Since the discovery of opioid receptors over two decades ago, an increasing body of work has emerged supporting the concept of multiple opioid receptors. Molecular cloning has identified three opioid receptor types - μ, δ, and κ - confirming pharmacological studies that previously postulated the existence of these three receptors. The cloned opioid receptors are highly homologous and belong to the family of seven-transmembrane, G protein-coupled receptors. With the development of novel opioid ligands, subtypes of the μ, δ, and κ receptors have been proposed, although the molecular basis of these subtypes has not been elucidated. In this review, we present the pharmacological data supporting the concept of multiple δ opioid receptor subtypes and offer hypothetical mechanisms which might generate these 'subtypes'.
|Original language||English (US)|
|Number of pages||23|
|Journal||Annual Review of Pharmacology and Toxicology|
|State||Published - May 31 1996|
- G protein-coupled receptor
- receptor heterogeneity
ASJC Scopus subject areas