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Tifluadom (KC 5103) induces suppression and latency changes on somatosensory evoked potentials which are reversed by opioid antagonists.

作者信息

Freye E, Hartung E, Schenk G K

出版信息

Life Sci. 1983;33 Suppl 1:537-40. doi: 10.1016/0024-3205(83)90559-3.

DOI:10.1016/0024-3205(83)90559-3
PMID:6319908
Abstract

Suppression of evoked potentials of the EEG are indicators of analgesia. Tifluadom induces latency changes which are reversed by the kappa-antagonist Mr 2266. Naloxone reverses peak suppression which indicates an additional interaction with the my-opioid-receptor. The specific benzodiazepine antagonist Ro 15-1788 is not effective in reversing peak-changes. Therefore nociceptive stimuli are modulated by tifluadom not only through the interaction with kappa- but also with my-opioid-receptors.

摘要

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