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Items: 1 to 20 of 102

1.

The action site of the synthetic kainoid (2S,3R,4R)-3-carboxymethyl-4-(4-methylphenylthio)pyrrolidine-2-carboxylic acid (PSPA-4), an analogue of Japanese mushroom poison acromelic acid, for allodynia (tactile pain).

Miyazaki S, Minami T, Mizuma H, Kanazawa M, Doi H, Matsumura S, Lu J, Onoe H, Furuta K, Suzuki M, Ito S.

Eur J Pharmacol. 2013 Jun 15;710(1-3):120-7. doi: 10.1016/j.ejphar.2012.10.023. Epub 2012 Nov 1.

PMID:
23124023
2.

A synthetic kainoid, (2S,3R,4R)-3-carboxymethyl-4-(phenylthio)pyrrolidine-2-carboxylic acid (PSPA-1) serves as a novel anti-allodynic agent for neuropathic pain.

Soen M, Minami T, Tatsumi S, Mabuchi T, Furuta K, Maeda M, Suzuki M, Ito S.

Eur J Pharmacol. 2007 Dec 1;575(1-3):75-81. Epub 2007 Aug 19.

PMID:
17826764
3.

Acute and late effects on induction of allodynia by acromelic acid, a mushroom poison related structurally to kainic acid.

Minami T, Matsumura S, Nishizawa M, Sasaguri Y, Hamanaka N, Ito S.

Br J Pharmacol. 2004 Jun;142(4):679-88. Epub 2004 May 24.

4.

Comparison of mechanisms of allodynia induced by acromelic acid A between early and late phases.

Omoto H, Matsumura S, Kitano M, Miyazaki S, Minami T, Ito S.

Eur J Pharmacol. 2015 Aug 5;760:42-8. doi: 10.1016/j.ejphar.2015.03.075. Epub 2015 Apr 8.

PMID:
25861935
6.

Presynaptic kainate receptors regulate spinal sensory transmission.

Kerchner GA, Wilding TJ, Li P, Zhuo M, Huettner JE.

J Neurosci. 2001 Jan 1;21(1):59-66.

7.

A marked increase in intracellular Ca2+ concentration induced by acromelic acid in cultured rat spinal neurons.

Ogata T, Nakamura Y, Tsuji K, Shibata T, Kataoka K, Ishida M, Shinozaki H.

Neuropharmacology. 1994 Sep;33(9):1079-85.

PMID:
7838320
9.
10.
11.

Desensitization of kainate receptors by kainate, glutamate and diastereomers of 4-methylglutamate.

Jones KA, Wilding TJ, Huettner JE, Costa AM.

Neuropharmacology. 1997 Jun;36(6):853-63.

PMID:
9225313
12.

Excitatory actions of mushroom poison (acromelic acid) on unmyelinated muscular afferents in the rat.

Taguchi T, Tomotoshi K, Mizumura K.

Neurosci Lett. 2009 Jun 5;456(2):69-73. doi: 10.1016/j.neulet.2009.03.102. Epub 2009 Apr 5.

PMID:
19429136
13.
14.

New, potent kainate derivatives: comparison of their affinity for [3H]kainate and [3H]AMPA binding sites.

Kwak S, Aizawa H, Ishida M, Shinozaki H.

Neurosci Lett. 1992 May 11;139(1):114-7.

PMID:
1341901
16.

Synthesis of an acromelic acid A analog-based 11C-labeled PET tracer for exploration of the site of action of acromelic acid A in allodynia induction.

Kanazawa M, Furuta K, Doi H, Mori T, Minami T, Ito S, Suzuki M.

Bioorg Med Chem Lett. 2011 Apr 1;21(7):2017-20. doi: 10.1016/j.bmcl.2011.02.018. Epub 2011 Feb 25.

PMID:
21354794
17.

Regional distribution of low affinity kainate receptors in brain of Macaca fascicularis determined by autoradiography using [3H](2S,4R)-4-methylglutamate.

Carroll FY, Finkelstein DI, Horne MK, Lawrence AJ, Crawford D, Paxinos G, Beart PM.

Neurosci Lett. 1998 Oct 16;255(2):71-4.

PMID:
9835217
18.
19.

LY339434, a GluR5 kainate receptor agonist.

Small B, Thomas J, Kemp M, Hoo K, Ballyk B, Deverill M, Ogden AM, Rubio A, Pedregal C, Bleakman D.

Neuropharmacology. 1998 Oct-Nov;37(10-11):1261-7.

PMID:
9849663
20.

Dicarboxyphenylglycines antagonize AMPA- but not kainate-induced depolarizations in neonatal rat motoneurones.

Thomas NK, Clayton P, Jane DE.

Eur J Pharmacol. 1997 Nov 5;338(2):111-6.

PMID:
9455991

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