d-Pro2-Endomorphin-1 andd-Pro2-Endomorphin-2, Respectively, Attenuate the Antinociception Induced by Endomorphin-1 and Endomorphin-2 Given Intrathecally in the Mouse-Reference-Cited by-同舟云学术

d-Pro2-Endomorphin-1 andd-Pro2-Endomorphin-2, Respectively, Attenuate the Antinociception Induced by Endomorphin-1 and Endomorphin-2 Given Intrathecally in the Mouse

Published:2002-11-01 Issue:2 Volume:303 Page:874-879
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Hung Kuei-chun,Wu Hsiang-en,Mizoguchi Hirokazu,Sakurada Shinobu,Okayama Toru,Fujimura Tsutomu,Murayama Kimie,Sakurada Tsukasa,Fujimoto James M.,Tseng Leon F.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference24 articles.

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3. Pharmacological characterization of endomorphin-1 and endomorphin-2 in mouse brain.;Goldberg;J Pharmacol Exp Ther,1998

4. Isolation of Relatively Large Amounts of Endomorphin-1 and Endomorphin-2 From Human Brain Cortex

5. Intrathecal morphine in mice: a new technique.;Hylden;Eur J Pharmacol,1980

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4. A Tyr-W-MIF-1 analog containing d-Pro2 discriminates among antinociception in mice mediated by different classes of μ-opioid receptors;European Journal of Pharmacology;2007-06

5. Endomorphin 1[ψ] and endomorphin 2[ψ], endomorphins analogues containing a reduced (CH2NH) amide bond between Tyr1 and Pro2, display partial agonist potency but significant antinociception;Life Sciences;2005-07