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Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis.

Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis. Research Abstract Details 

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  • Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis. Abstract Text:

    satoshi fujitaSatoshi Fujita,takashi abeTakashi Abe,micah j drummondMicah J Drummond,jerson g cadenasJerson G Cadenas,hans c dreyerHans C Dreyer,yoshiaki satoYoshiaki Sato,elena volpiElena Volpi,blake b rasmussenBlake B Rasmussen,satoshi fujitaSatoshi Fujita,takashi abeTakashi Abe,micah j drummondMicah J Drummond,jerson g cadenasJerson G Cadenas,hans c dreyerHans C Dreyer,yoshiaki satoYoshiaki Sato,elena volpiElena Volpi,blake b rasmussenBlake B Rasmussen,

    Low-intensity resistance exercise training combined with blood flow restriction (REFR) increases muscle size and strength as much as conventional resistance exercise with high loads. However, the cellular mechanism(s) underlying the hypertrophy and strength gains induced by REFR are unknown. We have recently shown that both the mammalian target of rapamycin (mTOR) signaling pathway and muscle protein synthesis (MPS) were stimulated after an acute bout of high-intensity resistance exercise in humans. Therefore, we hypothesized that an acute bout of REFR would enhance mTOR signaling and stimulate MPS. We measured MPS and phosphorylation status of mTOR-associated signaling proteins in six young male subjects. Subjects were studied once during blood flow restriction (REFR, bilateral leg extension exercise at 20% of 1 repetition maximum while a pressure cuff was placed on the proximal end of both thighs and inflated at 200 mmHg) and a second time using the same exercise protocol but without the pressure cuff [control (Ctrl)]. MPS in the vastus lateralis muscle was measured by using stable isotope techniques, and the phosphorylation status of signaling proteins was determined by immunoblotting. Blood lactate, cortisol, and growth hormone were higher following REFR compared with Ctrl (P < 0.05). Ribosomal S6 kinase 1 (S6K1) phosphorylation, a downstream target of mTOR, increased concurrently with a decreased eukaryotic translation elongation factor 2 (eEF2) phosphorylation and a 46% increase in MPS following REFR (P < 0.05). MPS and S6K1 phosphorylation were unchanged in the Ctrl group postexercise. We conclude that the activation of the mTOR signaling pathway appears to be an important cellular mechanism that may help explain the enhanced muscle protein synthesis during REFR.

    Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis. Publishing Authors By Initials

    s fujitaS Fujita,t abeT Abe,mj drummondMJ Drummond,jg cadenasJG Cadenas,hc dreyerHC Dreyer,y satoY Sato,e volpiE Volpi,bb rasmussenBB Rasmussen,s fujitaS Fujita,t abeT Abe,mj drummondMJ Drummond,jg cadenasJG Cadenas,hc dreyerHC Dreyer,y satoY Sato,e volpiE Volpi,bb rasmussenBB Rasmussen,

    For similar abstracts research abstracts see: abstracts research

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    Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of applied physiology (Bethesda, Md. : 198

    VOLUME: 103

    Page Numbers: 903-10

    Journal Abbreviation: J. Appl. Physiol.

    ISSN: 8750-7587

    DAY: 14

    MONTH: 06

    YEAR: 2007

    Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis. Information

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    LANGUAGE: eng

    NlmUniqueID: 8502536

    Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis. Keywords Mesh Terms:

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    Grant and Affiliation Information for Blood flow restriction during low-intensity resistance exercise increases S6K1 phosphorylation and muscle protein synthesis.

    AFFILIATION: Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA. fujita@k.u-tokyo.ac.jp

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCRR

    GRANT: S10-RR-16650

    ACRONYM: RR

    MEDLINETA: J Appl Physiol

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