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Publication Detail
Human monoclonal IgG anticardiolipin antibodies induce nitric oxide synthase expression.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Journal Article
  • Authors:
    Alves JD, Clapp BR, Stidwill R, Chen PP, Hingorani AD, Singer M, Isenberg DA
  • Publication date:
    04/2006
  • Pagination:
    246, 253
  • Journal:
    Atherosclerosis
  • Volume:
    185
  • Issue:
    2
  • Status:
    Published
  • Country:
    Ireland
  • Print ISSN:
    0021-9150
  • PII:
    S0021-9150(05)00398-9
  • Language:
    eng
  • Keywords:
    Animals, Antibodies, Anticardiolipin, Antibodies, Monoclonal, Aorta, Blood Pressure, Enzyme Inhibitors, Humans, Immunoglobulin G, Immunohistochemistry, In Vitro Techniques, Male, NG-Nitroarginine Methyl Ester, Nitric Oxide, Nitric Oxide Synthase, Nitric Oxide Synthase Type II, Nitric Oxide Synthase Type III, Phenylephrine, Rats, Rats, Sprague-Dawley, Renal Artery, Vasoconstriction, Vasoconstrictor Agents
Abstract
OBJECTIVE: Antiphospholipid antibodies are associated with increased risk of thrombosis, particularly as in antiphospholipid syndrome. This study aims to determine the acute effects of anticardiolipin antibodies on nitric oxide production and vascular function. METHODS: Ex vivo aortic rings from male Sprague Dawley rats were incubated with IgG monoclonal anticardiolipin antibody (IS4) or a non-specific IgG control. In organ baths, response to phenylephrine and acetlycholine was determined alone and with nitro-L-arginine methyl ester (L-NAME), 1,400 W, D-arginine, L-arginine, sodium nitroprusside and cardiolipin. In vivo antibodies were injected into anaesthetised, spontaneously breathing male Sprague Dawley rats. Haemodynamic variables and serum nitric oxide were measured. Immunohistochemistry for iNOS and eNOS was performed in kidney vessels. RESULTS: Phenylepherine contraction was decreased in the IS4 group compared to controls (p < 0.001). L-NAME, 1,400 W and cardiolipin, abolished this effect. L-Arginine caused significant relaxation in the IS4 group (p = 0.005). Mean arterial pressure in rats injected with IS4 was reduced compared to IgG and saline controls (p < 0.001). NO in plasma increased significantly after IS4 administration (p < 0.001). Immunohistochemistry showed increased iNOS expression in kidney arteries in the IS4 group, with no change in eNOS. CONCLUSION: Anticardiolipin antibodies induce NO production acutely via increased expression of iNOS in both ex vivo and in vivo models.
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