2022
DOI: 10.1080/1354750x.2022.2112290
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Insight into the role of myokines and myogenic regulatory factors under hypobaric hypoxia induced skeletal muscle loss

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Cited by 5 publications
(4 citation statements)
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“…Hypobaric Hypoxia: The simulated high-altitude environment was provided to animals through an animal decompression chamber. [4][5][6][7]79] An altitude of 7620 m, 8% O 2 , and pressure at 282 torr, along with 23-25 °C temperature, 45-55% humidity, and airflow of 2 l min −1 was maintained inside the chamber for the hypoxic group. The decompression chamber or hypoxia chamber was opened once a day to measure the body weight of the animals, change the bedding, and refill the water and food supply.…”
Section: Methodsmentioning
confidence: 99%
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“…Hypobaric Hypoxia: The simulated high-altitude environment was provided to animals through an animal decompression chamber. [4][5][6][7]79] An altitude of 7620 m, 8% O 2 , and pressure at 282 torr, along with 23-25 °C temperature, 45-55% humidity, and airflow of 2 l min −1 was maintained inside the chamber for the hypoxic group. The decompression chamber or hypoxia chamber was opened once a day to measure the body weight of the animals, change the bedding, and refill the water and food supply.…”
Section: Methodsmentioning
confidence: 99%
“…[3][4][5][6] Recently, we have also reported skeletal muscle as an endocrine organ that secretes myokines and myogenic regulatory factors for the repair and regeneration of HH-induced skeletal muscle loss. [7] A regulatory structure that also regulates skeletal muscle mass is microRNA. Recently, muscle-specific microRNAs are called "myomiR" [8] which have emerged as one of the critical regulators of skeletal muscle function.…”
Section: Introductionmentioning
confidence: 99%
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“…Associated mechanisms may include elevated neural precursor cell expressed developmentally down-regulated protein (NEDD)4 expression in muscle ( 42 ) and transforming growth factor (TGF)-mediated MSTN ( 43 ). Nevertheless, there are contrasting hypotheses that a high CO 2 environment can promote MSTN degradation by activating the AMPKα2-forkhead box O-like (FoxO) 3a-MuRF1 pathway ( 44 , 45 ). Studies on the mechanisms of COPD combined with sarcopenia have shown high heterogeneity in the fields of hypoxia and oxidative stress; however, the sample sizes of the relevant clinical studies are relatively small.…”
Section: Pathogenesismentioning
confidence: 99%