5 research outputs found
Immature Dentate Granule Cells Require Ntrk2/Trkb for the Formation of Functional Hippocampal Circuitry
Local or Not Local: Investigating the Nature of Striatal Theta Oscillations in Behaving Rats
International audienceVisual Abstract In the cortex and hippocampus, neuronal oscillations of different frequencies can be observed in local field potentials (LFPs). LFPs oscillations in the theta band (6-10 Hz) have also been observed in the dorsolateral striatum (DLS) of rodents, mostly during locomotion, and have been proposed to mediate behaviorally-relevant interactions between striatum and cortex (or between striatum and hippocampus). However, it is unclear if these theta oscillations are generated in the striatum. To address this issue, we recorded LFPs and spiking activity in the DLS of rats performing a running sequence on a motorized treadmill. We observed an increase in rhythmical activity of the LFP in the theta-band during run compared to rest periods. However, several observations suggest that these oscillations are mainly generated outside of the striatum. First, theta oscillations disappeared when Significance Statement In the cortex and hippocampus, neuronal network oscillations can be observed in the local field potentials (LFPs) and contribute to information transfer between brain regions. LFP oscillations can also be recorded in the striatum, even if, unlike the cortex and hippocampus, this brain region's anatomic organization does not favor the generation of dipolar sources. It is therefore unclear if these striatal oscillations are locally generated or reflect volume-conducted signals generated distally from the striatum. Here, we provide evidence that striatal theta oscillations of the LFPs recorded while rats performed a running sequence are largely contaminated by volume-conducted signals. We propose that theta LFP oscillations in the striatum do not accurately reflect local cellular activity and should be interpreted with caution
The Dorsal Striatum Energizes Motor Routines
International audienceThe dorsal striatum (dS) has been implicated in storing procedural memories and controlling movement kinematics. Since procedural memories are expressed through movements, the exact nature of the dS function has proven difficult to delineate. Here we challenged rats in complementary locomotion-based tasks designed to alleviate this confound. Surprisingly, dS lesions did not impair the rats' ability to remember the procedure for the successful completion of motor routines. However, the speed and initiation of the rewardoriented phase of the routines were irreversibly altered by the dS lesion. Further behavioral analyses combined with modeling in the optimal control framework indicated that these kinematic alterations were well-explained by an increased sensitivity to effort. Our work provides evidence supporting a primary role of the dS in modulating the kinematics of reward-oriented actions, a function that may be related to the optimization of the energetic costs of moving
Presynaptic GABAB Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
GABAB receptors are the G-protein-coupled receptors for GABA, the main inhibitory neurotransmitter in the central nervous system. Pharmacological activation of GABAB receptors regulates neurotransmission and neuronal excitability at pre- and postsynaptic sites. Electrophysiological activation of GABAB receptors in brain slices generally requires strong stimulus intensities. This raises the question as to whether behavioral stimuli are strong enough to activate GABAB receptors. Here we show that GABAB1a-/- mice, which constitutively lack presynaptic GABAB receptors at glutamatergic synapses, are impaired in their ability to acquire an operant learning task. In vivo recordings during the operant conditioning reveal a deficit in learning-dependent increases in synaptic strength at CA3-CA1 synapses. Moreover, GABAB1a-/- mice fail to synchronize neuronal activity in the CA1 area during the acquisition process. Our results support that activation of presynaptic hippocampal GABAB receptors is important for acquisition of a learning task and for learning-associated synaptic changes and network dynamics