Studies on the difference in the circumstances and the diseases between Japanese and Chinese

日本人和中国人的环境和疾病差异研究

基本信息

  • 批准号:
    05045047
  • 负责人:
  • 金额:
    $ 1.28万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for international Scientific Research
  • 财政年份:
    1993
  • 资助国家:
    日本
  • 起止时间:
    1993 至 无数据
  • 项目状态:
    已结题

项目摘要

Studies on the effects of various hypotensive drugs on left ventricular myocardial hypertrophy primarily by echocardiography have shown that calcium antagonists, angiotensin-converting enzyme inhibitors, alpha_2-blockers, and central sympatholytic drugs are effective for attenuating the condition, but that the effects of beta-blockers are unpredictable, and diuretics and direct vasodilators have no effects. However, the effects of hypotensive drugs have been suggested to vary among races, and there have been few studies in which the effects of hypotensive drugs on cardiac hypertrophy were compared internationally. Also, MRI has attracted attention as a method for measurement of the left ventricular weight, and comparison of the findings by MRI with those by conventional electrocardiography and echocardiography is interesting. This study is designed to evaluate anti-cardiac hypertrophy effects of various hypotensive drugs in Japanese and Chinese subjects by MRI as well as by echocaardio … More graphy and MRI.Objectives : Using cinemagnetic resonance imaging(MRI)and echocardiography(ECHO), we studied the effects of TCV-116, a specific antagonist for angiotensin II subtype 1 receptors, on hemodynamics and cardiac hypertrophy in patients with essential hypertension.Subjects and Methods : Twelve patients with essential hypertension received oral TCV-116 after a control period of placebo administration. Cine MRI images were acquired in the axial plane with a gradientecho technique, GRASS, with echo time of 13 msec, repetition time of 66 msec, and flip angle of 20 degrees. Simpson's rule was used forleft ventricular volume and mass measurements by MRI. Left ventricular volumes by ECHO were calculated using Teichholz's formula. Left ventricular mass(LVM)by ECHO was measured using American Society of Echocardiography measurements and the formula by Devereux et al. : LVM=0.8[1.04(IVS+LVID+PWT)^3-LVID^3)]+0.6g. (IVS : interventricularseptal thickness, PWT : posterior wall thickness, LVID : left ventricular internal dimension)Results : Final daily doses of TCV-116 were 8 mg in 7 patients, 4 mg in 3 patients and 2 mg in 2 patients. After TCV-116 administration, systolic BP decreased from 185*19(mean*SD)to 161*30 mmHg and diastolic BP from 108*10 to 96*13(n=12, p<0.005)while HR remained unchanged from 70*12 to 70*9 bpm(n=12, NS). Both MRI and ECHO revealed a significant decrease in LVM after TCV-116 administration(n=12, p<0.05). MRI revealed a significant decrease in TSR from 1888*473 to 1702*408 dynes-sec-cm^<-5>(n=11, p<0.05). No significant changes were observed in other hemodynamic parameters before and after TCV-116 administration.Conclusions : Inpatients with essential hypertension, TCV-116 administered orally at doses of 2-8 mg/day for 8-12 weeks reduced blood pressure and led to a regression of cardiac hypertrophy. No deficient changes were observed in other hemodynamic parameters.The above tests will be carried out and effects will be compared between Japanese and Chinese subjects in further studies. Less
Studies on the effects of various hypotensive drugs on left ventricular myocardial hypertrophy primary by echocardiography have shown that calcium antagonists, angiotensin-converting enzyme inhibitors, alpha_2-blockers, and central sympatholytic drugs are effective for attenuating the condition, but that the effects of beta-blockers are unpredictable, and diuretics and direct vasodilators have no effects.然而,已经提出降压药在种族之间有所不同,很少有研究在国际上比较了降压药对心脏肥大的影响。同样,MRI吸引了人们的注意,作为测量左心室重量的方法,并比较MRI与传统心电图和超声心动图的发现,很有趣。这项研究旨在评估MRI以及通过Echocaardio以及Echocaardio的日本和中国受试者的各种降压药的抗心肥力影响……更多的图形和MRI。目标:使用Cinemagnetic共鸣成像(MRI)和超声心动图(MRI)和超声心动图(ECHO)(echo),我们研究了TCV-116的特定敌人,一位特定的敌人,一位特定的敌人,是一位特定的敌人,,一名特定的敌人,是一种特定的敌人,是一种特定的敌人,启用了特定的敌人。基本高血压患者的血液动力学和心脏肥大。受试者和方法:在控制安慰剂后,十二例基本高血压患者接受了口服TCV-116。用梯形技术,草,回波时间为13毫秒,重复时间为66毫秒和20度的翻转角度,在轴向平面中获取了Cine MRI图像。 Simpson的规则被MRI使用了侧心体积和质量测量。使用Teichholz的公式计算出回声的左心室体积。通过美国超声心动图测量学会和Devereux等人的公式测量左心室质量(LVM):LVM = 0.8 [1.04(IVS+LVID+PWT)^3-LVID^3)]+0.6G。 (IVS:介入的厚度,PWT:后壁厚度,LVID:左心室内部尺寸)结果:7例患者的最终每日TCV-116剂量为8 mg,3例患者为4毫克,2例患者为2毫克。 TCV-116给药后,收缩压从185*19(平均*SD)降低到161*30 mmHg,舒张压从108*10至96*13(n = 12,p <0.005),而HR保持不变从70*12至70*9 bpm(n = 12,n = 12,ns)。 MRI和ECHO均显示TCV-116给药后LVM显着降低(n = 12,p <0.05)。 MRI显示TSR从1888*473到1702*408 Dynes-Sec-Cm^<-5>(n = 11,p <0.05)显着下降。 TCV-116给药之前和之后的其他血液动力学参数未观察到显着变化。结论:具有必不可少的高血压的住院患者,以2-8 mg/天的剂量口服TCV-116,持续8-12周,降低了血压,导致了心脏肥大的回归。在其他血液动力学参数中未观察到不足的变化。将进行上述测试,并在进一步的研究中比较日本和中国受试者之间的影响。较少的

项目成果

期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
I.Nakae,L.Quan,K.Hashimoto,Y.Sugimoto,T.Tsutamoto and M.Kinoshita: "Mechanism of the Vasodilatory Action of Nicorandil on Coronary Circulation in Dogs" Cardiovascular Drugs and Therapy. 8. 73-81 (1994)
I.Nakae,L.Quan,K.Hashimoto,Y.Sugimoto,T.Tsutamoto和M.Kinoshita:“尼可地尔对狗冠状动脉循环的血管舒张作用的机制”心血管药物和治疗。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
I.Nakae, L.Quan, K.Hashimoto, Y.Sugimoto, T.Tsutamoto and M.Kinoshita: "Mechanism of the Vasodilatory Action of Nicorandil on Coronary Circulation in Dogs" Cardiovascular Drugs and Therapy. 8. 73-81 (1994)
I.Nakae、L.Quan、K.Hashimoto、Y.Sugimoto、T.Tsutamoto 和 M.Kinoshita:“尼可地尔对狗冠状动脉循环的血管舒张作用机制”心血管药物和治疗。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

OKADA Yoshio其他文献

OKADA Yoshio的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('OKADA Yoshio', 18)}}的其他基金

Immunohistologial study on the expression of developmental intestinal epithelial antigens in embryogenesis and oncogenesis.
胚胎发生和肿瘤发生中发育肠上皮抗原表达的免疫组织学研究。
  • 批准号:
    14570499
  • 财政年份:
    2002
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Curriculum Development based on the children's learning ability
基于孩子学习能力的课程开发
  • 批准号:
    11680270
  • 财政年份:
    1999
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Design and synthesis of μ-selective opioidomimetic peptides
μ选择性阿片样肽的设计与合成
  • 批准号:
    11694326
  • 财政年份:
    1999
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Infectious disease, and hepatic and gastrointestinal disease in Japan and China
日本和中国的传染病、肝脏和胃肠道疾病
  • 批准号:
    07045049
  • 财政年份:
    1995
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Gene cloning of a novel apomucin expressed in human gastric surface epithelia and parietal cells
人胃表面上皮和壁细胞表达的新型阿普粘蛋白的基因克隆
  • 批准号:
    07670608
  • 财政年份:
    1995
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Gastrointestinal and hematologic diseases in Japan and China
日本和中国的胃肠道和血液疾病
  • 批准号:
    06045020
  • 财政年份:
    1994
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Basic Researches on Cell Fusion and Their Application to Cell Technology
细胞融合基础研究及其在细胞技术中的应用
  • 批准号:
    01102028
  • 财政年份:
    1989
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for Co-operative Research (A).
Experimental Sutdies for Application of the Heterogeneous Lung as Oxygenator
应用异质肺作为氧合器的实验研究
  • 批准号:
    01440056
  • 财政年份:
    1989
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (A)
FUNDAMENTAL AND CLINICAL RESEARCH ON THE RELATIONSHIP BETWEEN PULMONARY LYMPHATIC SYSTEMS AND THE PATHOGENESIS OF VARIOUS LUNG DISEASES
肺淋巴系统与多种肺部疾病发病关系的基础和临床研究
  • 批准号:
    60440062
  • 财政年份:
    1985
  • 资助金额:
    $ 1.28万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (A)

相似国自然基金

基于磷脂酶PLA2G6调控NLRP3炎症小体激活探讨西洋参抑制心脏肥大的机制研究
  • 批准号:
    82360787
  • 批准年份:
    2023
  • 资助金额:
    32.00 万元
  • 项目类别:
    地区科学基金项目
沉默因子REST介导心脏肥大α-MHC反转调节的染色质重塑机制
  • 批准号:
  • 批准年份:
    2020
  • 资助金额:
    58 万元
  • 项目类别:
    面上项目
基于甘油磷脂代谢研究西洋参抑制心脏肥大的作用机制
  • 批准号:
    81960732
  • 批准年份:
    2019
  • 资助金额:
    34 万元
  • 项目类别:
    地区科学基金项目
糖尿病心肌病中HuR调控成纤维细胞分泌导致心肌肥大EVs的机制研究
  • 批准号:
    81903607
  • 批准年份:
    2019
  • 资助金额:
    21.0 万元
  • 项目类别:
    青年科学基金项目
右美托咪定预处理抑制肥大细胞脱颗粒在心脏抗I/R损伤中的机制研究
  • 批准号:
    81860050
  • 批准年份:
    2018
  • 资助金额:
    35.0 万元
  • 项目类别:
    地区科学基金项目

相似海外基金

Examining the Function of a Novel Protein in the Cardiac Junctional Membrane Complex
检查心脏连接膜复合体中新型蛋白质的功能
  • 批准号:
    10749672
  • 财政年份:
    2024
  • 资助金额:
    $ 1.28万
  • 项目类别:
The role of BET proteins in pathological cardiac remodeling
BET蛋白在病理性心脏重塑中的作用
  • 批准号:
    10538142
  • 财政年份:
    2023
  • 资助金额:
    $ 1.28万
  • 项目类别:
Nanowired humam cardiac organoid derived exosomes for heart repair
纳米线人类心脏类器官衍生的外泌体用于心脏修复
  • 批准号:
    10639040
  • 财政年份:
    2023
  • 资助金额:
    $ 1.28万
  • 项目类别:
Virtual drug screen reveals context-dependent inhibition of cardiomyocyte hypertrophy
虚拟药物筛选揭示了心肌细胞肥大的情境依赖性抑制
  • 批准号:
    10678351
  • 财政年份:
    2023
  • 资助金额:
    $ 1.28万
  • 项目类别:
A role for cardiomyocyte pannexin 1 in non-ischemic heart failure
心肌细胞pannexin 1在非缺血性心力衰竭中的作用
  • 批准号:
    10680109
  • 财政年份:
    2023
  • 资助金额:
    $ 1.28万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了