TY - JOUR
T1 - Endogenous opioid peptide responses to opioid and anti-inflammatory medications following eccentric exercise-induced muscle damage
AU - Kraemer, William J.
AU - Joseph, Michael F.
AU - Volek, Jeff S.
AU - Hoffman, Jay R.
AU - Ratamess, Nicholas A.
AU - Newton, Robert U.
AU - Fragala, Maren S.
AU - French, Duncan N.
AU - Rubin, Martyn A.
AU - Scheett, Timothy P.
AU - McGuigan, Michael R.
AU - Thomas, Gwendolyn A.
AU - Gomez, Ana L.
AU - Häkkinen, Keijo
AU - Maresh, Carl M.
N1 - Funding Information:
This study was supported in part by a grant from Knoll Pharmaceuticals Corporation now Abbott Laboratories, Abbott Park, IL, USA. We thank all of the participants and laboratory and medical staffs for their dedicated work on this project.
PY - 2010/1
Y1 - 2010/1
N2 - To determine the effects of Vicoprofen®, Ibuprofen, and a placebo on the responses of endogenous opioid peptides following eccentric exercise-induced muscle damage 36 healthy men (age: 22.8 years; height: 178.8 ± 6.2 cm; body mass: 78.9 ± 13.7 kg; body fat: 15.8 ± 6.5%) volunteered to participate in the study. Each participant was evaluated for pain 24 h post and randomly assigned to an experimental group: VIC (Vicoprofen®), IBU (Ibuprofen), or P (placebo). Medication was given four times daily (i.e., VIC (hydrocodone bitartrate 7.5 mg with Ibuprofen 200 mg) and IBU 200 mg). Blood was obtained at rest and at 0, 24, 48, 72, 96 and 120 h following the eccentric exercise damage protocol. No significant changes for B-END were observed in the resting values over the recovery period among any of the treatment conditions. Conversely for plasma P-F, VIC and IBU had significantly (P < 0.05) higher plasma concentrations of P-F above placebo at 24, 48, 72, and 96 and 120 h with VIC higher than IBU and placebo conditions at 48, 72, 96, and 120 h. Significant resting elevations were observed for P-F from pre-exercise at 48, 72, 96, and 120 h for VIC; at 72 and 96 h for IBU and no changes in the placebo treatment. Less tissue damage (MRI analyses), improved physical function as well as reduced pain was observed for the VIC condition over IBU and placebo. These data indicate that exogenous medications appear to be differentially stimulating the peripheral (adrenal medulla) opioid neuroendocrine responses as measured by plasma concentrations.
AB - To determine the effects of Vicoprofen®, Ibuprofen, and a placebo on the responses of endogenous opioid peptides following eccentric exercise-induced muscle damage 36 healthy men (age: 22.8 years; height: 178.8 ± 6.2 cm; body mass: 78.9 ± 13.7 kg; body fat: 15.8 ± 6.5%) volunteered to participate in the study. Each participant was evaluated for pain 24 h post and randomly assigned to an experimental group: VIC (Vicoprofen®), IBU (Ibuprofen), or P (placebo). Medication was given four times daily (i.e., VIC (hydrocodone bitartrate 7.5 mg with Ibuprofen 200 mg) and IBU 200 mg). Blood was obtained at rest and at 0, 24, 48, 72, 96 and 120 h following the eccentric exercise damage protocol. No significant changes for B-END were observed in the resting values over the recovery period among any of the treatment conditions. Conversely for plasma P-F, VIC and IBU had significantly (P < 0.05) higher plasma concentrations of P-F above placebo at 24, 48, 72, and 96 and 120 h with VIC higher than IBU and placebo conditions at 48, 72, 96, and 120 h. Significant resting elevations were observed for P-F from pre-exercise at 48, 72, 96, and 120 h for VIC; at 72 and 96 h for IBU and no changes in the placebo treatment. Less tissue damage (MRI analyses), improved physical function as well as reduced pain was observed for the VIC condition over IBU and placebo. These data indicate that exogenous medications appear to be differentially stimulating the peripheral (adrenal medulla) opioid neuroendocrine responses as measured by plasma concentrations.
KW - Opiate-like
KW - Peptide F
KW - Proenkephalin
KW - Recovery
KW - Stress
KW - β-Endorphin
UR - http://www.scopus.com/inward/record.url?scp=72749103892&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=72749103892&partnerID=8YFLogxK
U2 - 10.1016/j.peptides.2009.09.031
DO - 10.1016/j.peptides.2009.09.031
M3 - Article
C2 - 19800931
AN - SCOPUS:72749103892
SN - 0196-9781
VL - 31
SP - 88
EP - 93
JO - Peptides
JF - Peptides
IS - 1
ER -