285 research outputs found
Carbon Monoxide Protects against Liver Failure through Nitric Oxide–induced Heme Oxygenase 1
Carbon monoxide (CO) and nitric oxide (NO) each have mechanistically unique roles in various inflammatory disorders. Although it is known that CO can induce production of NO and that NO can induce expression of the cytoprotective enzyme heme oxygenase 1 (HO-1), there is no information whether the protective effect of CO ever requires NO production or whether either gas must induce expression of HO-1 to exert its functional effects. Using in vitro and in vivo models of tumor necrosis factor α–induced hepatocyte cell death in mice, we find that activation of nuclear factor κB and increased expression of inducible NO are required for the protective effects of CO, whereas the protective effects of NO require up-regulation of HO-1 expression. When protection from cell death is initiated by CO, NO production and HO-1 activity are each required for the protective effect showing for the first time an essential synergy between these two molecules in tandem providing potent cytoprotection
Gamma-loud quasars: a view with BeppoSAX
We present SAX observations of the -ray emitting quasars
0836+710, 1510-089 and 2230+114. All the objects have been detected in the PDS
up to 100 keV and have extremely flat power-law spectra above 2 keV (=0.3--0.5). 0836+710 shows absorption higher than the galactic value and
marginal evidence for the presence of the redshifted 6.4 keV Iron line.
1510-089 shows a spectral break around 1 keV, with the low energy spectrum
steeper (=1.6) than the high energy power-law (=0.3). The
data are discussed in the light of current Inverse Compton models for the high
energy emission.Comment: 4 pages, 2 figures, to appear in the proceedings of the conference
"X-Ray Astronomy '99", Bologna, Italy, September 199
Rms-flux relation in the optical fast variability data of BL Lacertae object S5 0716+714
The possibility that BL Lac S5 0716+714 exhibits a linear root mean square
(rms)-flux relation in its IntraDay Variability (IDV) is analysed. The results
may be used as an argument in the existing debate regarding the source of
optical IDV in Active Galactic Nuclei. 63 time series in different optical
bands were used. A linear rms-flux relation at a confidence level higher than
65% was recovered for less than 8% of the cases. We were able to check if the
magnitude is log-normally distributed for eight timeseries and found, with a
confidence > 95%, that this is not the case.Comment: Accepted by Astrophysics and Space Scienc
Inhibition of platelet aggregation by carbon monoxide-releasing molecules (CO-RMs): comparison with NO donors
Carbon monoxide (CO) and CO-releasing molecules (CO-RMs) inhibit platelet aggregation in vitro. Herein, we compare the anti-platelet action of CORM-3, which releases CO rapidly (t½ 1 min), and CORM-A1, which slowly releases CO (t½ = 21 min). The anti-platelet effects of NO donors with various kinetics of NO release were studied for comparison. The effects of CO-RMs and NO donors were analyzed in washed human platelets (WP), platelets rich plasma (PRP), or whole blood (WB) using aggregometry technique. CORM-3 and CORM-A1 inhibited platelet aggregation in human PRP, WP, or WB, in a concentration-dependent manner. In all three preparations, CORM-A1 was more potent than CORM-3. Inhibition of platelets aggregation by CORM-A1 was not significantly affected by a guanylate cyclase inhibitor (ODQ) and a phosphodiesterase-5 inhibitor, sildenafil. In contrast, inhibition of platelet aggregation by NO donors was more potent with a fast NO releaser (DEA-NO, t½ = 2 min) than slow NO releasers such as PAPA-NO (t½ = 15 min) or other slow NO donors. Predictably, the anti-platelet effect of DEA-NO and other NO donors was reversed by ODQ while potentiated by sildenafil. In contrast to NO donors which inhibit platelets proportionally to the kinetics of NO released via activation of soluble guanylate cyclase (sGC), the slow CO-releaser CORM-A1 is a superior anti-platelet agent as compared to CORM-3 which releases CO instantly. The anti-platelet action of CO-RMs does not involve sGC activation. Importantly, CORM-A1 or its derivatives representing the class of slow CO releasers display promising pharmacological profile as anti-platelet agents
Heme oxygenase-1 prevents smoke induced B-cell infiltrates: a role for regulatory T cells?
<p>Abstract</p> <p>Background</p> <p>Smoking is the most important cause for the development of COPD. Since not all smokers develop COPD, it is obvious that other factors must be involved in disease development. We hypothesize that heme oxygenase-1 (HO-1), a protective enzyme against oxidative stress and inflammation, is insufficiently upregulated in COPD.</p> <p>The effects of HO-1 modulation on cigarette smoke induced inflammation and emphysema were tested in a smoking mouse model.</p> <p>Methods</p> <p>Mice were either exposed or sham exposed to cigarette smoke exposure for 20 weeks. Cobalt protoporphyrin or tin protoporphyrin was injected during this period to induce or inhibit HO-1 activity, respectively. Afterwards, emphysema development, levels of inflammatory cells and cytokines, and the presence of B-cell infiltrates in lung tissue were analyzed.</p> <p>Results</p> <p>Smoke exposure induced emphysema and increased the numbers of inflammatory cells and numbers of B-cell infiltrates, as well as the levels of inflammatory cytokines in lung tissue. HO-1 modulation had no effects on smoke induced emphysema development, or the increases in neutrophils and macrophages and inflammatory cytokines. Interestingly, HO-1 induction prevented the development of smoke induced B-cell infiltrates and increased the levels of CD4<sup>+</sup>CD25<sup>+ </sup>T cells and Foxp3 positive cells in the lungs. Additionally, the CD4<sup>+</sup>CD25<sup>+ </sup>T cells correlated positively with the number of Foxp3 positive cells in lung tissue, indicating that these cells were regulatory T cells.</p> <p>Conclusion</p> <p>These results support the concept that HO-1 expression influences regulatory T cells and indicates that this mechanism is involved in the suppression of smoke induced B-cell infiltrates. The translation of this interaction to human COPD should now be pursued.</p
Observations of a Correlated Gamma-Ray and Optical Flare for BL Lacertae
The latest observations of BL Lacertae with the EGRET instrument on CGRO show
that the gamma-ray flux was four times higher than the previous detection.
Within the 1997 July 15-22 observation there was a dramatic factor of 2.5
increase in the gamma-ray flux, with a sharp peak of about 8 hours, and
apparently preceding a brief optical flare by several hours. The gamma-ray
photon spectral index was significantly harder than that for the previous
detection.Comment: 11 pages, 3 figures. To be published in the Astrophysical Journal
Letter
Heme oxygenase-1 and carbon monoxide in pulmonary medicine
Heme oxygenase-1 (HO-1), an inducible stress protein, confers cytoprotection against oxidative stress in vitro and in vivo. In addition to its physiological role in heme degradation, HO-1 may influence a number of cellular processes, including growth, inflammation, and apoptosis. By virtue of anti-inflammatory effects, HO-1 limits tissue damage in response to proinflammatory stimuli and prevents allograft rejection after transplantation. The transcriptional upregulation of HO-1 responds to many agents, such as hypoxia, bacterial lipopolysaccharide, and reactive oxygen/nitrogen species. HO-1 and its constitutively expressed isozyme, heme oxygenase-2, catalyze the rate-limiting step in the conversion of heme to its metabolites, bilirubin IXα, ferrous iron, and carbon monoxide (CO). The mechanisms by which HO-1 provides protection most likely involve its enzymatic reaction products. Remarkably, administration of CO at low concentrations can substitute for HO-1 with respect to anti-inflammatory and anti-apoptotic effects, suggesting a role for CO as a key mediator of HO-1 function. Chronic, low-level, exogenous exposure to CO from cigarette smoking contributes to the importance of CO in pulmonary medicine. The implications of the HO-1/CO system in pulmonary diseases will be discussed in this review, with an emphasis on inflammatory states
Non-invasive measurements of exhaled NO and CO associated with methacholine responses in mice
<p>Abstract</p> <p>Background</p> <p>Nitric oxide (NO) and carbon monoxide (CO) in exhaled breath are considered obtainable biomarkers of physiologic mechanisms. Therefore, obtaining their measures simply, non-invasively, and repeatedly, is of interest, and was the purpose of the current study.</p> <p>Methods</p> <p>Expired NO (E<sub>NO</sub>) and CO (E<sub>CO</sub>) were measured non-invasively using a gas micro-analyzer on several strains of mice (C57Bl6, IL-10<sup>-/-</sup>, A/J, MKK3<sup>-/-</sup>, JNK1<sup>-/-</sup>, NOS-2<sup>-/- </sup>and NOS-3<sup>-/-</sup>) with and without allergic airway inflammation (AI) induced by ovalbumin systemic sensitization and aerosol challenge, compared using independent-sample t-tests between groups, and repeated measures analysis of variance (ANOVA) within groups over time of inflammation induction. E<sub>NO </sub>and E<sub>CO </sub>were also measured in C57Bl6 and IL-10-/- mice, ages 8–58 weeks old, the relationship of which was determined by regression analysis. S-methionyl-L-thiocitrulline (SMTC), and tin protoporphyrin (SnPP) were used to inhibit neuronal/constitutive NOS-1 and heme-oxygenase, respectively, and alter NO and CO production, respectively, as assessed by paired t-tests. Methacholine-associated airway responses (AR) were measured by the enhanced pause method, with comparisons by repeated measures ANOVA and post-hoc testing.</p> <p>Results</p> <p>E<sub>NO </sub>was significantly elevated in naïve IL-10<sup>-/- </sup>(9–14 ppb) and NOS-2<sup>-/- </sup>(16 ppb) mice as compared to others (average: 5–8 ppb), whereas E<sub>CO </sub>was significantly higher in naïve A/J, NOS-3<sup>-/- </sup>(3–4 ppm), and MKK3<sup>-/- </sup>(4–5 ppm) mice, as compared to others (average: 2.5 ppm). As compared to C57Bl6 mice, AR of IL-10<sup>-/-</sup>, JNK1<sup>-/-</sup>, NOS-2<sup>-/-</sup>, and NOS-3<sup>-/- </sup>mice were decreased, whereas they were greater for A/J and MKK3<sup>-/- </sup>mice. SMTC significantly decreased E<sub>NO </sub>by ~30%, but did not change AR in NOS-2<sup>-/- </sup>mice. SnPP reduced E<sub>CO </sub>in C57Bl6 and IL-10<sup>-/- </sup>mice, and increased AR in NOS-2<sup>-/- </sup>mice. E<sub>NO </sub>decreased as a function of age in IL-10<sup>-/- </sup>mice, remaining unchanged in C57Bl6 mice.</p> <p>Conclusion</p> <p>These results are consistent with the ideas that: 1) E<sub>NO </sub>is associated with mouse strain and knockout differences in NO production and AR, 2) alterations of E<sub>NO </sub>and E<sub>CO </sub>can be measured non-invasively with induction of allergic AI or inhibition of key gas-producing enzymes, and 3) alterations in AR may be dependent on the relative balance of NO and CO in the airway.</p
Sub-Milliarcsecond Imaging of Quasars and Active Galactic Nuclei. II. Additional Sources
We report further results from our imaging survey at 15GHz (lambda=2 cm) with
the Very Long Baseline Array. This paper presents single epoch images for 39
sources, bringing the total number of objects in the sample to 171. Our sample
is representative of a complete unbiased sample and it will be used for
statistical analysis of source properties. We compare the observed brightness
temperatures derived from our VLBA observations to those derived from total
intensity variations at 22 and 37 GHz. These are consistent with intrinsic
brightness temperatures in the range 10^10 to 10^12 K. We also present three
new spectroscopic redshift values: z=0.517+/-0.001 for 0026+346,
z=1.591+/-0.003 for 0727-115, and z=0.2016+/-0.0004 for 1155+251.
Images from this VLBA 2 cm survey are available on the Internet under
http://www.cv.nrao.edu/2cmsurvey.Comment: 21 pages, 6 figures, 4 tables, 1 appendix. Accepted for publication
(August 2002 issue) at The Astronomical Journal. Needs aastex.cls,
amsfonts.sty, amssymb.sty, apj.bst, natbib.st
Recommended from our members
Heme oxygenase-1 regulates cell proliferation via carbon monoxide-mediated inhibition of T-type Ca2+ channels
Induction of the antioxidant enzyme heme oxygenase-1 (HO-1) affords cellular protection and suppresses proliferation of vascular smooth muscle cells (VSMCs) associated with a variety of pathological cardiovascular conditions including myocardial infarction and vascular injury. However, the underlying mechanisms are not fully understood. Over-expression of Cav3.2 T-type Ca2+ channels in HEK293 cells raised basal [Ca2+]i and increased proliferation as compared with non-transfected cells. Proliferation and [Ca2+]i levels were reduced to levels seen in non-transfected cells either by induction of HO-1 or exposure of cells to the HO-1 product, carbon monoxide (CO) (applied as the CO releasing molecule, CORM-3). In the aortic VSMC line A7r5, proliferation was also inhibited by induction of HO-1 or by exposure of cells to CO, and patch-clamp recordings indicated that CO inhibited T-type (as well as L-type) Ca2+ currents in these cells. Finally, in human saphenous vein smooth muscle cells, proliferation was reduced by T-type channel inhibition or by HO-1 induction or CO exposure. The effects of T-type channel blockade and HO-1 induction were non-additive. Collectively, these data indicate that HO-1 regulates proliferation via CO-mediated inhibition of T-type Ca2+ channels. This signalling pathway provides a novel means by which proliferation of VSMCs (and other cells) may be regulated therapeutically
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