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31. |
Dual Functionality of Cyclooxygenase-2 as a Regulator of Tumor Necrosis Factor–Mediated G1Shortening and Nitric Oxide–Mediated Inhibition of Vascular Smooth Muscle Cell Proliferation |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 8,
2003,
Page 1015-1021
Asifa Haider,
Irene Lee,
Jerzy Grabarek,
Zbigniew Darzynkiewicz,
Nicholas Ferreri,
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摘要:
Background—Cyclooxygenase (COX)-2 contributes to vascular smooth muscle cell (VSMC) proliferation induced by tumor necrosis factor (TNF) and angiotensin II. The present study demonstrates, however, that depending on prevailing conditions, COX-2–derived prostanoids may also inhibit VSMC proliferation.Methods and Results—TNF-&agr; stimulated proliferation of VSMCs by shortening the G1phase of the cell cycle. This effect was abolished by NS-398, a selective COX-2 inhibitor. Addition of TNF did not affect the protein-to-DNA ratio, measured by flow cytometry, suggesting that TNF does not induce VSMC hypertrophy. Inhibition of nitric oxide synthase (NOS) activity attenuated TNF-mediated increases in prostaglandin (PG) I2synthesis, whereas thromboxane (TX) A2production and COX-2 protein expression were unaffected. Moreover, inhibition of NOS activity increased TNF-mediated proliferation by ≈23%. Thus, NO preferentially stimulates PGI2production, suggesting that production of NO by VSMCs challenged with TNF limits the ability of the cytokine to increase proliferation. NO donors increased COX-2 protein expression and PGI2synthesis, had no effect on TXA2production, and decreased cell numbers by 50%, indicating that expression of COX-2 per se might not be sufficient to support proliferation. The effects of NO donors were prevented when COX-2 activity was inhibited with NS-398.Conclusions—The COX-2–dependent proliferative response of VSMCs to TNF was modulated in an NO-dependent manner, and PGI2derived from COX-2 might contribute to the antiproliferative effect of NO donors.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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32. |
Ultrasound-Targeted Microbubble Destruction Can Repeatedly Direct Highly Specific Plasmid Expression to the Heart |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 8,
2003,
Page 1022-1026
Raffi Bekeredjian,
Shuyuan Chen,
Peter Frenkel,
Paul Grayburn,
Ralph Shohet,
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摘要:
Background—Noninvasive, tissue-specific delivery of therapeutic agents would be a valuable clinical tool. We have previously shown that ultrasound-targeted microbubble destruction can direct expression of an adenoviral reporter to the heart. The present study shows that this method can be applied to selectively deliver plasmid vectors to the heart.Methods and Results—We used albumin and lipid microbubbles containing plasmids with a luciferase transgene to target the heart in rats. After 4 days, organs were harvested and analyzed for reporter gene expression. In a second set of experiments, the hearts of rats treated with plasmids were harvested at various time points during a 4-week period. Both luciferase activity and mRNA concentrations were measured. Luciferase transfection with plasmids showed highly specific gene expression in the heart, with hardly any activity in control organs. Time course evaluation showed high transgene expression in the first 4 days, with a rapid decline thereafter. Repeated treatment produced a second peak of transgene expression with similar decay.Conclusions—Ultrasound-mediated destruction of microbubbles directs plasmid transgene expression to the heart with much greater specificity than viral vectors and can be regulated by repeated treatments. This noninvasive technique is a promising method for cardiac gene therapy.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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33. |
Cisapride-Induced Transmural Dispersion of Repolarization and Torsade de Pointes in the Canine Left Ventricular Wedge Preparation During Epicardial Stimulation |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 8,
2003,
Page 1027-1033
José Di Diego,
Luiz Belardinelli,
Charles Antzelevitch,
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摘要:
Background—Cisapride, a gastrointestinal prokinetic agent, was recently withdrawn from the market because of its propensity to induce torsade de pointes (TdP) arrhythmias. The present study examines the electrophysiological actions of cisapride in the isolated arterially perfused canine left ventricular wedge preparation.Methods and Results—Transmembrane action potentials from epicardial and M regions and a pseudo-ECG were simultaneously recorded. Cisapride (0.1 to 5 &mgr;mol/L) was added to the coronary perfusate. Cisapride prolonged the QT interval and increased transmural dispersion of repolarization (TDR) at relatively low but not at high concentrations. TdP could be induced with programmed electrical stimulation only at a low concentration of drug (0.2 &mgr;mol/L), when TDR was maximally prolonged. Moreover, TdP could only be induced during epicardial (but not endocardial) activation of the wedge, which was found to augment TDR. At higher concentrations of cisapride, QT was further prolonged, TDR was diminished, and TdP could no longer be induced. Tpeak–Tendinterval and Tpeak–Tendarea provided reasonable electrocardiographic indices of TDR.Conclusion—Our data (1) demonstrate a biphasic concentration/response relationship for the effect of cisapride to induce long-QT syndrome and TdP, (2) show the value of the left ventricular wedge preparation in identifying drugs that pose an arrhythmic risk, (3) support the hypothesis that risk for development of TdP is related to the increase in TDR rather than to prolongation of the QT interval, and (4) indicate that epicardial activation of the left ventricle, as occurs during biventricular pacing, can facilitate the development of TdP under long-QT conditions.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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34. |
Visualization of Left Main Coronary Dissection by Magnetic Resonance Coronary Angiography |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 8,
2003,
Page 1034-1035
Mihaela Tebeica,
Srirama Swaminathan,
Neil Weissman,
Prithvi Rai,
Anthon Fuisz,
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PDF (84KB)
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ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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