l-NAME prevents GM1 ganglioside-induced vasodilation in the rat brain

Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. It has been recently described that GM1 induces vasodilation. However, the mechanisms underlying GM1-induced vasodilation were not evaluated to date. Therefore,...

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Veröffentlicht in:Neurochemistry international 2008-12, Vol.53 (6), p.362-369
Hauptverfasser: Furian, Ana Flávia, Oliveira, Mauro Schneider, Magni, Danieli Valnes, Souza, Mauren Assis, Bortoluzzi, Vanessa Trindade, Bueno, Lívia Maronesi, Royes, Luiz Fernando Freire, Mello, Carlos Fernando
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Sprache:eng
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Zusammenfassung:Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. It has been recently described that GM1 induces vasodilation. However, the mechanisms underlying GM1-induced vasodilation were not evaluated to date. Therefore, in this study we investigated whether the nonspecific NOS inhibitor l-NAME prevents GM1-induced vasodilation in rats. The systemic injection of GM1 (50 mg/kg, i.p.) increased the outer diameter of pial vessels by 50% in anesthetized animals at 30 min, and this effect was fully prevented by the administration of the nitric oxide synthase inhibitor N G-nitro- l-arginine methyl ester ( l-NAME, 60 mg/kg, i.p. 15 min before GM1 injection). A 30 min exposure of cerebral cortex slices to GM1 (100 μM) increased the content of nitrite plus nitrate (NOx) by 50%. Addition of l-NAME (100 μM) to the incubation medium fully prevented GM1-induced NOx increase. Conversely, a 60 min exposure of slices to GM1 (100 μM) decreased NOx content, revealing a biphasic effect of GM1. Our results suggest that NO plays an important role in the vasodilation induced by GM1.
ISSN:0197-0186
1872-9754
DOI:10.1016/j.neuint.2008.07.011