Search Results - "Tillu, Dipti V"
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Extracellular phosphorylation of a receptor tyrosine kinase controls synaptic localization of NMDA receptors and regulates pathological pain
Published in PLoS biology (18-07-2017)“…Extracellular phosphorylation of proteins was suggested in the late 1800s when it was demonstrated that casein contains phosphate. More recently, extracellular…”
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IL-6- and NGF-induced rapid control of protein synthesis and nociceptive plasticity via convergent signaling to the eIF4F complex
Published in The Journal of neuroscience (10-11-2010)“…Despite the emergence of translational control pathways as mediators of nociceptive sensitization, effector molecules and mechanisms responsible for modulating…”
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Resveratrol Engages AMPK to Attenuate ERK and mTOR Signaling in Sensory Neurons and Inhibits Incision-Induced Acute and Chronic Pain
Published in Molecular pain (23-01-2012)“…Background: Despite advances in our understanding of basic mechanisms driving post-surgical pain, treating incision-induced pain remains a major clinical…”
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Targeting Adenosine Monophosphate-Activated Protein Kinase (AMPK) in Preclinical Models Reveals a Potential Mechanism for the Treatment of Neuropathic Pain
Published in Molecular pain (21-09-2011)“…Neuropathic pain is a debilitating clinical condition with few efficacious treatments, warranting development of novel therapeutics. We hypothesized that…”
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Spinal dopaminergic projections control the transition to pathological pain plasticity via a D1/D5-mediated mechanism
Published in The Journal of neuroscience (22-04-2015)“…The mechanisms that lead to the maintenance of chronic pain states are poorly understood, but their elucidation could lead to new insights into how pain…”
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Protease-activated receptor 2 activation is sufficient to induce the transition to a chronic pain state
Published in Pain (Amsterdam) (01-05-2015)“…Protease-activated receptor type 2 (PAR2) is known to play an important role in inflammatory, visceral, and cancer-evoked pain based on studies using PAR2…”
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Development and evaluation of small peptidomimetic ligands to protease-activated receptor-2 (PAR2) through the use of lipid tethering
Published in PloS one (13-06-2014)“…Protease-activated receptor-2 (PAR2) is a G-Protein Coupled Receptor (GPCR) activated by proteolytic cleavage to expose an attached, tethered ligand (SLIGRL)…”
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Temporal and sex differences in the role of BDNF/TrkB signaling in hyperalgesic priming in mice and rats
Published in Neurobiology of pain (01-01-2019)“…Highlights • The effect of TrkB-Fc on hyperalgesic priming is sexually dimorphic in mice. • The effect of TrkB-Fc on hyperalgesic priming is equivalent in male…”
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Pharmacological activation of AMPK inhibits incision-evoked mechanical hypersensitivity and the development of hyperalgesic priming in mice
Published in Neuroscience (17-09-2017)“…[Display omitted] •A novel resveratrol-based topical cream alleviates acute postoperative pain and hyperalgesic priming.•Combination treatments of resveratrol…”
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Spinal protein kinase M ζ underlies the maintenance mechanism of persistent nociceptive sensitization
Published in The Journal of neuroscience (04-05-2011)“…Sensitization of the pain pathway is believed to promote clinical pain disorders. We hypothesized that the persistence of a sensitized state in the spinal…”
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Local Translation and Retrograde Axonal Transport of CREB Regulates IL-6-Induced Nociceptive Plasticity
Published in Molecular pain (04-07-2014)“…Transcriptional regulation of genes by cyclic AMP response element binding protein (CREB) is essential for the maintenance of long-term memory. Moreover,…”
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The novel PAR2 ligand C391 blocks multiple PAR2 signalling pathways in vitro and in vivo
Published in British journal of pharmacology (01-09-2015)“…Background and Purpose Proteinase‐activated receptor‐2 (PAR2) is a GPCR linked to diverse pathologies, including acute and chronic pain. PAR2 is one of the…”
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BDNF Regulates Atypical PKC at Spinal Synapses to Initiate and Maintain a Centralized Chronic Pain State
Published in Molecular pain (20-03-2013)“…Background Chronic pain is an important medical problem affecting hundreds of millions of people worldwide. Mechanisms underlying the maintenance of chronic…”
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Lanthanide Labeling of a Potent Protease Activated Receptor‑2 Agonist for Time-Resolved Fluorescence Analysis
Published in Bioconjugate chemistry (17-10-2012)“…Protease activated receptor-2 (PAR2) is one of four G-protein coupled receptors (GPCRs) that can be activated by exogenous or endogenous proteases, which…”
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Development of highly potent protease‐activated receptor 2 agonists via synthetic lipid tethering
Published in The FASEB journal (01-04-2013)“…Protease‐activated receptor‐2 (PAR2) is a G‐protein coupled receptor (GPCR) associated with a variety of pathologies. However, the therapeutic potential of…”
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The Protease-activated Receptor-2-specific Agonists 2-Aminothiazol-4-yl-LIGRL-NH2 and 6-Aminonicotinyl-LIGRL-NH2 Stimulate Multiple Signaling Pathways to Induce Physiological Responses in Vitro and in Vivo
Published in The Journal of biological chemistry (27-05-2011)“…Protease-activated receptor-2 (PAR2) is one of four protease-activated G-protein-coupled receptors. PAR2 is expressed on multiple cell types where it…”
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Spinal Dopaminergic Projections Control the Transition to Pathological Pain Plasticity via a D 1 /D 5 -Mediated Mechanism
Published in The Journal of neuroscience (22-04-2015)“…The mechanisms that lead to the maintenance of chronic pain states are poorly understood, but their elucidation could lead to new insights into how pain…”
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Correction: Extracellular phosphorylation of a receptor tyrosine kinase controls synaptic localization of NMDA receptors and regulates pathological pain
Published in PLoS biology (01-11-2021)“…[This corrects the article DOI: 10.1371/journal.pbio.2002457.]…”
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The novel PAR 2 ligand C 391 blocks multiple PAR 2 signalling pathways in vitro and in vivo
Published in British journal of pharmacology (01-09-2015)“…Background and Purpose Proteinase‐activated receptor‐2 ( PAR 2) is a GPCR linked to diverse pathologies, including acute and chronic pain. PAR 2 is one of the…”
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