L-<em>trans</em>-<wbr/>Pyrrolidine-<wbr/>2,4-dicarboxylic Acid

L-trans–Pyrrolidine-2,4-dicarboxylic Acid

CAT N°: 24268
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From 48.00 40.80

L-trans-Pyrrolidine-2,4-dicarboxylic acid (L-trans-2,4-PDC) is an inhibitor of L-glutamate transport (Ki = 4.6 ?M in rat brain synaptosomes).{40981} It inhibits radioligand binding to NMDA receptors by 13% but has no effect on AMPA or kainate receptors when used at a concentration of 100 ?M. L-trans-2,4-PDC is neurotoxic to astrocyte-rich and astrocyte-poor rat cortical cultures (EC50s = 320 and 50 ?M, respectively), an effect that can be reversed by the NMDA antagonist MK-801 (Item No. 10009019) and glutamate-pyruvate transaminase but not the non-NMDA glutamate receptor antagonist CNQX (Item No. 14618).{40982} It induces efflux of the non-metabolizable glutamate analog [3H]-D-aspartate in an extracellular sodium-dependent manner. In vivo, L-trans-2,4-PDC (0.05-0.2 ?g/side) prevents amphetamine-induced hyperlocomotion in a dose-dependent manner in rats when injected directly into the nucleus accumbens.{40983} It also increases bladder intercontraction interval (ICI) without affecting postvoid residual or basal pressure in rats.{40984}

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