Therapeutic potential of pharmacologically targeting arteriolar myogenic tone

被引:65
作者
Hill, Michael A. [1 ,2 ]
Meininger, Gerald A. [1 ,2 ]
Davis, Michael J. [1 ,2 ]
Laher, Ismail [3 ]
机构
[1] Univ Missouri, Dalton Cardiovasc Res Ctr, Columbia, MO 65211 USA
[2] Univ Missouri, Dept Med Pharmacol & Physiol, Columbia, MO 65211 USA
[3] Univ British Columbia, Dept Pharmacol & Therapeut, Vancouver, BC V6T 1Z3, Canada
基金
美国国家卫生研究院;
关键词
VASCULAR SMOOTH-MUSCLE; LIGHT-CHAIN PHOSPHORYLATION; CA2+-ACTIVATED K+ CHANNELS; RHO-KINASE; CA2+ SPARKS; MYOSIN PHOSPHORYLATION; ACTIN CYTOSKELETON; CEREBRAL-ARTERIES; G-PROTEINS; SARCOPLASMIC-RETICULUM;
D O I
10.1016/j.tips.2009.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The arteriolar myogenic response, which is defined as vasoconstriction to increases in intraluminal pressure and, conversely, dilation to a reduction in pressure, is key in the setting of vascular resistance, local control of microvascular blood flow through autoregulation, and in the control of capillary hydrostatic pressure. Although considerable progress has been made in the quest for understanding the underlying sensory apparatus and cellular mechanisms, fundamental questions remain particularly if this pathway is to be considered as a target for novel strategies of pharmacological intervention. We propose that an ability to 're-set' myogenic tone would enable modification of systemic vascular resistance and pressure while at the same time preserving existing interactions with neurohumoral regulatory mechanisms. The challenge, therefore, is to identify steps unique to the myogenic signaling pathway to enable specific pharmacological targeting.
引用
收藏
页码:363 / 374
页数:12
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