Targeting the Nociceptin/Orphanin FQ Receptor for Scleroderma Therapy
Abstract
Scleroderma is a debilitating disease of the connective tissue that affects about 75,000100,000 individuals in the United States and accounts for an estimated $400 million in total annual medical costs. There is no treatment that stops or cures scleroderma: novel therapies are therefore urgently needed. The overall objective of this proposal is to demonstrate that small molecule compounds that target receptor-ligand pair NOP receptorNociceptin/Orphanin FQ can limit the damage and malfunctions that occur in the immune system and in blood vessels during scleroderma. We anticipate that our approach will demonstrate that a single drug can limit inflammation, heal blood vessel damage, and increase blood flow.
Document Details
- Document Type
- Technical Report
- Publication Date
- Dec 01, 2015
- Accession Number
- AD1005084
Entities
People
- Brian Zabel
Organizations
- Palo Alto Veterans Institute for Research