Prostaglandin H synthase and vascular function

被引:184
作者
Davidge, ST
机构
[1] Univ Alberta, Perinatal Res Ctr, Dept Obstet Gynecol, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Perinatal Res Ctr, Dept Physiol, Edmonton, AB T6G 2S2, Canada
关键词
endothelium; cyclooxygenase; prostaglandin; thromboxane; eicosanoid;
D O I
10.1161/hh2001.098351
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prostaglandin H synthase (PGHS) is a rate-limiting enzyme in the production of prostaglandins and thromboxane, which are important regulators of vascular function. Under normal physiological conditions, PGHS-dependent vasodilators (such as prostacyclin) modulate vascular tone. However, PGHS-dependent vasoconstriction (mediated by thromboxane and/or its immediate precursor, PGH,) predominates in some vascular pathologies (eg, systemic hypertension, diabetes, cerebral ischemia, and aging). This review will discuss the role of PGHS-dependent modulation of vascular function in a number of vascular beds (systemic, pulmonary, cerebral, and uterine) with an emphasis on vascular pathophysiology. Moreover, the specific contributions of the different isoforms (PGHS-1 and PGHS-2) are discussed. Understanding the role of PGHS in vascular function is of particular importance because they are the targets of the commonly used nonsteroidal antiinflammatory drugs (NSAIDs), which include aspirin and ibuprofen. Importantly, with the advent of specific PGHS-2 inhibitors for treatment of conditions such as chronic inflammatory disease, it is an opportune time to review the data regarding PGHS-dependent modulation of vascular function.
引用
收藏
页码:650 / 660
页数:11
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