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N-Oleoyldopamine (OLDA) is an endogenous lipid metabolite formed by the condensation of oleic acid and dopamine. It acts as a selective agonist for the transient receptor potential vanilloid type 1 (TRPV1), also known as the vanilloid receptor 1 (VR1). OLDA is found in mammalian brain tissue and has been shown to modulate activity of midbrain dopaminergic neurons through multiple mechanisms. It is equipotent to capsaicin at TRPV1 receptors and can induce hyperalgesia and nocifensive behavior in animal models. Additionally, OLDA is a potent inhibitor of 5-lipoxygenase[6][7][4].
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