ArticlePDF Available

Book Review: The Oxford Handbook of the Neurobiology of Pain by J. N. Wood

Authors:
Book Review
Wood, J. N. (Ed.). (2020). The Oxford Handbook of the Neurobiology of Pain. Oxford,
England: Oxford University Press. 864 pp.: ISBN 9780190860509, £160 Hardback.
Reviewed by: M. Catherine Bushnell ,Harold Grifth Professor Emerita, McGill
University, Montreal, Quebec, Canada; Scientist Emerita, National Institutes of Health,
Bethesda, MD, USA
Until recently, pain was viewed as an unpleasant symptom of disease or injury that needed to be
either alleviated or tolerated, but that did not inict harm in and of itself. We now know that
pain is much more than a symptom and, when chronic, can be viewed as a disease itself. The
opioid crisis, along with an aging population and the novel threat of pain related to long
COVID, has drawn new light to the consequences of pain and led to the search for a better under-
standing of pain mechanisms and possible non-opioid treatments.
The Oxford Handbook of the Neurobiology of Pain is a timely offering, providing a comprehen-
sive compendium of scholarly articles about pain, ranging from the history of pain research,
through non-human models, to detailed chapters about mechanisms at peripheral and central
nervous system levels, and nally pain conditions and treatment modalities. Individual chapters
are dedicated to some common chronic pain syndromes, such as headache, visceral pain, neuro-
pathic pain and cancer pain. Other chapters delve into molecular mechanisms, pain genetics, neu-
roimmune interactions and pain, and developmental aspects of pain.
The handbook is not organized into sections, and there is little coordination between chapters,
leading to a fair amount of redundancy, particularly in terms of primary afferent and spinal cord
mechanisms. This is not necessarily bad, since it allows readers to select individual chapters to
read, without committing to a thorough perusal of the more than 800 pages of text. Each chapter
has enough autonomy to be a stand-alone analysis of the topic and serve as a fundamental resource
for scientists and trainees working in the eld.
A stellar array of more than 50 experts in the eld have contributed to the handbook, each pre-
senting state-of-the art analyses of their topic. It is not possible to address each chapter individually,
but some highlights include an engrossing historical overview of purported pain mechanisms and
analgesic treatments throughout the ages (Chapter 1) and a thought-provoking analysis of the trans-
lation from rodent models to humans that clearly shows the problems but presents an optimistic
view of the future (Chapter 2).
A number of chapters offer an excellent reference for the serious pain scientist, with detailed
analyses of most aspects of nociception. Chapters are dedicated to the dorsal root ganglia (5),
heat and cold pain (7), noxious mechanoreception (8), signaling channels in the periphery and
dorsal horn (9-12, 21, 26, 27), and dorsal horn mechanisms (16).
Perception
12
© The Author(s) 2021
Article reuse guidelines:
sagepub.com/journals-permissions
DOI: 10.1177/03010066211053569
journals.sagepub.com/home/pec
The chapters on basic pain mechanisms may be too detailed for clinicians or neuroscientists not
specializing in pain, but other chapters could be extremely useful to the research-minded clinician
by providing a link between pre-clinical data and clinical syndromes. Such chapters include a dis-
cussion of sympathetic nervous system and pain (6); neuroimmune interactions and pain (13),
developmental and sex-related aspects of pain (14), mechanisms of migraine pain (19), relationship
between sleep and pain (20), the diversity of neuropathic pain conditions (22), the transition from
acute to chronic (23), cancer pain (24) and opioid mechanisms (25).
Although the handbook is quite comprehensive, there are some important gaps in the topics. In
terms of pre-clinical models, it was nice to see the inclusion of a chapter on invertebrate models of
nociception, but a discussion of human and non-human primate studies of nociception is conspicu-
ously absent. Additionally, although several chapters discuss descending pain modulation systems
and their role in pharmacological pain modulation, there is little discussion of non-pharmacological
pain treatments and their mechanisms. Given the problems with opioids and the uneven effective-
ness of other pharmacological treatments for chronic pain, a deep dive into non-pharmacological
pain treatments would have been welcome.
In conclusion, The Oxford Handbook of the Neurobiology of Pain is an outstanding collection of
chapters addressing a wide range of topics in the eld. With a few gaps, it is inclusive of both basic
and clinical aspects of pain. The volume should appeal most to the dedicated pain scientist, but it
could also be a useful tool for clinicians and students. At a price-tag of more than $200 US, and with
free reviews of many topics available within scientic journals, the appeal of this book to trainees
may, unfortunately, be diminished. Nevertheless, it is a denitive volume that brings together the
important issues in the eld of pain, discussed by the most preeminent experts.
ORCID iD
M. Catherine Bushnell https://orcid.org/0000-0001-5207-9767
2Perception 0(0)
Article
The pancreas is a heterocrine gland that has both exocrine and endocrine parts. Most pancreatic cancer begins in the cells that line the ducts of the pancreas and is called pancreatic ductal adenocarcinoma (PDAC). PDAC is the most encountered pancreatic cancer type. One of the most important characteristic features of PDAC is neuropathy which is primarily due to perineural invasion (PNI). PNI develops tumor microenvironment which includes overexpression of fibroblasts cells, macrophages, as well as angiogenesis which can be responsible for neuropathy pain. In tumor microenvironment inactive fibroblasts are converted into an active form that is cancer‐associated fibroblasts (CAFs). Neurotrophins they also increase the level of Substance P, calcitonin gene‐related peptide which is also involved in pain. Matrix metalloproteases are the zinc‐associated proteases enzymes which activates proinflammatory interleukin‐1β into its activated form and are responsible for release and activation of Substance P which is responsible for neuropathic pain by transmitting pain signal via dorsal root ganglion. All the molecules and their role in being responsible for neuropathic pain are described below.
ResearchGate has not been able to resolve any references for this publication.