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Differential involvement of opioidergic and serotonergic systems in the antinociceptive activity of N-arachidonoyl-phenolamine (AM404) in the rat: comparison with paracetamol
by
Ruggieri, Valentina
, Pini, Luigi Alberto
, Sandrini, Maurizio
, Vitale, Giovanni
in
Acetaminophen - pharmacology
/ Analgesics, Non-Narcotic - pharmacology
/ Animals
/ Arachidonic Acids - pharmacology
/ Biomedical and Life Sciences
/ Biomedicine
/ Frontal Lobe - drug effects
/ Frontal Lobe - metabolism
/ Hydroxyindoleacetic Acid - metabolism
/ Male
/ Neurosciences
/ Original Article
/ Pain - drug therapy
/ Pain Measurement
/ Pharmacology/Toxicology
/ Pons - drug effects
/ Pons - metabolism
/ Rats
/ Rats, Wistar
/ Receptor, Serotonin, 5-HT1A - drug effects
/ Receptor, Serotonin, 5-HT1A - metabolism
/ Receptors, Opioid, kappa - drug effects
/ Receptors, Opioid, kappa - metabolism
/ Receptors, Opioid, mu - drug effects
/ Receptors, Opioid, mu - metabolism
/ Receptors, Serotonin, 5-HT2 - drug effects
/ Receptors, Serotonin, 5-HT2 - metabolism
/ Receptors, Serotonin, 5-HT3 - drug effects
/ Receptors, Serotonin, 5-HT3 - metabolism
/ Serotonin - metabolism
2008
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Differential involvement of opioidergic and serotonergic systems in the antinociceptive activity of N-arachidonoyl-phenolamine (AM404) in the rat: comparison with paracetamol
by
Ruggieri, Valentina
, Pini, Luigi Alberto
, Sandrini, Maurizio
, Vitale, Giovanni
in
Acetaminophen - pharmacology
/ Analgesics, Non-Narcotic - pharmacology
/ Animals
/ Arachidonic Acids - pharmacology
/ Biomedical and Life Sciences
/ Biomedicine
/ Frontal Lobe - drug effects
/ Frontal Lobe - metabolism
/ Hydroxyindoleacetic Acid - metabolism
/ Male
/ Neurosciences
/ Original Article
/ Pain - drug therapy
/ Pain Measurement
/ Pharmacology/Toxicology
/ Pons - drug effects
/ Pons - metabolism
/ Rats
/ Rats, Wistar
/ Receptor, Serotonin, 5-HT1A - drug effects
/ Receptor, Serotonin, 5-HT1A - metabolism
/ Receptors, Opioid, kappa - drug effects
/ Receptors, Opioid, kappa - metabolism
/ Receptors, Opioid, mu - drug effects
/ Receptors, Opioid, mu - metabolism
/ Receptors, Serotonin, 5-HT2 - drug effects
/ Receptors, Serotonin, 5-HT2 - metabolism
/ Receptors, Serotonin, 5-HT3 - drug effects
/ Receptors, Serotonin, 5-HT3 - metabolism
/ Serotonin - metabolism
2008
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Differential involvement of opioidergic and serotonergic systems in the antinociceptive activity of N-arachidonoyl-phenolamine (AM404) in the rat: comparison with paracetamol
by
Ruggieri, Valentina
, Pini, Luigi Alberto
, Sandrini, Maurizio
, Vitale, Giovanni
in
Acetaminophen - pharmacology
/ Analgesics, Non-Narcotic - pharmacology
/ Animals
/ Arachidonic Acids - pharmacology
/ Biomedical and Life Sciences
/ Biomedicine
/ Frontal Lobe - drug effects
/ Frontal Lobe - metabolism
/ Hydroxyindoleacetic Acid - metabolism
/ Male
/ Neurosciences
/ Original Article
/ Pain - drug therapy
/ Pain Measurement
/ Pharmacology/Toxicology
/ Pons - drug effects
/ Pons - metabolism
/ Rats
/ Rats, Wistar
/ Receptor, Serotonin, 5-HT1A - drug effects
/ Receptor, Serotonin, 5-HT1A - metabolism
/ Receptors, Opioid, kappa - drug effects
/ Receptors, Opioid, kappa - metabolism
/ Receptors, Opioid, mu - drug effects
/ Receptors, Opioid, mu - metabolism
/ Receptors, Serotonin, 5-HT2 - drug effects
/ Receptors, Serotonin, 5-HT2 - metabolism
/ Receptors, Serotonin, 5-HT3 - drug effects
/ Receptors, Serotonin, 5-HT3 - metabolism
/ Serotonin - metabolism
2008
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Differential involvement of opioidergic and serotonergic systems in the antinociceptive activity of N-arachidonoyl-phenolamine (AM404) in the rat: comparison with paracetamol
Journal Article
Differential involvement of opioidergic and serotonergic systems in the antinociceptive activity of N-arachidonoyl-phenolamine (AM404) in the rat: comparison with paracetamol
2008
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Overview
It is recognized that paracetamol undergoes a metabolic transformation to
N
-arachydonylphenolamine (AM404), a CB
1
receptor ligand and anandamide uptake inhibitor. Using hot-plate and paw pressure tests, we decided to establish whether AM404 may act through opioidergic and serotonergic mechanisms. Thus, we pretreated rats with opioid μ
1
(naloxonazine) and κ (MR2266) or 5-HT
1A
(NAN-190), 5-HT
2
(ketanserin), and 5-HT
3
(ondansetron) receptor antagonists. We investigated the possible changes in 5-hydroxyindoleacetic acid/serotonin ratio in the frontal cortex and pons. The antinociceptive effect of AM404 (10 mg/kg, intrapertoneally) or paracetamol (400 mg/kg, intrapertoneally) in either test was abolished by naloxonazine or MR2266. Ondansetron prevented AM404 activity; NAN-190 and ketanserin were ineffective. Ketanserin antagonized paracetamol activity; NAN-190 and ondansetron were inactive. AM404 did not change serotonergic activity, while paracetamol decreased serotonin turnover. The diverse antinociceptive potency of the compounds might be explained by the different influence on the serotonergic system, despite a similar involvement of opioidergic one.
Publisher
Springer-Verlag
Subject
/ Analgesics, Non-Narcotic - pharmacology
/ Animals
/ Arachidonic Acids - pharmacology
/ Biomedical and Life Sciences
/ Hydroxyindoleacetic Acid - metabolism
/ Male
/ Rats
/ Receptor, Serotonin, 5-HT1A - drug effects
/ Receptor, Serotonin, 5-HT1A - metabolism
/ Receptors, Opioid, kappa - drug effects
/ Receptors, Opioid, kappa - metabolism
/ Receptors, Opioid, mu - drug effects
/ Receptors, Opioid, mu - metabolism
/ Receptors, Serotonin, 5-HT2 - drug effects
/ Receptors, Serotonin, 5-HT2 - metabolism
/ Receptors, Serotonin, 5-HT3 - drug effects
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