viernes, 2 de agosto de 2019

An Itch to Scratch: NCATS, NIDCR Scientists Identify Potential New Approach to Chronic Problem | National Center for Advancing Translational Sciences

An Itch to Scratch: NCATS, NIDCR Scientists Identify Potential New Approach to Chronic Problem | National Center for Advancing Translational Sciences

national institute of dental and craniofacial research

An Itch to Scratch: NCATS, NIDCR Scientists Identify Potential New Approach to Chronic Problem

Nerves involved in detecting an itch and sensing pain.
Nerves that stimulate skin are grouped in structures next to the spinal cord. Here, nerves in such a structure—called a dorsal root ganglion—that are involved in detecting an itch are labeled green. Nerves involved in sensing pain, temperature and other stimuli are shown in magenta.

Credit: Hans Juergen Solinski, National Institute of Dental and Craniofacial Research
Chronic itch goes beyond being just a simple annoyance; it can greatly affect a person’s quality of life. While scientists have some clues to its causes, effective therapies have been elusive.
Now, using a technique called quantitative high-throughput screening to sort through more than 86,000 compounds at the same time, researchers at NCATS and the National Institute of Dental and Craniofacial Research (NIDCR) report a new strategy that may eventually help alleviate chronic itch. They’ve shown that blocking a receptor, or docking station, found on the surface of both mouse and human spinal cord neurons could be key.
Several years ago, Mark Hoon, Ph.D., and his colleagues at NIDCR found a receptor, Npr1, on mouse spinal cord neurons for a protein associated with itch. The protein fit into Npr1 like a key into a lock, helping turn on the itch sensation. Npr1 appeared to be a potential target for drugs to halt itch.
Hoon contacted NCATS scientist James Inglese, Ph.D., and his team for help in identifying compounds that could block Npr1 activity. The researchers developed a series of assays, or tests, and used robots to screen compounds in human cells, finding approximately 1,400 molecules worth examining more closely. They then developed additional assays to narrow the list to 15 compounds. They showed a subset of these compounds could halt both human and mouse versions of the receptor from working. A follow-up study in mice showed that blocking the receptor reduced scratching.
Next, the scientists will examine more candidate compounds and determine how they block Npr1. They hope the findings will help them choose which compounds to study further and chemically modify as potential anti-itch drugs. Hoon, Inglese and their colleagues reported the results online July 10 in Science Translational Medicine(link is external).

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