Past events

One of the most remarkable functions of the human brain is the ability to recall a personal experience from the past and reenact it vividly in our mind, in a way that allows us to reflect upon the memory and derive from it relevant information that can guide our future behavior. My doctoral research explored the neuronal mechanisms that enable this core cognitive function in the human brain. Using rare electrophysiological recordings obtained from neurosurgical patients for clinical purposes I investigated and characterized the complex bidirectional interactions that occur between the hippocampus and the cerebral cortex during retrieval of conscious, reportable memories. My results are twofold. I first show that 1-2 seconds before the onset of individual recollections the hippocampus elicits transient electrical oscillations known as Sharp Wave Ripples (SWRs). Such oscillatory events have been extensively studied in animal models in recent years and were shown to reflect massive synchronization events during which millions of pyramidal neurons on the hippocampus output pathway fire simultaneously. My results demonstrate that the SWR events are selective to memory contents and play a major role in coordinating the re-activation of hippocampal-neocortical memory representations during retrieval. I show a tight coupling between SWR events and visual cortex activation, and reveal a massive peri-ripple activation of the default mode network. Second, I show that the cortex uses a flexible, goal-directed, "baseline shift" mechanism that allows the imposition of predefined boundaries on spontaneous recollections. Specifically, the results demonstrate that when free recall is limited to a particular category, the average neuronal activity level in cortical sites that represent the targeted category is steadily and significantly enhanced throughout the free recall period. Such steady-state excitatory enhancement is likely to introduce a category-specific bias in the cortical input arriving at the hippocampus, which may facilitate the reactivation of memory traces belonging to the targeted category and not others. Altogether, the results place hippocampal SWRs firmly as a central mechanism in the retrieval of human declarative memory. They demonstrate a central role for SWRs in coordinating the hippocampus-cortical dialogue during recollection and point to a flexible "baseline shift" mechanism that can account for the remarkable ease and precision by which we can constrain this dialogue to support retrieval goals. Zoom link to join: https://weizmann.zoom.us/j/92146113977?pwd=VmhuMEhBcTRYZDNWMVJ4bGJrR0lIdz09 Meeting ID: 92146113977 Password: 803220

I will discuss two studies from my laboratory, that reveal differential role of hypothalamic paraventricular and supraoptic oxytocin neurons, as well as anterior hypothalamic neurons in social decision making of adult male mice. Zoom link to join: https://weizmann.zoom.us/j/96608033618?pwd=SEdJUkR2ZzRBZ3laUUdGbWR1VFJTdz09 Meeting ID: 966 0803 3618 Password: 564068 Host: Dr. Rita Schmidt rita.schmidt@weizmann.ac.il tel: 9070

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The world around us is barely stable. To maintain constancy of perception, neuronal circuits adopt multiple mechanisms, each carefully tailored to grant the system with computational fidelity in the face of variable stimuli, yet to enable flexibility of computation in certain contexts. During my PhD I investigated the mechanisms that underlie retinal direction-selectivity. Using electrophysiology and modelling approaches, I will show how several mechanisms cooperate to maintain stability in the circuit’s response to moving objects carrying distinct characteristics. This stability is compromised when the retina is confronted by a repetitive light-adapting stimulus that changes the receptive field of cells in several layers of the circuit. Intriguingly, these changes in the cells’ receptive field expose antagonistic center-surround organization of direction coding: the center receptive field supports response to one direction, while the surround supports response to the opposite direction. Center-surround antagonism is thought to enhance spatial discrimination, but this is the first evidence for its contribution to retinal direction selectivity. This provides an example of how the retina elegantly implements computational motifs that are reminiscent of those found in higher brain regions, using just a handful of cell types, already at the first station of the visual system. (If you are not from the neuroscience field, please check out THIS). Zoom link to join: https://weizmann.zoom.us/j/91058452206?pwd=UFpBZkVrM1luUSttSGZUTHRiNUg5dz09 Meeting ID: 910 5845 2206 Password: 229240

Diffusion weighted MRI (DWI) is the main neuroimaging modality used in non-invasive investigations of tissue microstructure, and provides quantitative cytomorphological information on a spatial scale well below the nominal resolution of MRI. The main limitation of DWI is its lack of compartmental specificity, as its “reporter molecule” is water, ubiquitous in all tissue compartments and cell types. Brain metabolites are mostly confined to the intracellular space, and their concentrations vary across cell types. Several metabolites give rise to quantifiable magnetic resonance spectroscopy (MRS) signatures, and are thus considered as compartment-specific and sometimes cell-specific markers. Sensitization of MRS to diffusion results in a set of diffusion properties for a variety of intracellular metabolites, from which microstructural information specific to the intracellular space can be obtained. A proper choice of experimental settings can be used to investigate properties that range from cytoplasmic viscosity and tortuosity of the intracellular space, to overall cell morphological features. The specificity of some metabolites to different cell types such as neurons and astrocytes opens the way to studying morphological properties of different cell populations and monitoring their modulation by physiological changes in health and disease. The presentation will introduce methodological concepts of diffusion-weighted MRS, followed by simple examples that demonstrate the unique ability of diffusion-weighted MRS to characterize cell-type specific structural features. Special emphasis will be bestowed on experimental and modelling frameworks that merge the specificity of diffusion-weighted MRS with the sensitivity of DWI to gain insights on tissue microstructure beyond what each method can separately provide. Zoom link to join:https://weizmann.zoom.us/j/96608033618?pwd=SEdJUkR2ZzRBZ3laUUdGbWR1VFJTdz09 Meeting ID: 966 0803 3618 Password: 564068 Host: Dr. Rita Schmidt rita.schmidt@weizmann.ac.il tel: 9070

Although animals are known to heavily rely on chemical signals for intraspecies communication, the matter of human chemical communication remains greatly contentious. I will present evidence supporting the claim that humans, just like other animals, rely on bodily-odors to effectively navigate the social world. First, I will present a quantification of people’s overt olfactory-sampling behavior. Of approximately 400 respondents, 94% acknowledged engaging in smelling their close relationships, and approximately 60% acknowledged sniffing strangers. Next, we tested if this olfactory information is employed for socially-relevant behavioral decisions, such as trust, a key element in human socialization. We found that subliminal exposure to body-odor increased implicit trustworthiness attributed to anthropomorphic non-humans. Finally, I will describe the effect of a specific body-volatile, Hexadecanal (HEX), on human impulsive aggression. Using validated behavioral paradigms, we observed a remarkable dissociation: sniffing HEX blocked aggression in men, but triggered aggression in women. Using functional brain imaging, we uncovered a pattern of brain activity mirroring behavior: In both men and women, HEX increased activity in an area implicated in the perception of social cues. Hex then modulated functional connectivity in a brain network implicated in aggressive behavior in a sex-dependent manner. Altogether, the thesis puts forward the hypothesis that chemosignals are a form of human social communication. Under this premise, human sampling behavior of self and others’ body-volatiles provides one with important information that, in turn, affects behaviors central to human society, such as trust and aggression. Zoom link to join: https://weizmann.zoom.us/j/98031517872?pwd=U0EvNG5EdGJBL24zWmpKUlY1akdnZz09 Meeting ID: 980 3151 7872 Password: 976632

During early life the neural code must develop to appropriately transform sensory inputs into behavioural outputs. However little is known about how developments in neural representations directly impact on behaviour. By combining behavioural analysis with 2-photon calcium imaging at multiple timepoints from 4 to 15 dpf in the optic tectum of developing zebrafish larvae, we demonstrate a link between the maturity of neural coding in the visual brain and developmental changes in visually-guided behavior. We show that visually-driven hunting behavior improves from 4 to 15 days post-fertilization, becoming faster and more accurate. During the same period population activity in parts of the optic tectum refines, improving decoding and information transmission for particular spatial positions. Together these results show that developmental signatures of an emerging neural code can be directly related to observable properties of behaviour. Please click the link below to join: https://weizmann.zoom.us/j/96608033618?pwd=SEdJUkR2ZzRBZ3laUUdGbWR1VFJTdz09 Meeting ID: 966 0803 3618 Password: 564068 Host: Dr. Rita Schmidt rita.schmidt@weizmann.ac.il tel: 9070

The brain is rife with feedback connections within and between its regions, which almost inevitably should give rise to dynamic activity in the underlying neuronal populations. In the taste system of awake rats, neurons sequentially transition between activity states that correlate with taste perceptions such as identity, palatability, and novelty. In my talk I will present the current knowledge regarding taste information processing in the taste system and will add our recent description of sub-second novelty information transmission through a new circuit. Next, I will present unpublished data showing the dynamic changes in neuronal activity as taste memory is acquired and consolidated across 12 hours in behaving rats. Last, I will show how taste learning helps us investigating the early, pre-pathological, stages of Alzheimer’s disease. Zoom link to join: https://weizmann.zoom.us/j/96608033618?pwd=SEdJUkR2ZzRBZ3laUUdGbWR1VFJTdz09 Meeting ID: 966 0803 3618 Password: 564068 Host: Dr. Rita Schmidt rita.schmidt@weizmann.ac.il tel: 9070