THE DEVELOPMENT AND THE CLINICAL APPLICATION OF AN OPTICAL SYSTEM FOR THE SIMULTANEOUS DETERMINATION OF METABOLIC AND FUNCTIONAL CHANGES IN THE HEART AND BLOOD VESSELS.
用于同时测定心脏和血管代谢和功能变化的光学系统的开发和临床应用。
基本信息
- 批准号:03557043
- 负责人:
- 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 Developmental Scientific Research (B)
- 财政年份:1991
- 资助国家:日本
- 起止时间:1991 至 1993
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
(1) The development of a system for the simultaneous determination of metabolic and functional changes in the heart and blood vessels : A front-surface fluorometer with concentric optical fibers for double-wave length excitation (inner circle quartz fibers) and fluorescence detection (outer circle glass fibers) (CAM OF-2) was successfully and specifically designed and made with the collaboration of Japan Spectroscopic Co., Tokyo, Japan.(2) Using front-surface fluorometry of fura-2-loaded aortic valvular strips, the cytosolic Ca concentration, (Ca)i, of the endothelial cells in situ was firstly and quantitatively recorded. Both endothelin (ET)-1 and ET-3 elevated (Ca)i in the endothelial cells in situ. ET-1 elevated (Ca)i of a peak (the first phase) and sustained (the second phase) type. The second phase was exclusively extracellular Ca-dependent, Ca influx. Pertussis toxin (IAP) markedly inhibited the second phase. Thus, Ca influx induced by ET-1 is regulated by an IAP-sensitive G-protein in the endothelial cells in situ.(3) The effects of ethanol on the contractility of strips of porcine coronary artery, with and without endothelium, and following permeabilization with alpha -toxin, and on aortic valvular endothelial cells in situ were examined. It was found that ethanol contracted the coronaty artery both by increasing (Ca)i and by raising Ca sensitivity of the contractile apparatus, as mediated by GTP-binding protein. When the endothelium was exposed to ethanol, this contraction was prevented, presumably by releasing endothelium-derived relaxing factor (EDRF).(4) Using front-surface fluorometry and BCECF-loaded isolated perfused rat heart, pH changes of the myocardium was successfully recorded during ischemia-reperfusion. It was found that captoril, an angiotensin converting enzyme inhibitor, could partially inhibit the development of acidosis during ischemia.
(1)同时测定心脏和血管中代谢和功能变化的系统的开发:与Japan Spectroscopic Co.合作,成功地专门设计并制造了具有用于双波长激发(内环石英纤维)和荧光检测(外环玻璃纤维)的同心光纤的前表面荧光计(CAM OF-2),日本东京(2)利用荧光法测定了Fura-2负载的主动脉瓣条的前表面,首次定量记录了原位内皮细胞的胞浆Ca浓度(Ca)i。内皮素(ET)-1和ET-3均使内皮细胞内Ca ~(2+)升高。ET-1升高(Ca)i呈高峰(第一时相)和持续(第二时相)型。第二阶段是完全细胞外钙依赖性,钙内流。百日咳毒素(IAP)明显抑制第二时相。因此,由ET-1诱导的Ca内流在内皮细胞中由IAP敏感的G蛋白原位调节。(3)本文研究了乙醇对猪冠状动脉条(有内皮和无内皮)和α-毒素透化后收缩性的影响,以及对原位主动脉瓣内皮细胞的影响。结果表明,乙醇收缩冠状动脉的作用是通过增加(Ca)i和提高收缩器官的Ca敏感性两种途径实现的,这是由GTP结合蛋白介导的。当内皮细胞暴露于乙醇时,这种收缩被阻止,可能是通过释放内皮源性舒张因子(EDRF)。(4)应用前表面荧光法和负载BCECF的离体灌流大鼠心脏,成功地记录了缺血-再灌注过程中心肌pH的变化。发现血管紧张素转换酶抑制剂captoril可部分抑制缺血时酸中毒的发展。
项目成果
期刊论文数量(48)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Ushio-Fukai M: "Effects of isoprenaline on cytosolic calcium concentrations and on tension in the porcine coronary artery" J Physiol. 462. 679-696 (1993)
Ushio-Fukai M:“异丙肾上腺素对胞质钙浓度和猪冠状动脉张力的影响”J Physiol。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Aoki,H.: "Relationship between cytosolic calcium concentration and force in the papaverine-induced relaxation of medial strips of pig coronary artery." Br.J.Pharmacol.111. 489-496 (1994)
Aoki,H.:“胞质钙浓度与罂粟碱诱导的猪冠状动脉内侧条松弛的力之间的关系。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
K.Hirano: "Temporal changes in the calcium-force relation during histamine-induced contractions of strips of the coronary artery of the pig." Br J Pharmacol. 102. 27-34 (1991)
K.Hirano:“组胺诱导猪冠状动脉收缩期间钙-力关系的时间变化。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
H.Yamamoto: "Dextran sulfate inhibits the inositol 1,4,5-trisphosphate-induced Ca^<2+> release from skinned and cultured smooth muscle cells." Eur J Pharmacol. 206. 175-179 (1991)
H.Yamamoto:“硫酸葡聚糖抑制肌醇1,4,5-三磷酸诱导的Ca^2从剥皮和培养的平滑肌细胞中释放。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Natori Y: "Effects of L-NMMA and L-NNA on the selective ATP-induced enhancement of intratumoral blood flow." J Cereb Blood Flow Metab. 12. 120-127 (1992)
Natori Y:“L-NMMA 和 L-NNA 对选择性 ATP 诱导的瘤内血流增强的影响。”
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
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KANAIDE Hideo其他文献
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{{ truncateString('KANAIDE Hideo', 18)}}的其他基金
Development of a system for the continuous and simultaneous measurement of vascular intracellular signalings and metabolism
开发连续同步测量血管细胞内信号传导和代谢的系统
- 批准号:
13557067 - 财政年份:2001
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Molecular mechanisms of vasospasm : Intracellular signaling network underlying the Ca^<2+> of smooth muscle cells.
血管痉挛的分子机制:平滑肌细胞Ca^2 的细胞内信号网络。
- 批准号:
13470149 - 财政年份:2001
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Development of the optical system for continuous and multi-factorial monitoring of the intracellular signaling network in endothelial and smooth muscle cells in vascular strips.
开发光学系统,用于连续和多因素监测血管条内皮细胞和平滑肌细胞的细胞内信号网络。
- 批准号:
10557072 - 财政年份:1998
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for Scientific Research (B).
Studies on molecular cell biology of the inhibition of coronary vasoconstriction and intimal thickening.
抑制冠状血管收缩和内膜增厚的分子细胞生物学研究。
- 批准号:
07407022 - 财政年份:1995
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
TO DEVELOP A NEW SYSTEM TO CONTIMUOUSLY MONITOR THE FUNCTIONS AT THE CELLULAR AND MOLECULAR LEVELS OF THE VASCULAR ENDOTHELIAL AND SMOOTH MUSCLE CELLS IN VIVO.
开发一种新系统,在体内连续监测血管内皮细胞和平滑肌细胞的细胞和分子水平的功能。
- 批准号:
06557045 - 财政年份:1994
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
THE PATHOGENESIS OF AN INCREASE IN VASCULAR TONUS : THE DEVELOPMENT OF NEW VASODILATORS.
血管紧张度增加的发病机制:新血管扩张剂的开发。
- 批准号:
04454268 - 财政年份:1992
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
CELLULAR BIOLOGY OF ANTIANGINAL AGENTS ; DEVELOPMENT AND EVALUATION OF NEW DRUGS.
抗心绞痛药物的细胞生物学;
- 批准号:
01480250 - 财政年份:1989
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Ischemic Reperfusion Myocardial Injury ; Its Mechanism and Prevention.
缺血再灌注心肌损伤;
- 批准号:
61570422 - 财政年份:1986
- 资助金额:
$ 7.17万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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