e Epoxide Hydrolase Inhibitor - Efficacy in a DIO
Mouse Model plus Pharmacokinetics and Pharmacodynamics in Mice and Men"
(Whitcomb, R, Chen, D, Wang, J, Anandan, S-K, Gless, R and Webb, H).
This poster describes the direct correlation between the concentration
of AR9281 in blood and the activity of its target, sEH, in both mice
and humans. The data further demonstrate that AR9281 improves glucose
metabolism in rodent models of type 2 diabetes.
-- "A Novel Inhibitor of Soluble Epoxide Hydrolase, AR9281, Improves
Glucose Homeostasis in Diet-Induced Obese Mice" (Wong, K, Zhang, L-N,
Vincelette, J, Chen, D, Mehra, U, Cheng, Y, Gless, R, Anandan, S-K,
Webb, H).
Data presented in this poster show that in diet-induced obese mice,
AR9281 inhibits sEH and improves glucose tolerance in a highly-dose
dependent manner. Improvement of glucose tolerance by AR9281 is not
observed in sEH knock-out mice indicating that the action of AR9281 is
sEH mechanism-based. These positive effects are associated with
reductions in plasma insulin, IL-6, an inflammatory molecule elevated
in people with type 2 diabetes, and resistin, a hormone that plays a
role in predisposing obese individuals to diabetes.
-- "Improvement of Glucose Homeostasis by AR9281, a Novel Inhibitor of
Soluble Epoxide Hydrolase, in Diet-Induced Obese Mice Does Not Depend
on Active Nitric Oxide Synthase" (Vincelette, J, Chen, D, Mehra, U,
Cheng, Y, Gless, R, Anandan, S-K, MacIntyre, E and Wang, J).
Data presented in this poster show the correlation between treatment
with AR9281 and the lowering of the glucose levels after an oral
glucose tolerance test and demonstrate that these effects are not
inhibited by concurrent treatment with the nitric oxide synthase
inhibitor L-NAME (NG-nitro-L-arginine methyl est
'/>"/>SOURCE Arete Therapeutics Inc. Copyright©2009 PR Newswire. All rights reserved | |
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