Nitric Oxide-cGMP Signaling in Hypertension Current and Future Options for Pharmacotherapy

被引:53
作者
Ataei Ataabadi, Ehsan [1 ]
Golshiri, Keivan [1 ]
Juttner, Annika [1 ]
Krenning, Guido [2 ,3 ]
Danser, A. H. Jan [1 ]
Roks, Anton J. M. [1 ]
机构
[1] Erasmus MC, Dept Internal Med, Div Pharmacol & Vasc Med, Room Ee1418 POB 2040, NL-3000 CA Rotterdam, Netherlands
[2] Sulfateq BV, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Cardiovasc Regenerat Med, Groningen, Netherlands
关键词
hypertension; mitochondria; nitric oxide; oxidoreductase; soluble guanylyl cyclase; SOLUBLE GUANYLATE-CYCLASE; KINASE G I; ACETYLCHOLINE-INDUCED HYPOTENSION; ELECTRONIC CIGARETTE-SMOKING; REACTIVE OXYGEN; BLOOD-PRESSURE; ENDOTHELIAL DYSFUNCTION; STIMULATOR PRALICIGUAT; HEART-FAILURE; ORGAN DAMAGE;
D O I
10.1161/HYPERTENSIONAHA.120.15856
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
For the treatment of systemic hypertension, pharmacological intervention in nitric oxide-cyclic guanosine monophosphate signaling is a well-explored but unexploited option. In this review, we present the identified drug targets, including oxidases, mitochondria, soluble guanylyl cyclase, phosphodiesterase 1 and 5, and protein kinase G, important compounds that modulate them, and the current status of (pre)clinical development. The mode of action of these compounds is discussed, and based upon this, the clinical opportunities. We conclude that drugs that directly target the enzymes of the nitric oxide-cyclic guanosine monophosphate cascade are currently the most promising compounds, but that none of these compounds is under investigation as a treatment option for systemic hypertension.
引用
收藏
页码:1055 / 1068
页数:14
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