Search Results - "CHANDRAN, Prasant"
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Pharmacological modulation of movement-evoked pain in a rat model of osteoarthritis
Published in European journal of pharmacology (24-06-2009)“…This study was conducted to characterize movement-induced pain in a rat model of knee joint osteoarthritis and validate this behavioral assessment by…”
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Journal Article -
2
A-740003 [N-(1-{[(cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a novel and selective P2X7 receptor antagonist, dose-dependently reduces neuropathic pain in the rat
Published in The Journal of pharmacology and experimental therapeutics (01-12-2006)“…ATP-sensitive P2X(7) receptors are localized on cells of immunological origin including glial cells in the central nervous system. Activation of P2X(7)…”
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3
Default-mode-like network activation in awake rodents
Published in PloS one (18-11-2011)“…During wakefulness and in absence of performing tasks or sensory processing, the default-mode network (DMN), an intrinsic central nervous system (CNS) network,…”
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Indol-3-ylcycloalkyl Ketones: Effects of N1 Substituted Indole Side Chain Variations on CB2 Cannabinoid Receptor Activity
Published in Journal of medicinal chemistry (14-01-2010)“…Several 3-acylindoles with high affinity for the CB2 cannabinoid receptor and selectivity over the CB1 receptor have been prepared. A variety of 3-acyl…”
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Journal Article -
5
Central and peripheral sites of action for CB2 receptor mediated analgesic activity in chronic inflammatory and neuropathic pain models in rats
Published in British journal of pharmacology (01-01-2011)“…BACKGROUND AND PURPOSE Cannabinoid CB2 receptor activation by selective agonists has been shown to produce analgesic effects in preclinical models of…”
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Journal Article -
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Repeated dosing of ABT-102, a potent and selective TRPV1 antagonist, enhances TRPV1-mediated analgesic activity in rodents, but attenuates antagonist-induced hyperthermia
Published in Pain (Amsterdam) (01-03-2009)“…Transient receptor potential vanilloid type 1 (TRPV1) is a ligand-gated ion channel that functions as an integrator of multiple pain stimuli including heat,…”
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7
TRPV1-related modulation of spinal neuronal activity and behavior in a rat model of osteoarthritic pain
Published in Brain research (19-01-2011)“…Abstract The TRPV1 receptor functions as a molecular integrator, and blockade of this receptor modulates enhanced somatosensitivity across several animal…”
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Characterization of a cannabinoid CB2 receptor-selective agonist, A-836339 [2,2,3,3-tetramethyl-cyclopropanecarboxylic acid [3-(2-methoxy-ethyl)-4,5-dimethyl-3H-thiazol-(2Z)-ylidene]-amide], using in vitro pharmacological assays, in vivo pain models, and pharmacological magnetic resonance imaging
Published in The Journal of pharmacology and experimental therapeutics (01-01-2009)“…Studies demonstrating the antihyperalgesic and antiallodynic effects of cannabinoid CB(2) receptor activation have been largely derived from the use of…”
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9
Pharmacological modulation of brain activity in a preclinical model of osteoarthritis
Published in NeuroImage (Orlando, Fla.) (01-01-2013)“…The earliest stages of osteoarthritis are characterized by peripheral pathology; however, during disease progression chronic pain emerges—a major symptom of…”
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Journal Article -
10
Central and peripheral sites of action for CB 2 receptor mediated analgesic activity in chronic inflammatory and neuropathic pain models in rats
Published in British journal of pharmacology (01-01-2011)“…BACKGROUND AND PURPOSE Cannabinoid CB 2 receptor activation by selective agonists has been shown to produce analgesic effects in preclinical models of…”
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Journal Article -
11
The antihyperalgesic activity of a selective P2X7 receptor antagonist, A-839977, is lost in IL-1αβ knockout mice
Published in Behavioural brain research (01-12-2009)“…The pro-inflammatory cytokine interleukin-1β (IL-1β) has been implicated in both inflammatory processes and nociceptive neurotransmission. Activation of P2X7…”
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H 4 receptor antagonism exhibits anti-nociceptive effects in inflammatory and neuropathic pain models in rats
Published in Pharmacology, biochemistry and behavior (01-03-2010)“…The histamine H 4 receptor (H 4R) is expressed primarily on cells involved in inflammation and immune responses. To determine the potential role of H 4R in…”
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Journal Article -
13
Potentiation of analgesic efficacy but not side effects: Co-administration of an alpha 4 beta 2 neuronal nicotinic acetylcholine receptor agonist and its positive allosteric modulator in experimental models of pain in rats
Published in Biochemical pharmacology (15-10-2011)“…Positive modulation of the neuronal nicotinic acetylcholine receptor (nAChR) alpha 4 beta 2 subtype by selective positive allosteric modulator NS-9283 has…”
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14
Potentiation of analgesic efficacy but not side effects: Co-administration of an α4β2 neuronal nicotinic acetylcholine receptor agonist and its positive allosteric modulator in experimental models of pain in rats
Published in Biochemical pharmacology (15-10-2011)“…Positive allosteric modulator NS-9283 enhances NNR α4β2 agonist ABT-594 (up to 100 nmol/kg)-induced analgesic efficacy in animal models of pain, and cortical…”
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Journal Article Conference Proceeding -
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Antinociceptive effects of histamine H 3 receptor antagonist in the preclinical models of pain in rats and the involvement of central noradrenergic systems
Published in Brain research (01-10-2010)“…The histamine H 3 receptor is predominantly expressed in the central nervous system and plays a role in diverse physiological mechanisms. In the present study,…”
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Journal Article -
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Development of opioid tolerance with repeated transcutaneous electrical nerve stimulation administration
Published in Pain (Amsterdam) (01-03-2003)“…The analgesia produced by low and high frequency transcutaneous electrical nerve stimulation (TENS) is mediated by the release of μ- or δ-opioids, respectively…”
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H4 receptor antagonism exhibits anti-nociceptive effects in inflammatory and neuropathic pain models in rats
Published in Pharmacology, biochemistry and behavior (01-03-2010)“…The histamine H(4) receptor (H(4)R) is expressed primarily on cells involved in inflammation and immune responses. To determine the potential role of H(4)R in…”
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Journal Article -
18
Indol-3-yl-tetramethylcyclopropyl Ketones: Effects of Indole Ring Substitution on CB2 Cannabinoid Receptor Activity
Published in Journal of medicinal chemistry (27-03-2008)“…A series of potent indol-3-yl-tetramethylcyclopropyl ketones have been prepared as CB2 cannabinoid receptor ligands. Two unsubstituted indoles (5, 32) were the…”
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Journal Article -
19
Paradigm shift in translational neuroimaging of CNS disorders
Published in Biochemical pharmacology (15-06-2011)“…Structural MRI, task-evoked functional MRI and resting-state functional MRI in preclinical and clinical settings provide the capability of translational…”
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Journal Article -
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Antinociceptive effects of histamine H3 receptor antagonist in the preclinical models of pain in rats and the involvement of central noradrenergic systems
Published in Brain research (01-10-2010)“…Abstract The histamine H3 receptor is predominantly expressed in the central nervous system and plays a role in diverse physiological mechanisms. In the…”
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