Current therapies are largely inadequate to treat cold allodynia symptoms which arise from disorders such as nerve injury, inflammation, migraine headaches or chemotherapy-induced peripheral neuropathy. There is a large market for treating cold pain which results from the aforementioned disorders, and the opportunity to provide relief for millions of patients who suffer from neuropathic cold pain.
USC researchers have discovered therapeutic targets that control the effects of cold allodynia. It has been shown that cold allodynia is blocked in animals treated with neutralizing antibodies against the GFR-α3 ligand, Artemin. Heat and mechanical pain were unchanged, indicating that cold allodynia is mediated exclusively by a single molecular pathway. Artemin–GFRα3 signaling therefore can be targeted to selectively treat neuropathic cold pain.
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chemotherapy-induced peripheral neuropathy
discovered therapeutic targets
single molecular pathway
treating cold pain
neuropathic cold pain
