Subregional Differences in Medium Spiny Neuron Intrinsic Excitability Properties between Nucleus Accumbens Core and Shell in Male Rats

Abstract The nucleus accumbens (NAc) is known for its central role in reward and motivation (Day and Carelli, 2007; Floresco, 2015; Salgado and Kaplitt, 2015). Decades of research on the cellular arrangement, density, and connectivity of the NAc have identified two main subregions known as the core and shell (Záborszky et al., 1985; Berendse and Groenewegen, 1990; Zahm and Heimer, 1990). Although anatomically and functionally different, both the NAc core and shell are mainly comprised of GABAergic projection neurons known as medium spiny neurons (MSNs) (Matamales et al., 2009). Several studies have identified key morphologic differences between core and shell MSNs (Meredith et al., 1992; Forlano and Woolley, 2010) but few studies have directly addressed how core and shell MSNs differ in their intrinsic excitability (Pennartz et al., 1992; O’Donnell and Grace, 1993). Using whole-cell patch-clamp recordings in slices prepared from naive and rewarded male rats, we found that MSNs in the NAc shell were significantly more excitable than MSNs in the NAc core in both groups. In the shell, MSNs had significantly greater input resistance, lower cell capacitance, and a greater sag. This was accompanied by a lower action potential current threshold, a greater number of action potentials, and faster firing frequency compared with core MSNs. These subregional differences in intrinsic excitability could provide a potential physiological link to the distinct anatomic characteristics of core and shell MSNs and to their distinct functional roles in reward learning (Zahm, 1999; Ito and Hayen, 2011; Saddoris et al., 2015; West and Carelli, 2016).

[1]  A. Jasnow,et al.  Dissociable roles of the nucleus accumbens core and shell subregions in the expression and extinction of conditioned fear , 2021, Neurobiology of Stress.

[2]  S. George,et al.  Dopamine D1-D2 receptor heteromer expression in key brain regions of rat and higher species: Upregulation in rat striatum after cocaine administration , 2020, Neurobiology of Disease.

[3]  John Meitzen,et al.  Estradiol decreases medium spiny neuron excitability in female rat nucleus accumbens core. , 2020, Journal of neurophysiology.

[4]  C. Ferrario,et al.  Effects of the estrous cycle and ovarian hormones on cue-triggered motivation and intrinsic excitability of medium spiny neurons in the Nucleus Accumbens core of female rats , 2019, Hormones and Behavior.

[5]  C. Ferrario,et al.  Eating 'junk-food' has opposite effects on intrinsic excitability of nucleus accumbens core neurons in obesity-susceptible vs. -resistant rats. , 2019, Journal of neurophysiology.

[6]  M. Lobo,et al.  The Selective RhoA Inhibitor Rhosin Promotes Stress Resiliency Through Enhancing D1-Medium Spiny Neuron Plasticity and Reducing Hyperexcitability , 2019, Biological Psychiatry.

[7]  C. Jiménez-Rivera,et al.  Protein and surface expression of HCN2 and HCN4 subunits in mesocorticolimbic areas after cocaine sensitization , 2019, Neurochemistry International.

[8]  E. Valjent,et al.  Cell-Type- and Endocannabinoid-Specific Synapse Connectivity in the Adult Nucleus Accumbens Core , 2019, The Journal of Neuroscience.

[9]  Mark J. Thomas,et al.  Cell-type and region-specific nucleus accumbens AMPAR plasticity associated with morphine reward, reinstatement, and spontaneous withdrawal , 2019, bioRxiv.

[10]  Elyssa B. Margolis,et al.  Relative contributions and mapping of ventral tegmental area dopamine and GABA neurons by projection target in the rat , 2018, The Journal of comparative neurology.

[11]  John Meitzen,et al.  Electrophysiological properties of medium spiny neurons in the nucleus accumbens core of prepubertal male and female Drd1a-tdTomato line 6 BAC transgenic mice. , 2018, Journal of neurophysiology.

[12]  John Meitzen,et al.  Estrous cycle-induced sex differences in medium spiny neuron excitatory synaptic transmission and intrinsic excitability in adult rat nucleus accumbens core. , 2018, Journal of neurophysiology.

[13]  Cheryl F. Lichti,et al.  Environmental Enrichment and Social Isolation Mediate Neuroplasticity of Medium Spiny Neurons through the GSK3 Pathway , 2018, Cell reports.

[14]  N. Wu,et al.  Nucleus accumbens hyperpolarization-activated cyclic nucleotide-gated channels modulate methamphetamine self-administration in rats , 2016, Psychopharmacology.

[15]  Elizabeth A. West,et al.  Nucleus Accumbens Core and Shell Differentially Encode Reward-Associated Cues after Reinforcer Devaluation , 2016, The Journal of Neuroscience.

[16]  M. Sauvage,et al.  Environmental enrichment modulates intrinsic cellular excitability of hippocampal CA1 pyramidal cells in a housing duration and anatomical location-dependent manner , 2015, Behavioural Brain Research.

[17]  R. Wightman,et al.  Differential Dopamine Release Dynamics in the Nucleus Accumbens Core and Shell Reveal Complementary Signals for Error Prediction and Incentive Motivation , 2015, The Journal of Neuroscience.

[18]  M. Kaplitt,et al.  The Nucleus Accumbens: A Comprehensive Review , 2015, Stereotactic and Functional Neurosurgery.

[19]  Steven M. Graves,et al.  Nucleus accumbens shell excitability is decreased by methamphetamine self-administration and increased by 5-HT2C receptor inverse agonism and agonism , 2015, Neuropharmacology.

[20]  Alexxai V. Kravitz,et al.  Nucleus Accumbens Medium Spiny Neuron Subtypes Mediate Depression-Related Outcomes to Social Defeat Stress , 2015, Biological Psychiatry.

[21]  S. Floresco The nucleus accumbens: an interface between cognition, emotion, and action. , 2015, Annual review of psychology.

[22]  Michael Koch,et al.  Nucleus accumbens core and shell inactivation differentially affects impulsive behaviours in rats , 2014, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

[23]  J. Miranda,et al.  Cocaine Sensitization Increases Ih Current Channel Subunit 2 (HCN2) Protein Expression in Structures of the Mesocorticolimbic System , 2013, Journal of Molecular Neuroscience.

[24]  R. Wise,et al.  Synaptic and Behavioral Profile of Multiple Glutamatergic Inputs to the Nucleus Accumbens , 2012, Neuron.

[25]  G. Paxinos,et al.  Paxinos and Franklin's the Mouse Brain in Stereotaxic Coordinates , 2012 .

[26]  S. Chattarji,et al.  Enhanced intrinsic excitability and EPSP-spike coupling accompany enriched environment-induced facilitation of LTP in hippocampal CA1 pyramidal neurons. , 2012, Journal of neurophysiology.

[27]  T. Aosaki,et al.  Protein kinase C activity alters the effect of &mgr;-opioid receptors on inhibitory postsynaptic current in the striosomes , 2012, Neuroreport.

[28]  C. Woolley,et al.  Sex differences and effects of cocaine on excitatory synapses in the nucleus accumbens , 2011, Neuropharmacology.

[29]  R. Ito,et al.  Opposing Roles of Nucleus Accumbens Core and Shell Dopamine in the Modulation of Limbic Information Processing , 2011, The Journal of Neuroscience.

[30]  M. Podda,et al.  Dopamine D1-like receptor activation depolarizes medium spiny neurons of the mouse nucleus accumbens by inhibiting inwardly rectifying K+ currents through a cAMP-dependent protein kinase A-independent mechanism , 2010, Neuroscience.

[31]  J. Panksepp,et al.  Exposure to Cocaine Dynamically Regulates the Intrinsic Membrane Excitability of Nucleus Accumbens Neurons , 2010, The Journal of Neuroscience.

[32]  C. Woolley,et al.  Quantitative analysis of pre‐ and postsynaptic sex differences in the nucleus accumbens , 2009, The Journal of comparative neurology.

[33]  Mark J. Thomas,et al.  Similar Neurons, Opposite Adaptations: Psychostimulant Experience Differentially Alters Firing Properties in Accumbens Core versus Shell , 2009, The Journal of Neuroscience.

[34]  Y. Ben-Ari,et al.  Dopamine-Deprived Striatal GABAergic Interneurons Burst and Generate Repetitive Gigantic IPSCs in Medium Spiny Neurons , 2009, The Journal of Neuroscience.

[35]  Jean-Michel Deniau,et al.  Striatal Medium-Sized Spiny Neurons: Identification by Nuclear Staining and Study of Neuronal Subpopulations in BAC Transgenic Mice , 2009, PloS one.

[36]  R. Carelli,et al.  The Nucleus Accumbens and Pavlovian Reward Learning , 2007, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[37]  Yuchun Zhang,et al.  Involvement of Ih in Dopamine Modulation of Tonic Firing in Striatal Cholinergic Interneurons , 2007, The Journal of Neuroscience.

[38]  L. Vanderschuren,et al.  Involvement of dopamine D1 and D2 receptors in the nucleus accumbens core and shell in inhibitory response control , 2007, Psychopharmacology.

[39]  F. J. White,et al.  Dopamine D(2) receptor modulation of K(+) channel activity regulates excitability of nucleus accumbens neurons at different membrane potentials. , 2006, Journal of neurophysiology.

[40]  M. Roitman,et al.  Nucleus accumbens neurons encode Pavlovian approach behaviors: evidence from an autoshaping paradigm , 2006, The European journal of neuroscience.

[41]  T. Svensson,et al.  Differential effects of acute and chronic nicotine on dopamine output in the core and shell of the rat nucleus accumbens , 2005, Journal of Neural Transmission.

[42]  R. Shigemoto,et al.  Immunohistochemical localization of Ih channel subunits, HCN1–4, in the rat brain , 2004, The Journal of comparative neurology.

[43]  T. Robbins,et al.  Differential control over cocaine-seeking behavior by nucleus accumbens core and shell , 2004, Nature Neuroscience.

[44]  S. Siegelbaum,et al.  Hyperpolarization-activated cation currents: from molecules to physiological function. , 2003, Annual review of physiology.

[45]  R. Carelli Nucleus accumbens cell firing during goal-directed behaviors for cocaine vs. ‘natural’ reinforcement , 2002, Physiology & Behavior.

[46]  G. Di Chiara Nucleus accumbens shell and core dopamine: differential role in behavior and addiction. , 2002, Behavioural brain research.

[47]  J. Bargas,et al.  D2 Dopamine Receptors in Striatal Medium Spiny Neurons Reduce L-Type Ca2+ Currents and Excitability via a Novel PLCβ1–IP3–Calcineurin-Signaling Cascade , 2000, The Journal of Neuroscience.

[48]  Charles J. Wilson,et al.  Intrinsic Membrane Properties Underlying Spontaneous Tonic Firing in Neostriatal Cholinergic Interneurons , 2000, The Journal of Neuroscience.

[49]  R. Warren,et al.  Postnatal development of electrophysiological properties of nucleus accumbens neurons. , 2000, Journal of neurophysiology.

[50]  L. Kaczmarek,et al.  Cloning and localization of the hyperpolarization-activated cyclic nucleotide-gated channel family in rat brain. , 2000, Brain research. Molecular brain research.

[51]  R. Malenka,et al.  Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens. , 2000, Annual review of neuroscience.

[52]  D. S. Zahm,et al.  Functional‐anatomical Implications of the Nucleus Accumbens Core and Shell Subterritories , 1999, Annals of the New York Academy of Sciences.

[53]  P. Kalivas,et al.  Expression of D1 receptor, D2 receptor, substance P and enkephalin messenger RNAs in the neurons projecting from the nucleus accumbens , 1997, Neuroscience.

[54]  J. Bargas,et al.  D1 Receptor Activation Enhances Evoked Discharge in Neostriatal Medium Spiny Neurons by Modulating an L-Type Ca2+ Conductance , 1997, The Journal of Neuroscience.

[55]  A. Grace,et al.  Dopaminergic Reduction of Excitability in Nucleus Accumbens Neurons Recorded in Vitro , 1996, Neuropsychopharmacology.

[56]  H. Pape,et al.  Queer current and pacemaker: the hyperpolarization-activated cation current in neurons. , 1996, Annual review of physiology.

[57]  G. Meredith,et al.  Effects of dopamine depletion on the morphology of medium spiny neurons in the shell and core of the rat nucleus accumbens , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[58]  A. Grace,et al.  Physiological and morphological properties of accumbens core and shell neurons recorded in vitro , 1993, Synapse.

[59]  H. Groenewegen,et al.  Morphological differences between projection neurons of the core and shell in the nucleus accumbens of the rat , 1992, Neuroscience.

[60]  H. Groenewegen,et al.  Compartmental distribution of ventral striatal neurons projecting to the mesencephalon in the rat , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[61]  D. Zahm An electron microscopic morphometric comparison of tyrosine hydroxylase immunoreactive innervation in the neostriatum and the nucleus accumbens core and shell , 1992, Brain Research.

[62]  C. Pennartz,et al.  Differential membrane properties and dopamine effects in the shell and core of the rat nucleus accumbens studied in vitro , 1992, Neuroscience Letters.

[63]  A. Deutch,et al.  Pharmacological characterization of dopamine systems in the nucleus accumbens core and shell , 1992, Neuroscience.

[64]  D. S. Zahm,et al.  Specificity in the projection patterns of accumbal core and shell in the rat , 1991, Neuroscience.

[65]  M. Bardo,et al.  Autoradiographic localization of dopamine D1 and D2 receptors in rat nucleus accumbens: Resistance to differential rearing conditions , 1991, Neuroscience.

[66]  D. S. Zahm,et al.  Two transpallidal pathways originating in the rat nucleus accumbens , 1990, The Journal of comparative neurology.

[67]  R. North,et al.  Cation current activated by hyperpolarization in a subset of rat nucleus accumbens neurons. , 1990, Journal of neurophysiology.

[68]  H. Groenewegen,et al.  Organization of the thalamostriatal projections in the rat, with special emphasis on the ventral striatum , 1990, The Journal of comparative neurology.

[69]  R. Roth,et al.  Telencephalic Projections of the A8 Dopamine Cell Group , 1988, Annals of the New York Academy of Sciences.

[70]  L. Heimer,et al.  Cholecystokinin innervation of the ventral striatum: A morphological and radioimmunological study , 1985, Neuroscience.

[71]  H. Groenewegen,et al.  Organization of the efferent projections of the nucleus accumbens to pallidal, hypothalamic, and mesencephalic structures: A tracing and immunohistochemical study in the cat , 1984, The Journal of comparative neurology.