TY - JOUR
T1 - Regulation of psychomotor functions by dopamine
T2 - Integration of various approaches
AU - Sasa, Masashi
AU - Nishi, Akinori
AU - Kobayashi, Kazuto
AU - Sano, Hiromi
AU - Momiyama, Toshihiko
AU - Uramura, Kazuhide
AU - Yada, Toshihiko
AU - Mori, Norio
AU - Suzuki, Katsuaki
AU - Minabe, Yoshio
PY - 2003
Y1 - 2003
N2 - (1) The basal ganglia circuitry mediates a wide rage of brain functions such as motor control, behavioral planning, and reward prediction. Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons but also is involved in the pattern formation of their firing. The striatopallidal neurons containing dopamine D2 receptor plays a dual role in motor coordination dependent on DA transmission. (2) Activation of presynaptic D2-like receptors on GABAergic terminals onto striatal cholinergic interneurons selectively blocks N-type Ca2+ channels, thereby inhibiting GABA release. In addition, contribution of N-type channels and D2-like receptor-mediated presynaptic inhibition decreases in parallel with development, implying some relationship between basal ganglia-related function or dysfunction and age. (3) As an approach to determine dopamine neuronal activity, we monitored neuronal activities by measuring cytosolic Ca2+ concentration in VTA dopamine neurons. The present study indicates that VTA dopamine neurons are the direct targets of orexin-A and psychostimulants, and the [Ca2+]i signaling is thought to play a significant role in the regulation of dopamine neuronal activity. (4) The excitability of neostriatal neurons is regulated by a balance of glutamatergic and dopaminergic inputs. Glutamate has been shown to modulate dopaminergic signaling. Studies on the regulation of DARPP-32 phosphorylation by glutamate provide a molecular basis for both the synergistic and antagonistic effects of glutamate on dopaminergic signaling. (5) Impairment of function of stem/progenitor cells may be implicated in the pathogenesis of schizophrenia. To test this hypothesis, several experiments are currently ongoing in our laboratory, and the preliminary results obtained are described here.
AB - (1) The basal ganglia circuitry mediates a wide rage of brain functions such as motor control, behavioral planning, and reward prediction. Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons but also is involved in the pattern formation of their firing. The striatopallidal neurons containing dopamine D2 receptor plays a dual role in motor coordination dependent on DA transmission. (2) Activation of presynaptic D2-like receptors on GABAergic terminals onto striatal cholinergic interneurons selectively blocks N-type Ca2+ channels, thereby inhibiting GABA release. In addition, contribution of N-type channels and D2-like receptor-mediated presynaptic inhibition decreases in parallel with development, implying some relationship between basal ganglia-related function or dysfunction and age. (3) As an approach to determine dopamine neuronal activity, we monitored neuronal activities by measuring cytosolic Ca2+ concentration in VTA dopamine neurons. The present study indicates that VTA dopamine neurons are the direct targets of orexin-A and psychostimulants, and the [Ca2+]i signaling is thought to play a significant role in the regulation of dopamine neuronal activity. (4) The excitability of neostriatal neurons is regulated by a balance of glutamatergic and dopaminergic inputs. Glutamate has been shown to modulate dopaminergic signaling. Studies on the regulation of DARPP-32 phosphorylation by glutamate provide a molecular basis for both the synergistic and antagonistic effects of glutamate on dopaminergic signaling. (5) Impairment of function of stem/progenitor cells may be implicated in the pathogenesis of schizophrenia. To test this hypothesis, several experiments are currently ongoing in our laboratory, and the preliminary results obtained are described here.
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U2 - 10.1254/fpj.122.215
DO - 10.1254/fpj.122.215
M3 - Review article
C2 - 12939539
AN - SCOPUS:0141591554
SN - 0015-5691
VL - 122
SP - 215
EP - 225
JO - Folia Pharmacologica Japonica
JF - Folia Pharmacologica Japonica
IS - 3
ER -