AUTONOMIC RECEPTOR FUNCTION IN MYOCARDIAL ISCHEMIA
心肌缺血中的自主受体功能
基本信息
- 批准号:3364332
- 负责人:
- 金额:$ 5.57万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1990
- 资助国家:美国
- 起止时间:1990-07-01 至 1994-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
One hour of myocardial ischemia results in increased beta-adrenergic
receptor density but uncoupling of the beta-adrenergic receptor from
adenylate cyclase associated with decreases in the GTP regulatory protein,
G(s-alpha). The goals of this research proposal are directed at examining
the mechanism and time course of these changes as well as whether the
changes are reversible with coronary artery reperfusion. One major feature
is the combined study of physiology in the conscious animal instrumented
for measurement of subendocardial and subepicardial wall motion in ischemic
and nonischemic zones with biochemical measurements from the same hearts.
Coronary artery occlusion and reperfusion will be verified by direct
measurement of coronary blood flow (Doppler technique) and regional
myocardial blood flow (radioactive microsphere technique). The second
critical feature of the experimental design is the study of the changes in
subendocardial and subepicardial regions of the ischemic zone compared with
respective control values in the subendocardium and subepicardium in the
non-ischemic zone from the same hearts. Specifically ,beta-adrenergic
receptor agonist and antagonist binding, adenylate cyclase activity, cyclic
AMP, and GTP regulatory proteins will be examined in models of acute
myocardial ischemia. After determining the time course of changes in
autonomic receptors and coupling to adenylate cyclase, it will be
determined whether the changes are reversible by coronary artery
reperfusion.Another major goal is to determine whether changes are
transmural or affected regionally across the myocardial wall varying with
the level of ischemia across the myocardial wall. These experiments will be
compared where ischemia is more intense subendocardially and where ischemia
is equally intense in subepi- and subendocardium. In addition to examining
the responsiveness of in vivo myocardial wall motion and cellular changes
to beta-adrenergic stimulation with isoproterenol, mechanisms will be
addressed by examining the effects of coronary artery occlusion and
reperfusion in the presence and absence of alpha- and beta-adrenergic
receptor blockades and also in the desensitized heart, induced by
chronically elevated norepinephrine levels.
心肌缺血一小时会导致肾上腺素能增高
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Dorothy Eileen Vatner其他文献
Dorothy Eileen Vatner的其他文献
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{{ truncateString('Dorothy Eileen Vatner', 18)}}的其他基金
Adenylyl Cyclase Type 5 Inhibition to Treat Myocardial Infarction
腺苷酸环化酶 5 型抑制治疗心肌梗死
- 批准号:
9764847 - 财政年份:2018
- 资助金额:
$ 5.57万 - 项目类别:
INHIBITION OF ADENYLYL CYCLASE TYPE 5: HEALTHFUL AGING PROTECTION
抑制 5 型腺苷酸环化酶:健康的抗衰老保护
- 批准号:
9321949 - 财政年份:2016
- 资助金额:
$ 5.57万 - 项目类别:
SFRP2, cell survival, and coronary vascular angiogenesis
SFRP2、细胞存活和冠状血管生成
- 批准号:
8875747 - 财政年份:2013
- 资助金额:
$ 5.57万 - 项目类别:
SFRP2, cell survival, and coronary vascular angiogenesis
SFRP2、细胞存活和冠状血管生成
- 批准号:
8563199 - 财政年份:2013
- 资助金额:
$ 5.57万 - 项目类别:
Rescue of Beta-Adrenergic Cardiomyopathy by Inhibition of Adenylyl Cyclase
通过抑制腺苷酸环化酶来挽救β-肾上腺素能心肌病
- 批准号:
7638978 - 财政年份:2009
- 资助金额:
$ 5.57万 - 项目类别:
Rescue of Beta-Adrenergic Cardiomyopathy by Inhibition of Adenylyl Cyclase
通过抑制腺苷酸环化酶来挽救β-肾上腺素能心肌病
- 批准号:
7787533 - 财政年份:2009
- 资助金额:
$ 5.57万 - 项目类别:
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