Protein Information

ID 10
Name calmodulin
Synonyms CALM; CAM; CALM 1; CALM 2; CALM 3; CALM1; CALM2; CALM3…

Compound Information

ID 1468
Name HCH
CAS 1,2,3,4,5,6-hexachlorocyclohexane

Reference

PubMed Abstract RScore(About this table)
2054651 Yamada K, Saltarelli MD, Coyle JT: Effects of calmodulin antagonists on sodium-dependent high-affinity choline uptake. Brain Res. 1991 Feb 22;542(1):132-4.
The effects of calmodulin (CaM) antagonists were investigated on the sodium-dependent high-affinity choline uptake (SDHACU) as assessed by the specific binding of [3H] hemicholinium-3 ([3H] HCh-3) and high-affinity [3H] choline uptake. Potassium depolarization caused a significant 2-fold increase in the specific binding of [3H] HCh-3 in slices of rat striatum in vitro. CaM antagonists, including trifluoperazine (TFP), W-5, W-7, promethazine and haloperidol, dose-dependently inhibited potassium depolarization-stimulated [3H] HCh-3 binding with IC50s of 20, 40, 70, 30 and 48 (microM), respectively. Scatchard analysis revealed that the inhibitory effect of TFP resulted from a decrease in Bmax but no change in Kd of [3H] HCh-3 binding. Potassium depolarization of slices also stimulated high-affinity [3H] choline uptake, which was completely inhibited by 10 microM TFP. These results are discussed in relation to the regulatory mechanisms of SDHACU.
32(0,1,1,2)