PMID- 15036397 OWN - NLM STAT- MEDLINE DCOM- 20040720 LR - 20211203 IS - 0531-5565 (Print) IS - 1873-6815 (Electronic) IS - 0531-5565 (Linking) VI - 39 IP - 3 DP - 2004 Mar TI - Effects of aerobic exercise training on the protein kinase B (PKB)/mammalian target of rapamycin (mTOR) signaling pathway in aged skeletal muscle. PG - 379-85 AB - The protein kinase B (PKB)/mammalian target of rapamycin (mTOR) signaling pathway is thought to play a critical role in the regulation of protein synthesis and skeletal muscle mass. The purpose of the present study was to determine the effects of voluntary wheel running on the PKB/mTOR signaling pathway in muscles from aged mice (20-22 months). The total levels of mTOR were 65% higher in gastrocnemius muscles from aged mice subjected to wheel running compared to aged sedentary mice (p-0.002) PKB phosphorlation on Ser473 was 45% higher in gastrocnemius muscles from aged mice subjected to wheel running compared to aged sedentary mice (p=0.01) The total abundance of PKB was 50% higher in gastrocnemius muscles from wheel running mice compared to aged controls (p=0.005). Three months of wheel running did not alter the total amount of p70 S6K in gastrocnemius muscle. Protein synthesis, as assessed by [(14)C]phenylalanine incorporation into protein was significantly higher in soleus muscles from aged mice subjected to wheel running compared to aged sedentary mice (p-0.001) These findings indicate the aerobic exercise training may attenuate the age-related decline in protein synthesis, a process that appears to be due, in part, to increases in mTOR and PKB. FAU - Reynolds, Thomas H 4th AU - Reynolds TH 4th AD - Department of Internal Medicine, Division of Geriatric Medicine, University of Michigan and the GRECC, Ann Arbor Veterans Affairs Healthcare System, Ann Arbor, MI, USA. treynolds@ithaca.edu FAU - Reid, Pamela AU - Reid P FAU - Larkin, Lisa M AU - Larkin LM FAU - Dengel, Donald R AU - Dengel DR LA - eng GR - K01 AG000701-04/AG/NIA NIH HHS/United States GR - T32 AG000114/AG/NIA NIH HHS/United States GR - K01-AG00710/AG/NIA NIH HHS/United States GR - T32-AG00114/AG/NIA NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PL - England TA - Exp Gerontol JT - Experimental gerontology JID - 0047061 RN - 0 (Muscle Proteins) RN - 0 (Proto-Oncogene Proteins) RN - EC 2.7.11.1 (Protein Serine-Threonine Kinases) RN - EC 2.7.11.1 (Proto-Oncogene Proteins c-akt) RN - W36ZG6FT64 (Sirolimus) SB - IM MH - Aging/*physiology MH - Animals MH - Male MH - Mice MH - Mice, Inbred Strains MH - Muscle Contraction/physiology MH - Muscle Proteins/biosynthesis MH - Muscle, Skeletal/*metabolism MH - *Physical Conditioning, Animal MH - Protein Serine-Threonine Kinases/*metabolism MH - Proto-Oncogene Proteins/*metabolism MH - Proto-Oncogene Proteins c-akt MH - Signal Transduction/*physiology MH - Sirolimus/*metabolism MH - Specific Pathogen-Free Organisms PMC - PMC2714731 MID - NIHMS116631 EDAT- 2004/03/24 05:00 MHDA- 2004/07/21 05:00 PMCR- 2009/07/23 CRDT- 2004/03/24 05:00 PHST- 2003/09/30 00:00 [received] PHST- 2003/12/15 00:00 [revised] PHST- 2003/12/16 00:00 [accepted] PHST- 2004/03/24 05:00 [pubmed] PHST- 2004/07/21 05:00 [medline] PHST- 2004/03/24 05:00 [entrez] PHST- 2009/07/23 00:00 [pmc-release] AID - S0531556503003607 [pii] AID - 10.1016/j.exger.2003.12.005 [doi] PST - ppublish SO - Exp Gerontol. 2004 Mar;39(3):379-85. doi: 10.1016/j.exger.2003.12.005.