Cellular mechanism for anti-analgesic action of agonists of the κ-opioid receptor

Author:

Pan Z. Z.,Tershner S. A.,Fields H. L.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference29 articles.

1. Matthes, H. W. D. et al. Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the μ-opioid-receptor gene. Nature 383, 819–823 (1996).

2. Reisine, T. & Pasternak, G. in Goodman and Gilman's the Pharmacological Basis of Therapeutics (eds Hardman, J. G. & Limbird, L. E.) 521–555 (McGraw-Hill, New York, (1996)).

3. Zadina, J. E., Hackler, L., Ge, L.-J. & Kastin, A. J. Apotent and selective endogenous agonist for the μ-opiate receptor. Nature 386, 499–502 (1997).

4. Bhargava, H. N. Diversity of agents that modify opioid tolerance, physical dependence, abstinence syndrome and self-administrative behavior. Pharmacol. Rev. 46, 293–324 (1994).

5. Millan, M. J. κ-Opioid receptors and analgesia. Trends Pharmacol. Sci. 11, 70–76 (1990).

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