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The mGluR2 receptor agonist, DCG-IV, has been hypothesised to promote memory formation by disinhibiting mitral cell activity in the accessory olfactory bulb (AOB), leading to increased feedback inhibition from granule cells. We tested a key aspect of this hypothesis by recording DCG-IV effects on mitral cell activity in the AOB of urethane anaesthetised mice. Animals received 1 μl infusion of artificial cerebro-spinal fluid or 10, or 100 pmol of DCG-IV into the AOB. A recording electrode was located in the mitral cell layer and a reference electrode in the granule cell layer. There was no single unit activity in the latter. Single unit activity in the mitral cell layer was recorded before, during and after drug infusion. Local infusions of DCG-IV not only did not disinhibit mitral cells but actually reduced their firing frequency. The effect appeared during the infusion and was dose-dependent. The 10 pmol DCG-IV-induced decrease in spike rate was deeper and lasted longer than 100 pmol effect. Trends to return to the preinfusion levels were observed in both groups by the end of 60-min post-infusion period. Thus, this study failed to find a disinhibitory effect of DCG-IV on mitral cells that had been predicted on the basis of in vitro data. These findings challenge the established hypothesis that the memory inducing effects of DCG-IV are mediated by mitral cell disinhibition.
The pedunculopontine tegmental nucleus (PPN) belongs to the brainstem system which synchronizes hippocampal activity. Theta relevant intra-PPN circuitry involves its cholinergic, GABA-ergic and glutamatergic neurons and Substance P as neuromodulator. Evidence that PPN opioid elements also modulate the hippocampal theta is provided here. In urethane-anesthetized rats a unilateral microinjection of morphine (MF) (1.5 and 5 µg) increased the maximal peak power of tail pinch-induced theta. The higher dose also increased the corresponding frequency. When the theta was evoked by intra-PPN injection of carbachol (10 µg), the addition of MF (5 µg) prolonged theta latency and shortened the duration of the theta. These effects of MF were blocked by naloxone (5 µg). The results obtained suggest that the PPN opioid system can enhance or suppress the hippocampal theta depending on the actual level of PPN activation.
BACKGROUND AND AIMS: The amygdala has been proposed to act as a “relevance detector” involved in the processing of behaviorally relevant or significant stimuli. We investigated that putative function of the amygdala in the context of human social values, such as achievement, honesty or stimulation. METHODS: We used functional magnetic resonance imaging (fMRI) during a behavioral task of social values rating. During the task, participants were presented with different social values and asked to rate their importance as guiding principles in their lives. We used the conjunction analysis of values and their ratings to localize brain regions where value ratings modulated activity evoked by value processing. RESULTS: The conjunction analysis with the amygdala mask revealed that amygdala activity during value processing correlated with value rating scores. Moreover, the rating scores modified activity in the visual cortex during the response phase, when participants were pressing response buttons, so that higher scores were associated with stronger activation. CONCLUSIONS: The results suggest that the amygdala can code the subjective importance of social values. The increased activity in the visual cortex with higher rating scores may reflect amplified processing within the ventral visual stream, mediated by the amygdala. An intriguing possibility is that excitatory feedback from the amygdala in response to more important/significant stimuli during task performance could enhance functional connectivity between the amygdala and visual cortex. To investigate if that connectivity differed according to the ratings of value importance, a psychophysiological interaction analysis will be performed in further analysis.
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