Effects of tamoxifen on L-glutamate transporters of astrocytes

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Abstract

Tamoxifen (Tam) decreased the clearance of L-glutamate (L-Glu) by cultured astrocytes at 1 pM, 1 nM, and 1 μM, but became toxic at 10 μM. When L-Glu transporters were mostly inhibited by threo-β-benzyloxyaspartate (TBOA) (1 mM) or D,L-threo-β-hydroxyaspartate (THA) (1 mM), Tam (1 nM) did not change extracellular L-Glu concentration, confirming that Tam attenuates L-Glu transport through L-Glu transporters. ICI182,780, LY294002, and U0126 inhibited the effect of Tam dose-dependently, suggesting the involvement of estrogen receptors (ERs), the phosphatidylinositol 3-kinase (PI3K) cascade, and the mitogen-activated protein kinase (MAPK) cascade in the effect of Tam. ©2008 The Japanese Pharmacological Society.

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Sato, K., Saito, Y., Oka, J. I., Ohwada, T., & Nakazawa, K. (2008). Effects of tamoxifen on L-glutamate transporters of astrocytes. Journal of Pharmacological Sciences, 107(2), 226–230. https://doi.org/10.1254/jphs.08039SC

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