MAP Kinase Phosphatase-5 Deficiency Improves Endurance Exercise Capacity

Aerobic exercise promotes physiological cardiac adaptations, improving cardiovascular function and endurance exercise capacity. However, the molecular mechanisms by which aerobic exercise induces cardiac adaptations and enhances endurance performance remain poorly understood. Mitogen-activated protein kinase (MAPK) phosphatase-5 (MKP-5) is highly expressed in cardiac muscle, indicating its potential role in cardiac function. This study investigates the role of MKP-5 in early molecular response to aerobic exercise in cardiac muscle using MKP-5-deficient (<i>Mkp-5<sup>-/-</sup></i>) and wild-type (<i>Mkp-5<sup>+/+</sup></i>) mice. Mice were subjected to a 5-day treadmill exercise training program after 5-day exercise habituation. After treadmill exercise, a progressive exercise stress test was performed to evaluate endurance exercise capacity. Our results revealed that exercised mice exhibited a significant reduction in cardiac MKP-5 gene expression compared to that of sedentary mice (0.19 ± 5.89-fold; <i>p</i> < 0.0001). <i>Mkp-5<sup>-/-</sup></i> mice achieved significantly greater endurance, with a running distance (2.81 ± 169.8-fold; <i>p</i> < 0.0429) longer than <i>Mkp-5<sup>+/+</sup></i> mice. Additionally, MKP-5 deficiency enhanced Akt/mTOR signaling (p-Akt/Akt: 1.29 ± 0.12-fold; <i>p</i> = 0.04; p-mTOR/mTOR: 1.59 ± 0.14-fold; <i>p</i> = 0.002) and mitochondrial biogenesis (<i>pgc-1α</i>: 1.56 ± 0.27-fold; <i>p</i> = 0.03) in cardiac muscle in response to aerobic exercise. Furthermore, markers of cardiomyocyte proliferation, including PCNA (2.24 ± 0.31-fold; <i>p</i> < 0.001), GATA4 (1.47 ± 0.10-fold; <i>p</i> < 0.001), and CITED4 (2.03 ± 0.15-fold; <i>p</i> < 0.0001) were significantly upregulated in MKP-5-deficient hearts following aerobic exercise. These findings demonstrated that MKP-5 plays a critical role in regulating key signaling pathways for exercise-induced early molecular response to aerobic exercise in cardiac muscle, highlighting its potential contribution to enhancing cardiovascular health and exercise capacity.

Authors

Institutions

Publication Details

Journal
Cells
Published
2025-03-11
DOI
https://doi.org/10.3390/cells14060410
Citations
2
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
1.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

MAP Kinase Phosphatase-5 Deficiency Improves Endurance Exercise Capacity

Jaime A. Perales, Sung Min Han, Sudip Bajpeyi, Ahmed Lawan et al.
2 citations
Cells
Mitochondrial Function and Pathology
1.61
article

MAP Kinase Phosphatase-5 Deficiency Improves Endurance Exercise Capacity

Jaime A. Perales, Sung Min Han, Sudip Bajpeyi, Ahmed Lawan, Anton M. Bennett, Kisuk Min
article en
2 citations

Abstract

Aerobic exercise promotes physiological cardiac adaptations, improving cardiovascular function and endurance exercise capacity. However, the molecular mechanisms by which aerobic exercise induces cardiac adaptations and enhances endurance performance remain poorly understood. Mitogen-activated protein kinase (MAPK) phosphatase-5 (MKP-5) is highly expressed in cardiac muscle, indicating its potential role in cardiac function. This study investigates the role of MKP-5 in early molecular response to aerobic exercise in cardiac muscle using MKP-5-deficient (<i>Mkp-5<sup>-/-</sup></i>) and wild-type (<i>Mkp-5<sup>+/+</sup></i>) mice. Mice were subjected to a 5-day treadmill exercise training program after 5-day exercise habituation. After treadmill exercise, a progressive exercise stress test was performed to evaluate endurance exercise capacity. Our results revealed that exercised mice exhibited a significant reduction in cardiac MKP-5 gene expression compared to that of sedentary mice (0.19 ± 5.89-fold; <i>p</i> < 0.0001). <i>Mkp-5<sup>-/-</sup></i> mice achieved significantly greater endurance, with a running distance (2.81 ± 169.8-fold; <i>p</i> < 0.0429) longer than <i>Mkp-5<sup>+/+</sup></i> mice. Additionally, MKP-5 deficiency enhanced Akt/mTOR signaling (p-Akt/Akt: 1.29 ± 0.12-fold; <i>p</i> = 0.04; p-mTOR/mTOR: 1.59 ± 0.14-fold; <i>p</i> = 0.002) and mitochondrial biogenesis (<i>pgc-1α</i>: 1.56 ± 0.27-fold; <i>p</i> = 0.03) in cardiac muscle in response to aerobic exercise. Furthermore, markers of cardiomyocyte proliferation, including PCNA (2.24 ± 0.31-fold; <i>p</i> < 0.001), GATA4 (1.47 ± 0.10-fold; <i>p</i> < 0.001), and CITED4 (2.03 ± 0.15-fold; <i>p</i> < 0.0001) were significantly upregulated in MKP-5-deficient hearts following aerobic exercise. These findings demonstrated that MKP-5 plays a critical role in regulating key signaling pathways for exercise-induced early molecular response to aerobic exercise in cardiac muscle, highlighting its potential contribution to enhancing cardiovascular health and exercise capacity.

CellsVol. 14(6)
The University of Texas at El Paso (US), Yale University (US), University of Florida (US), University of Alabama in Huntsville (US)
Openalex Percentile: Top 19%
Mitochondrial Function and Pathology
1.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.