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Abstract Title:

HU-444, a Novel, Potent Anti-Inflammatory, Nonpsychotropic Cannabinoid.

Abstract Source:

J Pharmacol Exp Ther. 2015 Oct ;355(1):66-75. Epub 2015 Aug 13. PMID: 26272937

Abstract Author(s):

Christeene G Haj, Percy F Sumariwalla, Lumír Hanuš, Natalya M Kogan, Zhana Yektin, Raphael Mechoulam, Mark Feldmann, Ruth Gallily

Article Affiliation:

Christeene G Haj

Abstract:

Cannabidiol (CBD) is a component of cannabis, which does not cause the typical marijuana-type effects, but has a high potential for use in several therapeutic areas. In contrast toΔ(9)-tetrahydrocannabinol (Δ(9)-THC), it binds very weakly to the CB1 and CB2 cannabinoid receptors. It has potent activity in both in vitro and in vivo anti-inflammatory assays. Thus, it lowers the formation of tumor necrosis factor (TNF)-α, a proinflammatory cytokine, and was found to be an oral antiarthritic therapeutic in murine collagen-induced arthritis in vivo. However, in acidic media, it can cyclize to the psychoactive Δ(9)-THC. We report the synthesis of a novel CBD derivative, HU-444, which cannot be converted by acid cyclization into a Δ(9)-THC-like compound. In vitro HU-444 had anti-inflammatory activity (decrease of reactive oxygen intermediates and inhibition of TNF-α production by macrophages); in vivo it led to suppression of production of TNF-α and amelioration of liver damage as well as lowering of mouse collagen-induced arthritis. HU-444 did not cause Δ(9)-THC-like effects in mice. We believe that HU-444 represents a potential novel drug for rheumatoid arthritis and other inflammatory diseases.

Study Type : Animal Study

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