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Induction of COX-2 Expression by the Endocannabinoid Derivative R(+)-Methanandamide

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 525))

Abstract

Cannabinoids produce a broad array of potential therapeutical effects, including the reduction of nausea in cancer and AIDS patients undergoing chemotherapy [1]. In recent years, two G1 protein-coupled cannabinoid receptors, CB1 and CB2, have been identified and cloned. Whereas the CB2 receptor is preferentially expressed in the central nervous system [2], the CB2 receptor has been described as the predominant form expressed in peripheral immune cells [3]. The discovery of specific cannabinoid receptors was followed by the identification of two endogenous arachidonic acid derivatives, anandamide (N-arachidonylethanolamide) and 2-arachidonylglycerol, which exhibit specific binding affinity to cannabinoid receptors [4, 5]. However, emerging evidence suggests that various cannabinoid actions are mediated via cannabinoid receptor-independent pathways, comprising activation of mitogen-activated protein kinases (MAPKs) [6, 7], alteration of intracellular calcium [8] and cAMP levels [9, 10], inhibition of cytokine expression [11] and induction of histamine release [12].

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Hinz, B., Ramer, R., Brune, K. (2003). Induction of COX-2 Expression by the Endocannabinoid Derivative R(+)-Methanandamide. In: Yazici, Z., Folco, G.C., Drazen, J.M., Nigam, S., Shimizu, T. (eds) Advances in Prostaglandin, Leukotriene, and other Bioactive Lipid Research. Advances in Experimental Medicine and Biology, vol 525. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-9194-2_30

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  • DOI: https://doi.org/10.1007/978-1-4419-9194-2_30

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-4831-3

  • Online ISBN: 978-1-4419-9194-2

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