Memory improvement via stimulation of temporal cortex

Stimulation of temporal cortex with electrodes at memory encoding time boosted recall by 15%, in humans.

In the first phase, researchers listened to brain activity while subjects were memorizing nouns. They trained a model to try to predict, based on the brain activity at encoding time, if that word would be remembered or not. In the second phase, researchers ran the model while subjects were memorizing words, and if the model predicted that the word was more than 50% likely to be forgotten, they zapped the brain for 0.5 seconds (through a single pair of adjacent electrodes in the lateral temporal cortex, at amplitudes ranging from 0.5 mA to 1.5 mA (for electrodes deep in the cortex) or 3.5 mA (for the cortical surface) (amplitude was the maximum within this range such that stimulation didn’t appear to cause afterdischarges). Stimulation in this fashion improved recall by 15%. After stimulation, the classifier was more likely to say that the subject would remember the word, which might suggest that the stimulation improved recall by sometimes nudging the brain into a state that the classifier recognized as good for memory encoding.

As an aside, imo one should keep in mind that this doesn’t necessarily mean that this would be a good thing to do every time you are learning something. The way i like to think about this experiment is to imagine that you have some big machine that you don’t know how it works. The machine sometimes makes humming noises and other times it makes sputtering noises. You notice that when it makes the sputtering noise, this correlates somewhat with it not doing its job so well. So, whenever you hear a sputtering noise, you kick it really hard. Sometimes when you kick it, it makes it hum again. You record data and find out that if you kick it when it sputters, that improves output by 15%. That’s very interesting, but does it mean that it’s a good idea to kick the machine whenever it sputters? No — maybe kicking the machine damages it a little (or has some small probability of damaging it sometimes), or maybe the sputtering was something (such as a self-cleaning cycle) that the machine needs to do for its long-term health even at the cost of short-term performance. In other words, there is a clear gain to kicking the machine when it sputters, but it is unknown if there is also a subtle cost.

 

Youssef Ezzyat, Paul A. Wanda, Deborah F. Levy, Allison Kadel, Ada Aka, Isaac Pedisich, Michael R. Sperling, Ashwini D. Sharan, Bradley C. Lega, Alexis Burks, Robert E. Gross, Cory S. Inman, Barbara C. Jobst, Mark A. Gorenstein, Kathryn A. Davis, Gregory A. Worrell, Michal T. Kucewicz, Joel M. Stein, Richard Gorniak, Sandhitsu R. Das, Daniel S. Rizzuto & Michael J. Kahana. Closed-loop stimulation of temporal cortex rescues functional networks and improves memory.

 

https://www.wired.com/story/ml-brain-boost

Topological analysis of population activity in visual cortex

Singh, G., Memoli, F., Ishkhanov, T., Sapiro, G., Carlsson, G., & Ringach, D. L. (2008). Topological analysis of population activity in visual cortex. Journal of Vision, 8(8):11, 1–18, http://journalofvision.org/8/8/11/, doi:10.1167/8.8.11

From sparsely sampled data, we can attempt to estimate some of topological structure of the data.

Toplogical structure is here represented by Betti numbers. The paper explains this best:

Consider a world where objects are made of elastic rubber. Two objects are considered equivalent if they can be deformed into each other without tearing the material. If such a transformation between X and Y exists, we say they are topologically equivalent……it is evident that a possible reason for two objects not to be equivalent is that they differ in the number of holes. Thus, simply counting holes can provide a signature for the object at hand. Holes can exist in different dimensions. A one-dimensional hole is exposed when a one-dimensional loop (a closed curve) on the object cannot be deformed into a single point without tearing the loop. If two such loops can be deformed into one another they define the same hole, which should be counted only once. Analogous definitions can be invoked in higher dimensions. For example, a two-dimensional hole is revealed when a closed two-dimensional oriented surface on the object cannot be deformed into a single point.

This notion of counting holes of different dimensions is formalized by the definition of Betti numbers. The Betti numbers of an object X can be arranged in a sequence, b ( X )=( b 0 , b 1 , b 2 , I ), where b 0 represents the number of connected components, b 1 represents the number of one- dimensional holes, b 2 the number of two-dimensional holes, and so forth. An important property of Betti sequences is that if two objects are topologically equiv- alent (they can be deformed into each other) they share the same Betti sequence. One must note, as we will shortly illustrate, that the reverse is not always true: two objects can be different but have the same Betti sequence.

A technique is presented for estimating the Betti numbers of sampled data using “Rips complexes” and “barcodes”. To put this technique to use on neural data, the spiking of 5 cells (mostly “complex cells in the superficial layers”) with high spontaineous rate in V1 in Macaques were recorded from. The spikes were binned and a point cloud in 5D was constructed (so i think the coordinates of the point cloud representing the spike rate in each of the 5 dimensions).

This was done in two experimental conditions, when a stimulus was being presented, and when the eyes were occluded. In both cases, the topological structure varied between a circle and a sphere, although the circle structure was found with higher probability in the stimulus condition. The authors present a model of circular structure generated “if cortical activity is dominated by neuronal responses to stimulus orientation”, and a model of toroidal structure generated “A toroidal representation may arise from a neuronal population responding to two circular variables, such as orientation and color hue”. Note that a torus wasn’t actually observed in the data; a circle and a sphere was. In the conclusions the authors speculate what could have caused the sphere.

The authors conclude that the topology of spiking patterns for “both the data for spontaneous and driven conditions have similar topological structures, with the signatures of the circle and the sphere dominating the results”.

Neuroscience as a new national priority

President Obama: “Now, it’s time to get to work.”

NYT article: http://www.nytimes.com/2013/04/02/science/obama-to-unveil-initiative-to-map-the-human-brain.html

 

http://www.whitehouse.gov/sites/default/modules/wh_multimedia/EOP_OVP_player.swf

Hippocampus may still have a role in recalling old memories

Paraphrasing/adding to the article abstract: prevailing theory suggests that long-term memories are encoded via a two-phase process requiring temporary involvement of the hippocampus followed by permanent storage in the neocortex. However this group found that, even weeks later, after the memories are supposed to be independent of the hippocampus, they could disrupt recall by briefly suppressing hippocampal CA1. The suppression must be brief; if they suppress CA1 for a long time recall works again. This suggests that, long after memory formation, the memory is not primarily stored in the hippocampus, but the hippocampus is still somehow involved in recall. The research also implicates anterior cingulate cortex in recall. Abstract after the break.

Continue reading

Neurons with similar tuning more likely to be connected

From the abstract: … we determine synaptic connectivity between nearby layer 2/3 pyramidal neurons in vitro, the response properties of which were first characterized in mouse visual cortex in vivo. We found that connection probability was related to the similarity of visually driven neuronal activity. Neurons with the same preference for oriented stimuli connected at twice the rate of neurons with orthogonal orientation preferences. Neurons responding similarly to naturalistic stimuli formed connections at much higher rates than those with uncorrelated responses. Bidirectional synaptic connections were found more frequently between neuronal pairs with strongly correlated visual responses….

Ho Ko, Sonja B. Hofer, Bruno Pichler, Katherine A. Buchanan, P. Jesper Sjöström, Thomas D. Mrsic-Flogel. Functional specificity of local synaptic connections in neocortical networks. Nature. 2011 May 5;473(7345):87-91. Epub 2011 Apr 10.

Dopamine error

(pun intended). I am embarrassed to say that earlier today I remarked to a colleague that dopamine only encodes unexpected reward, not unexpected lack of reward. This is (afaik) incorrect. It has a baseline level of firing that goes down when there is an unexpected lack of reward (see fig 1 in Wolfram Schultz, Peter Dayan, P. Read Montague. A Neural Substrate of Prediction and Reward)

However, because it can only go down so far, the negative signal is clipped, which might have consequences (see Yael Niv, Michael O Duff, Peter Dayan. Dopamine, uncertainty and TD learning).

The previous article mentions that some other people think that maybe dopamine is tracking uncertainty as well as reward. This one talks about a theory that acetylcholine is related to expected uncertainty, and norepinephrine is related to unexpected uncertainty:
Angela Yu, Peter Dayan. Expected and Unexpected Uncertainty: ACh and NE in the Neocortex (huh, all those papers had Peter Dayan as one of the authors) (btw I haven’t read all of the papers I’m posting here)

Since we’re on the subject of temporal difference learning, I’ll mention that in my opinion temporal difference learning may be a model of how futures/speculators in financial markets are supposed to propagate future price changes back in time to the present (if you think of the market as a cognitive system). I haven’t formalized this idea yet, though.

Local sleep in awake rats

this experiment claims to show that

(1) when rats are sleep-deprived, small populations of rat brain neurons can fall asleep while the rest of the rat is awake, and
(2) this may correspond to performance degradation

summary:
http://arstechnica.com/science/news/2011/04/if-you-only-feel-half-awake-you-probably-are.ars

article:

http://www.nature.com/nature/journal/v472/n7344/full/nature10009.html

i haven’t read the actual article yet…