-
Je něco špatně v tomto záznamu ?
Endurance Training Inhibits the JAK2/STAT3 Pathway to Alleviate Sarcopenia
B. Yao, L. Li, X. Guan, J. Zhu, Q. Liu, B. Qu, H. Ding
Status minimální Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
PubMed Central
od 2020
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- Janus kinasa 2 * metabolismus MeSH
- kondiční příprava zvířat * fyziologie MeSH
- kosterní svaly metabolismus MeSH
- myši MeSH
- sarkopenie * metabolismus prevence a kontrola terapie MeSH
- signální transdukce * MeSH
- stárnutí metabolismus MeSH
- transkripční faktor STAT3 * metabolismus MeSH
- vytrvalostní trénink * MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Aging leads to a decrease in muscle function, mass, and strength in skeletal muscle of animals and humans. The transcriptome identified activation of the JAK/STAT pathway, a pathway that is associated with skeletal muscle atrophy, and endurance training has a significant effect on improving sarcopenia; however, the exact mechanism still requires further study. We investigated the effect of endurance training on sarcopenia. Six-month-old male SAMR1 mice were used as a young control group (group C), and the same month-old male SAMP8 mice were divided into an exercise group (group E) and a model group (group M). A 3-month running exercise intervention was performed on group E, and the other two groups were kept normally. Aging caused significant signs of sarcopenia in the SAMP8 mice, and endurance training effectively improved muscle function, muscle mass, and muscle strength in the SAMP8 mice. The expression of JAK2/STAT3 pathway factor was decreased in group E compared with group M, and the expression of SOCS3, the target gene of STAT3, and NR1D1, an atrophy-related factor, was significantly increased. Endurance training significantly improved the phenotypes associated with sarcopenia, and the JAK2/STAT3 pathway is a possible mechanism for the improvement of sarcopenia by endurance training, while NR1D1 may be its potential target. Keywords: Sarcopenia, Endurance training, Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3), Nuclear receptor subfamily 1, group D member 1 (Nr1d1).
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24009821
- 003
- CZ-PrNML
- 005
- 20250716154834.0
- 007
- ta
- 008
- 240606s2024 xr ad f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.935234 $2 doi
- 035 __
- $a (PubMed)38710060
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Yao, B. $u Institute of Sports Medicine and Health, Chengdu Sport University, Chengdu, Sichuan, China. yaobinyu222@163.com
- 245 10
- $a Endurance Training Inhibits the JAK2/STAT3 Pathway to Alleviate Sarcopenia / $c B. Yao, L. Li, X. Guan, J. Zhu, Q. Liu, B. Qu, H. Ding
- 520 9_
- $a Aging leads to a decrease in muscle function, mass, and strength in skeletal muscle of animals and humans. The transcriptome identified activation of the JAK/STAT pathway, a pathway that is associated with skeletal muscle atrophy, and endurance training has a significant effect on improving sarcopenia; however, the exact mechanism still requires further study. We investigated the effect of endurance training on sarcopenia. Six-month-old male SAMR1 mice were used as a young control group (group C), and the same month-old male SAMP8 mice were divided into an exercise group (group E) and a model group (group M). A 3-month running exercise intervention was performed on group E, and the other two groups were kept normally. Aging caused significant signs of sarcopenia in the SAMP8 mice, and endurance training effectively improved muscle function, muscle mass, and muscle strength in the SAMP8 mice. The expression of JAK2/STAT3 pathway factor was decreased in group E compared with group M, and the expression of SOCS3, the target gene of STAT3, and NR1D1, an atrophy-related factor, was significantly increased. Endurance training significantly improved the phenotypes associated with sarcopenia, and the JAK2/STAT3 pathway is a possible mechanism for the improvement of sarcopenia by endurance training, while NR1D1 may be its potential target. Keywords: Sarcopenia, Endurance training, Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3), Nuclear receptor subfamily 1, group D member 1 (Nr1d1).
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a sarkopenie $x metabolismus $x prevence a kontrola $x terapie $7 D055948
- 650 12
- $a Janus kinasa 2 $x metabolismus $7 D053614
- 650 12
- $a transkripční faktor STAT3 $x metabolismus $7 D050796
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a myši $7 D051379
- 650 12
- $a kondiční příprava zvířat $x fyziologie $7 D010805
- 650 12
- $a signální transdukce $7 D015398
- 650 12
- $a vytrvalostní trénink $7 D000076663
- 650 _2
- $a kosterní svaly $x metabolismus $7 D018482
- 650 _2
- $a stárnutí $x metabolismus $7 D000375
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Li, L.
- 700 1_
- $a Guan, X.
- 700 1_
- $a Zhu, J.
- 700 1_
- $a Liu, Q.
- 700 1_
- $a Qu, B.
- 700 1_
- $a Ding, H.
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 73, č. 2 (2024), s. 295-304
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/38710060 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y - $z 0
- 990 __
- $a 20240606 $b ABA008
- 991 __
- $a 20250716154817 $b ABA008
- 999 __
- $a min $b bmc $g 2283484 $s 1219651
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 73 $c 2 $d 295-304 $e 20240430 $i 1802-9973 $m Physiological research $n Physiol Res $x MED00003824
- LZP __
- $b NLK116 $a Pubmed-20240606