کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10738333 | 1046702 | 2011 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
The acute-phase protein serum amyloid A induces endothelial dysfunction that is inhibited by high-density lipoprotein
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کلمات کلیدی
HPSS•NOPBMCODQSAASGCcGMPDPIMCP-1guanosine 3′,5′-cyclic monophosphate - guanosine 3 '، 5'-cyclic monophosphateO2•− - O2 • -l-arginine - آرژینین الACh - آهAcetylcholine - استیل کولینl-Arg - ال-آرژینینinflammation - التهاب( توروم) HAEC - اینSoluble guanylyl cyclase - حلال گویینیل سیکلاسEndothelial function - دسترسپذیری یا دستیابیپذیریdiphenyliodonium - دیفنیلیدونیمFree radicals - رادیکال آزادSuperoxide anion radical - رادیکال آنیون سوپراکسیدserum amyloid A - سرم آمیلوئید Ahuman aortic endothelial cell - سلول اندوتلیال آئورت انسانEndothelial cell - سلول های اندوتلیالperipheral blood mononuclear cells - سلول های تک هسته ای خون محیطیTissue factor - عامل بافتNitric oxide - نیتریک اکسیدMonocyte chemotactic protein-1 - پروتئین chemotactic monocyte-1Acute-phase protein - پروتئین حاد فازSNP - چندریختی تک-نوکلئوتید
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
سالمندی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
The acute-phase protein serum amyloid A (SAA) is elevated during inflammation and may be deposited in atheroma where it promotes atherosclerosis. We investigated the proatherogenic effects of SAA on the vascular endothelium and their regulation by high-density lipoprotein (HDL). Exposure of human aortic endothelial cells (HAEC) to SAA (0.25-25 μg/ml) decreased nitric oxide (
- NO) synthesis/bioavailability, although the endothelial NO synthase monomer-to-dimer ratio was unaffected. SAA (10 μg/ml) stimulated a Ca2+ influx linked to apocynin-sensitive superoxide radical anion (O2
- â) production. Gene expression for arginase-1, nuclear factor κB (NF-κB), interleukin-8, and tissue factor (TF) increased within 4 h of SAA stimulation. Enzymatically active Arg-1/2 was detected in HAEC cultured with SAA for 24 h. Therefore, in addition to modulating
- NO bioavailability by stimulating O2
- â production in the endothelium, SAA modulated vascular l-Arg bioavailability. SAA also diminished relaxation of preconstricted aortic rings induced by acetylcholine, and added superoxide dismutase restored the vascular response. Preincubation of HAEC with HDL (100 or 200, but not 50, μg/ml) before (not after) SAA treatment ameliorated the Ca2+ influx and O2
- â production; decreased TF, NF-κB, and Arg-1 gene expression; and preserved overall vascular function. Thus, SAA may promote endothelial dysfunction by modulating
- NO and l-Arg bioavailability, and HDL pretreatment may be protective. The relative HDL to SAA concentrations may regulate the proatherogenic properties of SAA on the vascular endothelium.
- NO) synthesis/bioavailability, although the endothelial NO synthase monomer-to-dimer ratio was unaffected. SAA (10 μg/ml) stimulated a Ca2+ influx linked to apocynin-sensitive superoxide radical anion (O2
- â) production. Gene expression for arginase-1, nuclear factor κB (NF-κB), interleukin-8, and tissue factor (TF) increased within 4 h of SAA stimulation. Enzymatically active Arg-1/2 was detected in HAEC cultured with SAA for 24 h. Therefore, in addition to modulating
- NO bioavailability by stimulating O2
- â production in the endothelium, SAA modulated vascular l-Arg bioavailability. SAA also diminished relaxation of preconstricted aortic rings induced by acetylcholine, and added superoxide dismutase restored the vascular response. Preincubation of HAEC with HDL (100 or 200, but not 50, μg/ml) before (not after) SAA treatment ameliorated the Ca2+ influx and O2
- â production; decreased TF, NF-κB, and Arg-1 gene expression; and preserved overall vascular function. Thus, SAA may promote endothelial dysfunction by modulating
- NO and l-Arg bioavailability, and HDL pretreatment may be protective. The relative HDL to SAA concentrations may regulate the proatherogenic properties of SAA on the vascular endothelium.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Free Radical Biology and Medicine - Volume 51, Issue 7, 1 October 2011, Pages 1390-1398
Journal: Free Radical Biology and Medicine - Volume 51, Issue 7, 1 October 2011, Pages 1390-1398
نویسندگان
Paul K. Witting, Changjie Song, Kenneth Hsu, Susan Hua, Sarah N. Parry, Roshanak Aran, Carolyn Geczy, Saul Benedict Freedman,