Selective modifiers of glutathione biosynthesis and ‘repriming’ of vascular smooth muscle photorelaxation

Autor: Rebecca J Pritchard, Ian L. Megson, Frederick W. Flitney, Kesson S. Magid, Sally A Holmes
Rok vydání: 2000
Předmět:
Zdroj: British Journal of Pharmacology. 130:1575-1580
ISSN: 0007-1188
Popis: Photorelaxation of vascular smooth muscle (VSM) is caused by the release of nitric oxide (NO) from a finite molecular store that can be depleted by irradiating pre-contracted arteries with visible light. The ability of an ‘exhausted’ vessel to respond to a further period of illumination is lost temporarily but then recovers slowly as the photosensitive store is reconstituted in the dark. The recovery process, termed repriming, displays an absolute requirement for endothelium-derived NO and is inhibited by pre-treating arteries with ethacrynic acid, a thiol-alkylating agent. Here we demonstrate that agents that up- or down-regulate glutathione (GSH) biosynthesis influence the extent to which the store is regenerated in the dark. Isolated rat tail arteries (RTAs) were perfused internally with Krebs solution containing phenylephrine (PE; mean [PE]±s.e.mean: 5.78±0.46 μM) and periodically exposed to laser light (λ=514.5 nm, 6.3 mW cm−2 for 6 min). Photorelaxations of control RTAs were compared with those from either (a) vessels taken from animals previously injected i.p. with buthionine sulphoximine (BSO), an inhibitor of γ-glutamylcysteine synthetase (three injections, 100 mg kg−1 at 8 h intervals); or (b) isolated RTAs that were perfused ex vivo with oxothiazolidine (OXO), a precursor of cysteine (10−4 M OXO for 60 min). RTAs from BSO-treated animals exhibited attenuated photorelaxations: the mean (±s.e.mean) amplitude of the response recorded after 72 min recovery in the dark was 12.4±1.6% versus 21.4±2.9% for control arteries (n=5; P
Databáze: OpenAIRE
Externí odkaz: