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Retinal adaptation and invariance to changes in higher-order stimulus statistics

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 Added by Gasper Tkacik
 Publication date 2012
  fields Biology
and research's language is English




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Adaptation in the retina is thought to optimize the encoding of natural light signals into sequences of spikes sent to the brain. However, adaptation also entails computational costs: adaptive code is intrinsically ambiguous, because output symbols cannot be trivially mapped back to the stimuli without the knowledge of the adaptive state of the encoding neuron. It is thus important to learn which statistical changes in the input do, and which do not, invoke adaptive responses, and ask about the reasons for potential limits to adaptation. We measured the ganglion cell responses in the tiger salamander retina to controlled changes in the second (contrast), third (skew) and fourth (kurtosis) moments of the light intensity distribution of spatially uniform temporally independent stimuli. The skew and kurtosis of the stimuli were chosen to cover the range observed in natural scenes. We quantified adaptation in ganglion cells by studying two-dimensional linear-nonlinear models that capture well the retinal encoding properties across all stimuli. We found that the retinal ganglion cells adapt to contrast, but exhibit remarkably invariant behavior to changes in higher-order statistics. Finally, by theoretically analyzing optimal coding in LN-type models, we showed that the neural code can maintain a high information rate without dynamic adaptation despite changes in stimulus skew and kurtosis.



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The ability of the organism to distinguish between various stimuli is limited by the structure and noise in the population code of its sensory neurons. Here we infer a distance measure on the stimulus space directly from the recorded activity of 100 neurons in the salamander retina. In contrast to previously used measures of stimulus similarity, this neural metric tells us how distinguishable a pair of stimulus clips is to the retina, given the noise in the neural population response. We show that the retinal distance strongly deviates from Euclidean, or any static metric, yet has a simple structure: we identify the stimulus features that the neural population is jointly sensitive to, and show the SVM-like kernel function relating the stimulus and neural response spaces. We show that the non-Euclidean nature of the retinal distance has important consequences for neural decoding.
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We present a theoretical study aiming at model fitting for sensory neurons. Conventional neural network training approaches are not applicable to this problem due to lack of continuous data. Although the stimulus can be considered as a smooth time dependent variable, the associated response will be a set of neural spike timings (roughly the instants of successive action potential peaks) which have no amplitude information. A recurrent neural network model can be fitted to such a stimulus-response data pair by using maximum likelihood estimation method where the likelihood function is derived from Poisson statistics of neural spiking. The universal approximation feature of the recurrent dynamical neuron network models allow us to describe excitatory-inhibitory characteristics of an actual sensory neural network with any desired number of neurons. The stimulus data is generated by a Phased Cosine Fourier series having fixed amplitude and frequency but a randomly shot phase. Various values of amplitude, stimulus component size and sample size are applied in order to examine the effect of stimulus to the identification process. Results are presented in tabular form at the end of this text.
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Objective. Clinical trials previously demonstrated the spectacular capacity to elicit visual percepts in blind patients affected with retinal diseases by electrically stimulating the remaining neurons on the retina. However, these implants restored very limited visual acuity and required transcutaneous cables traversing the eyeball, leading to reduced reliability and complex surgery with high postoperative infection risks. Approach. To overcome the limitations imposed by cables, a retinal implant architecture in which near-infrared illumination carries both power and data through the pupil is presented. A high efficiency multi-junction photovoltaic cell transduces the optical power to a CMOS stimulator capable of delivering flexible interleaved sequential stimulation through a diamond microelectrode array. To demonstrate the capacity to elicit a neural response with this approach while complying with the optical irradiance safety limit at the pupil, fluorescence imaging with a calcium indicator is used on a degenerate rat retina. Main results. The power delivered by the laser at safe irradiance of 4 mW/mm2 is shown to be sufficient to both power the stimulator ASIC and elicit a response in retinal ganglion cells (RGCs), with the ability to generate of up to 35 000 pulses per second at the average stimulation threshold. Significance. This confirms the feasibility of wirelessly generating a response in RGCs with a digital stimulation controller that can deliver complex multipolar stimulation patterns at high repetition rates.
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