Honore P - Search Results

1

Spinal nerve ligation in mouse upregulates TRPV1 heat function in injured IB4-positive nociceptors.

Vilceanu D, Honore P, Hogan QH, Stucky CL. Vilceanu D, et al. Among authors: honore p. J Pain. 2010 Jun;11(6):588-99. doi: 10.1016/j.jpain.2009.09.018. Epub 2009 Dec 16. J Pain. 2010. PMID: 20015699 Free PMC article.

2

Repeated dosing of ABT-102, a potent and selective TRPV1 antagonist, enhances TRPV1-mediated analgesic activity in rodents, but attenuates antagonist-induced hyperthermia.

Honore P, Chandran P, Hernandez G, Gauvin DM, Mikusa JP, Zhong C, Joshi SK, Ghilardi JR, Sevcik MA, Fryer RM, Segreti JA, Banfor PN, Marsh K, Neelands T, Bayburt E, Daanen JF, Gomtsyan A, Lee CH, Kort ME, Reilly RM, Surowy CS, Kym PR, Mantyh PW, Sullivan JP, Jarvis MF, Faltynek CR. Honore P, et al. Pain. 2009 Mar;142(1-2):27-35. doi: 10.1016/j.pain.2008.11.004. Epub 2009 Jan 9. Pain. 2009. PMID: 19135797

3

Additive antinociceptive effects of the selective Nav1.8 blocker A-803467 and selective TRPV1 antagonists in rat inflammatory and neuropathic pain models.

Joshi SK, Honore P, Hernandez G, Schmidt R, Gomtsyan A, Scanio M, Kort M, Jarvis MF. Joshi SK, et al. Among authors: honore p. J Pain. 2009 Mar;10(3):306-15. doi: 10.1016/j.jpain.2008.09.007. Epub 2008 Dec 13. J Pain. 2009. PMID: 19070548 Free article.

4

A-995662 [(R)-8-(4-methyl-5-(4-(trifluoromethyl)phenyl)oxazol-2-ylamino)-1,2,3,4-tetrahydronaphthalen-2-ol], a novel, selective TRPV1 receptor antagonist, reduces spinal release of glutamate and CGRP in a rat knee joint pain model.

Puttfarcken PS, Han P, Joshi SK, Neelands TR, Gauvin DM, Baker SJ, Lewis GR, Bianchi BR, Mikusa JP, Koenig JR, Perner RJ, Kort ME, Honore P, Faltynek CR, Kym PR, Reilly RM. Puttfarcken PS, et al. Among authors: honore p. Pain. 2010 Aug;150(2):319-326. doi: 10.1016/j.pain.2010.05.015. Epub 2010 Jun 19. Pain. 2010. PMID: 20621685

5

Involvement of the TTX-resistant sodium channel Nav 1.8 in inflammatory and neuropathic, but not post-operative, pain states.

Joshi SK, Mikusa JP, Hernandez G, Baker S, Shieh CC, Neelands T, Zhang XF, Niforatos W, Kage K, Han P, Krafte D, Faltynek C, Sullivan JP, Jarvis MF, Honore P. Joshi SK, et al. Among authors: honore p. Pain. 2006 Jul;123(1-2):75-82. doi: 10.1016/j.pain.2006.02.011. Epub 2006 Mar 20. Pain. 2006. PMID: 16545521

6

Central pituitary adenylate cyclase 1 receptors modulate nociceptive behaviors in both inflammatory and neuropathic pain states.

Davis-Taber R, Baker S, Lehto SG, Zhong C, Surowy CS, Faltynek CR, Scott VE, Honore P. Davis-Taber R, et al. Among authors: honore p. J Pain. 2008 May;9(5):449-56. doi: 10.1016/j.jpain.2008.01.329. Epub 2008 Mar 12. J Pain. 2008. PMID: 18337184 Free article.

7

Analgesic profile of intrathecal P2X(3) antisense oligonucleotide treatment in chronic inflammatory and neuropathic pain states in rats.

Honore P, Kage K, Mikusa J, Watt AT, Johnston JF, Wyatt JR, Faltynek CR, Jarvis MF, Lynch K. Honore P, et al. Pain. 2002 Sep;99(1-2):11-9. doi: 10.1016/s0304-3959(02)00032-5. Pain. 2002. PMID: 12237180

8

Ketoprofen produces profound inhibition of spinal c-Fos protein expression resulting from an inflammatory stimulus but not from noxious heat.

Buritova J, Honoré P, Besson JM. Buritova J, et al. Among authors: honore p. Pain. 1996 Oct;67(2-3):379-89. doi: 10.1016/0304-3959(96)03138-7. Pain. 1996. PMID: 8951933

9

Are there long-term changes in the basal or evoked Fos expression in the dorsal horn of the spinal cord of the mononeuropathic rat?

Catheline G, Le Guen S, Honoré P, Besson JM. Catheline G, et al. Among authors: honore p. Pain. 1999 Mar;80(1-2):347-57. doi: 10.1016/s0304-3959(98)00234-6. Pain. 1999. PMID: 10204748

10

TNP-ATP, a potent P2X3 receptor antagonist, blocks acetic acid-induced abdominal constriction in mice: comparison with reference analgesics.

Honore P, Mikusa J, Bianchi B, McDonald H, Cartmell J, Faltynek C, Jarvis MF. Honore P, et al. Pain. 2002 Mar;96(1-2):99-105. doi: 10.1016/s0304-3959(01)00434-1. Pain. 2002. PMID: 11932066

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