Using Large Language Models to Map Grammar in the Brain

Post by Anastasia Sares

The takeaway

This study shows that grammatical features are encoded by individual neurons in the brain, distinct from other characteristics of the speech signal. Grammar-sensitive neurons are distributed throughout the left hemisphere in a way that is hard to detect when averaging regional activity.

What's the science?

Since the time of Broca, scientists have developed more and more detailed maps of the language-processing areas of the human brain. They have used a variety of brain imaging techniques, including functional magnetic resonance imaging (fMRI), electroencephalography (EEG), and others. All of these techniques have been helpful, but still lack the precise detail of single-neuron recording that is done routinely in animals. The only time that electrodes are implanted in human brains is when they are already undergoing an operation, such as for epilepsy. During those times when the brain is exposed, researchers can gather precious single-neuron data.

One challenge about studying human language processing is the complexity of language itself. In everyday conversation, we are free to put together words in a myriad of forms and sentence structures. Most of the time, studies of language involve presenting pre-designed words, phrases, or sentences that have a feature we are interested in (for example, sentences with different relationships between the subject and the object). However, this eliminates the natural spontaneity of language production, and so we can’t be sure if the brain activity we observe is reflecting what our brains do daily.

Fortunately, the technology behind large language models (some of which are now commonly referred to as “AI,” though not all of them are on the same scale) has given us the ability to represent natural language production in a way that computers can digest, and we can identify interesting features without having to design awkward stimuli. This week in Nature, Cai and colleagues combined natural language processing and recordings from electrodes implanted in the brains of epilepsy patients to map human language production, including grammatical features.

How did they do it?

The authors had access to eight people who were undergoing surgery for epilepsy. At the time of their operations, the patients consented to have an array of electrodes temporarily implanted in their brains so that the researchers could gather data about the firing of individual neurons. Depending on the patient, these electrode arrays were located in different spots in the brain, so the researchers had a variety of brain regions represented.

After implantation, the researchers recorded brain activity through the electrodes while asking the participant questions and allowing them to respond freely. They recorded these conversations and applied natural language processing algorithms to classify each sample of speech. In addition to representing the individual words, this approach extracts both grammatical relationships and the hierarchical structure of phrases (see image below). By labeling these features, the authors could then look at which parts of the brain were selectively responding to parts of speech, hierarchical features, or specific conversation contexts.

What did they find?

About 9% of neurons responded specifically to a word’s part of speech (noun, adjective, verb, etc). About 16% of neurons responded to constituency depth (how deep the word was in the nested hierarchy of the sentence), and so on. These neurons had very little overlap with each other, or with neurons that tracked other features of the speech (like the meaning of the word itself, or whether the pitch of the spoken word was high or low). Interestingly, these neurons that responded to different grammatical features were scattered throughout various brain regions, which may explain why it has been hard to pinpoint grammatical processing in the brain by summing up large amounts of activity. In addition, these grammar-selective neurons appeared in both hemispheres of the brain, but the most strongly predictive ones were in the left hemisphere, which lines up with decades of research confirming that language is processed on the left side of the brain (for most people).

What's the impact?

The results of this study inform debates about how the brain processes language. First, it supports the idea that certain high-level features of language can be coded by single neurons, rather than being only a result of multiple neurons firing in a pattern. These results also suggest that the popular but simplistic “modular” approach, where “region X is responsible for function Y,” doesn’t really work here: grammar-sensitive neurons are scattered throughout the left hemisphere.

Access the original scientific publication here. 

How Word Processing and Facial Recognition Adapt After Stroke

Post by Amanda Engstrom

The takeaway

Within the brain, facial recognition is lateralized to the right, and word processing is lateralized to the left. In individuals who suffer an early stroke in the left hemisphere, both word processing and facial recognition occur on the right without any impairment to facial recognition ability.

What's the science?

In the neurotypical human brain, the fusiform face area (FFA), a region within the ventro-occipital temporal cortex (vOTC), responds preferentially to faces. Face processing is right-lateralized, meaning the right hemisphere of the FFA is more active and dominant than the left. Conversely, language and visual word form processing are left-lateralized in a region called the visual word form area (VWFA) within the left VOTC. It has been hypothesized that these two lateralization patterns are linked: as children learn to read, the VWFA establishes itself in the left vOTC, either displacing or blocking the expansion of facial processing there, causing face processing to rely more heavily on the right vOTC. While correlations between literacy and face lateralization support this idea, evidence of direct competition between word and face processing remains mixed. This week in the Journal of Neuroscience, Seydell-Greenwald and colleagues used functional MRI (fMRI) to test whether face processing is altered in individuals who suffered a left-hemisphere perinatal stroke (LHPS) and consequently developed right-lateralized language and word processing. 

How did they do it?

The authors performed fMRI on 15 individuals with LHPS (mean age 19 years) who had previously established right-hemisphere language dominance and right-lateralized VWFA and compared them to 14 neurotypical individuals (mean age 16 years) with typical left-hemisphere language dominance. Both groups were fluent readers with comparable language comprehension scores. Participants completed a visual localizer task in which they viewed rapid sequences of images from three categories: faces, places, and word forms, allowing the authors to map and compare the lateralization of face and word form processing across groups. Participants then completed the Cambridge Face Memory Test, a standardized assessment of unfamiliar face recognition, requiring them to learn six faces and then identify them across different viewing angles and conditions. Together, these two tasks allowed the authors to assess both the neural lateralization of face processing and its behavioral consequences in individuals with LHPS relative to unaffected control participants. 

What did they find?

Control participants showed the typical pattern of left-lateralization for word forms and right-lateralization for faces, while the LHPS group was right-lateralized for both. This indicates that when word processing reorganizes to the right hemisphere after an early stroke, face processing does not compensate by shifting to the left. Instead, both functions are supported by the same hemisphere. There were no significant differences in the strength, spatial extent, or peak activation of face responses between the two groups, and both groups showed a positive correlation between face lateralization and word form lateralization, meaning stronger right-lateralization for words was associated with stronger right-lateralization for faces. Lastly, LHPS participants performed slightly but not significantly worse than controls on the Cambridge Face Memory Test, and both groups scored within normal range. Together, these findings suggest that sharing the right vOTC with word form processing does not meaningfully compromise the neural representation of faces or the ability to recognize them. 

What's the impact?

This study was the first to show that although the neurotypical brain delineates facial processing and visual word processing to either the right or left hemisphere, respectively, patients who have experienced early stroke to the left hemisphere can process both faces and written words together in the right hemisphere without any meaningful cost to either. This challenges the long-standing idea that the typical opposite-hemisphere arrangement of face and word processing is driven by competition. These findings provide insight into the key drivers of lateralizing specific neuronal pathways and demonstrate the remarkable capacity of the developing brain to reorganize after injury. 

Access the original scientific publication here.

Can Brain Stimulation Help Jump-Start Awareness?

Post by Annika Matthiesen

The takeaway

Stimulating specific brain regions may help “jump-start” brain activity in patients who have limited awareness and disrupted brain communication. While the effects were modest, the study suggests this noninvasive approach could help support recovery of awareness and responsiveness.

What’s the science?

People with severe disorders of consciousness have limited awareness and responsiveness because communication between different parts of the brain can be disrupted. Currently, there are very few effective treatments to improve wakefulness or recovery in these patients. This week in NeuroImage, Sangare and colleagues aim to improve brain activity and awareness in patients with limited wakefulness through brain stimulation.

How did they do it?

The authors studied 18 patients with disorders of consciousness. The authors used brain stimulation on the frontal cortex, an area at the front of the brain involved in higher-level thinking and control. Before and during treatment, the researchers measured how patients responded to sounds, sights, movement, and attempts to communicate. They also used EEG to record the brain’s electrical activity through sensors placed on the scalp, to track changes in brain function. Patients received stimulation or no stimulation (control), and the authors compared their responses before and after treatment. Six months later, the researchers followed up again to see whether any changes lasted over time.

What did they find?

The researchers found some signs that the brain stimulation may have helped improve patients’ responsiveness and awareness, as the treatment group showed slightly greater behavioral improvement than the control group after stimulation. However, they did not observe changes in the overall level of consciousness. EEG results showed more active and complex brain activity in certain regions after treatment, which may suggest stronger communication between different parts of the brain. Overall, stimulation increased electrical activity across seven areas throughout the brain, although these changes did not consistently lead to major improvements in consciousness or behavior. Together, the findings suggest the stimulation may influence brain function, but larger studies are needed to determine whether it can produce meaningful recovery for patients with severe disorders of consciousness.

What’s the impact?

This study found that brain stimulation may help improve brain activity and responsiveness in patients with limited wakefulness by strengthening communication across different parts of the brain. If future studies confirm these findings, noninvasive brain stimulation could offer a safe way to improve awareness and brain communication in people with a wide array of serious neurological conditions.

Access the original scientific publication here.