Investigation of Regression of Atherosclerotic Lesion through Regulation of Nitric Oxide Related Responses -Treatment by Gene Transfer of Nitric Oxide Synthase-
Investigation of Regression of Atherosclerotic Lesion through Regulation of Nitric Oxide Related Responses -Treatment by Gene Transfer of Nitric Oxide Synthase-
批准号:
09470166
负责人:
IGUCHI Akihisa
金额:
$7.17万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1999
中文摘要
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英文摘要
We determined the effect of endothelial and inducible nitric oxide synthase (eNOS, iNOS) gene transfer using adenovirus vector on the advanced lesion of atherosclerosis. We prepared adenovirus vector of eNOS and iNOS cDNA. The abdominal aortae of 40 male and oophorectomized female rabbits were injured by balloon catheter and they were fed with HCD [standard diet and 1% cholesterol] for 12 weeks. After treatment, we made sure the size and character of atherosclerosis in thoracic (HCD induced) and abdominal (endothelial injury plus HCD) aorta using IVUS (intra vascular ultra sonography). Then, we transferred gene of eNOS, iNOS and eNOS plus iNOS onto atherosclerotic lesion of thoracic and abdominal aorta using dispatch blood flow reserved catheter. As the control, cDNA vector of β-galactosidase was transferred. After 3 and 7 days of gene transfer, the change of size and character of atherosclerosis in thoracic and abdominal aorta was examined using IVUS, and then, animals were sacrificed … More and examined as below. Basal and stimulated NO release was estimated by an NO selective electrode as well as vascular response and the plasma NO metabolites. Surface involvement and area occupied by atherosclerotic lesion were also evaluated. An immunohistochemical study was done. The area occupied by macrophage derived foam cells was numbered. HCD mediated increased plasma lipid levels were not affected by gene transfer of each vector. Not only atherosclerosis in the thoracic aorta but also severe atherosclerosis in the abdominal aorta was partially improved by eNOS and iNOS gene transfer. The acetylcholine-induced NO-mediated relaxation was severely impaired in HCD supplemented balloon injured rabbits. The impaired abdominal aortic relaxation of balloon injured and atherogenic diet supplemented rabbits was slightly restored by eNOS and iNOS gene transfer. The above results suggest that gene transfer of eNOS and iNOS could regress the advanced lesion of severe mechanisms and more effective combined virus vector will be elucidated from now. Less
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Hayashi T.Iguchi A.他2名: "Estriol replacement improves endothelial function and bone mineral density in elderly women"J gerontology. (印刷中). (2000)
Hayashi T. Iguchi A. 和其他 2 人:“雌三醇替代可改善老年女性的内皮功能和骨矿物质密度”J gerontology(出版中)。
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Hayashi T.Iguchi A.他3名: "Physiological concentration of 17β estradiol retards the progression of severe atherosclerosis induced by cholesterol diet plus balloon injury via NO."Arterioscler Thromb Vasc Biol. (印刷中). (2000)
Hayashi T. Iguchi A. 和其他 3 人:“17β 雌二醇的生理浓度可延缓由胆固醇饮食和 NO 造成的球囊损伤引起的严重动脉粥样硬化的进展。”Arterioscler Thromb Vasc Biol(出版中)。
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Hayashi T., Iguchi A. 他3名: "Physiological concen*m*on of 17β****diol re**nts the prog**ion of severe ******len*is induced by cholemen**diet plus b*llo** injury vi* NO."Arterioscler Thromb Vasc Biol.. (印刷中). (2000)
Hayashi T.、Iguchi A. 和其他 3 人:“17β****二醇的生理浓度*m*on与胆碱引起的严重******len*的进展有关**饮食加上 b*llo** 损伤 vi* NO。“Arterioscler Thromb Vasc Biol..(印刷中)。(2000)
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Hayashi T., Iguchi A. 他6名: "dehydrosplandn***ne re***ds *the***l**mls fom**** through the co*emion to e*rogen The po****e role of **s*oxl**"Arterioscler Thromb Vasc Biol.. (印刷中). (2000)
Hayashi T.、Iguchi A. 和其他 6 人:“deHydrossplandn***ne re***ds *the***l**mls fom**** through the co*emion to e*rogen The po*** * **s*oxl** 的作用“Arterioscler Thromb Vasc Biol..(印刷中)。(2000)
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Hayashi T,Iguchi A.: "Nipradilol:A β-adrenoceptor antagonist with nitric oxide-releasing action." Cardiovase Drug Reviews. 16. 212-236 (1998)
Hayashi T、Iguchi A.:“尼普地洛:具有一氧化氮释放作用的 β-肾上腺素受体拮抗剂。”Cardiovase Drug Reviews 16. 212-236 (1998)。
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