Trends in Neurosciences
Volume 32, Issue 2, February 2009, Pages 118-126
Journal home page for Trends in Neurosciences

Review
Historical perspective
A brief history of human brain mapping

https://doi.org/10.1016/j.tins.2008.11.001Get rights and content

Human functional brain mapping as we presently know it began when the experimental strategies of cognitive psychology were combined with modern brain-imaging techniques (first positron emission tomography and then functional magnetic resonance imaging) to examine how brain function supports mental activities. This marriage of disciplines and techniques galvanized the field of cognitive neuroscience, which has rapidly expanded to include a broad range of the social sciences in addition to basic scientists interested in the neurophysiology, cell biology and genetics of the imaging signals. Although much of this work has transpired over the past couple of decades, its roots can be traced back more than a century.

Introduction

Over the past 30 years the field of cognitive neuroscience has emerged as an important growth area in neuroscience. Cognitive neuroscience combines the experimental strategies of cognitive psychology with various techniques to actually examine how brain function supports mental activities. Leading this research in normal humans are the techniques of functional brain imaging: positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) along with electroencephalography (EEG), electrocorticography (ECoG), magnetoencephalography (MEG) and, most recently, optical imaging with near-infrared spectroscopy (NIRS).

It is easy to conclude that much of the work leading to the emergence of functional brain imaging in particular and cognitive neuroscience in general has transpired over the past decade or so because of much recent prominence at scientific meetings and in the scientific literature. Additionally, it has received substantial media attention probably related to the human fascination with brain-mind questions. In truth, crucial work has been occurring for more than a century.

To place current work in perspective, I present a brief historical overview (Figure 1) of some of the concepts, events and personalities that have shaped functional brain imaging as we know it today. I call upon not only published accounts of many events and discoveries but also recollections shared with me by those who have lived through the remarkable events of the past several decades. Such views serve to not only breathe life into the science but also carry the caveat that they are necessarily colored by one's own involvement.

I focus on human brain imaging with PET and fMRI recognizing that other techniques, particularly electrical (e.g. EEG, MEG and ECoG), also have and will continue to have an important role. I begin with a discussion of the physiology of brain imaging with PET and fMRI.

Section snippets

Physiology

The signals obtained with PET and fMRI are based on changes in blood flow, oxygen consumption and glucose utilization that relate in a surprisingly precise way to the cellular activity of the brain, including astrocytes and neurons. The details of these relationships are presented, discussed and debated elsewhere 1, 2, 3, 4, 5, 6. Here, some basic facts necessary to understand the history of functional brain imaging are briefly presented.

X-ray computed tomography

In 1971 Godfrey Hounsfield introduced X-ray computed tomography (or CT as it is now called) at Atkinson Morley's Hospital in London. In creating CT, Hounsfield had arrived at a practical solution to the problem of creating three-dimensional transaxial tomographic images of an intact object from data obtained by passing highly focused X-ray beams through the object and recording their attenuation. Hounsfield's invention received enormous attention and quite literally changed the way in which we

Metabolism versus blood flow

Work on the neural correlates of human behaviors with PET began with studies of brain glucose metabolism and the tracer 18F-2-fluoro-2-deoxy-d-glucose (FDG). This was an extension of the autoradiographic deoxyglucose technique (Box 3) developed by Sokoloff and his colleagues (National Institutes of Health) for studies in laboratory animals [32]. Sokoloff had demonstrated the sensitivity of this technique to functional changes in neuronal activity in a wide-ranging group of animal experiments

Stereotaxy

As PET images of task-induced changes in regional blood flow started to accumulate, an old problem resurfaced. How do you objectively relate functional imaging data to brain anatomy? This problem was neither new to functional brain imaging with PET nor previously unexplored.

The solution came in the form of a technique called ‘stereotaxy’, which was first developed by Horsley and Clarke for animal research in 1908 and much later applied by to humans by neurosurgeons (for additional details see

The present

It is easy to be optimistic about the human brain-mapping agenda. Its growth, particularly since the advent of fMRI BOLD imaging, has been dramatic. However, challenges do arise because of the immense diversity of this agenda.

Neuroscientists interested in brain function from a cellular and molecular perspective now are obliged to understand not only the concepts and strategies of cognitive psychology but also a wide array of behavioral disciplines covered under the rubric of social neuroscience

The future

As we look to the future, changes clearly appear on the horizon. It might be too strong to suggest that we are facing a paradigm shift [67], but certainly some reorientation is taking place in terms of how we understand brain function. Although this reorientation has received substantial stimulation from imaging work with PET and fMRI, it has its roots in more than a century of discussions on the nature of brain functions.

Since the 19th century, and possibly longer, two perspectives on brain

Acknowledgements

My work has been generously supported by the National Institutes of Health (National Institute of Neurological Disorders and Stroke, www.ninds.nih.gov; National Heart, Lung, and Blood Institute, www.nhlbi.nih.gov; and National Institute of Mental Health, www.nimh.nih.gov) for nearly 40 years. In addition, I have received support from the Charles A. Dana Foundation (www.dana.org), the James S. McDonnell Foundation (www.jsmf.org), the John D. and Catherine T. MacArthur Foundation (www.macfound.org

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