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Larazotide is a peptide antagonist of alpha3beta4 subunit-containing nicotinic acetylcholine receptors (nAChRs). It selectively inhibits epibatidine-induced calcium mobilization in HEK293 cells expressing human alpha3beta4 subunit-containing nAChRs over HEK293 cells expressing alpha4beta2 subunit-containing nAChRs (IC50s = 91 and 276 nM, respectively). Larazotide (100 µM) decreases inflammatory cytokine-induced tight junction dysfunction in isolated rat intestinal epithelial cells. In vivo, larazotide (0. 3, and 30 µg/kg) inhibits nicotine self-administration and varenicline-induced reinstatement of nicotine-seeking behavior in rats. It also increases intestinal epithelial cell bridging and decreases intestinal damage without reducing liver damage in a rat model of thioacetamide-induced acute liver failure.. Solulibility: DMSO: Sparingly Soluble: 1-10 mg/ml: PBS pH 7.2: Sparingly Soluble: 1-10 mg/ml.
Keywords:
AT-1001, Gly-Gly-Val-Leu-Val-Gln-Pro-Gly, glycylglycyl-L-valyl-L-leucyl-L-valyl-L-glutaminyl-L-prolyl-glycine, monoacetate salt
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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