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Anisetty, N.

Publications and source records attributed to Anisetty, N..

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Transient dopamine response on medium spiny neuron subtypes in switching approach-avoidance outcomes against action bias - A framework for exploration in action selection

An ensemble of direct and indirect pathway medium spiny neurons (dMSN and iMSN), compete via their neural activity to drive the decision to approach or avoid an object, respectively. Dopamine acting as a reward prediction error (RPE) signal causes experience-dependent synaptic changes in dMSN and iMSN, thereby shifting the dominance of neural activity to approach or avoidance signalling. These changes create bias in the striatal neuronal ensemble and restrict the choice to approach or avoidance in further iterations. However, organisms often exhibit behaviour where they choose undesirable or exploratory actions in anticipation of future reward or avoid desirable actions in anticipation of future risk. These against-bias decisions or exploratory decisions are not accounted for by the existing neuronal framework. To bridge this gap, we postulate that transient motivational dopamine released from dopaminergic axons locally at sub-second timescales can cause temporary switch in dominance of neural activity between dMSN and iMSN leading to such adaptive decisions. By accounting for bias towards approach or avoidance or neither through synaptic weightages and accounting for differential affinity of DA to D1R and D2R, changes in dMSN and iMSN excitability at different levels of motivational dopamine was analysed. Furthermore, the spiking activity of striatal neuronal ensemble comprising of dMSN projecting directly and iMSN projecting indirectly onto the output nuclei of basal ganglia i.e. SNr neurons was simulated. This led to promising findings that demonstrate how SNr neuronal activity can generate outcomes that work against the cortico-striatal synaptic bias towards approach or avoidance. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=192 HEIGHT=200 SRC="FIGDIR/small/630270v2_ufig1.gif" ALT="Figure 1"> View larger version (33K): org.highwire.dtl.DTLVardef@fa322org.highwire.dtl.DTLVardef@9f27e1org.highwire.dtl.DTLVardef@f35d84org.highwire.dtl.DTLVardef@1808ed4_HPS_FORMAT_FIGEXP M_FIG C_FIG (Source: Created in BioRender. Anisetty, N. (2025) https://BioRender.com/a96f199)

neuroscience↗

Impact of dopaminergic modulation on the state transitions of striatal medium spiny neuron sub-types - a computational study

Medium spiny neurons (MSN) of the striatum are known for their bistable membrane potential leading to two states: a hyperpolarized down-state and a depolarized up-state. Glutamatergic inputs from the hippocampus play a key role in switching the cell to the up-state. This gating is known to play a key role in regulating when other synaptic inputs, such as from the cortex, should generate action potentials and when they should be considered as noise. Any deviations from this pattern of state transitions indicates abnormal gating that has implications in conditions such as schizophrenia. Although dopamine is reported to modulate ion channels of MSN sub-types - dMSN and iMSN - its influence on the state transition times and up-state dwell times are not yet examined. We address this lacuna using biophysically constrained spiny models of dMSN and iMSN with explicit dopamine receptors. Our findings indicate a significant increase in up-state dwell time for dMSN and a significant decrease for iMSN when the % activation of DA receptors was increased. Additionally, a strong correlation between state transition times and spiking frequencies of MSN sub-types was observed.

neuroscience↗