Abstract:
:Although clofibrate has been shown to inhibit platelet aggregation that is caused by thrombin, ADP and epinephrine, by blocking the release of arachidonic acid from platelet phospholipids [8], here we have demonstrated that clofibrate enhanced platelet aggregation by arachidonic acid and PLC and reversed the effects of PGE1 on platelet cAMP concentration and on PLC-induced secretion of [14C]-5HT in similar, concentration-dependent manners. Taken together, these findings strongly suggest that the proaggregatory effect of clofibrate is mediated by a lowering of cAMP in platelets.
journal_name
Biochem Pharmacoljournal_title
Biochemical pharmacologyauthors
Huzoor-Akbar,Witiak DT,Newman HA,Fertel RH,Feller DRdoi
10.1016/0006-2952(82)90434-8subject
Has Abstractpub_date
1982-06-01 00:00:00pages
2125-8issue
11eissn
0006-2952issn
1873-2968pii
0006-2952(82)90434-8journal_volume
31pub_type
杂志文章abstract::Accumulating evidence indicates that dysfunction in amino acid neurotransmission contributes to the pathophysiology of depression. Consequently, the modulation of amino acid neurotransmission represents a new strategy for antidepressant development. While glutamate receptor ligands are known to have antidepressant eff...
journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/j.bcp.2009.04.008
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abstract::The localization of [3H]forskolin binding to microscope slide mounted sections of rat kidney has been examined using autoradiography. Saturation studies showed [3H]forskolin binding to two sites, a high affinity site (KD = 8.7 nM, Bmax = 0.14 pmol/mg protein) and a low affinity site (KD = 6.7 microM, Bmax = 11.0 pmol/...
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/0006-2952(89)90628-x
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journal_title:Biochemical pharmacology
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doi:10.1016/0006-2952(94)90283-6
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
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更新日期:2019-01-01 00:00:00
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journal_title:Biochemical pharmacology
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更新日期:2005-02-01 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
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更新日期:2003-07-15 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/0006-2952(94)90587-8
更新日期:1994-11-16 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/j.bcp.2016.08.004
更新日期:2016-10-15 00:00:00
abstract::Nuclear factor-kappaB (NFKB) is a transcription factor with a pivotal role in inducing genes involved in physiological processes as well as in the response to injury and infection. A model has been proposed whereby the diverse agents that activate NFkappaB do so by increasing oxidative stress within the cell. Activati...
journal_title:Biochemical pharmacology
pub_type: 杂志文章,评审
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更新日期:2000-01-01 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
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更新日期:2009-03-15 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/0006-2952(89)90554-6
更新日期:1989-08-15 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/0006-2952(94)90123-6
更新日期:1994-02-11 00:00:00
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journal_title:Biochemical pharmacology
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/j.bcp.2011.04.015
更新日期:2011-08-01 00:00:00
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pub_type: 杂志文章
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更新日期:2005-02-01 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
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pub_type: 杂志文章
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更新日期:2000-07-01 00:00:00
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更新日期:2016-02-15 00:00:00
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journal_title:Biochemical pharmacology
pub_type: 杂志文章
doi:10.1016/0006-2952(90)90199-u
更新日期:1990-03-01 00:00:00
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pub_type: 杂志文章
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更新日期:1985-04-01 00:00:00
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pub_type: 杂志文章
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更新日期:1994-04-20 00:00:00