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It suggested that the observed increase in the amount of GluR1 -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunits, NR2A NMDA receptor subunits, metabotropic receptor mGluR1, and PSD95 (a scaffolding protein of the PSD), but also the decrease in the quantity of Shank (another scaffolding protein), were due to an inhibition of proteasome activity
Zuo P, Ogita K, Suzuki T, Han D, Yoneda Y
S2CID 52020890
Its structure was confirmed by mass spectrometry and amino acid analysis [2]
Understanding this relationship helps you distinguish between the medication working as intended and the medication causing problems that need addressing
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