cardamonin and Pain

Topics: Administration, Oral; Analgesics; Animals; Chalcones; Disease Models, Animal; Dose-Response Relationship, Drug; Glutamic Acid; Injections, Intraperitoneal; Mice; Pain; Plant Extracts; Receptors, Opioid; TRPV Cation Channels; Zingiberaceae

Recently, we reported that Alpinia katsumadai (AK) has anti-nociceptive activity in vivo and that cardamonin (CDN) from AK suppresses the activity and expression of transglutaminase-2 (Tgase-2). However, it remains unknown whether CDN contributes to the anti-nociceptive activities of AK in vivo. We examined the anti-inflammatory effects of CDN in MG63 osteoblast-like cells and Raw264.7 macrophage-like cells treated with interleukin-1β treatment. CDN suppressed the expression of Tgase-2, cyclooxygenase-2 (COX-2), and p65 (nuclear factor-κB) in a concentration-dependent manner, and restored the expression of IκB in MG63 and Raw264.7 cells. However, CDN did not inhibit the activity of COX-2. Gene silencing of Tgase-2 reduced the COX-2 expression in MG63 cells. Phenylbenzoquinone (PBQ)-induced writhing, carrageenan-induced hyperalgesia, and rota-rod test were used to evaluate the anti-nociceptive activity in vivo. CDN (3-30 mg/kg, orally administered) significantly inhibited PBQ-induced writhing. CDN also produced a significant, dose-dependent increase in the withdrawal response latencies in carrageenan-induced hyperalgesia. The effects of CDN on PBQ-induced writhing were not caused by impaired motor functions. These results suggest that CDN might be helpful in controlling the pain from inflammatory diseases.

Topics: Alpinia; Analgesics; Animals; Benzoquinones; Carrageenan; Cell Line; Chalcones; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Gene Expression; GTP-Binding Proteins; Humans; Male; Medicine, Korean Traditional; Mice; Mice, Inbred ICR; Pain; Plants, Medicinal; Protein Glutamine gamma Glutamyltransferase 2; Rats; Rats, Sprague-Dawley; RNA, Small Interfering; Transglutaminases