Hallucinations Induced in Lab Could Be Key to Better Understanding and Treatment

Summary: Inducing hallucinations using visual stimuli in a lab setting enables more objective and reliable testing.

Source: University of New South Wales

Cognitive neuroscientists from UNSW Sydney say if we really want to understand and treat the pathological hallucinations that affect people with physical and mental illnesses, the best place to start is in the laboratory.

Inducing hallucinations in the general population using visual stimulation procedures works similarly to illusions, and enables more objective and repeatable testing. It’s also much less distressing to the test subject than studying pathological hallucinations experienced by people with conditions like Parkinson’s disease or schizophrenia.

“By nature, [lab-induced hallucinations] can be induced in almost anyone at any time,” the neuroscientists write in an opinion piece published recently in Philosophical Transactions B journal.

“This can help to curb the current overreliance on studying pathological hallucinations, thereby reducing burdens placed on patients and simplifying recruitment and testing logistics.”

Seeing something that isn’t there

Most people naturally think of visual hallucinations as being realistic images or scenes, such as seeing humans or spiders (what we call ‘complex’ hallucinations). However, a hallucination in its broadest sense can be defined as the experience of seeing something that is not there. As such, visual hallucinations can also include seeing basic geometric shapes or colours (referred to as ‘simple’ hallucinations), and scientists can trigger both simple and complex hallucinations in the laboratory.

Professor Joel Pearson, the senior author of the opinion piece, says work the group did in 2016 showed that you could induce hallucinations in people reliably and safely using specific types of flickering lights.

“We showed that you could use flickering lights in an annulus – basically a flickering white ring like a doughnut on a black background – and you could induce hallucinations of little dark blobs which rotate around the ring,” he says.

“And you could use that to try and study the mechanisms behind visual hallucinations. But those flicker hallucinations are just the tip of the iceberg, and there are many other techniques for inducing hallucinations that are similar to pathological hallucinations in terms of the experience and underlying neural processes.”

Prof. Pearson says one of the trickier problems is working out which techniques can tell us something about pathological hallucinations.

“A lot of this work shows that it’s hard to separate hallucinations from illusions and veridical (reality-based) perception. Current hallucination definitions are too black and white, and aren’t up to the task of classifying many of these lab-induced experiences.”

Spectrum of experience

Professor Pearson and fellow authors Dr Sebastian Rogers and Dr Rebecca Keogh use a continuous spectrum of experience to distinguish hallucinations from other types of perception, based on the similarity between the physical stimulation of the senses (the light that enters the eye) and the actual conscious experience (the image we ‘see’ or experience).

This shows a distorted woman
Hallucinations have been difficult to study and can be distressing for the person experiencing them, but hallucinations induced in the lab are much more benign. Image is credited to UNSW

Veridical perception (involving a strong relationship between what is ‘in reality’ and what one sees) is at one end of this spectrum and hallucinations (a weak relationship between what is present in reality and with what one sees) is at the other, with illusions falling somewhere in between.

According to lead author Dr Rogers, “the thesis of the idea is that the further a lab-induced experience is toward the hallucination end of the spectrum, the more it can tell us about other types of hallucination”.

“If you really don’t want to call one of these lab-induced experiences a hallucination, that’s fine by us. We don’t really mind what the name is, we care most about whether we can study it to learn about pathological and other hallucinations. It’s a way to investigate hallucinatory processes any time we want in the lab, with anyone.”

Dr Keogh says, “once we understand the underlying mechanisms, that is, what in the brain leads to seeing things that aren’t there, then we’ll be able to develop treatments. There are very few treatments for hallucinations at the moment, and most are medications that can lead to unwanted side effects.

“Using lab hallucination models can allow us to develop new avenues for more targeted treatments, such as electrical or magnetic brain stimulation.”

About this psychology research news

Source: University of New South Wales
Contact: Press Office – University of New South Wales
Image: The image credited to University of New South Wales

Original Research: Closed access.
Hallucinations on demand: the utility of experimentally induced phenomena in hallucination research” by Sebastian Rogers, Rebecca Keogh and Joel Pearson.  Philosophical Transactions B


Abstract

Hallucinations on demand: the utility of experimentally induced phenomena in hallucination research

Despite the desire to delve deeper into hallucinations of all types, methodological obstacles have frustrated development of more rigorous quantitative experimental techniques, thereby hampering research progress. Here, we discuss these obstacles and, with reference to visual phenomena, argue that experimentally induced phenomena (e.g. hallucinations induced by flickering light and classical conditioning) can bring hallucinations within reach of more objective behavioural and neural measurement. Expanding the scope of hallucination research raises questions about which phenomena qualify as hallucinations, and how to identify phenomena suitable for use as laboratory models of hallucination. Due to the ambiguity inherent in current hallucination definitions, we suggest that the utility of phenomena for use as laboratory hallucination models should be represented on a continuous spectrum, where suitability varies with the degree to which external sensory information constrains conscious experience. We suggest that existing strategies that group pathological hallucinations into meaningful subtypes based on hallucination characteristics (including phenomenology, disorder and neural activity) can guide extrapolation from hallucination models to other hallucinatory phenomena. Using a spectrum of phenomena to guide scientific hallucination research should help unite the historically separate fields of psychophysics, cognitive neuroscience and clinical research to better understand and treat hallucinations, and inform models of consciousness.

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