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Items: 1 to 20 of 121

1.

Differential antinociceptive effects of intrathecal administration of C-terminal esterified endomorphin-2 analogues in mice.

Wang CL, Xiang Q, Diao YX, Ren YK, Gu N.

Eur J Pain. 2014 Sep;18(8):1157-64. doi: 10.1002/j.1532-2149.2014.00462.x. Epub 2014 Feb 21.

PMID:
24677379
2.

The antinociceptive properties of endomorphin-1 and endomorphin-2 in the mouse.

Tseng LF.

Jpn J Pharmacol. 2002 Jul;89(3):216-20. Review.

3.
4.

Possible involvement of dynorphin A-(1-17) release via mu1-opioid receptors in spinal antinociception by endomorphin-2.

Mizoguchi H, Watanabe H, Hayashi T, Sakurada W, Sawai T, Fujimura T, Sakurada T, Sakurada S.

J Pharmacol Exp Ther. 2006 Apr;317(1):362-8. Epub 2006 Jan 4.

5.

Dynorphinergic mechanism mediating endomorphin-2-induced antianalgesia in the mouse spinal cord.

Wu HE, Sun HS, Darpolar M, Leitermann RJ, Kampine JP, Tseng LF.

J Pharmacol Exp Ther. 2003 Dec;307(3):1135-41. Epub 2003 Oct 13.

6.

Differential antinociception induced by spinally administered endomorphin-1 and endomorphin-2 in the mouse.

Ohsawa M, Mizoguchi H, Narita M, Nagase H, Kampine JP, Tseng LF.

J Pharmacol Exp Ther. 2001 Aug;298(2):592-7.

7.

Differential antinociceptive effects induced by intrathecally administered endomorphin-1 and endomorphin-2 in the mouse.

Sakurada S, Hayashi T, Yuhki M, Orito T, Zadina JE, Kastin AJ, Fujimura T, Murayama K, Sakurada C, Sakurada T, Narita M, Suzuki T, Tan-no K, Tseng LF.

Eur J Pharmacol. 2001 Sep 21;427(3):203-10.

PMID:
11567650
8.

A Tyr-W-MIF-1 analog containing D-Pro2 discriminates among antinociception in mice mediated by different classes of mu-opioid receptors.

Nakayama D, Watanabe C, Watanabe H, Mizoguchi H, Sakurada T, Sakurada S.

Eur J Pharmacol. 2007 Jun 1;563(1-3):109-16. Epub 2007 Feb 8.

PMID:
17343845
10.

Differential antinociceptive effects of endomorphin-1 and endomorphin-2 in the mouse.

Tseng LF, Narita M, Suganuma C, Mizoguchi H, Ohsawa M, Nagase H, Kampine JP.

J Pharmacol Exp Ther. 2000 Feb;292(2):576-83.

11.

Spinal analgesic actions of the new endogenous opioid peptides endomorphin-1 and -2.

Stone LS, Fairbanks CA, Laughlin TM, Nguyen HO, Bushy TM, Wessendorf MW, Wilcox GL.

Neuroreport. 1997 Sep 29;8(14):3131-5.

PMID:
9331928
12.

MGM-9 [(E)-methyl 2-(3-ethyl-7a,12a-(epoxyethanoxy)-9-fluoro-1,2,3,4,6,7,12,12b-octahydro-8-methoxyindolo[2,3-a]quinolizin-2-yl)-3-methoxyacrylate], a derivative of the indole alkaloid mitragynine: a novel dual-acting mu- and kappa-opioid agonist with potent antinociceptive and weak rewarding effects in mice.

Matsumoto K, Takayama H, Narita M, Nakamura A, Suzuki M, Suzuki T, Murayama T, Wongseripipatana S, Misawa K, Kitajima M, Tashima K, Horie S.

Neuropharmacology. 2008 Aug;55(2):154-65. doi: 10.1016/j.neuropharm.2008.05.003. Epub 2008 May 9.

PMID:
18550129
13.

Morphine can produce analgesia via spinal kappa opioid receptors in the absence of mu opioid receptors.

Yamada H, Shimoyama N, Sora I, Uhl GR, Fukuda Y, Moriya H, Shimoyama M.

Brain Res. 2006 Apr 14;1083(1):61-9. Epub 2006 Mar 10.

PMID:
16530171
14.

Analgesic effect of endomorphin-1.

Li ZH, Shan LD, Jiang XH, Guo SY, Yu GD, Hisamitsu T, Yin QZ.

Acta Pharmacol Sin. 2001 Nov;22(11):976-80.

15.

The antinociceptive effects of endomorphin-1 and endomorphin-2 in diabetic mice.

Kamei J, Zushida K, Ohsawa M, Nagase H.

Eur J Pharmacol. 2000 Mar 10;391(1-2):91-6.

PMID:
10720639
16.
17.

5-HT spinal antinociception involves mu opioid receptors: cross tolerance and antagonist studies.

Goodchild CS, Guo Z, Freeman J, Gent JP.

Br J Anaesth. 1997 May;78(5):563-9.

PMID:
9175973
18.
19.

Antinociceptive effects of intrathecal endomorphin-1 and -2 in rats.

Horvath G, Szikszay M, Tömböly C, Benedek G.

Life Sci. 1999;65(24):2635-41.

PMID:
10619371
20.

Characterization of opioid activities of endomorphin analogs with C-terminal amide to hydrazide conversion.

Wang CL, Ren YK, Xiang Q, Wang Y, Gu N, Lu C, Wang R.

Neuropeptides. 2013 Oct;47(5):297-304. doi: 10.1016/j.npep.2013.09.001. Epub 2013 Sep 19.

PMID:
24084335

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