Scinovex
reviewTop 10% cited

Molecular Mechanisms of Opioid Receptor-dependent Signaling and Behavior

Anesthesiology · 2011 · Vol. 115(6) · pp. 1363–1381
Ream Al‐HasaniMichael R. Bruchas

Abstract

Opioid receptors have been targeted for the treatment of pain and related disorders for thousands of years and remain the most widely used analgesics in the clinic. Mu (μ), kappa (κ), and delta (δ) opioid receptors represent the originally classified receptor subtypes, with opioid receptor like-1 (ORL1) being the least characterized. All four receptors are G-protein coupled and activate inhibitory G proteins. These receptors form homo- and heterodimeric complexes and signal to kinase cascades and scaffold a variety of proteins.The authors discuss classic mechanisms and developments in understanding opioid tolerance and opioid receptor signaling and highlight advances in opioid molecular pharmacology, behavioral pharmacology, and human genetics. The authors put into context how opioid receptor signaling leads to the modulation of behavior with the potential for therapeutic intervention. Finally, the authors conclude there is a continued need for more translational work on opioid receptors in vivo.

Neuropeptides and Animal PhysiologyReceptor Mechanisms and SignalingPharmacological Receptor Mechanisms and EffectsReceptorOpioidMedicineOpioid receptorκ-opioid receptorSignal transductionPharmacologyContext (archaeology)Neuroscienceδ-opioid receptor

MeSH terms

Analgesics, OpioidAnimalsDrug ToleranceHumansPainReceptors, OpioidSignal TransductionMice
Citations
1,022
FWCI
7.14
field-weighted impact
References
191
Percentile
98%
vs. same field & year
Citations per year
References
Differential regulation and properties of MAPKs
Oncogene · 2007 · 1,408 citations
The stress-activated protein kinase pathways
Cellular and Molecular Life Sciences · 1999 · 648 citations
Glial activation: a driving force for pathological pain
Trends in Neurosciences · 2001 · 1,083 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.