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Journal Abstract Search

468 related items for PubMed ID: 18571771

  • 21. Nonopioidergic mechanism mediating morphine-induced antianalgesia in the mouse spinal cord.
    Wu HE, Thompson J, Sun HS, Leitermann RJ, Fujimoto JM, Tseng LF.
    J Pharmacol Exp Ther; 2004 Jul; 310(1):240-6. PubMed ID: 14999057
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  • 23. Differentiation of opioid receptor preference by [Dmt1]endomorphin-2-mediated antinociception in the mouse.
    Jinsmaa Y, Fujita Y, Shiotani K, Miyazaki A, Li T, Tsuda Y, Okada Y, Ambo A, Sasaki Y, Bryant SD, Lazarus LH.
    Eur J Pharmacol; 2005 Feb 10; 509(1):37-42. PubMed ID: 15713427
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  • 24. Structure-constrained endomorphin analogs display differential antinociceptive mechanisms in mice after spinal administration.
    Wang Y, Zhou J, Liu X, Zhao L, Wang Z, Zhang X, Wang K, Wang L, Wang R.
    Peptides; 2017 May 10; 91():40-48. PubMed ID: 28363796
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  • 26. The antinociceptive properties of endomorphin-1 and endomorphin-2 in the mouse.
    Tseng LF.
    Jpn J Pharmacol; 2002 Jul 10; 89(3):216-20. PubMed ID: 12184724
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  • 32. The spinal antinociceptive effects of endomorphins in rats: behavioral and G protein functional studies.
    Xie H, Woods JH, Traynor JR, Ko MC.
    Anesth Analg; 2008 Jun 10; 106(6):1873-81. PubMed ID: 18499626
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  • 33. Distinct physiological role of amidino-TAPA-sensitive and DAMGO-insensitive μ-opioid receptor splice variants in the mouse spinal cord.
    Mizoguchi H, Watanabe C, Higashiya T, Takeda S, Moriyama K, Aoki Y, Kon-no T, Takagi H, Yonezawa A, Sato T, Sakurada T, Sakurada S.
    Eur J Pharmacol; 2013 Jul 05; 711(1-3):80-6. PubMed ID: 23623932
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  • 35. Spinal pretreatment with antisense oligodeoxynucleotides against exon-1, -4, or -8 of mu-opioid receptor clone leads to differential loss of spinal endomorphin-1-and endomorphin-2-induced antinociception in the mouse.
    Wu HE, Mizoguchi H, Terashvili M, Leitermann RJ, Hung KC, Fujimoto JM, Tseng LF.
    J Pharmacol Exp Ther; 2002 Nov 05; 303(2):867-73. PubMed ID: 12388674
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  • 36. Kappa1- and kappa2-opioid receptors mediating presynaptic inhibition of dopamine and acetylcholine release in rat neostriatum.
    Schoffelmeer AN, Hogenboom F, Mulder AH.
    Br J Pharmacol; 1997 Oct 05; 122(3):520-4. PubMed ID: 9351509
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  • 37. Dynorphin A-(1-13) potently improves the impairment of spontaneous alternation performance induced by the mu-selective opioid receptor agonist DAMGO in mice.
    Itoh J, Ukai M, Kameyama T.
    J Pharmacol Exp Ther; 1994 Apr 05; 269(1):15-21. PubMed ID: 7909556
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  • 40. Different motivational effects induced by the endogenous mu-opioid receptor ligands endomorphin-1 and -2 in the mouse.
    Narita M, Ozaki S, Ioka M, Mizoguchi H, Nagase H, Tseng LF, Suzuki T.
    Neuroscience; 2001 Apr 05; 105(1):213-8. PubMed ID: 11483313
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