INT76095
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Cyclooxygenase-2 (COX-2), inducible NO synthase (iNOS) and IL-1beta gene expressions were quantified by transcription of mRNA followed by real time and quantitative polymerase chain reaction. | |||||||||||||||
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It may be possible that iNOS induction and expression dependent on synergistic signals to macrophage/monocyte [45,46], and cytokines and virus products may be acting as different stimuli. | |||||||||||||||
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Replicating dengue viruses may be necessary for optimal iNOS induction, since rates of iNOS+ cells were much higher than when the inactivated virus was used. | |||||||||||||||
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Infectious virus, if not crucial, certainly play an important role in inducing iNOS. | |||||||||||||||
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[12-14] is consistent with induction of iNOS during acute disease as reported here for both in vivo and in vitro infection. | |||||||||||||||
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The highest incidence of iNOS activation was from 6 to 10 days of disease (8 out of 20 patients). | |||||||||||||||
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The inducible isoform of nitric oxide synthase (iNOS) may be expressed early in the inflammatory process. | |||||||||||||||
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These data suggest that cAMP is required for the induction of iNOS in ECs and that NO may directly impair adenylate cyclase activity, preventing iNOS activation. | |||||||||||||||
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These data suggest that cAMP is required for the induction of iNOS in ECs and that NO may directly impair adenylate cyclase activity, preventing iNOS activation. | |||||||||||||||
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Exposure of ECs to the NO donor, SNAP, before the addition of LPS + IFN, blocked iNOS induction, whereas preincubation of ECs with inhibitors of NOS, before morphine or anandamide exposure, restored LPS + IFN induction of iNOS, suggesting a direct impact of NO on the regulation of iNOS activity. | |||||||||||||||
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Nitric oxide (NO), when produced via inducible NO synthase (iNOS) in excess under pathological conditions (e.g., inflammation, endotoxemia, and septic shock), may lead to tissue injury and organ dysfunction. | |||||||||||||||
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Interestingly, NAC increased the IL-1beta and iNOS mRNA levels but did not significantly modify COX-2 mRNA expression. | |||||||||||||||
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Nitric oxide (NO) generated from inducible NO synthase (iNOS) participates in immune and inflammatory responses in many tissues. | |||||||||||||||
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This injury results from initial COX inhibition and other local events, with translocation of indigenous luminal bacteria, leading to induction of NO synthase isoform, iNOS, and subsequent production of the cytotoxic moiety, peroxynitrite from NO and superoxide. | |||||||||||||||
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This injury results from initial COX inhibition and other local events, with translocation of indigenous luminal bacteria, leading to induction of NO synthase isoform, iNOS, and subsequent production of the cytotoxic moiety, peroxynitrite from NO and superoxide. | |||||||||||||||
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Increased STAT-1 and iNOS mRNA levels were also observed in DRGs from FIV-infected animals relative to mock-infected controls. | |||||||||||||||
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FIV infection up-regulated inducible NO synthase (iNOS), STAT-1, and TNF-alpha mRNA levels in DRG cultures. | |||||||||||||||
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The present studies indicate that FIV infection of DRGs directly contributes to axonal and neuronal injury through a mechanism involving macrophage immune activation, which is mediated by STAT-1 and iNOS activation. | |||||||||||||||
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The inactivated virus consistently induced low rates of INOS+ monocytes, however differences were statistically insignificant when compared to controls. | |||||||||||||||
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Among 11 patients with normal platelet levels merely 4 had significantly elevated iNOS+ cell ratios. | |||||||||||||||
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General Comments
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