Role of 20-hydroxyeicosatetraenoic acid (20-HETE) in vascular system
Author:
Affiliation:
1. Medicinal Research Laboratory, Taisho Pharmaceutical Co., Ltd.
2. Department of Physiology and Medicine and Kidney Disease Center, Medical College of Wisconsin
Publisher
Japan Society of Smooth Muscle Research
Subject
General Medicine,Physiology
Link
https://www.jstage.jst.go.jp/article/jsmr/41/4/41_4_175/_pdf
Reference116 articles.
1. Alonso-Galicia, M., Sun, C.W., Falck, J.R., Harder, D.R. and Roman, R.J. (1998). Contribution of 20-HETE to the vasodilator actions of nitric oxide in renal arteries. Am. J. Physiol. 275: F370-F378.
2. Alonso-Galicia, M., Falck, J.R., Reddy, K.M. and Roman, R.J. (1999). 20-HETE agonists and antagonists in the renal circulation. Am. J. Physiol. 277: F790-F796.
3. Alonso-Galicia, M., Maier, K.G., Greene, A.S., Cowley, A.W. Jr. and Roman, R.J. (2002). Role of 20-hydroxyeicosatetraenoic acid in the renal and vasoconstrictor actions of angiotensin II. Am. J. Physiol. 283: R60-R68.
4. Amaral, S.L., Maier, K.G., Schippers, D.N., Roman, R.J. and Greene, A.S. (2003). CYP4A metabolites of arachidonic acid and VEGF are mediators of skeletal muscle angiogenesis. Am. J. Physiol. 284: H1528-H1535.
5. Bednar, M.M., Gross, C.E., Balazy, M.K., Belosludtsev, Y., Colella, D.T., Falck, J.R. and Balazy, M. (2000). 16(R)-hydroxy-5,8,11,14-eicosatetraenoic acid, a new arachidonate metabolite in human polymorphonuclear leukocytes. Biochem. Pharmacol. 60: 447-455.
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