2019
DOI: 10.3389/fendo.2019.00517
|View full text |Cite
|
Sign up to set email alerts
|

Non and Epigenetic Mechanisms in Regulation of Adaptive Thermogenesis in Skeletal Muscle

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
8
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 9 publications
(8 citation statements)
references
References 68 publications
0
8
0
Order By: Relevance
“…In the case of the offspring at postnatal day 245, an increase in irisin but not in Pgc-1 α was observed, which could indicate that the regulation of thermogenesis in skeletal muscle is mediated by another pathway. 40 Sarcolipin plays a role in metabolism and muscle thermogenesis through Ca 2þ -ATPase of the endoplasmic reticulum (SERCA), 41 and in an animal model of obesity induced by a HFD, sarcolipin/ SERCA expression is decreased. However, irisin treatment increased the expression of both genes.…”
Section: Discussionmentioning
confidence: 99%
“…In the case of the offspring at postnatal day 245, an increase in irisin but not in Pgc-1 α was observed, which could indicate that the regulation of thermogenesis in skeletal muscle is mediated by another pathway. 40 Sarcolipin plays a role in metabolism and muscle thermogenesis through Ca 2þ -ATPase of the endoplasmic reticulum (SERCA), 41 and in an animal model of obesity induced by a HFD, sarcolipin/ SERCA expression is decreased. However, irisin treatment increased the expression of both genes.…”
Section: Discussionmentioning
confidence: 99%
“…TAAR1 also stimulates cAMP-dependent calcium flux, leading to CaMKII-dependent activation of MEK/ERK signaling. Given that augmented Ca 2+ -handling is associated with skeletal muscle thermogenesis 28 , it is possible that T1AM could also induce thermogenesis in the heart via enhanced Ca 2+ -handling by the activation of PKA or MAPK signaling. However, in the present study, we did not see any significant effects of PKA inhibitor on the actions of T1AM (Supplementary Figs.…”
Section: Discussionmentioning
confidence: 99%
“…We found two CpG sites, in the gene CLK2 and near the gene TOR4 , that were associated with SaO2. CDC like kinase 2 or CLK2 suppresses PPARGC1A transcriptional activity on gluconeogenic genes ( Sahu et al, 2019 ) and thus downregulates hepatic gluconeogenesis and glucose output. We found CLK2 methylation to be positively associated with SaO 2 , suggesting that CLK2 expression is potentially decreased in hypoxic conditions, given methylation is linked to gene repression.…”
Section: Discussionmentioning
confidence: 99%