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      Excitatory and inhibitory effects of dopamine on neuronal activity of the caudate nucleus neurons in vitro

      , , ,
      Brain Research
      Elsevier BV

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          Abstract

          Effects of dopamine on the rat caudate nucleus neurons were examined in a slice preparation using an intracellular recording technique. Perfusion of the bath with a low concentration (1 microM) of dopamine produced a depolarization concomitant with an increase in the spontaneous firing and the number of action potentials evoked by a depolarizing pulse applied into the cells. In contrast, higher concentrations (100-500 microM) of dopamine inhibited the spontaneous and current-induced firings without apparent effects on the resting membrane potential. In addition, during application of a high concentration (100 microM) of dopamine there was a marked elevation of the threshold potential of the action potential elicited by a higher depolarizing current. Simultaneous application of haloperidol (0.5-5 microM) antagonized both excitatory and inhibitory effects induced by the low and high concentrations of dopamine, respectively. In addition, the excitatory effect induced by a low concentration (1 microM) of dopamine was antagonized by domperidone (0.5 microM), a selective D2 receptor antagonist, while the inhibitory effect by a high concentration (100 microM) was blocked by SCH 23390, a selective D1 receptor antagonist. These results strongly suggest that the postsynaptic sites of caudate nucleus neurons have at least two subtypes of dopamine receptors (D1 and D2 receptors) that mediate inhibitory and excitatory responses of the neuron to dopamine, respectively.

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          Author and article information

          Journal
          Brain Research
          Brain Research
          Elsevier BV
          00068993
          August 1987
          August 1987
          : 418
          : 2
          : 262-272
          Article
          10.1016/0006-8993(87)90094-1
          2890403
          d409b39e-2617-4ad4-829f-b38b4f21c117
          © 1987

          https://www.elsevier.com/tdm/userlicense/1.0/

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