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United States Department of Agriculture

Agricultural Research Service

Title: Phenylpropenic Acid Amide, N-Caffeoyltyramine, Increases Camp Via Beta 2-Adrenoceptors in Human Monocytic U937 Cells; Its Effects on Monocyte Activation

Authors
item Park, Jae
item Schoene, Norberta

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: December 15, 2004
Publication Date: April 6, 2005
Citation: Park, J.B., Schoene, N.W. 2005. Phenylpropenic acid amide, n-caffeoyltyramine, increases camp via beta 2-adrenoceptors in human monocytic u937 cells; its effects on monocyte activation. [Abstract]. Experimental Biology 830(5):830.

Interpretive Summary: No Interpretive Summary is required for a meeting abstract.

Technical Abstract: N-caffeoyltyramine is a phenylpropenic acid amide found in numerous plants, including Lycium chinense (Chinese Wolfberry). In this study, N-caffeoyltyramine and its natural analogues (N-cinnamoyltyramine, N-coumaroyltyramine, N-feruloyltyramine, and N-sinapoyltyramine) were investigated to determine their potency as beta-adrenoceptors in human monocytic U937 cells because they have chemical structures strikingly similar to a beta-adrenergic drug, dobutamine. Among the phytochemicals tested in this study, N-caffeoyltyramine was the most potent compound, increasing cAMP at concentrations lower than 0.5 microM via beta-adrenoceptors. Several beta-adrenoceptor agonists were compared with N-caffeoyltyramine in producing cAMP in U937 cells, and the decreasing order of the potency was isoproterenol N-caffeoyltyramine salbutamol > arterenol > dobutamine. Using beta subtype selective antagonists (atenolol (beta1) and butoxamine (beta2)), N-caffeoyltyramine was found to increase cAMP mainly via beta 2-adrenoceptor in U937 cells. cAMP is involved in numerous cellular processes including monocyte activation leading to severe insults to a site of vascular injury. Therefore, effects of N-caffeoyltyramine on monocyte activation markers were also investigated in this study.

Last Modified: 12/17/2014
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