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They not only directly activate the expression of GAD65/67 and VGAT, ensuring the GABAergic properties of interneurons, but also regulate genes such as Arx, guiding interneurons to migrate from the ventral forebrain to the cortex and form inhibitory circuits

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A classic pharmacokinetic study in the Annals of Internal Medicine (Levine et al., 2004) found that a modeled 50 g IV dose produced peak plasma levels around 13,400 mol/L, versus 220 mol/L for the maximum tolerated oral regimen roughly 3070 times higher plasma concentrations with IV administration