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Serotonergic Neurotransmission System Modulator, Vortioxetine, and Dopaminergic D2/D3 Receptor Agonist, Ropinirole, Attenuate Fibromyalgia-Like Symptoms in Mice

Molecules (Basel, Switzerland), 2021-04, Vol.26 (8), p.2398

2021

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Interventional and preventive effects of aripiprazole and ceftriaxone used alone or in combination on oxaliplatin-induced tactile and cold allodynia in mice

Biomedicine & pharmacotherapy, 2019-03, Vol.111, p.882-890

2019

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Chemotherapy-induced peripheral neuropathy: part 1—current state of knowledge and perspectives for pharmacotherapy

Pharmacological reports, 2020-06, Vol.72 (3), p.486-507

Sałat, Kinga

2020

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Chemotherapy-induced peripheral neuropathy—part 2: focus on the prevention of oxaliplatin-induced neurotoxicity

Pharmacological reports, 2020-06, Vol.72 (3), p.508-527

Sałat, Kinga

2020

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Phenylalanine-Based AMPA Receptor Antagonist as the Anticonvulsant Agent with Neuroprotective Activity-In Vitro and In Vivo Studies

Molecules (Basel, Switzerland), 2022-01, Vol.27 (3), p.875

2022

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Antiepileptic Drug Tiagabine Does Not Directly Target Key Cardiac Ion Channels Kv11.1, Nav1.5 and Cav1.2

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3522

2021

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Novel GPR18 Ligands in Rodent Pharmacological Tests: Effects on Mood, Pain, and Eating Disorders

International journal of molecular sciences, 2023-05, Vol.24 (10), p.9046

2023

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Lipopolysaccharide-Induced Model of Neuroinflammation: Mechanisms of Action, Research Application and Future Directions for Its Use

Molecules (Basel, Switzerland), 2022-08, Vol.27 (17), p.5481

2022

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Naturally Inspired Molecules for Neuropathic Pain Inhibition-Effect of Mirogabalin and Cebranopadol on Mechanical and Thermal Nociceptive Threshold in Mice

Molecules (Basel, Switzerland), 2023-11, Vol.28 (23), p.7862

2023

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The Microglial Activation Inhibitor Minocycline, Used Alone and in Combination with Duloxetine, Attenuates Pain Caused by Oxaliplatin in Mice

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3577

2021

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8-Hydroxyquinolylnitrones as multifunctional ligands for the therapy of neurodegenerative diseases

Acta pharmaceutica Sinica. B, 2023-05, Vol.13 (5), p.2152-2175

2023

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Wide-Range Measurement of Thermal Preference-A Novel Method for Detecting Analgesics Reducing Thermally-Evoked Pain in Mice

Molecules (Basel, Switzerland), 2021-01, Vol.26 (3), p.612

2021

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Behavioral effects of buspirone in a mouse model of posttraumatic stress disorder

Behavioural brain research, 2020-03, Vol.381, p.112380-112380, Article 112380

2020

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An overview of the pharmacological properties and potential applications of natural monoterpenes

Mini reviews in medicinal chemistry, 2014-01, Vol.14 (14), p.1156

2014

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Dopamine D2/D3 receptor agonists attenuate PTSD-like symptoms in mice exposed to single prolonged stress

Neuropharmacology, 2019-09, Vol.155, p.1-9

2019

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The Magic of Crystal Structure-Based Inhibitor Optimization: Development of a Butyrylcholinesterase Inhibitor with Picomolar Affinity and in Vivo Activity

Journal of medicinal chemistry, 2018-01, Vol.61 (1), p.119-139

2018

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Phencyclidine and Scopolamine for Modeling Amnesia in Rodents: Direct Comparison with the Use of Barnes Maze Test and Contextual Fear Conditioning Test in Mice

Neurotoxicity research, 2018-10, Vol.34 (3), p.431-441

2018

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Antidepressant-like effects of ketamine, norketamine and dehydronorketamine in forced swim test: Role of activity at NMDA receptor

Neuropharmacology, 2015-12, Vol.99, p.301-307

2015

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Transient receptor potential channels - emerging novel drug targets for the treatment of pain

Current medicinal chemistry, 2013-04, Vol.20 (11), p.1409

2013

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Evaluation of cebranopadol, a dually acting nociceptin/orphanin FQ and opioid receptor agonist in mouse models of acute, tonic, and chemotherapy-induced neuropathic pain

Inflammopharmacology, 2018-04, Vol.26 (2), p.361-374

2018

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Structure-activity relationship study of tryptophan-based butyrylcholinesterase inhibitors

European journal of medicinal chemistry, 2020-12, Vol.208, p.112766-112766, Article 112766

2020

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Antinociceptive activity of transient receptor potential channel TRPV1, TRPA1, and TRPM8 antagonists in neurogenic and neuropathic pain models in mice

Journal of Zhejiang University. B. Science, 2015-03, Vol.16 (3), p.167-178

2015

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Anticonvulsant active inhibitor of GABA transporter subtype 1, tiagabine, with activity in mouse models of anxiety, pain and depression

Pharmacological reports, 2015-06, Vol.67 (3), p.465-472

2015

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Nitrogen, oxygen or sulfur containing heterocyclic compounds as analgesic drugs used as modulators of the nitroxidative stress

Mini reviews in medicinal chemistry, 2013-03, Vol.13 (3), p.335

2013

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Antidepressant-like activity of venlafaxine and clonidine in mice exposed to single prolonged stress – A model of post-traumatic stress disorder. Pharmacodynamic and molecular docking studies

Brain research, 2017-10, Vol.1673, p.1-10

2017

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Serotonergic Neurotransmission System Modulator, Vortioxetine, and Dopaminergic D2/D3 Receptor Agonist, Ropinirole, Attenuate Fibromyalgia-Like Symptoms in Mice

Interventional and preventive effects of aripiprazole and ceftriaxone used alone or in combination on oxaliplatin-induced tactile and cold allodynia in mice

Chemotherapy-induced peripheral neuropathy: part 1—current state of knowledge and perspectives for pharmacotherapy

Chemotherapy-induced peripheral neuropathy—part 2: focus on the prevention of oxaliplatin-induced neurotoxicity

Phenylalanine-Based AMPA Receptor Antagonist as the Anticonvulsant Agent with Neuroprotective Activity-In Vitro and In Vivo Studies

Antiepileptic Drug Tiagabine Does Not Directly Target Key Cardiac Ion Channels Kv11.1, Nav1.5 and Cav1.2

Novel GPR18 Ligands in Rodent Pharmacological Tests: Effects on Mood, Pain, and Eating Disorders

Lipopolysaccharide-Induced Model of Neuroinflammation: Mechanisms of Action, Research Application and Future Directions for Its Use

Naturally Inspired Molecules for Neuropathic Pain Inhibition-Effect of Mirogabalin and Cebranopadol on Mechanical and Thermal Nociceptive Threshold in Mice

The Microglial Activation Inhibitor Minocycline, Used Alone and in Combination with Duloxetine, Attenuates Pain Caused by Oxaliplatin in Mice

8-Hydroxyquinolylnitrones as multifunctional ligands for the therapy of neurodegenerative diseases

Wide-Range Measurement of Thermal Preference-A Novel Method for Detecting Analgesics Reducing Thermally-Evoked Pain in Mice

Behavioral effects of buspirone in a mouse model of posttraumatic stress disorder

An overview of the pharmacological properties and potential applications of natural monoterpenes

Dopamine D2/D3 receptor agonists attenuate PTSD-like symptoms in mice exposed to single prolonged stress

The Magic of Crystal Structure-Based Inhibitor Optimization: Development of a Butyrylcholinesterase Inhibitor with Picomolar Affinity and in Vivo Activity

Phencyclidine and Scopolamine for Modeling Amnesia in Rodents: Direct Comparison with the Use of Barnes Maze Test and Contextual Fear Conditioning Test in Mice

Antidepressant-like effects of ketamine, norketamine and dehydronorketamine in forced swim test: Role of activity at NMDA receptor

Transient receptor potential channels - emerging novel drug targets for the treatment of pain

Evaluation of cebranopadol, a dually acting nociceptin/orphanin FQ and opioid receptor agonist in mouse models of acute, tonic, and chemotherapy-induced neuropathic pain

Structure-activity relationship study of tryptophan-based butyrylcholinesterase inhibitors

Antinociceptive activity of transient receptor potential channel TRPV1, TRPA1, and TRPM8 antagonists in neurogenic and neuropathic pain models in mice

Anticonvulsant active inhibitor of GABA transporter subtype 1, tiagabine, with activity in mouse models of anxiety, pain and depression

Nitrogen, oxygen or sulfur containing heterocyclic compounds as analgesic drugs used as modulators of the nitroxidative stress

Antidepressant-like activity of venlafaxine and clonidine in mice exposed to single prolonged stress – A model of post-traumatic stress disorder. Pharmacodynamic and molecular docking studies

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