abstract methods introduction results conclusions

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52.4±5.1 ml/kg/min) underwent a resting muscle biopsy from their right vastus lateralis (VL) then completed a HIIT ... Significant phosphorylation of TBC1D4 was also detected in MHC I at 90 min post- exercise compared to ... 48 hr no exercise.
Fiber Type-Specific Activation of AMPK Following Acute High Intensity Interval Exercise in Concurrently Trained Men

Kinesiology

James R.

1 Bagley ,

Kara K.

2 Lazauskas ,

Irene S.

2 Tobias ,

Jeremy

2 Siu ,

Nathan

2 Serrano ,

Cameron

2 Yen

& Andrew J.

2 Galpin

1 Muscle

Physiology Laboratory, Department of Kinesiology, College of Health & Social Sciences, San Francisco State University 2 Biochemistry & Molecular Exercise Physiology Laboratory, Center for Sport Performance, California State University, Fullerton

METHODS

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48 hr no exercise 12 hr food/caffeine fast No medications or PEDs Standardized meal Food log for 7 days prior Hydration check

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Fast

Visit 1: VO2max test and anthropometrics Visit 2: biopsies/HIIT experiment (7-14 d after Visit 1) 4 vastus lateralis biopsies (alternating right, left, right, left) 6 HIIT rounds, cycle erg. (~100% VO2max for 1.5 min, 40% for 2.5 min) Gas exchange monitored during HIIT

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TBC1D1 Expression

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Figure 6: A) Representative CNIA lane view images of TBC1D1 (B) expression and (C) phosphorylation in MHC I vs. MHC IIa fibers before and after HIIT. Significance: * (relative to MHC I), ^ (relative to Rest).

ABSTRACT

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Figure 7: A) Representative CNIA lane view images of TBC1D4 (B) expression and (C) phosphorylation in MHC I vs. MHC IIa fibers before and after HIIT. Significance: * (relative to MHC I), ^ (relative to Rest).

CONCLUSIONS Preserve

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9 participants 4 time points 30 fibers per biopsy = 1,080 fibers

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MHC I Select and Combine Fibers

9 participants, 4 time points 2 fiber types, = 72 samples

MHC IIa CNIA Analysis Tubulin

 HIIT exercise induced: 1. FT-specific activation of AMPK 2. FT-specific differences in phosphorylation of AMPKα and all three substrates measured 3. Delayed phosphorylation responses in TBC1D1 and TBC1D4 Application: Athletes with different fiber type compositions may require different post-exercise nutritional timing strategies.

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A) MHC I

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Biopsy FT Percemtage

PURPOSE: AMP-activated protein kinase (AMPK) is an energy-sensing regulator of cellular metabolism that is activated during acute exercise. Previous human skeletal muscle studies analyzed AMPK activation in mixed fiber type (FT) biopsy samples, though recent investigations show that AMPK’s properties are dependent on myosin heavy chain (MHC) FT (i.e., slow- vs. fast-twitch). The purpose of this study was to assess the phosphorylation of AMPK and three of its substrates (markers of AMPK activity), ACC, TBC1D1 and TBC1D4, in slow (MHC I) vs. fast (MHC IIa) skeletal muscle fibers from concurrently trained men following acute high intensity interval training (HIIT) exercise. METHODS: Nine concurrently trained males (age 31±2 y; height 178±9 cm; mass 84±10 kg; VO2max 52.4±5.1 ml/kg/min) underwent a resting muscle biopsy from their right vastus lateralis (VL) then completed a HIIT bout consisting of 6 rounds (Intervals: 1.5 min at 90-100% VO2max, then 2.5 min at ~40%). A second biopsy (left VL) was performed immediately after completion of the final exercise round with a third and fourth biopsy collected at 90 min and 180 min post-HIIT. Single muscle fibers were mechanically isolated for MHC analysis via SDS-PAGE to identify FT and combined into MHC I and MHC IIa pools of 5-8 fibers. FT-specific phosphorylation of AMPKα, ACC, TBC1D1 and TBC1D4 was quantified via capillary nanoimmunoassay (CNIA). RESULTS: AMPKα phosphorylation was significantly (p