Review Article

Heterotrimeric G-proteins and their role in opioid receptor function

Gabriella Fábián*

Department of Zoology and Cell Biology, University of Szeged, Szeged, Hungary

Heterotrimeric G-proteins are signal transducers of heptahelical receptors. They consist of a and bg subunits, both capable of interacting with several different effectors. Specific domains in their structures enable them to connect different intracellular signaling cascades, such as the adenylyl cyclase, phosphoinositol-bisphosphate or MAP kinase pathways. Their activity is synchronized by several components, one of them being a new protein family termed RGS (regulators of G-protein signaling). Members of this family inhibit the G-protein function. The intracellular localization of G-proteins indicates their role in plasma membrane-independent processes. Opioid receptors transmit their signals mainly via Gi/o proteins. Although the heterogeneity of opioid ligands (peptides and alkaloids) and their receptors (m, d, k and suggested subtypes in these classes) reveals a complicated picture, their unique characteristic of a high dependence capacity can not be explained without the analysis of the G-protein function. Acta Biol Szeged 45(1-4):13-21 (2001) PDF

Key Words: signal transduction, G-proteins, opioid receptor, tolerance

*Corresponding author. E-mail: fabiang@bio.u-szeged.hu