HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Role of group II secretory phospholipase A2 in atherosclerosis: 1. Increased atherogenesis and altered lipoproteins in transgenic mice expressing group IIa phospholipase A2.

Abstract
Some observations have suggested that the extracellular group IIa phospholipase A2 (sPLA2), previously implicated in chronic inflammatory conditions such as arthritis, may contribute to atherosclerosis. We have examined this hypothesis by studying transgenic mice expressing the human enzyme. Compared with nontransgenic littermates, the transgenic mice exhibited dramatically increased atherosclerotic lesions when maintained on a high-fat, high-cholesterol diet. Surprisingly, the transgenic mice also exhibited significant atherosclerotic lesions when maintained on a low-fat chow diet. Immunohistochemical staining indicated that sPLA2 was present in the atherosclerotic lesions of the transgenic mice. On both chow and atherogenic diets, the transgenic mice exhibited decreased levels of HDLs and slightly increased levels of LDLs compared with nontransgenic littermates. These data indicate that group IIa sPLA2 may promote atherogenesis, in part, through its effects on lipoprotein levels. These data also provide a possible mechanism for the observation that there is an increased incidence of coronary artery disease in many chronic inflammatory diseases.
AuthorsB Ivandic, L W Castellani, X P Wang, J H Qiao, M Mehrabian, M Navab, A M Fogelman, D S Grass, M E Swanson, M C de Beer, F de Beer, A J Lusis
JournalArteriosclerosis, thrombosis, and vascular biology (Arterioscler Thromb Vasc Biol) Vol. 19 Issue 5 Pg. 1284-90 (May 1999) ISSN: 1079-5642 [Print] United States
PMID10323781 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Cholesterol, Dietary
  • Dietary Fats
  • Lipids
  • Lipoproteins, LDL
  • Lipoproteins, VLDL
  • Esterases
  • Phospholipases A
  • Group II Phospholipases A2
  • Phospholipases A2
  • Aryldialkylphosphatase
Topics
  • Animals
  • Arteriosclerosis (enzymology, etiology, genetics)
  • Aryldialkylphosphatase
  • Cholesterol, Dietary (toxicity)
  • Diet, Atherogenic
  • Dietary Fats (toxicity)
  • Esterases (deficiency)
  • Female
  • Genetic Predisposition to Disease
  • Group II Phospholipases A2
  • Humans
  • Lipids (blood)
  • Lipoproteins, LDL (biosynthesis)
  • Lipoproteins, VLDL (biosynthesis)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Mice, Transgenic
  • Phospholipases A (genetics, physiology)
  • Phospholipases A2

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: