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Tan-No, K. et al.

Koichi Tan-No, Masakazu Shimoda, Mai Sugawara, Osamu Nakagawasai, Fukie Niijima, Hiromi Watanabe, Seiichi Furuta, Takumi Sato, Susumu Satoh, Yuichiro Arai, Jolanta Kotlinska, Jerzy Silberring, Lars Terenius, Takeshi Tadano,

Cysteine protease inhibitors suppress the development of tolerance to morphine antinociception.

The effects of various protease inhibitors on the development of antinociceptive tolerance to morphine were examined in mice. Intrathecal (i.t.) administration of morphine (0.01-1 nmol) produced a dose-dependent and significant antinociceptive effect in the 0.5% formalin test. When the doses of morphine (mg/kg, s.c. per injection) were given as pretreatment twice daily for two days [first day (30) and second day (60)], i.t. administration of morphine (0.1 nmol) was inactive due to antinociceptive tolerance on the third day. Tolerance to i.t. morphine was significantly suppressed by the i.t. injection of N-ethylmaleimide or Boc-Tyr-Gly-NHO-Bz, inhibitors of cysteine proteases involved in dynorphin degradation, as well as by dynorphin A, dynorphin B and (-) U-50,488, a selective kappa-opioid receptor agonist. On the other hand, amastatin, an aminopeptidase inhibitor, phosphoramidon, an endopeptidase 24.11 inhibitor, lisinopril, an angiotensin-converting enzyme inhibitor, and phenylmethanesulfonyl fluoride, a serine protease inhibitor, were inactive. These results suggest that cysteine protease inhibitors suppress the development of morphine tolerance presumably through the inhibition of dynorphin degradation.[1]

References

Cysteine protease inhibitors suppress the development of tolerance to morphine antinociception. Tan-No, K., Shimoda, M., Sugawara, M., Nakagawasai, O., Niijima, F., Watanabe, H., Furuta, S., Sato, T., Satoh, S., Arai, Y., Kotlinska, J., Silberring, J., Terenius, L., Tadano, T. Neuropeptides (2008) [Pubmed]

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