2012
DOI: 10.2460/ajvr.73.1.19
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Efficacy of ABT-116, an antagonist of transient receptor potential vanilloid type 1, in providing analgesia for dogs with chemically induced synovitis

Abstract: HDA had no apparent effect on sodium urate-induced lameness; LDA did attenuate the lameness but not as completely as firocoxib treatment. High rectal temperature is an adverse effect of oral ABT-116 administration that may be of clinical concern.

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Cited by 16 publications
(23 citation statements)
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“…Indeed, a variant of TRPV1 has been associated to a reduced risk of pain in OA . All together, these data support an important role for TRPV1 antagonists to relieve OA pain, even though two of them, ABT‐116 and AZD1386, failed to give significant pain relief in this pathology . Furthermore, we have to consider that OA is a complex pathology where TRPV1 is only one pain target …”
Section: Pathophysiological Rolesmentioning
confidence: 79%
“…Indeed, a variant of TRPV1 has been associated to a reduced risk of pain in OA . All together, these data support an important role for TRPV1 antagonists to relieve OA pain, even though two of them, ABT‐116 and AZD1386, failed to give significant pain relief in this pathology . Furthermore, we have to consider that OA is a complex pathology where TRPV1 is only one pain target …”
Section: Pathophysiological Rolesmentioning
confidence: 79%
“…Consisitent with these findings, in a randomized, double‐blinded, prospective clinical trial with client‐owned dogs suffering from severe hip osteoarthritic pain, the TRPV1 antagonist ABT‐116 showed only marginal analgesic activity over placebo (Malek et al ., ). ABT‐116 did not attenuate lameness in dogs with experimentally induced urate synovitis either at doses at which it caused seriously high rectal temperatures (Cathcart et al ., ). The striking difference in the analgesic activity of TRPV1 antagonists between rodent (where it potently reduces experimental osteoarthritic pain; Honore et al ., ; Puttfarcken et al ., ) and canine (without clinical benefits, see earlier) models of human osteoarthritic pain is puzzling and concerning.…”
Section: Pain and Trp Channelsmentioning
confidence: 97%
“…Taken together, these findings identify TRPV1 as a promising target to relieve OA pain. However, the TRPV1 antagonist -4-(trifluoromethyl)phenyl)methyl)-N9-(1-methyl-1H-indazol-4-yl)] did not provide any significant pain relief in dogs with experimental synovitis (Cathcart et al, 2012) or naturally occurring, age-related hip OA (Malek et al, 2012), and AZD1386 (Fig. 9) was withdrawn from clinical trials in patients with OA after a periodic review of the data failed to show any clinical benefit (Svensson et al, 2010;Miller et al, 2014).…”
Section: Transient Receptor Potential Channels: Acquired Diseasesmentioning
confidence: 99%