Autor: |
Nikolaev MV; I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry , Russian Academy of Sciences , St. Petersburg 194223 , Russia., Komarova MS; I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry , Russian Academy of Sciences , St. Petersburg 194223 , Russia., Tikhonova TB; I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry , Russian Academy of Sciences , St. Petersburg 194223 , Russia., Korosteleva AS; I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry , Russian Academy of Sciences , St. Petersburg 194223 , Russia., Potapjeva NN; I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry , Russian Academy of Sciences , St. Petersburg 194223 , Russia., Tikhonov DB; I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry , Russian Academy of Sciences , St. Petersburg 194223 , Russia. |
Abstrakt: |
The chemical structures of some antidepressants are similar to those of recently described amine-containing ligands of acid-sensing ion channels (ASICs). ASICs are expressed in brain neurons and participate in numerous CNS functions. As such, they can be related to antidepressant action or side effects. We therefore studied the actions of a series of antidepressants on recombinant ASIC1a and ASIC2a and on native ASICs in rat brain neurons. Most of the tested compounds prevented steady-state ASIC1a desensitization evoked by conditioning acidification to pH 7.1. Amitriptyline also potentiated ASIC1a responses evoked by pH drops from 7.4 to 6.5. We conclude that amitriptyline has a twofold effect: it shifts activation to less acidic values while also shifting steady-state desensitization to more acidic values. Chlorpromazine, desipramine, amitriptyline, fluoxetine, and atomoxetine potentiated ASIC2a response. Tianeptine caused strong inhibition of ASIC2a. Both potentiation and inhibition of ASIC2a were accompanied by the slowdown of desensitization, suggesting distinct mechanisms of action on activation and desensitization. In experiments on native heteromeric ASICs, tianeptine and amitriptyline demonstrated the same modes of action as on ASIC2a although with reduced potency. |