pH-Resolved ATP Synthesis in Skeletal Muscle: Concept, Implementation, and Assessment Using Dynamic 31P Magnetic Resonance Spectroscopy at 7T

<b>Background/Objectives:</b> Dynamic changes in inorganic phosphate (Pi), phosphocreatine (PCr), and pH during post-exercise recovery reflect underlying muscle energetics and mitochondrial ATP synthesis, but the conventional single-pool model assuming uniform metabolic response fails to address myofiber composition and pH-dependent metabolic heterogeneity in skeletal muscle. This study aimed to characterize the interplay between pH, Pi, and PCr, and to develop an analytical method for assessing pH-resolved ATP synthesis using <sup>31</sup>P MRS. <b>Methods:</b> Five healthy subjects underwent dynamic <sup>31</sup>P MRS scans during plantar flexion exercise. ATP synthesis was evaluated from post-exercise PCr and Pi recovery time courses using the single-pool model, and from Pi recovery time courses using a multi-pool model in which the Pi signal lineshape was segmented into four pH-specific pools: alkaline (pH 7.3 ± 0.2), neutral (pH 7.0 ± 0.1), mildly acidic (pH 6.8 ± 0.1), and moderately acidic (pH 6.6 ± 0.1). <b>Results:</b> The single-pool model showed that during exercise, Pi increased proportionally to PCr depletion, and both Pi and PCr recovered monoexponentially immediately after exercise with τPi 33±9 s<τPCr (40 ±9 s); ATP remained stable while pH exhibited a "heart-beat" pattern, characterized by an initial alkalization followed by neutralization during exercise, a post-exercise acidic undershoot, and a subsequent slow recovery (τpH≫τPCr). The four-pool model demonstrated a pronounced pH dependence of Pi recovery, with slower recovery at lower pH (τPi: 19 ± 6 s at pH 7.3, 25 ± 7 s at pH 7.0, 32 ± 11 s at pH 6.8, and 46 ± 17 s at pH 6.6). Pi recovery is slowed with aging under acidic conditions, with little or no effect observed at neutral or alkaline pH. These results provide new insights into skeletal muscle metabolic heterogeneity, reflecting how different myofiber microenvironments modulate ATP synthesis. <b>Conclusions:</b> By overcoming the constraints of the single-pool model, the proposed multi-pool framework uncovers pH-dependent ATP synthesis and provides direct evidence of pronounced metabolic heterogeneity in skeletal muscle during exercise and recovery.

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Journal
Diagnostics
Published
2026-03-02
DOI
https://doi.org/10.3390/diagnostics16050744
Primary Topic
Cardiovascular and exercise physiology
Type
article
Field-Weighted Citation Impact
0.00

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article

pH-Resolved ATP Synthesis in Skeletal Muscle: Concept, Implementation, and Assessment Using Dynamic 31P Magnetic Resonance Spectroscopy at 7T

Ren Jimin, Staci Shearin, JARETT BERRY, Wanpen Vongpatanasin et al.
Diagnostics
Cardiovascular and exercise physiology
article

pH-Resolved ATP Synthesis in Skeletal Muscle: Concept, Implementation, and Assessment Using Dynamic 31P Magnetic Resonance Spectroscopy at 7T

Ren Jimin, Staci Shearin, JARETT BERRY, Wanpen Vongpatanasin, N Patel, Ross Querry
article en

Abstract

<b>Background/Objectives:</b> Dynamic changes in inorganic phosphate (Pi), phosphocreatine (PCr), and pH during post-exercise recovery reflect underlying muscle energetics and mitochondrial ATP synthesis, but the conventional single-pool model assuming uniform metabolic response fails to address myofiber composition and pH-dependent metabolic heterogeneity in skeletal muscle. This study aimed to characterize the interplay between pH, Pi, and PCr, and to develop an analytical method for assessing pH-resolved ATP synthesis using <sup>31</sup>P MRS. <b>Methods:</b> Five healthy subjects underwent dynamic <sup>31</sup>P MRS scans during plantar flexion exercise. ATP synthesis was evaluated from post-exercise PCr and Pi recovery time courses using the single-pool model, and from Pi recovery time courses using a multi-pool model in which the Pi signal lineshape was segmented into four pH-specific pools: alkaline (pH 7.3 ± 0.2), neutral (pH 7.0 ± 0.1), mildly acidic (pH 6.8 ± 0.1), and moderately acidic (pH 6.6 ± 0.1). <b>Results:</b> The single-pool model showed that during exercise, Pi increased proportionally to PCr depletion, and both Pi and PCr recovered monoexponentially immediately after exercise with τPi 33±9 s<τPCr (40 ±9 s); ATP remained stable while pH exhibited a "heart-beat" pattern, characterized by an initial alkalization followed by neutralization during exercise, a post-exercise acidic undershoot, and a subsequent slow recovery (τpH≫τPCr). The four-pool model demonstrated a pronounced pH dependence of Pi recovery, with slower recovery at lower pH (τPi: 19 ± 6 s at pH 7.3, 25 ± 7 s at pH 7.0, 32 ± 11 s at pH 6.8, and 46 ± 17 s at pH 6.6). Pi recovery is slowed with aging under acidic conditions, with little or no effect observed at neutral or alkaline pH. These results provide new insights into skeletal muscle metabolic heterogeneity, reflecting how different myofiber microenvironments modulate ATP synthesis. <b>Conclusions:</b> By overcoming the constraints of the single-pool model, the proposed multi-pool framework uncovers pH-dependent ATP synthesis and provides direct evidence of pronounced metabolic heterogeneity in skeletal muscle during exercise and recovery.

DiagnosticsVol. 16(5)
The University of Texas at Tyler (US), Southwestern Medical Center (US), Advanced Imaging Research (United States) (US), The University of Texas Southwestern Medical Center (US)
University of Texas Southwestern Medical Center, Associazione Italiana per la Ricerca sul Cancro, National Institutes of Health
Openalex Percentile: Top 35%
Cardiovascular and exercise physiology
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