Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2808466 | Neuropeptides | 2006 | 11 Pages |
Abstract
In all patients CSF concentrations of N-acetyl-β-endorphin IRM and β-lipotropin IRM were found to be increased after terminating the propofol infusion with spinal anesthesia still effective at tB. Patients did not feel pain at times tA, tB or tD; however, they reported moderate to considerable pain at tC. There were no correlations of postoperative pain severity at tC with ACTH, β-endorphin(1-31) or N-acetyl-β-endorphin IRM concentrations in CSF. In contrast, we observed significant inverse correlations (Spearman's rank correlation coefficients between â0.83 and â0.85, p < 0.01) for postoperative pain severity with β-lipotropin IRM concentrations in CSF at tC, and, in addition, at tA, tB and tD; thus, postoperative pain severity appeared to be dependent on a central system controlling sensitivity to pain, linked to a POMC system releasing β-lipotropin IRM into CSF and already active at times tA and tB. We conclude that β-lipotropin IRM in CSF might be considered to serve as a predictor of sensitivity to postoperative pain.
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Authors
Reginald Matejec, Axel Schulz, Jörg Mühling, Holger Uhlich, Rolf-Hasso Bödeker, Gunter Hempelmann, Hansjörg Teschemacher,