Search Results - BROAD, Lisa M.
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Activation of Muscarinic M1 Acetylcholine Receptors Induces Long-Term Potentiation in the Hippocampus
Published in Cerebral cortex (New York, N.Y. 1991) (01-01-2016)“…Muscarinic M1 acetylcholine receptors (M1Rs) are highly expressed in the hippocampus, and their inhibition or ablation disrupts the encoding of spatial memory…”
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2
5-I A-85380 and TC-2559 differentially activate heterologously expressed α4β2 nicotinic receptors
Published in European journal of pharmacology (06-06-2006)“…The neuronal nicotinic acetylcholine receptor α4 and β2 subunits expressed in heterologous expression systems assemble into at least two distinct subunit…”
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3
Acetylcholine modulates gamma frequency oscillations in the hippocampus by activation of muscarinic M1 receptors
Published in The European journal of neuroscience (01-06-2017)“…Modulation of gamma oscillations is important for the processing of information and the disruption of gamma oscillations is a prominent feature of…”
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4
M1 muscarinic allosteric modulators slow prion neurodegeneration and restore memory loss
Published in The Journal of clinical investigation (01-02-2017)“…The current frontline symptomatic treatment for Alzheimer's disease (AD) is whole-body upregulation of cholinergic transmission via inhibition of…”
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5
The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
Published in Experimental physiology (01-01-2024)“…A metabotropic glutamate receptor coupled to phospholipase D (PLD‐mGluR) was discovered in the hippocampus over three decades ago. Its pharmacology and direct…”
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6
TRPV3 in Drug Development
Published in Pharmaceuticals (Basel, Switzerland) (09-09-2016)“…Transient receptor potential vanilloid 3 (TRPV3) is a member of the TRP (Transient Receptor Potential) super-family. It is a relatively underexplored member of…”
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7
Pharmacological analysis of intracellular Ca2+ signalling: problems and pitfalls
Published in Trends in pharmacological sciences (Regular ed.) (01-09-1998)“… In this review, Colin Taylor and Lisa Broad summarize the more serious problems associated with some of the commonly used drugs, and describe specific situations in which the multiple effects of drugs on Ca2…”
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Mechanisms of capacitative calcium entry
Published in Journal of cell science (15-06-2001)“…Capacitative Ca(2+) entry involves the regulation of plasma membrane Ca(2+) channels by the filling state of intracellular Ca(2+) stores in the endoplasmic…”
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In vitro pharmacological and rat pharmacokinetic characterization of LY3020371, a potent and selective mGlu 2/3 receptor antagonist
Published in Neuropharmacology (01-03-2017)“…Metabotropic glutamate (mGlu ) receptors are of considerable interest owing to their role in modulating glutamate transmission via presynaptic, postsynaptic…”
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10
Current status of muscarinic M1 and M4 receptors as drug targets for neurodegenerative diseases
Published in Neuropharmacology (01-07-2018)“…The cholinergic signalling system has been an attractive pathway to seek targets for modulation of arousal, cognition, and attention which are compromised in…”
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11
Identification and pharmacological profile of a new class of selective nicotinic acetylcholine receptor potentiators
Published in The Journal of pharmacology and experimental therapeutics (01-09-2006)“…Here we report the discovery, by high-throughput screening, of three novel (2-amino-5-keto)thiazole compounds that act as selective potentiators of nicotinic…”
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12
From structure to clinic: Design of a muscarinic M1 receptor agonist with potential to treatment of Alzheimer's disease
Published in Cell (24-11-2021)“…Current therapies for Alzheimer's disease seek to correct for defective cholinergic transmission by preventing the breakdown of acetylcholine through…”
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13
Biased M1-muscarinic-receptor-mutant mice inform the design of next-generation drugs
Published in Nature chemical biology (01-03-2020)“…Cholinesterase inhibitors, the current frontline symptomatic treatment for Alzheimer’s disease (AD), are associated with low efficacy and adverse effects. M1…”
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14
A non-capacitative pathway activated by arachidonic acid is the major Ca2+ entry mechanism in rat A7r5 smooth muscle cells stimulated with low concentrations of vasopressin
Published in The Journal of physiology (15-05-1999)“…Depletion of the Ca 2+ stores of A7r5 cells stimulated Ca 2+ , though not Sr 2+ , entry. Vasopressin (AVP) or platelet-derived growth factor (PDGF) stimulated…”
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15
TRPA1 Antagonist LY3526318 Inhibits the Cinnamaldehyde‐Evoked Dermal Blood Flow Increase: Translational Proof of Pharmacology
Published in Clinical pharmacology and therapeutics (01-11-2023)“…Transient receptor potential Ankyrin 1 (TRPA1) is an ion channel expressed by sensory neurons, where it mediates pain signaling. Consequently, it has emerged…”
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Bitopic Binding Mode of an M 1 Muscarinic Acetylcholine Receptor Agonist Associated with Adverse Clinical Trial Outcomes
Published in Molecular pharmacology (01-06-2018)“…The realization of the therapeutic potential of targeting the M muscarinic acetylcholine receptor (mAChR…”
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Identification and pharmacological profile of SPP1, a potent, functionally selective and brain penetrant agonist at muscarinic M1 receptors
Published in British journal of pharmacology (01-01-2019)“…Background and Purpose We aimed to identify and develop novel, selective muscarinic M1 receptor agonists as potential therapeutic agents for the symptomatic…”
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18
An Antibody Biosensor Establishes the Activation of the M1 Muscarinic Acetylcholine Receptor during Learning and Memory
Published in The Journal of biological chemistry (22-04-2016)“…Establishing the in vivo activation status of G protein-coupled receptors would not only indicate physiological roles of G protein-coupled receptors but would…”
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Synthesis and Pharmacological Characterization of C4 β -Amide-Substituted 2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylates. Identification of (1 S,2 S,4 S,5 R,6 S)-2-Amino-4-[(3-methoxybenzoyl)amino]bicyclo[3.1.0]hexane-2,6-dicarboxylic Acid (LY2794193), a Highly Potent and Selective mGlu 3 Receptor Agonist
Published in Journal of medicinal chemistry (22-03-2018)“…Multiple therapeutic opportunities have been suggested for compounds capable of selective activation of metabotropic glutamate 3 (mGlu ) receptors, but small…”
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Pharmacological characterisation of ligand- and voltage-gated ion channels expressed in human iPSC-derived forebrain neurons
Published in Psychopharmacology (01-03-2014)“…Introduction Genetic causes, or predisposition, are increasingly accepted to be part of the ethiopathogenesis of many neuropsychiatric diseases. While genes…”
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