1995
DOI: 10.1002/ajh.2830500417
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High‐density lipoprotein fails to inhibit serotonin‐induced activation of blood platelets

Abstract: High-density lipoprotein (HDL) of 100-400 micrograms/ml did not prevent morphological alterations of human blood platelets treated with serotonin (1-5 microM). Highly concentrated HDL (1,200 micrograms/ml) appeared to activate platelets in vitro. These findings indicate that whole HDL may not inhibit agonist-induced platelet activation.

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Cited by 2 publications
(2 citation statements)
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“…During the rolling process, platelets become bind to scavenger receptors, but oxidized LDL can bind to the receptors and promote foam cell formation 8) . A number of studies have shown a close relationship between platelet activation and lipoproteins such as LDL, oxidized LDL and HDL [9][10][11][12][13][14][15] . Oxidized LDL can be transported by platelets to macrophages, leading to foam cell formation 9) .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…During the rolling process, platelets become bind to scavenger receptors, but oxidized LDL can bind to the receptors and promote foam cell formation 8) . A number of studies have shown a close relationship between platelet activation and lipoproteins such as LDL, oxidized LDL and HDL [9][10][11][12][13][14][15] . Oxidized LDL can be transported by platelets to macrophages, leading to foam cell formation 9) .…”
Section: Introductionmentioning
confidence: 99%
“…Platelets are activated by LDL or oxidized LDL, and the activation inhibited by HDL [9][10][11][12] ; however, several reports have indicated that HDL activates platelets in vitro [13][14][15] ; highly concentrated HDL appears to activate platelets in vitro 13) . ApoE-rich HDL2 inhibits aggregation of platelets stimulated with ADP in vitro, but HDL3 accelerates aggregation 14) .…”
mentioning
confidence: 99%