Search bioRxivSearch

Biology subjects

Ahmadian, Y.

Publications and source records attributed to Ahmadian, Y..

5 recordsLinked to original sources

Heading direction with respect to a reference point modulates place-cell activity

Utilizing electrophysiological recordings from CA1 pyramidal cells in freely moving mice, we find that a majority of neural responses are modulated by the heading-direction of the animal relative to a point within or outside their enclosure that we call a reference point. Our findings identify a novel representation in the neuronal responses in the dorsal hippocampus.

neuroscience

Sniff invariant odor coding

Sampling regulates stimulus intensity and temporal dynamics at the sense organ. Despite variations in sampling behavior, animals must make veridical perceptual judgments about external stimuli. In olfaction, odor sampling varies with respiration, which influences neural responses at the olfactory periphery. Nevertheless, rats were able to perform fine odor intensity judgments despite variations in sniff kinetics. To identify the features of neural activity supporting stable intensity perception, in awake mice we measured responses of Mitral/Tufted (MT) cells to different odors and concentrations across a range of sniff frequencies. Amplitude and latency of the MT cells responses vary with sniff duration. A fluid dynamics (FD) model based on odor concentration kinetics in the intranasal cavity can account for this variability. Eliminating sniff waveform dependence of MT cell responses using the FD model significantly improves concentration decoding. This suggests potential schemes for sniff waveform invariant odor concentration coding.\n\nHighlightsO_LIOdor concentration discrimination does not depend on sniff frequency\nC_LIO_LIAmplitude and latency of MT cell responses vary with sniff frequency\nC_LIO_LIA fluid dynamic based model accounts for sniff dependent variability in the responses\nC_LIO_LITransforming MT cell responses with this model achieves sniff invariant coding\nC_LI

neuroscience

Capturing the diversity of biological tuning curves using generative adversarial networks

Tuning curves characterizing the response selectivities of biological neurons often exhibit large degrees of irregularity and diversity across neurons. Theoretical network models that feature heterogeneous cell populations or random connectivity also give rise to diverse tuning curves. However, a general framework for fitting such models to experimentally measured tuning curves is lacking. We address this problem by proposing to view mechanistic network models as generative models whose parameters can be optimized to fit the distribution of experimentally measured tuning curves. A major obstacle for fitting such models is that their likelihood function is not explicitly available or is highly intractable to compute. Recent advances in machine learning provide ways for fitting generative models without the need to evaluate the likelihood and its gradient. Generative Adversarial Networks (GAN) provide one such framework which has been successful in traditional machine learning tasks. We apply this approach in two separate experiments, showing how GANs can be used to fit commonly used mechanistic models in theoretical neuroscience to datasets of measured tuning curves. This fitting procedure avoids the computationally expensive step of inferring latent variables, e.g., the biophysical parameters of individual cells or the particular realization of the full synaptic connectivity matrix, and directly learns model parameters which characterize the statistics of connectivity or of single-cell properties. Another strength of this approach is that it fits the entire, joint distribution of experimental tuning curves, instead of matching a few summary statistics picked a priori by the user. More generally, this framework opens the door to fitting theoretically motivated dynamical network models directly to simultaneously or non-simultaneously recorded neural responses.

neuroscience

Learning Fast And Slow: Deviations From The Matching Law Can Reflect An Optimal Strategy Under Uncertainty

Behavior which deviates from our normative expectations often appears irrational. A classic example concerns the question of how choice should be distributed among multiple alternatives. The so-called matching law predicts that the fraction of choices made to any option should match the fraction of total rewards earned from the option. This choice strategy can maximize reward in a stationary reward schedule. Empirically, however, behavior often deviates from this ideal. While such deviations have often been interpreted as reflecting noisy, suboptimal, decision-making, here we instead suggest that they reflect a strategy which is adaptive in nonstationary and uncertain environments. We analyze the results of a dynamic foraging task. Animals exhibited significant deviations from matching, and animals turned out to be able to collect more rewards when deviation was larger. We show that this behavior can be understood if one considers that animals had incomplete information about the environments dynamics. In particular, using computational models, we show that in such nonstationary environments, learning on both fast and slow timescales is beneficial. Learning on fast timescales means that an animal can react to sudden changes in the environment, though this inevitably introduces large fluctuations (variance) in value estimates. Concurrently, learning on slow timescales reduces the amplitude of these fluctuations at the price of introducing a bias that causes systematic deviations. We confirm this prediction in data - monkeys indeed solved the bias-variance tradeoff by combining learning on both fast and slow timescales. Our work suggests that multi-timescale learning could be a biologically plausible mechanism for optimizing decisions under uncertainty.

neuroscience

Stabilized supralinear network dynamics account for stimulus-induced changes of noise variability in the cortex

Variability and correlations in cortical activity are ubiquitously modulated by stimuli. Correlated variability is quenched following stimulus onset across multiple cortical areas, suppressing low-frequency components of the LFP and of Vm-LFP coherence. Modulation of Fano factors and correlations in area MT is tuned for stimulus direction. What circuit mechanisms underly these behaviors? We show that a simple model circuit, the stochastic Stabilized Supralinear Network (SSN), robustly explains these results. Stimuli modulate variability by modifying two forms of effective connectivity between activity patterns that characterize excitatory-inhibitory (E/I) circuits. Increases in the strength with which activity patterns inhibit themselves reduce correlated variability, while increases in feedforward connections between patterns (transforming E/I imbalance into balanced fluctuations) increase variability. These results suggest an operating regime of cortical dynamics that involves fast fluctuations and fast responses to stimulus changes, unlike previous models of variability suppression through suppression of chaos or networks with multiple attractors.

neuroscience