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[Role of hepatic lipases, cholesterol ester transfer proteins and LCAT in the postprandial phase].
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- Author(s): van Tol A;van Tol A
- Source:
Klinische Wochenschrift [Klin Wochenschr] 1990; Vol. 68 Suppl 22, pp. 23-8.
- Publication Type:
English Abstract; Journal Article; Research Support, Non-U.S. Gov't; Review
- Language:
German
- Additional Information
- Transliterated Title:
Die Rolle der hepatischen Lipase (HTGL), der Cholesterinester-Transfer-Proteine und der LCAT in der posprandialen Phase.
- Source:
Publisher: Springer Verlag Country of Publication: Germany NLM ID: 2985205R Publication Model: Print Cited Medium: Print ISSN: 0023-2173 (Print) Linking ISSN: 00232173 NLM ISO Abbreviation: Klin Wochenschr Subsets: MEDLINE
- Publication Information:
Original Publication: Berlin : Springer Verlag
- Subject Terms:
- Abstract:
Hepatic, heparin-releaseable lipase is a multifunctional enzyme that may act on all lipoprotein classes present in plasma from fasted subjects. Recent evidence suggests that the enzyme also plays a role in the metabolism of chylomicronremnants. Its activity is impaired in normolipidemic patients with coronary heart disease, which also have a delayed removal of chylomicronremnants from plasma. Therefore hepatic lipase, in addition to lipoprotein lipase, plays an important role in postprandial lipoprotein metabolism. The activity levels of lecithin: cholesterol acyltransferase (LCAT) and cholesterylester transfer protein (CETP) are virtually unchanged after the ingestion of an oral fat load by normolipidemic subjects. However, the net mass transfer of cholesterylesters out of HDL into apo B-containing lipoproteins (chylomicronremnants, VLDL/IDL/LDL) is strongly increased. All triglyceride-rich lipoprotein fractions accumulate postprandially and, as a result of CETP action, become enriched in cholesterylesters. Defects in hepatic remnant removal may result in influx of remnants into the arterial wall. In patients with hyperlipidemia (and increased risk for atherosclerosis) the CETP-mediated formation of cholesterylester-rich remnants may operate, not only during the postprandial phase, but continuously.
- Number of References:
35
- Accession Number:
0 (CETP protein, human)
0 (Carrier Proteins)
0 (Cholesterol Ester Transfer Proteins)
0 (Cholesterol Esters)
0 (Dietary Fats)
0 (Glycoproteins)
0 (Triglycerides)
EC 2.3.1.43 (Phosphatidylcholine-Sterol O-Acyltransferase)
EC 3.1.1.34 (Lipoprotein Lipase)
- Publication Date:
Date Created: 19900101 Date Completed: 19910523 Latest Revision: 20071115
- Publication Date:
20221213
- Accession Number:
2087075
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