Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men: No protective effect of anti-inflammatory medication

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Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men : No protective effect of anti-inflammatory medication. / Dideriksen, K.; Reitelseder, S.; Boesen, A. P.; Zillmer, M.; Agergaard, J.; Kjaer, M.; Holm, L.

In: Physiological Reports, Vol. 12, No. 4, e15958, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Dideriksen, K, Reitelseder, S, Boesen, AP, Zillmer, M, Agergaard, J, Kjaer, M & Holm, L 2024, 'Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men: No protective effect of anti-inflammatory medication', Physiological Reports, vol. 12, no. 4, e15958. https://doi.org/10.14814/phy2.15958

APA

Dideriksen, K., Reitelseder, S., Boesen, A. P., Zillmer, M., Agergaard, J., Kjaer, M., & Holm, L. (2024). Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men: No protective effect of anti-inflammatory medication. Physiological Reports, 12(4), [e15958]. https://doi.org/10.14814/phy2.15958

Vancouver

Dideriksen K, Reitelseder S, Boesen AP, Zillmer M, Agergaard J, Kjaer M et al. Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men: No protective effect of anti-inflammatory medication. Physiological Reports. 2024;12(4). e15958. https://doi.org/10.14814/phy2.15958

Author

Dideriksen, K. ; Reitelseder, S. ; Boesen, A. P. ; Zillmer, M. ; Agergaard, J. ; Kjaer, M. ; Holm, L. / Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men : No protective effect of anti-inflammatory medication. In: Physiological Reports. 2024 ; Vol. 12, No. 4.

Bibtex

@article{f8a49936516c427987a5bc7265b1413d,
title = "Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men: No protective effect of anti-inflammatory medication",
abstract = "Muscle inactivity may reduce basal and postprandial muscle protein synthesis (MPS) rates in humans. Anti-inflammatory treatment alleviates the MPS impairments in younger individuals. The present study explored the influence of nonsteroidal anti-inflammatory drugs (NSAIDs) upon MPS during a period of inactivity in older humans. Eighteen men (age 60–80 years) were allocated to ibuprofen (1200 mg/day, Ibu) or control (Plc) groups. One lower limb was cast immobilized for 2 weeks. Postabsorptive and postprandial MPS was measured before and after the immobilization by L-[ring-13C6]-phenylalanine infusion. The protein expression of select anabolic signaling molecules was investigated by western blot. Basal (0.038 ± 0.002%/h and 0.039 ± 0.005%/h, Plc and Ibu, respectively) and postprandial (0.064 ± 0.004%/h and 0.067 ± 0.010%/h, Plc and Ibu, respectively) MPS rate were higher pre-immobilization compared to basal (0.019 ± 0.005%/h and 0.020 ± 0.010%/h, Plc and Ibu, respectively) and postprandial (0.033 ± 0.005%/h and 0.037 ± 0.006%/h, Plc and Ibu, respectively) MPS rate post-immobilization (p < 0.001). NSAID treatment did not affect the suppression of MPS (p > 0.05). The anabolic signaling were in general reduced after immobilization (p < 0.05). These changes were unaffected by NSAID treatment (p > 0.05). Basal and postprandial MPS dropped markedly after 2 weeks of lower limb immobilization. NSAID treatment neither influenced the reduction in MPS nor the anabolic signaling after immobilization in healthy older individuals.",
keywords = "anabolic resistance, ibuprofen, muscle disuse, muscle inactivity, muscle protein synthesis signaling, myofibrillar FSR",
author = "K. Dideriksen and S. Reitelseder and Boesen, {A. P.} and M. Zillmer and J. Agergaard and M. Kjaer and L. Holm",
note = "Publisher Copyright: {\textcopyright} 2024 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.",
year = "2024",
doi = "10.14814/phy2.15958",
language = "English",
volume = "12",
journal = "Physiological Reports",
issn = "2051-817X",
publisher = "Wiley Periodicals, Inc.",
number = "4",

}

RIS

TY - JOUR

T1 - Lower basal and postprandial muscle protein synthesis after 2 weeks single-leg immobilization in older men

T2 - No protective effect of anti-inflammatory medication

AU - Dideriksen, K.

AU - Reitelseder, S.

AU - Boesen, A. P.

AU - Zillmer, M.

AU - Agergaard, J.

AU - Kjaer, M.

AU - Holm, L.

N1 - Publisher Copyright: © 2024 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.

PY - 2024

Y1 - 2024

N2 - Muscle inactivity may reduce basal and postprandial muscle protein synthesis (MPS) rates in humans. Anti-inflammatory treatment alleviates the MPS impairments in younger individuals. The present study explored the influence of nonsteroidal anti-inflammatory drugs (NSAIDs) upon MPS during a period of inactivity in older humans. Eighteen men (age 60–80 years) were allocated to ibuprofen (1200 mg/day, Ibu) or control (Plc) groups. One lower limb was cast immobilized for 2 weeks. Postabsorptive and postprandial MPS was measured before and after the immobilization by L-[ring-13C6]-phenylalanine infusion. The protein expression of select anabolic signaling molecules was investigated by western blot. Basal (0.038 ± 0.002%/h and 0.039 ± 0.005%/h, Plc and Ibu, respectively) and postprandial (0.064 ± 0.004%/h and 0.067 ± 0.010%/h, Plc and Ibu, respectively) MPS rate were higher pre-immobilization compared to basal (0.019 ± 0.005%/h and 0.020 ± 0.010%/h, Plc and Ibu, respectively) and postprandial (0.033 ± 0.005%/h and 0.037 ± 0.006%/h, Plc and Ibu, respectively) MPS rate post-immobilization (p < 0.001). NSAID treatment did not affect the suppression of MPS (p > 0.05). The anabolic signaling were in general reduced after immobilization (p < 0.05). These changes were unaffected by NSAID treatment (p > 0.05). Basal and postprandial MPS dropped markedly after 2 weeks of lower limb immobilization. NSAID treatment neither influenced the reduction in MPS nor the anabolic signaling after immobilization in healthy older individuals.

AB - Muscle inactivity may reduce basal and postprandial muscle protein synthesis (MPS) rates in humans. Anti-inflammatory treatment alleviates the MPS impairments in younger individuals. The present study explored the influence of nonsteroidal anti-inflammatory drugs (NSAIDs) upon MPS during a period of inactivity in older humans. Eighteen men (age 60–80 years) were allocated to ibuprofen (1200 mg/day, Ibu) or control (Plc) groups. One lower limb was cast immobilized for 2 weeks. Postabsorptive and postprandial MPS was measured before and after the immobilization by L-[ring-13C6]-phenylalanine infusion. The protein expression of select anabolic signaling molecules was investigated by western blot. Basal (0.038 ± 0.002%/h and 0.039 ± 0.005%/h, Plc and Ibu, respectively) and postprandial (0.064 ± 0.004%/h and 0.067 ± 0.010%/h, Plc and Ibu, respectively) MPS rate were higher pre-immobilization compared to basal (0.019 ± 0.005%/h and 0.020 ± 0.010%/h, Plc and Ibu, respectively) and postprandial (0.033 ± 0.005%/h and 0.037 ± 0.006%/h, Plc and Ibu, respectively) MPS rate post-immobilization (p < 0.001). NSAID treatment did not affect the suppression of MPS (p > 0.05). The anabolic signaling were in general reduced after immobilization (p < 0.05). These changes were unaffected by NSAID treatment (p > 0.05). Basal and postprandial MPS dropped markedly after 2 weeks of lower limb immobilization. NSAID treatment neither influenced the reduction in MPS nor the anabolic signaling after immobilization in healthy older individuals.

KW - anabolic resistance

KW - ibuprofen

KW - muscle disuse

KW - muscle inactivity

KW - muscle protein synthesis signaling

KW - myofibrillar FSR

U2 - 10.14814/phy2.15958

DO - 10.14814/phy2.15958

M3 - Journal article

C2 - 38406891

AN - SCOPUS:85186213870

VL - 12

JO - Physiological Reports

JF - Physiological Reports

SN - 2051-817X

IS - 4

M1 - e15958

ER -

ID: 384607703