Rudolph, U. | bioRxiv Science

bioRxiv2022

Control of contextual memory through interneuronal α5-GABAA receptors

{gamma}-aminobutyric acid type A receptors that incorporate 5 subunits (5-GABAARs) are highly enriched in the hippocampus and are strongly implicated in control of learning and memory. Receptors located on pyramidal neuron dendrites have long been considered responsible, but here we report that their selective knockout from either interneurons (5-i-KO) or pyramidal neurons (5-pyr-KO) interferes with the ability of the general anesthetic etomidate to suppress contextual conditioning. Using Ca2+ imaging of CA1 pyramidal neuron activity in freely exploring mice to assess hippocampal function directly, we found that etomidate blocked the development of place cells and spatial engrams in wild type (WT) and 5-pyr-KO mice, but not in 5-i-KO mice. In addition, 5-i-KO mice developed weaker spatial engrams than WT mice under control conditions. These findings show that interneuronal 5-GABAARs serve a physiological role in promoting spatial learning, and that they mediate the suppression of hippocampus-dependent memory by etomidate.

neuroscience↗

bioRxiv2020

Identification of amyloid beta oligomers in locus coeruleus (LC) neurons of Alzheimer's patients and their impact on LC oxidative stress, inhibitory neurotransmitter receptors and neuronal excitability

Amyloid {beta} oligomers (A{beta}O) are potent modulators of two key Alzheimers pathological processes, namely synaptic dysfunction and tau tangle formation in various brain regions. Remarkably, the impact of A{beta}O in one of the earliest brain regions to exhibit Alzheimers pathology, the locus coeruleus (LC), remains to be determined. Of particular importance is the effect of A{beta}O on the excitability of individual LC neurons. This parameter determines brain-wide noradrenaline (NA) release, and thus NA-mediated brain functions, including cognition, emotion and immune function, which are all severely compromised in Alzheimers. Using a mouse model of increased A{beta} production (APP-PSEN1), together with correlative histopathological analyses in post mortem Alzheimers patient samples, we determined the impact of A{beta} pathology on various correlates of LC neuronal integrity. A{beta}O immunoreactivity in the LC of APP-PSEN1 mice was replicated in patient samples, presenting as individual clusters located both intraneuronally, in mitochondrial compartments, as well as extracellularly in association with inhibitory synapses. No specific signal was detected in either patient control or wild type mouse samples. Accompanying this A{beta}O expression profile was LC neuronal hyperexcitability and indicators of oxidative stress in APP-PSEN1 mice. LC hyperexcitability arose from a diminished inhibitory effect of GABA, due to impaired expression and function of the GABA-A receptor (GABAAR) 3 subunit. Importantly, this altered LC 3-GABAAR expression profile overlapped with A{beta}O expression in both APP-PSEN1 mice and Alzheimers patient samples. Finally, strychnine-sensitive glycine receptors (GlyRs) remained resilient to A{beta}O-induced changes and their activation reversed LC hyperexcitability. Alongside this first demonstration of A{beta}O expression in the LC of Alzheimers patients, the study is also first to reveal a direct association between A{beta}O and LC neuronal excitability. GlyR-3-GABAAR modulation of A{beta}O-dependent LC hyperexcitability could delay the onset of cognitive and psychiatric symptoms arising from LC-NA deficits, thereby significantly diminishing the disease burden for Alzheimers patients.

neuroscience↗