Photobiomodulation on bax and Bcl-2 proteins and SIRT1/PGC-1 α axis mRNA expression levels of aging rat skeletal muscle

Fang Hui Li, Yan Ying Liu, Fei Qin, Qing Luo, Hai Ping Yang, Quan Guang Zhang, Timon Cheng Yi Liu

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Objective. This study aimed to analyze the effects of low level laser irradiation (LLLI) on Bax and IGF-1 and Bcl-2 protein contents and SIRT1/PGC-1α axis mRNA expression levels to prevent sarcopenia in aged rats. Material and Methods. Twenty female Sprague Dawley rats (18 months old) were randomly divided into two groups (n = 10 per group): control (CON) and LLLI groups. The gallium-aluminum-arsenium (GaAlAs) laser irradiation at 810 nm was used in the single point contact mode (3.75 J/cm2; 0.4 cm 2; 125 mW/cm2; 30 s). Bax, Bcl-2, and IGF-1 proteins and SIRT1/PGC-1α axis mRNA expression were assessed 24 h after LLLI on gastrocnemius in aged rat. Results. Gastrocnemius muscle weights, gastrocnemius mass/body mass, Bcl-2/BAX ratio, Bcl-2 protein, IGF-1 protein, and the mRNA contents in SIRT1, PGC-1α, NRF1, TMF, and SOD2 were significantly (P < 0.05) increased by LLLI compared to CON group without LLLI. However, levels of BAX protein and caspase 3 mRNA were significantly attenuated by LLLI compared to CON group (P < 0.05). Conclusion. LLLI at 810 nm inhibits sarcopenia associated with upregulation of Bcl-2/BAX ratio and IGF-1 and SIRT1/PGC-1α axis mRNA expression in aged rats. This indicates that LLLI has potential to decrease progression of myocyte apoptosis in sarcopenic muscles.

Original languageEnglish (US)
Article number384816
JournalInternational Journal of Photoenergy
Volume2014
DOIs
StatePublished - 2014

ASJC Scopus subject areas

  • General Chemistry
  • Atomic and Molecular Physics, and Optics
  • Renewable Energy, Sustainability and the Environment
  • General Materials Science

Fingerprint

Dive into the research topics of 'Photobiomodulation on bax and Bcl-2 proteins and SIRT1/PGC-1 α axis mRNA expression levels of aging rat skeletal muscle'. Together they form a unique fingerprint.

Cite this