Use of DREADD Technology to Identify Novel Targets for Antidiabetic Drugs

G protein-coupled receptors (GPCRs) form a superfamily of plasma membrane receptors that couple to four major families of heterotrimeric G proteins, G s , G i , G q , and G 12 . GPCRs represent excellent targets for drug therapy. Since the individual GPCRs are expressed by many different cell types,...

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Veröffentlicht in:Annual review of pharmacology and toxicology 2021-01, Vol.61 (1), p.421-440
Hauptverfasser: Wang, Lei, Zhu, Lu, Meister, Jaroslawna, Bone, Derek B.J, Pydi, Sai P, Rossi, Mario, Wess, Jürgen
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Sprache:eng
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Zusammenfassung:G protein-coupled receptors (GPCRs) form a superfamily of plasma membrane receptors that couple to four major families of heterotrimeric G proteins, G s , G i , G q , and G 12 . GPCRs represent excellent targets for drug therapy. Since the individual GPCRs are expressed by many different cell types, the in vivo metabolic roles of a specific GPCR expressed by a distinct cell type are not well understood. The development of designer GPCRs known as DREADDs (designer receptors exclusively activated by a designer drug) that selectively couple to distinct classes of heterotrimeric G proteins has greatly facilitated studies in this area. This review focuses on the use of DREADD technology to explore the physiological and pathophysiological roles of distinct GPCR G protein cascades in several metabolically important cell types. The novel insights gained from these studies should stimulate the development of GPCR-based treatments for major metabolic diseases such as type 2 diabetes and obesity.
ISSN:0362-1642
1545-4304
DOI:10.1146/annurev-pharmtox-030220-121042