Ibuprofen or ozagrel increases NO release and l-nitro arginine induces TXA2 release from cultured porcine basilar arterial endothelial cells
| Autor: | Takeshi Obi, Shigeru Ishiguro, Yoriko Hashiguchi, Atsushi Miyamoto, Akira Nishio |
|---|---|
| Rok vydání: | 2007 |
| Předmět: |
Time Factors
Arginine Swine Physiology Thromboxane Prostaglandin Ibuprofen In Vitro Techniques Pharmacology Nitric Oxide Nitroarginine Nitric oxide Thromboxane A2 chemistry.chemical_compound medicine.artery Basilar artery medicine Animals Ozagrel Cyclooxygenase Inhibitors Aorta Abdominal Enzyme Inhibitors Cells Cultured Dose-Response Relationship Drug biology Endothelial Cells Thromboxane B2 Vasodilation Nitric oxide synthase chemistry Biochemistry Vasoconstriction Basilar Artery biology.protein Methacrylates Molecular Medicine Imines Thromboxane-A Synthase Cyclooxygenase Nitric Oxide Synthase |
| Zdroj: | Vascular Pharmacology. 46:85-90 |
| ISSN: | 1537-1891 |
| Popis: | The vascular resting tone of the porcine basilar artery appears to be mostly maintained by a balance between spontaneously released nitric oxide (NO) from endothelial cells and thromboxane (TX) A(2) from endothelial and smooth muscle cells. However the precise role of the interaction between the above two substances in the control of vascular tone is unclear. We attempted to clarify the interaction between NO and TXA(2) using cultured porcine basilar arterial endothelial cells. The cultured endothelial cells produced NO spontaneously, while TXB(2) (a stable metabolite of TXA(2)) production remained below the detection limit. Ibuprofen (a COX inhibitor) and ozagrel (a TXA(2) synthetase inhibitor) significantly increased the spontaneous production of NO, which was not affected by 1400W (an iNOS inhibitor). l-Nitro arginine (a NOS inhibitor) significantly induced TXB(2) production. These results suggest that NO may inhibit COX or TXA(2) synthetase, and that therefore inhibition of NOS might disinhibit COX or TXA(2) synthetase, subsequently inducing TXA(2) production. On the other hand, as TXA(2) and other contractility-related prostaglandin(s) may inhibit NOS, therefore the inhibition of COX or TXA(2) synthetase might disinhibit NOS, and then increase the spontaneous production of NO in porcine basilar arterial endothelial cells. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect