We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Objectives
- Definitions
- Evolutionary roles and key differences between pain and itch
- Types of pain and itch
- Pain-relief vs. itch-suppression
- Peripheral differences
- Painful reflex
- Inflammation and pain mediators
- Peripheral pain receptors
- Identification of pain receptors: TRPV1 and Piezo2
- Pain-specific activation of pERK in spinal cord dorsal horn neurons
- Pruritus (itch) in humans
- Animals feel itch
- Mouse behaviors of pain (wiping) and itch (scratching)
- Inflammation and itch mediators
- Peripheral itch receptors
- Loss of chloroquine (CQ)-induced itch in Mrgpr-clusterΔ−/− mice
- Ablation of MrgprA3+ neurons attenuates all itch behaviors in mice
- Itch mediators and signaling
- GRP/GRP receptor (GRPR) mediates the itch sensation in the spinal cord
- Spinal cord GRPR+ neurons are essential for acute and chronic itch
- Loss of inhibitory interneurons enhances itch in Bhlhb5 mutant mice
- Pain and itch pathways
- Spinal cord mechanical itch by TLR5+/Ucn3+ pathway
- Coding theories of pain and itch
- Itch pathway in the brain
- Drug-induced pain and itch
- Imiquimod induces scratching via TLR7
- TLR7 expression in mouse DRG neurons
- Intrathecal morphine induces itch via inhibitory neurons (disinhibition)
- Morphine suppresses inhibitory synaptic transmission in the spinal inhibitory neurons
- Morphine induces analgesia via SST+ excitatory neurons in the spinal cord
- Cutaneous T-cell lymphoma (CTCL) with chronic itch
- A mouse model of CTCL exhibits tumor growth and chronic itch
- Lymphoma is highly innervated by nerve fibers in mouse CTCL model
- IL-31/IL-31R pathway contributes to pruritus in mouse CTCL model
- IL-31R/TRPV1 upregulation in pruricepive neurons of DRG in CTCL
- Intrathecal gabapentin reduces neuropathic itch in last phases
- miR-711, produced by lymphoma, induces itch, but not pain, via TRPA1
- Glial cells and neuro-glial interactions in chronic pain
- Glial cells (astrocytes) in chronic itch
- Conclusions
- The translational revolution of itch
- Acknowledgements
- Financial disclosures
Topics Covered
- Pain mediators and receptors
- Pruritus in humans and animals
- Itch mediators and receptors
- Pain and itch pathway
- Coding theories of pain and itch
- Drug induced pain and itch
- Cutaneous T-cell lymphoma (CTCL) with chronic itch
- Neuro-glial interactions in chronic pain
- Translational revolution of itch
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Ji, R. (2026, September 30). Itch vs. pain [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved October 1, 2026, from https://doi.org/10.69645/WHIZ5320.Export Citation (RIS)
Publication History
- Published on September 30, 2026
Financial Disclosures
- There are no commercial/financial matters to disclose.
A selection of talks on Physiology & Anatomy
Transcript
Please wait while the transcript is being prepared...
0:00
This is Ru-Rong Ji
from Duke University,
Center for Translational
Pain Medicine.
Today, I will be discussing
the topic of itch versus pain.
0:13
My talk has three
major objectives:
Understanding pain
and itch mechanisms,
exploring mediators, receptors,
and circuits of pain and itch,
finally, dissecting
clinical relevance and
treatments for chronic
pain and itch.
What is pain?
0:34
According to the definition of
International Association
for the Study of Pain (IASP)
pain is an unpleasant sensory
and emotional experience
associated with actual or
potential tissue damage.
It serves as a
protective mechanism
alerting the body
to injury or danger
and eliciting
behavioral responses
to minimize harm, such as
the withdrawal reflex.
What is itch? Like pain,
itch, or pruritus,
is an unpleasant
sensory experience
that triggers the
urge to scratch.
It is distinct from pain,
but shares overlapping
neural pathways.
Itch serves a
function by alerting
organisms to
irritants, allergens,
or parasites, eliciting
protective behaviors,
such as scratching or grooming.
In some cases,
scratching also causes
pleasure by activating the
reward system in the brain.
1:39
The evolutionary roles
of pain and itch.
Pain and itch have evolved
as adaptive survival mechanisms.
Pain serves for
avoidance, protection,
and prevention, as well
as healing promotion,
adaptive learning such
as no pain, no gain.
Itch serves for
irritant protection,
parasite defense,
and wound healing.