Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 104, Issue 51, Pages 20588-20593Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.0706980105
Keywords
G-protein-coupled receptors; rimonabant; inflammatory pain; drugs of abuse
Categories
Funding
- NIDA NIH HHS [K05 DA019521, DA019521] Funding Source: Medline
Ask authors/readers for more resources
To date, the endogenous ligands described for cannabinoid receptors have been derived from membrane lipids. To identify a peptide ligand for CB1 cannabinoid receptors, we used the recently described conformation-state sensitive antibodies and screened a panel of endogenous pepticles from rodent brain or adipose tissue. This led to the identification of hemopressin (PVNFKFLSH) as a pepticle ligand that selectively binds CB, cannabinoid receptors. We find that hemopressin is a CB, receptor-selective antagonist, because it is able to efficiently block signaling by CB, receptors but not by other members of family A G protein-coupled receptors (including the closely related CB2 receptors). Hemopressin also behaves as an inverse agonist of CB, receptors, because it is able to block the constitutive activity of these receptors to the same extent as its well characterized antagonist, rimonabant. Finally, we examine the activity of hemopressin in vivo using different models of pain and find that it exhibits antinociceptive effects when administered by either intrathecal, intraplantar, or oral routes, underscoring hemopressin's therapeutic potential. These results represent a demonstration of a pepticle ligand for CB, cannabinoid receptors that also exhibits analgesic properties. These findings are likely to have a profound impact on the development of novel therapeutics targeting CB, receptors.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available