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- W2019954351 abstract "The μ-opioid receptor (MOR) is the primary target for opioid analgesics. MOR induces analgesia through the inhibition of second messenger pathways and the modulation of ion channels activity. Nevertheless, cellular excitation has also been demonstrated, and proposed to mediate reduction of therapeutic efficacy and opioid-induced hyperalgesia upon prolonged exposure to opioids. In this mini-perspective, we review the recently identified, functional MOR isoform subclass, which consists of six transmembrane helices (6TM) and may play an important role in MOR signaling. There is evidence that 6TM MOR signals through very different cellular pathways and may mediate excitatory cellular effects rather than the classic inhibitory effects produced by the stimulation of the major (7TM) isoform. Therefore, the development of 6TM and 7TM MOR selective compounds represents a new and exciting opportunity to better understand the mechanisms of action and the pharmacodynamic properties of a new class of opioids." @default.
- W2019954351 created "2016-06-24" @default.
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- W2019954351 date "2015-10-01" @default.
- W2019954351 modified "2023-10-01" @default.
- W2019954351 title "μ-Opioid receptor 6-transmembrane isoform: A potential therapeutic target for new effective opioids" @default.
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- W2019954351 doi "https://doi.org/10.1016/j.pnpbp.2014.11.009" @default.
- W2019954351 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4646084" @default.
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