Skip to main content
. 2017 Mar 6;149(3):335–353. doi: 10.1085/jgp.201611720

Table 1. Drugs used in this study.

Drug Action Concentration Application method
L-AP4 Activates group III mGluRs 4 or 50 µM Bath, puffer
BAPTA Chelates Ca2+ 10 mM Intracellular
Cd2+ Blocks neurotransmitter release 1 mM Bath
CGP 52432 Blocks GABAB receptors 5 µM Bath
Concanavalin A Blocks desensitization of kainate receptors 300 µg/ml Bath
CPPG Blocks group III mGluRs 200 or 600 µM Bath, puffer
Cyclothiazide Blocks desensitization of AMPA receptors 60 µM Bath
Isradipine Blocks L-type Ca2+ channels 10 µM Bath, puffer
MK-801 Blocks NMDA receptors 1 mM Intracellular
MMPIP Blocks mGluR7 10 µM Bath
NMDA Activates NMDA receptors 5 mM Puffer
Picrotoxin Blocks GABAA receptors 100 or 200 µM Bath, puffer
SCH 23390 Blocks D1-class dopamine receptors 60 nM Bath (2–8 h)
Spiperone Blocks D2-class dopamine receptors 60 nM Bath (2–8 h)
Strychnine Blocks glycine receptors 5 or 10 µM Bath, puffer
TBOA Blocks glutamate transporters 25 µM Bath
TPMPA Blocks GABAC receptors 15 or 30 µM Bath, puffer