Abstract

The formation of prostaglandin E2 (PGE2) is associated with adverse inflammatory effects. However, long-term treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) comes with risk of severe side effects. Therefore, alternative ways to inhibit PGE2 are warranted. We have investigated the effects of tea extracts and the polyphenols epigallocatechin gallate (EGCG) and quercetin on PGE2 formation, determined by immunoassay, and protein expression, determined by immunoblotting, of cytosolic phospholipase A2 (cPLA2), cyclooxygenase 2 (COX-2) and microsomal PGE synthase-1 (mPGES-1) in human monocytes. Green and black tea extracts, and with a lower potency, Rooibos tea extract, inhibited lipopolysaccharide (LPS) and calcium ionophore-induced PGE2 formation. In addition, all tea extracts inhibited the LPS-induced expression of mPGES-1, and the green and black tea extracts also inhibited, to a lesser extent, COX-2 expression. The tea extracts only marginally reduced cPLA2 expression and had no effect on COX-1 expression. EGCG, present in green and black tea, and quercetin, present in all three teas, also inhibited PGE2 formation and expression of mPGES-1, COX-2 and cPLA2. Cell-based and cell-free assays were also performed to evaluate direct effects on the enzymatic activity of COX and PGE synthases. Mainly, the cell-free assay demonstrated partial inhibition by the tea extracts and polyphenols. However, the inhibition required higher doses compared to the effects demonstrated on protein expression. In conclusion, green and black tea, and to a lesser extent Rooibos tea, are potent inhibitors of PGE2 formation in human monocytes, and mediate their effects by inhibiting the expression of the enzymes responsible for PGE2 formation, especially mPGES-1.

Highlights

  • Introduction published maps and institutional affilConsumption of tea has been attributed health beneficial effects, and it has been suggested to reduce the risk of, e.g., cardiovascular diseases and cancer [1,2]

  • We investigated the inhibitory effects of green tea, black tea, Rooibos tea extracts, and the polyphenols epigallocatechin gallate (EGCG) and quercetin on the formation of prostaglandin E2 (PGE2) and the expression of the enzymes involved in its formation in human monocytes

  • Human monocytes were pretreated with LPS for 24 h prior to assessment of the amount of PGE2 formed by the cells in response to a 45 min stimulation with the calcium ionophore A23187

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Summary

Introduction

Consumption of tea has been attributed health beneficial effects, and it has been suggested to reduce the risk of, e.g., cardiovascular diseases and cancer [1,2]. The main catechin found in green tea is epigallocatechin gallate (EGCG), and it is a major constituent of the polyphenols, but epicatechin gallate, epigallocatechin and catechin gallate are present [3,4]. EGCG is the most well-studied of the tea flavonoids, and it has been suggested to have beneficial effects in humans, predominantly due to its antioxidant properties [5,6]. Its content of EGCG is lower than of green tea due to oxidation of the catechins, resulting in dimers and polymers of the catechins, named theaflavins and thearubigins [3]

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