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MECHANICS OF PULMONARY VASCULAR SMOOTH MUSCLE

MECHANICS OF PULMONARY VASCULAR SMOOTH MUSCLE
肺血管平滑肌的力学
批准号:
3355393
负责人:
JOHN N EVANS
金额:
$15.33万
依托单位国家:
美国
项目类别:
财政年份:
1987
资助国家:
美国
项目状态:
已结题
起止时间:
1987-07-01 至 1993-06-30

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中文摘要
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英文摘要
The long term goal of this proposal is to understand changes that occur in the function of vascular smooth muscle in pulmonary hypertension (PH). The basic mechanical properties of isolated vessels will be studied in normal rats and those with pulmonary hypertension induced by chronic exposure to hypobaric hypoxia. Hypoxic induced PH is characterized by extensive vascular remodeling including increased amounts of smooth muscle, extension of that muscle peripherally and increases in connective tissue. The increased resistance is a function of increased passive wall stiffness and altered smooth muscle contractile function. This proposal will characterize the properties of the smooth muscle cells of pulmonary arterial and venous vessels from normal and hypertensive rats. Circumference: tension and force: velocity relationships will be determined and related to contractile protein content and morphologic characteristics. Maximal active stress will be determined and related to the amount of actin and myosin. This basic characterization will be completed on large and small vessels from both arterial and venous system. In addition, single pulmonary vascular smooth muscle cells will be isolated and studied independent of the vessel wall and surrounding cells. The dependence of pharmacologic response of pulmonary vessels on circumference will be assessed. This proposal will provide unique data concerning the properties of pulmonary vascular smooth muscle in the normal as well as hypertensive vascular bed. This type of characterization will provide insight into the function of this circulation and changes responsible for the development of pulmonary hypertension.
期刊论文(4)
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会议论文
Spontaneous production of PDGF A-chain homodimer by rat lung fibroblasts in vitro.
体外大鼠肺成纤维细胞自发产生 PDGF A 链同二聚体。
DOI: 10.1152/ajplung.1992.263.2.l185
发表时间: 1992
期刊: The American journal of physiology
影响因子: --
作者: [Fabisiak,JP, Absher,M, Evans,JN, Kelley,J]
通讯作者: Kelley,J
Increased expression of PDGF-B (c-sis) mRNA in rat lung precedes DNA synthesis and tissue repair during chronic hyperoxia.
慢性高氧期间,大鼠肺中 PDGF-B (c-sis) mRNA 的表达增加先于 DNA 合成和组织修复。
DOI: 10.1165/ajrcmb/1.3.181
发表时间: 1989
期刊: American journal of respiratory cell and molecular biology
影响因子: 6.4
作者: [Fabisiak,JP, Evans,JN, Kelley,J]
通讯作者: Kelley,J
DOI: 10.1164/ajrccm/138.4.945
发表时间: 1988
期刊: The American review of respiratory disease
影响因子: --
作者: [Coflesky,JT, Evans,JN]
通讯作者: Evans,JN
DOI: 10.1378/chest.99.3_supplement.52s
发表时间: 1991
期刊: Chest
影响因子: 9.6
作者: [Fabisiak,JP, Evans,JN, Absher,M, Gannon,D, Kelley,J]
通讯作者: Kelley,J
CONSTRUCTION OF TRANSGENIC ANIMAL CARE FACILITY
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