Comparative studies on morphine- and stress-induced analgesia and the development of tolerance to the effects: Implication of protein synthesis mechanism in the process.

TAKAHASHI Masakatsu, IZUMI Reiko, KANETO Hiroshi

doi:10.1254/jjp.37.197

Comparative studies were made on morphine and stress-induced analgesia (SIA) and also on the development of tolerance to the effects. Cycloheximide (CYH), a potent protein synthesis inhibitor, did not affect the analgesic effect of morphine, but effectively suppressed the development of tolerance. CYH, however, potentiated both foot shock (FS) and immobilized-water immersion (IW) SIAs and inhibited the development of tolerance to FS-SIA. Incorporation of ³H-leucine into the TCA-insoluble fraction of mouse brain regions was inhibited by morphine, and the inhibition was reversed by the pretreatment with CYH. The inhibitory effect of morphine was lost in morphine tolerant animals. At the peak of SIA, incorporation of ³H-leucine was not changed in FS-SIA, but significantly inhibited in IW-SIA, and these effects were not modified by the pretreatment with CYH. The reduced incorporation of ³H-leucine in IW-SIA tolerant animals was partially reversed by CYH. Thus, the protein synthesis mechanism is greatly influenced by morphine or stresses, but the direct evidence for the implication of the mechanism in the process of producing analgesia and tolerance formation could not be demonstrated. However, differences in the underlying mechanisms were apparent between morphine and SlAs and also between FS and IW-SIA.

Comparative studies on morphine- and stress-induced analgesia and the development of tolerance to the effects: Implication of protein synthesis mechanism in the process.

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