about
Local anaesthetic activity of beta-caryophylleneMolecular simplification of 1,4-diazabicyclo[4.3.0]nonan-9-ones gives piperazine derivatives that maintain high nootropic activity.Satiety factor oleoylethanolamide recruits the brain histaminergic system to inhibit food intakeDM235 (sunifiram): a novel nootropic with potential as a cognitive enhancer.Pharmacological characterization of DM232 (unifiram) and DM235 (sunifiram), new potent cognition enhancers.Antihyperalgesic activity of verbascoside in two models of neuropathic pain.Reversible antisense inhibition of Shaker-like Kv1.1 potassium channel expression impairs associative memory in mouse and ratEnlarging the NSAIDs family: ether, ester and acid derivatives of the 1,5-diarylpyrrole scaffold as novel anti-inflammatory and analgesic agents.Silencing of the RNA-binding protein HuR attenuates hyperalgesia and motor disability in experimental autoimmune encephalomyelitis.Antihistamine antinociception is mediated by Gi-protein activation.Amitriptyline and clomipramine activate Gi-protein signaling pathway in the induction of analgesia.The RNA-binding protein HuD promotes spinal GAP43 overexpression in antiretroviral-induced neuropathy.Contribution of G inhibitory protein alpha subunits in paradoxical hyperalgesia elicited by exceedingly low doses of morphine in mice.Alpha-2 agonists induce amnesia through activation of the Gi-protein signalling pathway.The new HDAC1 inhibitor LG325 ameliorates neuropathic pain in a mouse model.4-methyl benzylamine stimulates food consumption and counteracts the hypophagic effects of amphetamine acting on brain Shaker-like Kv1.1 channelsSpinal RyR2 pathway regulated by the RNA-binding protein HuD induces pain hypersensitivity in antiretroviral neuropathy.St. John's wort relieves pain in an animal model of migraine.A prolonged protein kinase C-mediated, opioid-related antinociceptive effect of st John's Wort in mice.Increase of neurofilament-H protein in sensory neurons in antiretroviral neuropathy: Evidence for a neuroprotective response mediated by the RNA-binding protein HuD.Different involvement of type 1, 2, and 3 ryanodine receptors in memory processesPKC-mediated HuD-GAP43 pathway activation in a mouse model of antiretroviral painful neuropathy.Methylamine, but not ammonia, is hypophagic in mouse by interaction with brain Kv1.6 channel subtype.Hypofunctionality of Gi proteins as aetiopathogenic mechanism for migraine and cluster headache.Memory facilitation and stimulation of endogenous nerve growth factor synthesis by the acetylcholine releaser PG-9.Effect of pertussis toxin on baclofen- and diphenhydramine-induced amnesia.Influence of potassium channel modulators on cognitive processes in mice.Chiral aryloxyalkylamines: Selective 5-HT(1B/1D) activation and analgesic activity.St. John's Wort reduces neuropathic pain through a hypericin-mediated inhibition of the protein kinase Cgamma and epsilon activity.Novel ester and acid derivatives of the 1,5-diarylpyrrole scaffold as anti-inflammatory and analgesic agents. Synthesis and in vitro and in vivo biological evaluation.Supraspinal role of protein kinase C in oxaliplatin-induced neuropathy in rat.Involvement of potassium channels in amitriptyline and clomipramine analgesia.ERK1/2 phosphorylation is involved in the antidepressant-like action of 2,5-diphenyl-3-(4-fluorophenylseleno)-selenophene in mice.Indomethacin, caffeine and prochlorperazine alone and combined revert hyperalgesia in in vivo models of migraine.Reversal of NO-induced nociceptive hypersensitivity by St. John's wort and hypericin: NF-κB, CREB and STAT1 as molecular targets.Central cholinergic challenging of migraine by testing second-generation anticholinesterase drugs.St. John's Wort seed and feverfew flower extracts relieve painful diabetic neuropathy in a rat model of diabetes.Molecular interaction in the mouse PAG between NMDA and opioid receptors in morphine-induced acute thermal nociception.Synthesis, biological evaluation, and receptor docking simulations of 2-[(acylamino)ethyl]-1,4-benzodiazepines as kappa-opioid receptor agonists endowed with antinociceptive and antiamnesic activity.[(3-Chlorophenyl)piperazinylpropyl]pyridazinones and analogues as potent antinociceptive agents.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nicoletta Galeotti
@ast
Nicoletta Galeotti
@en
Nicoletta Galeotti
@es
Nicoletta Galeotti
@nl
Nicoletta Galeotti
@sl
type
label
Nicoletta Galeotti
@ast
Nicoletta Galeotti
@en
Nicoletta Galeotti
@es
Nicoletta Galeotti
@nl
Nicoletta Galeotti
@sl
prefLabel
Nicoletta Galeotti
@ast
Nicoletta Galeotti
@en
Nicoletta Galeotti
@es
Nicoletta Galeotti
@nl
Nicoletta Galeotti
@sl
P1053
N-1093-2015
P106
P1153
7006361716
P21
P2798
P31
P3829
P496
0000-0002-1812-9844