TY - CHAP
T1 - Electrophysiological characteristics of dopamine neurons
T2 - A 35-year update
AU - Shi, Wei Xing
N1 - Wei-Xing Shi Part of the Journal of Neural Transmission. Supplementa book series (NEURALTRANS, volume 73) This chapter consists of four sections. The first section provides a general description of the electrophysiological characteristics of dopamine (DA) neurons in both the substantia nigra and ventral tegmental area.
PY - 2009/1/1
Y1 - 2009/1/1
N2 - This chapter consists of four sections. The first section provides a general description of the electrophysiological characteristics of dopamine (DA) neurons in both the substantia nigra and ventral tegmental area. Emphasis is placed on the differences between DA and neighboring non-DA neurons. The second section discusses the ionic mechanisms underlying the generation of action potential in DA cells. Evidence is provided to suggest that these mechanisms differ not only between DA and non-DA neurons but also between DA cells located in different areas, with different projection sites and at different developmental stages. Some of the differences may play a critical role in the vulnerability of a DA neuron to cell death. The third section describes the firing patterns of DA cells. Data are presented to show that the current "80/160 ms" criteria for burst identification need to be revised and that the burst firing, originally described by Bunney et al., can be described as slow oscillations in firing rate. In the ventral tegmental area, the slow oscillations are, at least partially, derived from the prefrontal cortex and part of prefrontal information is transferred to DA cells indirectly through inhibitory neurons. The final section focuses on the feedback regulation of DA cells. New evidence suggests that DA autoreceptors are coupled to multiple effectors, and both D1 and D2-like receptors are involved in long-loop feedback control of DA neurons. Because of the presence of multiple feedback and nonfeedback pathways, the effect of a drug on a DA neuron can be far more complex than an inhibition or excitation. A better understanding of the intrinsic properties of DA neurons and their regulation by afferent input will, in time, help to point to the way to more effective and safer treatments for disorders including schizophrenia, drug addiction, and Parkinson's disease. © 2009 Springer-Verlag Vienna.
AB - This chapter consists of four sections. The first section provides a general description of the electrophysiological characteristics of dopamine (DA) neurons in both the substantia nigra and ventral tegmental area. Emphasis is placed on the differences between DA and neighboring non-DA neurons. The second section discusses the ionic mechanisms underlying the generation of action potential in DA cells. Evidence is provided to suggest that these mechanisms differ not only between DA and non-DA neurons but also between DA cells located in different areas, with different projection sites and at different developmental stages. Some of the differences may play a critical role in the vulnerability of a DA neuron to cell death. The third section describes the firing patterns of DA cells. Data are presented to show that the current "80/160 ms" criteria for burst identification need to be revised and that the burst firing, originally described by Bunney et al., can be described as slow oscillations in firing rate. In the ventral tegmental area, the slow oscillations are, at least partially, derived from the prefrontal cortex and part of prefrontal information is transferred to DA cells indirectly through inhibitory neurons. The final section focuses on the feedback regulation of DA cells. New evidence suggests that DA autoreceptors are coupled to multiple effectors, and both D1 and D2-like receptors are involved in long-loop feedback control of DA neurons. Because of the presence of multiple feedback and nonfeedback pathways, the effect of a drug on a DA neuron can be far more complex than an inhibition or excitation. A better understanding of the intrinsic properties of DA neurons and their regulation by afferent input will, in time, help to point to the way to more effective and safer treatments for disorders including schizophrenia, drug addiction, and Parkinson's disease. © 2009 Springer-Verlag Vienna.
KW - Amphetamine
KW - Antipsychotic drug
KW - Autoreceptor
KW - Burst
KW - Feedback control
KW - Non-DA neurons
KW - Pacemaker potential
KW - Prefrontal cortex
KW - SK channel
KW - Slow oscillation
KW - Striatum
KW - Substantia nigra
KW - Ventral tegmental area
KW - History, 21st Century
KW - Neurons/drug effects
KW - Dopamine Agents/pharmacology
KW - Ventral Tegmental Area/cytology
KW - Action Potentials/drug effects
KW - History, 20th Century
KW - Feedback, Physiological/drug effects
KW - Substantia Nigra/cytology
KW - Animals
KW - Electrophysiology/history
KW - Dopamine/metabolism
KW - In Vitro Techniques
KW - Ion Channels/drug effects
UR - https://link.springer.com/chapter/10.1007%2F978-3-211-92660-4_8
UR - https://www.mendeley.com/catalogue/dbfc7ad7-98d0-3fd6-8d97-fce635ed1fb9/
U2 - 10.1007/978-3-211-92660-4_8
DO - 10.1007/978-3-211-92660-4_8
M3 - Chapter
C2 - 20411771
SN - 9783211926598
T3 - Journal of Neural Transmission, Supplementa
SP - 103
EP - 119
BT - Birth, Life and Death of Dopaminergic Neurons in the Substantia Nigra
PB - Springer-Verlag Wien
ER -