Cholinergic Modulation of Synaptic Plasticity in VAChT-Modified Mice

The hippocampus is a region of the brain known for its role in learning and memory. The neural correlate of memory formation is believed to be changes in synaptic efficacy through processes broadly termed “synaptic plasticity”. Synaptic plasticity includes long term changes that increases (potentiation, LTP) or decreases (depression) synaptic strength. The hippocampus receives modulatory cholinergic afferents originating in the basal forebrain. This project investigates changes in bidirectional synaptic plasticity in gene-modified vesicular acetylcholine transporter protein-knockdown (VAChT-KD) mice, which express decreased acetylcholine secretion. Extracellular field recordings were performed on hippocampal slices to characterize synaptic physiology in the CA1- region glutamatergic synapses. VAChT-KD mice expressed reduced basal transmission and activity-dependent LTP, though depression was not changed. Furthermore, acute application of the cholinergic agonist carbachol rescued the LTP deficit. This project demonstrates that decreased cholinergic tone can affect hippocampal synaptic processes and suggests mechanisms by which cholinergic pathways may act on synapse physiology

Kainate receptor function in rodent subcortical visual processing.

Glutamate is found throughout the central nervous system and has been shown to be an important excitatory neurotransmitter in the visual system. There are two subdivisions of receptor on which this ubiquitous neurotransmitter acts, metabotropic (mGluR) and ionotropic (GluR) glutamate receptors. There are eight sub types of mGluR falling into three groups, and fifteen GluR subunits also divided into three groups. Kainate receptors (KARs) comprise one group of the ionotropic glutamate receptor subdivision. Relay cells of the lateral geniculate nucleus (LGN) are driven and modulated by a variety of NMDA, AMPA and metabotropic receptors. In addition, investigation into the involvement of mGluR, AMPA and NMDA receptor function in the synaptic processing of the superior colliculus (SC) has been well documented. It has been difficult, however, to establish specific KAR function in these brain structures due to lack of pharmacological agents acting solely at kainate receptors. In recent years such agents have become available, thus enabling the present study of GluR5 involvement in visual processing within the SC and LGN. The purpose of this body of work has been to assess the involvement of GluR5-containing Kainate receptors (KARs) in synaptic transmission between retinal ganglion cells (RGCs) and subcortical brain structures involved in the processing of visual information namely the superficial superior colliculus (SSC) and the lateral geniculate nucleus (LGN). The majority of the work focused on the function of KARs in the SSC. To elucidate the involvement of KARs in visual processing, both in vivo and in vitro methods were utilised. In vivo electrophysiology was used for extracellular recording of evoked activity of both SSC and LGN neurons in response to visual stimuli. This was carried out during intravenous injection of GluR5 antagonist. In vivo recording twinned with iontophoretic administration of GluR5-specific pharmacological compounds was also employed to investigate KAR participation in direct synaptic transmission between RGCs and the SSC neurons. The same technique was used to study KAR involvement in the phenomenon of response habituation exhibited by these neurons. To parallel in vivo protocols, in vitro SSC slice experiments were performed to study the effect of GluR5 agonists and antagonists on evoked postsynaptic currents. This enabled the administration of drugs at concentrations specific for GluR5 subunits whilst investigating GluR5 involvement in direct synaptic transmission between RGC input and SSC neurons. In addition, a paired pulse protocol was employed to propose a presynaptic location of GluR5-containing KARs at retinal input into the SSC. Furthermore, the use of GluR5- specific and GABAR-specific compounds during evoked current recording indicated the involvement of GluR5-containing receptors in the direct modulation of excitatory but not inhibitory input into the SSC. In summary, therefore, both in vivo and in vitro electrophysiology techniques were used to indicate a location and function for GluR5 KARs in the subcortical visual system of the rat. GluR5-containing receptors were found to modulate visual processing of both the LGN and SSC. It was unclear whether these receptors were located in the LGN itself due to the use of systemic injection protocols, however, iontophoresis of GluR5-selective drugs demonstrated a role in modulating visual responses within the SSC. The mechanism by which GluR5 receptors modulated responses in the SSC was further elucidated by a series of whole cell patch-clamp experiments which revealed that GluR5-containing receptors reduced synaptic transmission at excitatory inputs directly onto recorded cells and those connections with the intrinsic inhibitory circuitry of the SSC. In addition a paired-pulse protocol was used to determine that the decrease in excitatory transmission was caused by the presynaptic reduction of glutamatergic transmission

Activity-dependent changes in synaptic efficacy at glutamatergic and GABAergic connections in the immature hippocampus

During development, correlated network activity plays a crucial role in establishing functional synaptic contacts, thus contributing to the development of adult neuronal circuits. In the hippocampus, a region of the brain involved in the formation of declarative memories, network-driven giant depolarizing potentials or GDPs are generated by the synergistic action of glutamate and GABA, which at this developmental stage is depolarizing and excitatory. The depolarizing action of GABA during GDPs results in calcium flux via NMDA receptors and voltage-dependent calcium channels. Calcium, in turn activates different signaling pathways necessary for several developmental processes including synaptogenesis. In previous work from our laboratory it was demonstrated that GDPs and associated calcium transients act as coincident detectors for enhancing synaptic efficacy at poorly developed mossy fibre-CA3 synapses in a Hebbian type of way..

Activity-dependent regulation of GABA release at immature mossy fibers-CA3 synapses: role of the Prion protein

In adulthood, mossy fibers (MFs), the axons of granule cells of the dentate gyrus (DG), release glutamate onto CA3 principal cells and interneurons. In contrast, during the first week of postnatal life MFs release -aminobutyric acid (GABA), which, at this early developmental stage exerts a depolarizing and excitatory action on targeted cells. The depolarizing action of GABA opens voltage-dependent calcium channels and NMDA receptors leading to calcium entry and activation of intracellular signaling pathways involved in several developmental processes, thus contributing to the refinement of neuronal connections and to the establishment of adult neuronal circuits. The release of GABA has been shown to be down regulated by several neurotransmitter receptors which would limit the enhanced excitability caused by the excitatory action of GABA. It is worth noting that the immature hippocampus exhibits spontaneous correlated activity, the so called giant depolarizing potentials or GDPs that act as coincident detector signals for enhancing synaptic activity, thus contributing to several developmental processes including synaptogenesis. GDPs render the immature hippocampus more prone to seizures. Here, I explored the molecular mechanisms underlying synaptic transmission and activity-dependent synaptic plasticity processes at immature GABAergic MF-CA3 synapses in wild-type rodents and in mice lacking the prion protein (Prnp0/0 mice). In the first paper, I studied the functional role of kainate receptors (KARs) in regulating GABA release from MF terminals. Presynaptic KARs regulate synaptic transmission in several brain areas and play a central role in modulating glutamate release at adult MF-CA3 synapses. I found that functional presynaptic GluK1 receptors are present on MF terminals where they down regulate GABA release. Thus, application of DNQX or UBP 302, a selective antagonist for GluK1 receptors, strongly increased the amplitude of MF-GABAA-mediated postsynaptic currents (GPSCs). This effect was associated with a decrease in failure rate and increase in PPR, indicating a presynaptic type of action. GluK1 receptors were found to be tonically activated by glutamate present in the extracellular space, since decreasing the extracellular concentration of glutamate with a glutamate scavenger system prevented their activation and mimicked the effects of KAR antagonists. The depressant effect of GluK1 on GABA release was dependent on pertussis toxin (PTx)-sensitive G protein-coupled kainate receptors since it was prevented when hippocampal slices were incubated in the presence of a solution containing PTx. This effect was presynaptic since application of UBP 302 to cells patched with an intracellular solution containing GDP S still potentiated synaptic responses. In addition, the depressant effect of GluK1 on GABA release was prevented by U73122, which selectively inhibits phospholipase C, downstream to G protein activation. Interestingly, U73122, enhanced the probability of GABA release, thus unveiling the ionotropic type of action of kainate receptors. In line with this, we found that GluK1 receptors enhanced MF excitability by directly depolarizing MF terminals via calcium-permeable cation channels. We also explored the possible involvement of GluK1 in spike time-dependent (STD) plasticity and we found that GluK1 dynamically regulate the direction of STD-plasticity, since the pharmacological block of this receptor shifted spike-time dependent potentiation into depression. The mechanisms underlying STD-LTD at immature MF-CA3 synapses have been investigated in detail in the second paper. STD-plasticity is a Hebbian form of learning which consists in bi-directional modifications of synaptic strength according to the temporal order of pre and postsynaptic spiking. Interestingly, we found that at immature mossy fibers (MF)-CA3 synapses, STD-LTD occurs regardless of the temporal order of stimulation (pre versus post or viceversa). However, as already mentioned, while STD-LTD induced by positive pairing (pre before post) could be shifted into STD-LTP after blocking presynaptic GluK1 receptors, STD-LTD induced by negative pairing (post before pre) relied on the activation of CB1 receptors. At P3 but not at P21, endocannabinoids released by the postsynaptic cell during spiking-induced membrane depolarization retrogradely activated CB1 receptors, probably expressed on MF terminals and persistently depressed GABA release in the rat hippocampus. Thus, bath application of selective CB1 receptor antagonists prevented STD-LTD. Pharmacological tools allow identifying anandamide as the endogenous ligand responsible of activity-dependent depressant effect. To further assess whether STD-LTD is dependent on the activation of CB1 receptors, similar experiments were performed on WT-littermates and CB1-KO mice. While in WT mice the pairing protocol produced a persistent depression of MF-GPSCs as in rats, in CB1-KO mice failed to induce LTD. Consistent with these data, in situ hybridization experiments revealed detectable levels of CB1 mRNA in the granule cell layer of P3 but not of P21mice. These experiments strongly suggest that at immature MF-CA3 synapses STD-LTD is mediated by CB1 receptors, probably transiently expressed, during a critical time window, on MF terminals. In the third paper, I studied synaptic transmission and activity dependent synaptic plasticity at immature MF-CA3 synapses in mice devoid of the prion protein (Prnp0/0). The prion protein (PrPC) is a conserved glycoprotein widely expressed in the brain and involved in several neuronal processes including neurotransmission. If converted to a conformationally altered form, PrPSc can cause neurodegenerative diseases, such as Creutzfeldt-Jakob disease in humans. Previous studies aimed at characterizing Prnp0/0 mice have revealed only mild behavioral changes, including an impaired spatial learning, accompanied by electrophysiological and biochemical alterations. Interestingly, PrPC is developmentally regulated and in the hippocampus its expression parallels the maturation of MF. Here, we tested the hypothesis that at immature (P3-P7) MF-CA3 synapses, PrPC interferes with synaptic plasticity processes. To this aim, the rising phase of Giant Depolarizing Potentials (GDPs), a hallmark of developmental networks, was used to stimulate granule cells in the dentate gyrus in such a way that GDPs were coincident with afferent inputs. In WT animals, the pairing procedure induced a persistent increase in amplitude of MF-GPSCs. In contrast, in Prnp0/0 mice, the same protocol produced a long-term depression (LTD). LTP was postsynaptic in origin and required the activation of cAMP-dependent PKA signaling while LTD was presynaptic and was reliant on G protein-coupled GluK1 receptor and protein lipase C downstream to G protein activation. In addition, at emerging CA3-CA1 synapses of PrPC-deficient mice, stimulation of Schaffer collateral failed to induce LTP, known to be PKA-dependent. Finally, we also found that LTD in Prnp0/0 mice was mediated by GluK1 receptors, since UBP 302 blocked its induction. These data suggest that in the immature hippocampus PrPC controls the direction of synaptic plasticity

Direct presynaptic and indirect astrocyte-mediated mechanisms both contribute to endocannabinoid signaling in the pedunculopontine nucleus of mice

The pedunculopontine nucleus (PPN), a cholinergic nucleus of the reticular activating system, is known to be involved in the regulation of sleep and wakefulness. Endogenous and exogenous cannabinoids, by systemic or local administration to the pedunculopontine nucleus, can both influence sleep. We previously demonstrated that activation of astrocytes by cannabinoid type 1 (CB1) receptor agonists was able to modulate the membrane potential of PPN neurons, even in the presence of blockers of fast synaptic neurotransmission. In the present work, we provide evidence that synaptic inputs of PPN neurons are also affected by activation of presynaptic and astrocytic CB1 receptors. Using slice electrophysiology combined with calcium imaging, optogenetics and immunohistochemistry, we revealed a direct presynaptic inhibitory action on inhibitory postsynaptic currents, along with a mild increase of excitatory postsynaptic currents during CB1 receptor stimulation. Besides inhibition of excitatory and inhibitory neurotransmission through stimulation of presynaptic CB1 receptors, astrocyte- and mGluR-dependent tonic inhibition and excitation also developed. The mild stimulatory action of CB1 receptor activation on excitatory neurotransmission is the combination of astrocyte-dependent tonic excitation on excitatory neurons and the canonical presynaptic CB1 receptor activation and consequential inhibition of excitatory synaptic neurotransmission, whereas the astrocyte-dependent stimulatory action was not observed in inhibitory neurotransmission within the PPN. Our findings demonstrate that endocannabinoids act in the PPN via a dual pathway, consisting of a direct presynaptic and an indirect, astrocyte-mediated component, regulating synaptic strength and neuronal activity via independent mechanisms

NMDA RECEPTORS IN THE DORSAL VAGAL COMPLEX OF NORMAL AND DIABETIC MICE

The dorsal vagal complex (DVC), containing the nucleus of the solitary tract (NTS) and the dorsal motor nucleus of the vagus nerve (DMV), plays a pivotal role in autonomic regulation. Afferent fibers from peripheral organs and higher brain centers synapse in the NTS, which integrates these synaptic connections as well as information from systemically circulating hormones and metabolites. The integrated information is relayed to the dorsal motor nucleus of the vagus nerve (DMV), which in turn, projects motor fibers to elicit parasympathetic control of digestive and other viscera. Physiological functions mediated by the DVC are disrupted in diabetic patients and synaptic plasticity within the DVC has been linked to these complications. N-methyl-D-aspartic acid (NMDA) receptors have been extensively studied for their involvement in synaptic plasticity in a variety of central nervous system disorders; and their activation in the DVC modulates hepatic glucose production and feeding behavior. Although chronic disease can alter NMDA function, changes in DVC expression and/or sensitivity of NMDA receptors in diabetic states has not been addressed. Using whole cell electrophysiology, functional properties of the nuclei in the DVC were investigated in normoglycemic and type 1 diabetic mice. Preterminal NMDA (preNMDA) receptors were discovered to tonically modulate excitatory neurotransmission on terminals contacting DMV neurons. While these preNMDA receptors were not found to differentially modulate tonic excitatory neurotranmission, soma-dendritic NMDA receptor responses of NTS neurons were augmented in type 1 diabetic mice. Through the use single-cell PCR, increased NMDA receptor responses could be correlated to neurons that mediate excitatory neurotransmission and would argue that augmented NMDA receptor responses increase vagal output. In general, enhancing vagal output decreases activity of connected peripheral organs. Molecular approaches were employed to corroborate the observed functional NMDA receptors changes to their protein and mRNA expression levels. Overall, results argue that NMDA receptors are involved in synaptic plasticity in DVC of type 1 diabetic mice to enhance excitatory neurotransmission. This modulation may potentially serve as a physiological counter regulatory mechanism to control pathological disturbances of gastrointestinal homeostatic reflex responses

The Mammalian Interaural Time Difference Detection Circuit Is Differentially Controlled by GABAB Receptors during Development

Throughout development GABAB receptors (GABABRs) are widely expressed in the mammalian brain. In mature auditory brainstem neurons, GABABRs are involved in the short-term regulation of the strength and dynamics of excitatory and inhibitory inputs, thus modulating sound analysis. During development, GABABRs also contribute to long-term changes in input strength. Using a combination of whole-cell patch-clamp recordings in acute brain slices and immunostainings in gerbils, we characterized developmental changes in GABABR-mediated regulation of synaptic inputs to neurons in the medial superior olive (MSO), an auditory brainstem nucleus that analyzes interaural time differences (ITDs). Here, we show that, before hearing onset, GABABR-mediated depression of transmitter release is much stronger for excitation than inhibition, whereas in mature animals GABABRs mainly control the inhibition. During the same developmental period, GABABR immunoreactivity shifts from the dendritic to the somatic region of the MSO. Furthermore, only before hearing onset (postnatal day 12), stimulation of the fibers originating in the medial and the lateral nucleus of the trapezoid body (MNTB and LNTB) activates GABABRs on both the inhibitory and the excitatory inputs. After hearing onset, GAD65-positive endings devoid of glycine transporter reactivity suggest GABA release from sources other than the MNTB and LNTB. At this age, pharmacological increase of spontaneous synaptic release activates GABABRs only on the inhibitory inputs. This indicates not only a profound inhibitory effect of GABABRs on the major inputs to MSO neurons in neonatal animals but also a direct modulatory role of GABABRs for ITD analysis in the MSO of adult animals