Secretory non-pancreatic phospholipase A2: influence on lipoprotein metabolism
Journal of Lipid Research, ISSN: 0022-2275, Vol: 38, Issue: 11, Page: 2232-2239
1997
- 37Citations
- 9Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations37
- Citation Indexes37
- CrossRef37
- Captures9
- Readers9
Article Description
Lipoprotein metabolism is markedly altered during inflammation. The concentration of human secretory phospholipase A2 (sPLA2) can increase hundreds of fold in inflammatory fluids and in the circulation. It was detected in atherosclerotic lesions where many inflammatory genes are induced. As sPLA2 has been reported to act on lipoproteins as substrates, lipoprotein profiles in transgenic mice expressing sPLA2 were studied. HDL levels were markedly decreased in transgenic mice overexpressing sPLA2. HDL in the transgenics were smaller in size, with a significant decrease (11%) in phospholipid content compared to nontransgenic littermates. In sPLA2 transgenic mice and transgenic mice expressing both sPLA2 and human apolipoprotein B (apoB), the concentrations of apoB-containing lipoproteins were not altered. We conclude that sPLA2 alters HDL metabolism and could be responsible for the depressed levels of HDL that exist during chronic inflammatory diseases.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0022227520349373; http://dx.doi.org/10.1016/s0022-2275(20)34937-3; https://linkinghub.elsevier.com/retrieve/pii/S0022227520349373; https://api.elsevier.com/content/article/PII:S0022227520349373?httpAccept=text/xml; https://api.elsevier.com/content/article/PII:S0022227520349373?httpAccept=text/plain; https://dul.usage.elsevier.com/doi/; http://dx.doi.org/10.1016/s0022-2275%2820%2934937-3; https://dx.doi.org/10.1016/s0022-2275%2820%2934937-3
Elsevier BV
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