Neostriatum medium spiny direct pathway GABA cell

- - BG - NEOSTRIAT - PRINC - MSN - direct - gaba
Properties are:  Present   Absent 
Input Receptors
Intrinsic Currents
Output Transmitters
Distal equivalent dendrite
Neocortex L5/6 pyramidal GLU cell
 -Axon terminal.Glutamate
Neocortical Superficial Pyramidal Neuron terminals (T) and Thalamic Relay Neuron terminals (T)
Glutamate
From cerebral cortex (McGeer PL et al, 1977 [mammal]1 ).
Substantia nigra pars compacta DA cell
 -Axon terminal.Dopamine
Substantia Nigra Dopaminergic Cell terminals (T)
D1
Input from dopaminergic neurons in the substantia nigra; causes small depolarization? sometimes a decrease in firing rate; modulates anomalous rectification of dendritic membrane (I IR)?
I h
Large EPSPs activate I IR, increasing the membrane resistance, shortening the dendrites electrotonically, making the cell more sensitive to subsequent inputs (see
Middle equivalent dendrite
Neocortex L5/6 pyramidal GLU cell
 -Axon terminal.Glutamate
Neocortical Superficial Pyramidal Neuron terminals (T) and Thalamic Relay Neuron terminals (T)
Glutamate
From cerebral cortex (McGeer PL et al, 1977 [mammal]1 ).
Substantia nigra pars compacta DA cell
 -Axon terminal.Dopamine
Substantia Nigra Dopaminergic Cell terminals (T)
D1
Input from dopaminergic neurons in the substantia nigra; causes small depolarization? sometimes a decrease in firing rate; modulates anomalous rectification of dendritic membrane (I IR)?
I h
Large EPSPs activate I IR, increasing the membrane resistance, shortening the dendrites electrotonically, making the cell more sensitive to subsequent inputs (see
Proximal equivalent dendrite
Neocortex L5/6 pyramidal GLU cell
 -Axon terminal.Glutamate
Neocortical Superficial Pyramidal Neuron terminals (T) and Thalamic Relay Neuron terminals (T)
Glutamate
From cerebral cortex (McGeer PL et al, 1977 [mammal]1 ).
Substantia nigra pars compacta DA cell
 -Axon terminal.Dopamine
Substantia Nigra Dopaminergic Cell terminals (T)
D1
Input from dopaminergic neurons in the substantia nigra; causes small depolarization? sometimes a decrease in firing rate; modulates anomalous rectification of dendritic membrane (I IR)?
I h
Large EPSPs activate I IR, increasing the membrane resistance, shortening the dendrites electrotonically, making the cell more sensitive to subsequent inputs (see
Soma
D1
Activation of both D1- and D2-class receptors has been shown to modulate potassium and sodium currents in acutely isolated neostriatal neurons (Surmeier DJ and Kitai ST, 19932 ). Recordings in slices showed that D1 receptor activation can either inhibit or enhance evoked activity, depending on the level of membrane depolarization, by modulating an L-type Ca2+ conductance (Hernández-López S et al, 19973 ).
D2
Activation of both D1- and D2-class receptors has been shown to modulate potassium and sodium currents in acutely isolated neostriatal neurons (Surmeier DJ and Kitai ST, 19932 ).
Gaba
GABAergic responses evoked by electrical stimulations have been studied in slices (Kita T et al, 19854 ).
Muscarinic
Recording from dissociated neurons using intracellular and whole-cell voltage-clamp recordings showed that carbachol can act at M1-like muscarinic receptors to reduce the membrane K+ conductances and excite the neostriatal neurons (Hsu KS et al, 1996 [rat]5 ).
I K
I Na,t
Kinetic properties were studied using the whole-cell patch-clamp technique (Ogata N and Tatebayashi H, 1990 [guinea pig]6 ).
I L high threshold
Whole-cell voltage-clamp recordings showed that HVA currents were present in at least 95% of neostriatal neurons, but that the majority of them appeared to belong neither to the "L-type" nor the "N-type" classification (Hoehn K et al, 1993 [rat]8 ). However, recordings in slices showed that D1 receptor activation can either inhibit or enhance evoked activity, depending on the level of membrane depolarization, by modulating an L-type Ca2+ conductance (Hernández-López S et al, 19973 ).
I N
Whole-cell voltage-clamp recordings showed that HVA currents were present in at least 95% of neostriatal neurons, but that the majority of them appeared to belong neither to the "L-type" nor the "N-type" classification (Hoehn K et al, 1993 [rat]8 ).
I T low threshold
Whole-cell voltage-clamp recordings showed that a low-threshold transient (T-type) Ca2+ current was observed in 40% of neurons (Hoehn K et al, 1993 [rat]8 ). Another study suggested that adult neostriatal projection neurons do not express significant levels of LVA Ca2+ current (Bargas J et al, 1994 [rat]9 ).
I A
The contribution of a fast (IAt), and a slowly (IAs)-inactivating A-currents were studied in slices. The results suggest a role for these currents to define the limits on the depolarized state (Nisenbaum ES and Wilson CJ, 199510 ). With whole-cell patch clamp, two types of A-current were found in rat neostriatal neurons, one similar to previous descriptions in mammals and a second activated at considerably more depolarized potentials (Surmeier DJ et al, 198911 ). A slowly inactivating A current has also been studied (Gabel LA and Nisenbaum ES, 199812 ).
I h
The contribution of an inwardly rectifying current (IKir) were studied in slices. The results suggest that the hyperpolarized state is determined principally by this current (Nisenbaum ES and Wilson CJ, 199510 ).
I Potassium
A slow, noninactivating current may have a role to define the limits on the depolarized state, and to govern the spike discharge characteristics once the depolarized state has been reached (Nisenbaum ES and Wilson CJ, 199510 ). A non-inactivating, Ca-independent, K+ current may limit the amplitude of membrane depolarizations associated with prolonged excursions into the depolarized state (Nisenbaum ES et al, 1996 [rat]13 ).
I Calcium
Whole cell recordings from acutely dissociated neurons exhibited a R-type currents that were characterized as HVA by their rapid deactivation kinetics, half-activation and half-inactivation voltages, and sensitivity to depolarized holding potentials. In neocortical pyramidal neurons these currents inactivated at more negative potentials than in medium spiny neurons (Foehring RC et al, 200014 ).
I K,Ca
Calcium-dependent potassium channels are preferentially activated by calcium entry through N- and Q-type channels (Vilchis C et al, 200015 ).
I N
Calcium-dependent potassium channels are preferentially activated by calcium entry through N- and Q-type channels (Vilchis C et al, 200015 ).
I p,q
Calcium-dependent potassium channels are preferentially activated by calcium entry through N- and Q-type channels (Vilchis C et al, 200015 ).
I Na,p
Nomarski optics and infrared videomicroscopy were used to demonstrate the existence of a TTX-sensitive persistent Na+ conductance (INaP) in identified medium-sized neostriatal neurons (Cepeda C et al, 199516 ).
Axon hillock
I K
I Na,t
Axon fiber
Axon terminal
I N
Gaba Indirect spiny neurons, globus pallidus external neuron, globus pallidus internal neuron, substantia nigra reticulata neurons
I L high threshold
(Hernandez-Lopez S et al, 20007 ).
Classical References: first publications on each compartmental property; search PubMed for complete list
1.  McGeer PL, McGeer EG, Scherer U and Singh K. (1977) A glutamatergic corticostriatal path? Brain Res 128:369-73.
2.  Surmeier DJ and Kitai ST. (1993) D1 and D2 dopamine receptor modulation of sodium and potassium currents in rat neostriatal neurons. Prog Brain Res 99:309-24.
3.  Hernández-López S, Bargas J, Surmeier DJ, Reyes A and Galarraga E. (1997) D1 receptor activation enhances evoked discharge in neostriatal medium spiny neurons by modulating an L-type Ca2+ conductance. J Neurosci 17:3334-42.
4.  Kita T, Kita H and Kitai ST. (1985) Local stimulation induced GABAergic response in rat striatal slice preparations: intracellular recordings on QX-314 injected neurons. Brain Res 360:304-10.
5.  Hsu KS, Yang CH, Huang CC and Gean PW. (1996) Carbachol induces inward current in neostriatal neurons through M1-like muscarinic receptors. Neuroscience 73:751-60.
6.  Ogata N and Tatebayashi H. (1990) Sodium current kinetics in freshly isolated neostriatal neurones of the adult guinea pig. Pflugers Arch 416:594-603.
7.  Hernandez-Lopez S, Tkatch T, Perez-Garci E, Galarraga E, Bargas J, Hamm H and Surmeier DJ. (2000) D2 dopamine receptors in striatal medium spiny neurons reduce L-type Ca2+ currents and excitability via a novel PLC[beta]1-IP3-calcineurin-signaling cascade. J Neurosci 20:8987-95.
8.  Hoehn K, Watson TW and MacVicar BA. (1993) Multiple types of calcium channels in acutely isolated rat neostriatal neurons. J Neurosci 13:1244-57.
9.  Bargas J, Howe A, Eberwine J, Cao Y and Surmeier DJ. (1994) Cellular and molecular characterization of Ca2+ currents in acutely isolated, adult rat neostriatal neurons. J Neurosci 14:6667-86.
10.  Nisenbaum ES and Wilson CJ. (1995) Potassium currents responsible for inward and outward rectification in rat neostriatal spiny projection neurons. J Neurosci 15:4449-63.
11.  Surmeier DJ, Bargas J and Kitai ST. (1989) Two types of A-current differing in voltage-dependence are expressed by neurons of the rat neostriatum. Neurosci Lett 103:331-7.
12.  Gabel LA and Nisenbaum ES. (1998) Biophysical characterization and functional consequences of a slowly inactivating potassium current in neostriatal neurons. J Neurophysiol 79:1989-2002 [Journal] .
13.  Nisenbaum ES, Wilson CJ, Foehring RC and Surmeier DJ. (1996) Isolation and characterization of a persistent potassium current in neostriatal neurons. J Neurophysiol 76:1180-94 [Journal] .
14.  Foehring RC, Mermelstein PG, Song WJ, Ulrich S and Surmeier DJ. (2000) Unique properties of R-type calcium currents in neocortical and neostriatal neurons. J Neurophysiol 84:2225-36 [Journal] .
15.  Vilchis C, Bargas J, Ayala GX, Galván E and Galarraga E. (2000) Ca2+ channels that activate Ca2+-dependent K+ currents in neostriatal neurons. Neuroscience 95:745-52.
16.  Cepeda C, Chandler SH, Shumate LW and Levine MS. (1995) Persistent Na+ conductance in medium-sized neostriatal neurons: characterization using infrared videomicroscopy and whole cell patch-clamp recordings. J Neurophysiol 74:1343-8 [Journal] .