Search Results - "Hales, Tim G"
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The 5-HT3 receptor – the relationship between structure and function
Published in Neuropharmacology (01-01-2009)“…The 5-hydroxytryptamine type-3 (5-HT3) receptor is a cation-selective ion channel of the Cys-loop superfamily. 5-HT3 receptor activation in the central and…”
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2
The impact of adverse childhood experiences on multimorbidity: a systematic review and meta-analysis
Published in BMC medicine (15-08-2024)“…Adverse childhood experiences (ACEs) have been implicated in the aetiology of a range of health outcomes, including multimorbidity. In this systematic review…”
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3
The search for the “next” euphoric non-fentanil novel synthetic opioids on the illicit drugs market: current status and horizon scanning
Published in Forensic toxicology (01-01-2019)“…Purpose A detailed review on the chemistry and pharmacology of non-fentanil novel synthetic opioid receptor agonists, particularly N -substituted benzamides…”
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Editorial: Opioids in the time of the COVID-19 pandemic: from cellular mechanisms to public health policy
Published in Frontiers in pharmacology (2023)Get full text
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5
Src Kinase Inhibition Attenuates Morphine Tolerance without Affecting Reinforcement or Psychomotor Stimulation
Published in Anesthesiology (Philadelphia) (01-11-2017)“…Prolonged opioid administration leads to tolerance characterized by reduced analgesic potency. Pain management is additionally compromised by the hedonic…”
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Pharmacological and nutritional targeting of voltage-gated sodium channels in the treatment of cancers
Published in iScience (23-04-2021)“…Voltage-gated sodium (NaV) channels, initially characterized in excitable cells, have been shown to be aberrantly expressed in non-excitable cancer tissues and…”
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7
Cross-sectional study examining the epidemiology of chronic pain in Nepal
Published in Pain reports (01-03-2023)“…The World Health Organization recognizes chronic pain as a global public health concern; however, there is a bias towards research conducted in relatively…”
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Agonist‐ and antagonist‐induced up‐regulation of surface 5‐HT3A receptors
Published in British journal of pharmacology (01-08-2015)“…Background and Purpose The 5‐HT3 receptor is a member of the pentameric ligand‐gated ion channel family and is pharmacologically targeted to treat irritable…”
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Morphine‐induced mechanical hypersensitivity in mice requires δ receptors, β‐arrestin2, and c‐Src activity
Published in The Journal of physiology (01-04-2023)“…Morphine diminishes pain, but its long‐term use is compromised by tolerance and hyperalgesia. Studies implicate δ receptors, β‐arrestin2 and Src kinase in…”
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10
Tonically active GABAA receptors in hippocampal pyramidal neurons exhibit constitutive GABA-independent gating
Published in Molecular pharmacology (01-02-2007)“…Phasic and tonic inhibitory currents of hippocampal pyramidal neurons exhibit distinct pharmacological properties. Picrotoxin and bicuculline methiodide…”
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11
Engineering a surrogate human heteromeric α/β glycine receptor orthosteric site exploiting the structural homology and stability of acetylcholine-binding protein
Published in IUCrJ (01-11-2019)“…Protein-engineering methods have been exploited to produce a surrogate system for the extracellular neurotransmitter-binding site of a heteromeric human…”
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Novel structural determinants of single channel conductance and ion selectivity in 5-hydroxytryptamine type 3 and nicotinic acetylcholine receptors
Published in The Journal of physiology (15-02-2010)“…Nicotinic acetylcholine (nACh) and 5-hydroxytryptamine type 3 (5-HT 3 ) receptors are cation-selective ion channels of the pentameric ligand-gated ion channel…”
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13
Childhood maltreatment and chronic “all over” body pain in adulthood: a counterfactual analysis using UK Biobank
Published in Pain (Amsterdam) (15-11-2024)“…Abstract Evidence linking adverse childhood experiences and chronic pain in adulthood is largely cross-sectional, potentially subject to recall bias and does…”
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14
A Novel Class of Ligand-gated Ion Channel Is Activated by Zn2
Published in The Journal of biological chemistry (10-01-2003)“…In mammals, the superfamily of “Cys loop,” ligand-gated ion channels (LGICs), is assembled from a pool of more than 40 homologous subunits. These subunits have…”
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Early-life adversity increases morphine tolerance and persistent inflammatory hypersensitivity through upregulation of δ opioid receptors in mice
Published in Pain (Amsterdam) (01-10-2023)“…Exposure to severely stressful events during childhood is associated with poor health outcomes in later life, including chronic pain and substance use…”
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High Affinity Binding of Epibatidine to Serotonin Type 3 Receptors
Published in The Journal of biological chemistry (11-04-2008)“…Epibatidine and mecamylamine are ligands used widely in the study of nicotinic acetylcholine receptors (nAChRs) in the central and peripheral nervous systems…”
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Structural Determinants of Ca2+ Permeability and Conduction in the Human 5-Hydroxytryptamine Type 3A Receptor
Published in The Journal of biological chemistry (11-07-2008)“…Cation-selective cysteine (Cys)-loop transmitter-gated ion channels provide an important pathway for Ca2+ entry into neurones. We examined the influence on…”
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Traumatic needle damage to nerves during regional anesthesia: presentation of a novel mechanotransduction hypothesis
Published in Regional anesthesia and pain medicine (01-11-2022)“…Despite advances in needle positioning techniques, nerve damage still occurs after regional anesthesia. Recognized causes include local anesthetic toxicity,…”
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Potent Inactivation-Dependent Inhibition of Adult and Neonatal NaV1.5 Channels by Lidocaine and Levobupivacaine
Published in Anesthesia and analgesia (01-09-2018)“…BACKGROUND:Cardiotoxic effects of local anesthetics (LAs) involve inhibition of NaV1.5 voltage-gated Na channels. Metastatic breast and colon cancer cells also…”
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TRV130 partial agonism and capacity to induce anti‐nociceptive tolerance revealed through reducing available μ‐opioid receptor number
Published in British journal of pharmacology (01-04-2021)“…Background and Purpose β‐Arrestin2 recruitment to μ‐receptors may contribute to the development of opioid side effects. This possibility led to the development…”
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