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Potential role of hepatic lipase in the accrual of docosahexaenoic acid (DHA) in the brain
Author(s) -
Dhavamani Sugasini,
Yang Peng,
Ng Dominic,
Khetarpal Sumeet,
Vitali Cecilia,
Rader Daniel,
Subbaiah Papasani
Publication year - 2017
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.31.1_supplement.781.4
Subject(s) - lysophosphatidylcholine , docosahexaenoic acid , medicine , endocrinology , chemistry , lipase , transporter , hepatic lipase , calanus finmarchicus , enzyme , biochemistry , phosphatidylcholine , fatty acid , biology , polyunsaturated fatty acid , phospholipid , gene , ecology , crustacean , membrane , copepod
DHA is an essential fatty acid that is required for the normal development and function of the brain. Because of its inability to synthesize adequate amounts of DHA from the precursors, the brain has to acquire DHA through the blood brain barrier (BBB). Recent studies demonstrated the presence of a transporter at the BBB that specifically transports DHA into the brain in the form of lysophosphatidylcholine (LPC‐DHA). However, the mechanism by which LPC‐DHA is generated in the plasma is not known. Our previous studies showed that there are three different enzymes in plasma‐ lecithin cholesterol acyltransferase (LCAT), endothelial lipase (EL), and hepatic lipase (HL), which can generate LPC‐DHA from sn‐2 DHA PC of lipoproteins. In this study we determined the potential roles of these enzymes in the delivery of DHA to the brain by examining the brain DHA levels in the mice genetically deficient in each of these enzymes. The results show that the brain DHA levels of LCAT‐deficient mice (16.3%) or EL‐deficient mice (15.2%) were not significantly lower than those of their littermates. However, the concentration of brain DHA was significantly lower in HL knockout (KO) mice (13.5%) compared to their littermates (17.1%) (p<0.002). The DHA levels were also lower in the plasma but not in the liver, or heart of HL KO mice. Furthermore, the concentration of LPC‐DHA was significantly decreased in the plasma of HL KO mice. These results suggest that HL may be important for the supply of DHA to the brain by generating LPC‐DHA either in the plasma itself, or in the liver, followed by its secretion into plasma. Support or Funding Information Supported by NIH R01 HL 68685 (PVS)