Effect of isoprostanes on sympathetic neurotransmission in the human isolated iris-ciliary body

Citation
So. Awe et al., Effect of isoprostanes on sympathetic neurotransmission in the human isolated iris-ciliary body, NEUROCHEM R, 25(4), 2000, pp. 491-496
Citations number
29
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROCHEMICAL RESEARCH
ISSN journal
03643190 → ACNP
Volume
25
Issue
4
Year of publication
2000
Pages
491 - 496
Database
ISI
SICI code
0364-3190(200004)25:4<491:EOIOSN>2.0.ZU;2-0
Abstract
Isoprostanes (IsoP's) are prostaglandin-like compounds that are derived fro m free-radical catalyzed peroxidation of arachidonic acid independent of th e cyclcooxygenase enzyme. In the present study, we investigated the effect of IsoP's on norepinephrine (NE) release from human isolated iris-ciliary b odies. Isolated human iris-ciliary bodies were prepared for studies of [H-3 ]NE release using the superfusion method, Both 8-iso-prostaglandin F-2 alph a (F-2-IsoP) and the thromboxane (Tx) receptor agonist, U46619 enhanced fie ld-stimulated [H-3]NE release from isolated, superfused human iris-ciliary bodies without affecting basal tritium efflux. On the other hand, an equimo lar concentration (10 mu M) of 8-iso-prostaglandin E-2 (E-2-IsoP) inhibited evoked [H-3]NE overflow. The Tx-receptor antagonist, SQ 29548 blocked the enhancements of electrically-evoked [H-3]NE release induced by F-2-IsoP and U46619. However, the inhibitory responses elicited by E-2-IsoP was not ant agonized by SQ 29548. We conclude that IsoP's can produce both excitatory a nd inhibitory effects on sympathetic neurotransmission in human isolated ir is-ciliary bodies. The stimulatory effects of IsoP's on NE release may be m ediated by Tx-receptors.