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 |
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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. |
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ISSN: | 0197-0186 1872-9754 |
DOI: | 10.1016/j.neuint.2008.07.011 |