4.7 Article

Green tea catechins inhibit pancreatic phospholipase A2 and intestinal absorption of lipids in ovariectomized rats

Journal

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
Volume 17, Issue 7, Pages 492-498

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2006.03.004

Keywords

lipids; phosphatidylcholine; green tea; (-)-epigallocatechin gallate; phospholipase A(2); alpha-tocopherol; rats

Funding

  1. NCCIH NIH HHS [R21AT001363-01A2] Funding Source: Medline

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This study was conducted to examine whether the inhibition of intestinal lipid absorption by green tea is associated with the inhibitory effect of its catechins on pancreatic phospholipase A(2) (PLA(2)). PLA(2) activity was assayed by using 1,2-dioleoylphosphatidylcholine (DOPC), porcine pancreatic PLA2 and catechins at varying concentrations (0.075-1.80 mu mol/L). The amount of 1-oleoyl-2-bydroxyphosphatidylcholine liberated was determined by HPLC. The percentage of inhibition of PLA(2) by catechins at 0.6 mu mol increased in the order of (-)-epicatechin (23.3%), (+)-catechin (CAT; 24.8%), (-)-epigallocatechin (25.7%), (-)-epicatechin gallate (39.7%) and (-)-epigallocatechin gallate (EGCG; 64.9%). In an in vivo study, ovariectomized rats with lymph cannula were infused intraduodenally for 8 h with a triolein emulsion containing [dioleoyl-l-C-14]-phosphatidylcholine, DOPC, alpha-tocopherol (alpha TCH) and retinol (ROH) without (CAT0) or with CAT or EGCG. The lymphatic total C-14-radioactivity was significantly lowered by EGCG (45.5 +/- 4.9% dose) compared with CAT (56.2 +/- 5.2% dose) and CATO (64.7 +/- 2.0% dose). The C-14-radioactivity remaining in the small intestinal lumen and cecum was higher in EGCG (24.1% dose) than in CAT (9.5% dose) and CAT0 rats (9.0% dose). Significantly less C-14 radioactivity was incorporated into lymph triacylglycerol and cholesteryl ester in EGCG rats. The absorption of alpha TOH, used as a marker of extremely hydrophobic lipids, was significantly lower in EGCG (7.8 +/- 1.7 mu mol) than in CAT (14.4 +/- 2.8 mu mol) and CATO rats (16.8 +/- 2.1 mu mol). The absorption of ROH was unaffected, whereas oleic acid output was lower in EGCG rats. The results show that EGCG inhibits the intestinal absorption of lipids, which is in part associated with its inhibition of phosphatidylcholine hydrolysis. Data suggest that EGCG may inhibit the absorption of other highly lipophilic organic compounds.

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