHODS: To assess the role of MHCI in the disease, we examined transgenic SOD1G93A mice crossbred with β2 microglobulin-deficient mice, which express little if any MHCI on the cell surface and are defective for CD8+ T cells...
August 9, 2018: Molecular Neurodegeneration
https://www.readbyqxmd.com/read/30092568/roles-of-exosome-like-vesicles-released-from-inflammatory-c2c12-myotubes-regulation-of-myocyte-differentiation-and-myokine-expression
#6
Sujin Kim, Min-Jae Lee, Ji-Young Choi, Dong-Ho Park, Hyo-Bum Kwak, Sohee Moon, Je-Woo Koh, Hun-Kyu Shin, Ji-Kan Ryu, Chang-Shin Park, Jai Hyung Park, Ju-Hee Kang
BACKGROUND/AIMS: The complicated differentiation processes of cells in skeletal muscle against inflammation that induce muscle atrophy are not fully elucidated. Given that skeletal muscle is a secretory organ, we evaluated the effects of inflammation on myogenic signals and myokine expression, and the roles of inflammatory exosomes released by myotubes in myogenic differentiation. METHODS: Inflammation was induced by treatment of fully differentiated C2C12 myotubes with a cytokine mixture of TNF-α and INF-γ...
August 9, 2018: Cellular Physiology and Biochemistry
https://www.readbyqxmd.com/read/30091665/responses-of-skeletal-muscle-size-and-anabolism-are-reproducible-with-multiple-periods-of-unloading-reloading
#7
Kevin L Shimkus, Yasaman Shirazi-Fard, Michael P Wiggs, Shaik T Ullah, Camilo Pohlenz, Delbert M Gatlin, Chad C Carroll, Harry A Hogan, James D Fluckey
AIM: Mechanical unloading has long been understood to contribute to rapid and substantial adaptations within skeletal muscle, most notably muscle atrophy. Studies have often demonstrated that many of the alterations resulting from disuse are reversed with a reintroduction of load and have supported the concept of muscle plasticity. We hypothesized that adaptations during disuse and recovery was a repeatable/reproducible phenomenon, which we tested with repeated changes in mechanical load...
August 9, 2018: Journal of Applied Physiology
https://www.readbyqxmd.com/read/30091009/the-pattern-of-idiopathic-isolated-teres-minor-atrophy-with-regard-to-its-two-bundle-anatomy
#8
Yusuhn Kang, Joong Mo Ahn, Choong Guen Chee, Eugene Lee, Joon Woo Lee, Heung Sik Kang
OBJECTIVE: We aimed to analyze the pattern of teres minor atrophy with regard to its two-bundle anatomy and to assess its association with clinical factors. MATERIALS AND METHODS: Shoulder MRIs performed between January and December 2016 were retrospectively reviewed. Images were evaluated for the presence and pattern of isolated teres minor atrophy. Isolated teres minor atrophy was categorized into complete or partial pattern, and partial pattern was further classified according to the portion of the muscle that was predominantly affected...
August 8, 2018: Skeletal Radiology
https://www.readbyqxmd.com/read/30088953/mitochondrial-membrane-protein-associated-neurodegeneration-a-case-report-and-literature-review
#9
Pavel Dušek, David Školoudík, Jan Roth, Petr Dušek
Mitochondrial membrane protein-associated neurodegeneration (MPAN) is an autosomal recessive disorder caused by mutation in the C19orf12 gene. We report a compound heterozygous c.[32C>T];[205G>A;424A>G] (p.[Thr11Met];[Gly69Arg;Lys142Glu]) Czech patient who manifested with right foot dystonia, impaired handwriting, attention deficit, and signs of iron accumulation on brain MRI. Gradually, he developed dysarthria, spastic-dystonic gait, pedes cavi, and atrophy of leg muscles. Additionally, we report demographic parameters, clinical signs, and allelic frequencies of C19orf12 mutations of all published MPAN cases...
August 8, 2018: Neurocase
https://www.readbyqxmd.com/read/30087400/exercise-prevents-impaired-autophagy-and-proteostasis-in-a-model-of-neurogenic-myopathy
#10
Juliane C Campos, Leslie M Baehr, Kátia M S Gomes, Luiz R G Bechara, Vanessa A Voltarelli, Luiz H M Bozi, Márcio A C Ribeiro, Nikolas D Ferreira, José B N Moreira, Patricia C Brum, Sue C Bodine, Julio C B Ferreira
Increased proteolytic activity has been widely associated with skeletal muscle atrophy. However, elevated proteolysis is also critical for the maintenance of cellular homeostasis by disposing cytotoxic proteins and non-functioning organelles. We recently demonstrated that exercise activates autophagy and re-establishes proteostasis in cardiac diseases. Here, we characterized the impact of exercise on skeletal muscle autophagy and proteostasis in a model of neurogenic myopathy induced by sciatic nerve constriction in rats...
August 7, 2018: Scientific Reports
https://www.readbyqxmd.com/read/30084798/leucine-can-modulate-the-expression-of-proteins-related-to-protein-degradation-signalling-under-mtor-inhibition-in-c2c12-cells
#11
Bianca Cristine Favero-Santos, Maria Cristina Cintra Gomes-Marcondes
Many metabolic syndromes lead to energetic disturbs which ends to an intense catabolic state. The branched-chain amino acid leucine shows very positive effects on muscle protein metabolism. However, it is still not clear how leucine acts improving the protein turnover. This study aimed to evaluate in vitro the effects of leucine supplementation in minimising the signalling pathway of protein degradation when mTOR was inhibited. Our studies were conducted in murine C2C12 myotubes exposed to 2mM leucine or 2mM isoleucine in control situation and compared to the inhibition of mTOR by rapamycin...
July 30, 2018: Cellular and Molecular Biology
https://www.readbyqxmd.com/read/30084281/an-update-on-diagnostic-options-and-considerations-in-limb-girdle-dystrophies
#12
Corrado Angelini, Laura Giaretta, Roberta Marozzo
Limb Girdle Muscular Dystrophies (LGMD) encompasses a clinically heterogeneous group of rare, genetic progressive muscle disorders presenting with weakness and atrophy of predominant pelvic and shoulder muscles. The spectrum of disease severity ranges from severe childhood-onset muscular dystrophy to adult-onset dystrophy. Areas covered: The review presents an update of the clinical phenotypes and diagnostic options for LGMD including both dominant and recessive LGMD and consider their differential clinical and histopathological features...
August 7, 2018: Expert Review of Neurotherapeutics
https://www.readbyqxmd.com/read/30084072/muscle-profile-and-cognition-in-patients-with-alzheimer-s-disease-dementia
#13
Yeonsil Moon, Ye-Ji Choi, Jin Ok Kim, Seol-Heui Han
INTRODUCTION: Neurodegenerative disease is one of the main contributing factors affecting muscle atrophy. However, this intriguing brain-muscle axis has been explained by the unsubstantial mechanisms. Although there have been several studies that have evaluated the muscle profile and its relation to cognition in patients with dementia, there is still lack of data using standardized methods and only few published studies on Korean populations. The objective of this study is to evaluate the relationship of muscle mass and strength to cognition in patients with Alzheimer's disease dementia (AD)...
August 6, 2018: Neurological Sciences
https://www.readbyqxmd.com/read/30083183/aberrant-protein-turn-over-associated-with-myofibrillar-disorganization-in-fhl1-knockout-mice
#14
Jingjing Ding, Yan Fei Cong, Bo Liu, Jianing Miao, Lili Wang
Mutations in the FHL1 gene, and FHL1 protein deletion, are associated with rare hereditary myopathies and cardiomyopathies. FHL1-null mice develop age-dependent myopathy and increased autophagic activity. However, the molecular pathway involved in contractile function and increased autophagic activity in the FHL1-null mouse has not yet been fully elucidated. In this study, FHL1 protein was knocked out in mice using Transcription Activator-like Effector Nucleases (TALENs) and the IRS1-FOXO1/mTOR signaling pathway was investigated in skeletal muscles and heart...
2018: Frontiers in Genetics
https://www.readbyqxmd.com/read/30083128/a-novel-mutation-of-gars-in-a-chinese-family-with-distal-hereditary-motor-neuropathy-type-v
#15
Xueying Yu, Bin Chen, Hefei Tang, Wei Li, Ying Fu, Zaiqiang Zhang, Yaping Yan
Glycyl-tRNA synthetase ( GARS) gene mutations have been reported to be associated with Charcot-Marie-Tooth disease 2D and distal hereditary motor neuropathy type V (dHMN-V). In this study, we report a novel GARS mutation in a Chinese family with dHMN-V. Clinical, electromyogram, genetic, and functional data were explored. The proband was an 11-year-old girl presented with progressive distal limb muscle weakness and atrophy due to peripheral motor neuropathy for 1 year. Another five members from three successive generations of the family showed similar symptoms during their first to second decades and demonstrated an autosomal dominant inheritance...
2018: Frontiers in Neurology
https://www.readbyqxmd.com/read/30082698/the-detrimental-effects-of-glucocorticoids-exposure-during-pregnancy-on-offspring-s-cardiac-functions-mediated-by-hypermethylation-of-bone-morphogenetic-protein-4
#16
Jieying Peng, Yuhao Zhou, Zhiyu Zhang, Zhiming Wang, Lingtong Gao, Xiao Zhang, Zhou Fang, Guangyao Li, Huaiyan Chen, Hongxing Yang, Lu Gao
The intra-uterine and external environmental factors not only affect the early development of fetuses, their interaction with genesis will also substantially program the physiological functions of offspring throughout life. Synthetic glucocorticoid (GC) is widely used for the management of women at risk of preterm birth or undergone autoimmune diseases. However, excess GC might cause a number of chronic diseases in later life. In the present study, we set up a programming rat model by daily injection of dexamethasone (DEX) since 14...
August 6, 2018: Cell Death & Disease
https://www.readbyqxmd.com/read/30080421/contrast-enhanced-ultrasound-determines-supraspinatus-muscle-atrophy-after-cuff-repair-and-correlates-to-functional-shoulder-outcome
#17
Christian Fischer, Sascha Gross, Felix Zeifang, Gerhard Schmidmaier, Marc-André Weber, Pierre Kunz
BACKGROUND: Muscle degeneration as a consequence of rotator cuff tears is mainly assessed by magnetic resonance imaging. Contrast-enhanced ultrasound (CEUS) is a new functional imaging method to assess microvascular perfusion as a fundamental parameter of muscle tissue vitality. In this cross-sectional study, the authors evaluated supraspinatus muscle perfusion after cuff repair and analyzed its association with functional shoulder outcome and the grade of echogenicity in B-mode ultrasound indicating fatty infiltration...
August 6, 2018: American Journal of Sports Medicine
https://www.readbyqxmd.com/read/30080234/critical-evaluation-of-muscle-mass-loss-as-a-prognostic-marker-of-morbidity-in-critically-ill-patients-and-methods-for-its-determination
#18
Vera Joskova, Anna Patkova, Eduard Havel, Simona Najpaverova, Daniela Uramova, Miroslav Kovarik, Zdenek Zadak, Miloslav Hronek
OBJECTIVE: Loss of muscle mass in critically ill patients is associated with serious consequences, such as prolonged mechanical ventilation, intensive care unit confinement, and higher mortality. Thus, monitoring muscle mass, and especially its decline, should provide a useful indicator of morbidity and mortality. Performing evaluations according only to body mass index is imperfect, therefore the aim of this article was to evaluate appropriate methods for muscle mass loss determination in ICU patients...
August 6, 2018: Journal of Rehabilitation Medicine
https://www.readbyqxmd.com/read/30079931/epigenetics-in-ascending-thoracic-aortic-aneurysm-and-dissection
#19
Adeline Boileau, Mark E Lindsay, Jean-Baptiste Michel, Yvan Devaux
Thoracic aortic aneurysm (TAA) is an asymptomatic and progressive dilatation of the thoracic aorta. Ascending aortic dissection (AAD) is an acute intraparietal tear, occurring or not on a pre-existing dilatation. AAD is a condition associated with a poor prognosis and a high mortality rate. TAA and AAD share common etiology as monogenic diseases linked to transforming growth factor β signaling pathway, extracellular matrix defect, or smooth muscle cell protein mutations. They feature a complex pathogenesis including loss of smooth muscle cells, altered phenotype, and extracellular matrix degradation in aortic media layer...
February 2018: Aorta (Stamford, Conn.)
https://www.readbyqxmd.com/read/30079853/%C3%AE-1-acid-glycoprotein-inhibits-insulin-responses-by-glucose-oxidation-protein-synthesis-and-protein-breakdown-in-mouse-c2c12-myotubes
#20
T G Ramsay, L A Blomberg, T H Elsasser, T J Caperna
Increased plasma α-1 acid glycoprotein (AGP) is correlated with reduced growth rates in neonatal swine. The specific physiological mechanisms contributing to this relationship are unknown. This study was performed to determine if AGP can modify muscle metabolism by examining glucose oxidation and protein synthesis in the C2C12 muscle cell line. Cells were used for experiments 4 days post-fusion as myotubes. Myotubes were exposed to AGP for 24 h, with the last 4 h used to monitor 14C-glucose oxidation or to measure protein synthesis by incorporation of 3H-tyrosine...
August 6, 2018: Animal: An International Journal of Animal Bioscience
keyword
keyword
161529
1
2
Fetch more papers »
Fetching more papers... Fetching...
Read by QxMD. Sign in or create an account to discover new knowledge that matter to you.
Remove bar
Read by QxMD icon Read
×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"