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Updated: Dec 24, 2025

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An in vivo Rodent Model of Contraction-induced Injury and Non-invasive Monitoring of Recovery
Published on: May 11, 2011
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Early pH Changes in Musculoskeletal Tissues upon Injury-Aerobic Catabolic Pathway Activity Linked to Inter-Individual
Julia C Berkmann1,2, Aaron X Herrera Martin1,2, Agnes Ellinghaus3
1Julius Wolff Institut, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.
International Journal of Molecular Sciences
|April 9, 2020
Summary
Musculoskeletal injuries cause local tissue acidification in bone and muscle hematomas. This pH drop, linked to metabolic activity, may offer new therapeutic opportunities for controlled drug delivery.
Area of Science:
- Biomedical Engineering
- Orthopedics
- Regenerative Medicine
Background:
- Local pH changes are known to occur after bone fracture, but the kinetics and extent are unclear.
- It is unknown if pH acidification in fracture hematomas extends to adjacent muscle hematomas or is unique to bone healing.
Purpose of the Study:
- To investigate the in vivo pH changes in bone and muscle hematomas during the early phase after musculoskeletal injury.
- To determine the extent and pattern of acidification in preclinical models.
Main Methods:
- Simultaneous in vivo pH measurements in sheep and rat models post-fracture and muscle trauma (up to 48 hours).
- Histological and metabolomic analysis of rat fracture hematomas.
- In vivo pH monitoring in bone and muscle hematomas.
Main Results:
- Local acidification was observed in both bone and muscle hematomas in both animal models.
- Mean pH values in rat hematomas were 6.69 (bone) and 6.89 (muscle), with significant variations.
- Metabolomic data suggested a correlation between reduced tricarboxylic acid cycle activity and pH, indicating metabolic activity as a potential cause.
Conclusions:
- Early musculoskeletal hematomas exhibit significant local acidification.
- The observed pH changes are linked to metabolic processes within the injured tissue.
- This early acidification presents a potential target for developing novel therapies with spatially and temporally controlled drug release.
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