Platelet and vessel associated prostacyclin and thromboxane A2/prostaglandin endoperoxide receptors
Corresponding Author
K. JASCHONEK
Medizinische Klinik der Universität Tübingen, D-7400 Tübingen, FRG
2 Medizinische Klinik der Universität Tübingen, Otfried-Müller Straße 10, D-7400 Tübingen, FRGSearch for more papers by this authorC. P. MULLER
Medizinische Klinik der Universität Tübingen, D-7400 Tübingen, FRG
Search for more papers by this authorCorresponding Author
K. JASCHONEK
Medizinische Klinik der Universität Tübingen, D-7400 Tübingen, FRG
2 Medizinische Klinik der Universität Tübingen, Otfried-Müller Straße 10, D-7400 Tübingen, FRGSearch for more papers by this authorC. P. MULLER
Medizinische Klinik der Universität Tübingen, D-7400 Tübingen, FRG
Search for more papers by this authorAbstract
Abstract. Synthetic stable analogues of thromboxane A2 (TXA2), cyclic endoperoxides (PGH2) and prostacyclin (PGI2) opened up new opportunities for investigating the mechanisms of action of these compounds. They proved to be useful pharmacological probes for characterizing PGI2 and TXA2/PGH2 receptors. Over the past few years, new synthetic antagonists with high specificity allowed the modulation of biological responses to endogenous eicosanoids. These compounds will, therefore, considerably promote our understanding of the biological function and significance of arachidonate metabolites. The present review summarizes current concepts that have arisen concerning platelet and vascular PGI2 and TXA2/PGH2 receptors, their transmembrane signal transduction, as well as their possible implications in the pathophysiology of cardiovascular disease.
Abbreviations:
-
- Cyclic AMP
-
- 3‘, 5’-adenosine-monophosphate
-
- IP3
-
- inositol-1, 4, 5-trisphosphate
-
- GTP
-
- guanosine-5-triphosphate
-
- G
-
- guanyl nucleotide binding regulatory proteins
-
- PGH2
-
- cyclic endoperoxides
-
- PG
-
- prostaglandin
-
- PGI2
-
- prostacycli;n
-
- PI
-
- phosphoinositide
-
- TXA2
-
- thromboxane A2.
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