Literature DB >> 22664908

G protein-coupled receptors as therapeutic targets for multiple sclerosis.

Changsheng Du1, Xin Xie.   

Abstract

G protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants. They are considered as the most successful therapeutic targets for a broad spectrum of diseases. Multiple sclerosis (MS) is an inflammatory disease that is characterized by immune-mediated demyelination and degeneration of the central nervous system (CNS). It is the leading cause of non-traumatic disability in young adults. Great progress has been made over the past few decades in understanding the pathogenesis of MS. Numerous data from animal and clinical studies indicate that many GPCRs are critically involved in various aspects of MS pathogenesis, including antigen presentation, cytokine production, T-cell differentiation, T-cell proliferation, T-cell invasion, etc. In this review, we summarize the recent findings regarding the expression or functional changes of GPCRs in MS patients or animal models, and the influences of GPCRs on disease severity upon genetic or pharmacological manipulations. Hopefully some of these findings will lead to the development of novel therapies for MS in the near future.

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Year:  2012        PMID: 22664908      PMCID: PMC3750109          DOI: 10.1038/cr.2012.87

Source DB:  PubMed          Journal:  Cell Res        ISSN: 1001-0602            Impact factor:   25.617


  288 in total

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2.  Norepinephrine inhibits gamma-interferon-induced major histocompatibility class II (Ia) antigen expression on cultured astrocytes via beta-2-adrenergic signal transduction mechanisms.

Authors:  E M Frohman; B Vayuvegula; S Gupta; S van den Noort
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

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Review 4.  Neurological S1P signaling as an emerging mechanism of action of oral FTY720 (fingolimod) in multiple sclerosis.

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10.  Cannabinoids control spasticity and tremor in a multiple sclerosis model.

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  19 in total

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5.  Deficiency of the G protein Gαq ameliorates experimental autoimmune encephalomyelitis with impaired DC-derived IL-6 production and Th17 differentiation.

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6.  Single-cell profiling reveals GPCR heterogeneity and functional patterning during neuroinflammation.

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Review 9.  Trends in GPCR drug discovery: new agents, targets and indications.

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10.  Aurintricarboxylic acid ameliorates experimental autoimmune encephalomyelitis by blocking chemokine-mediated pathogenic cell migration and infiltration.

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