Research Topics
Species | Giovanna M ScotoSummaryAffiliation: University of Catania Country: Italy Publications
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Detail Information
Publications
Effects of intraplantar nocistatin and (±)-J 113397 injections on nociceptive behavior in a rat model of inflammationGiovanna M Scoto
Department of Drug Sciences Pharmacology and Toxicology Section, University of Catania, V le A Doria 6, 95125 Catania, Italy
Pharmacol Biochem Behav 100:639-44. 2012..Thus, it is likely that the peripheral N/OFQ/NOP receptor system contributes to the abnormal pain sensitivity in an inflammatory state...
Blockade of the nociceptin/orphanin FQ/NOP receptor system in the rat ventrolateral periaqueductal gray potentiates DAMGO analgesiaGiovanna M Scoto
Department of Pharmaceutical Sciences Pharmacology Section, University of Catania, V le A Doria 6, 95125 Catania, Italy
Peptides 28:1441-6. 2007..N/OFQ significantly blocked DAMGO (a selective MOP agonist) analgesia, while UFP-101 enhanced the effect of the opioid given at a subanalgesic dose. These results confirm our hypothesis of an antiopioid role for N/OFQ in the vlPAG...
Involvement of the Nociceptin/Orphanin FQ-NOP receptor system in the ventrolateral periaqueductal gray following mechanical allodynia in chronic painGiovanna M Scoto
Department of Pharmaceutical Sciences, University of Catania, V le A Doria 6, 95125 Catania, Italy
Life Sci 85:206-10. 2009..The aim of the present study was to identify the role of the vlPAG Nociceptin/Orphanin FQ/NOP receptor system in allodynia, a nociceptive behavioral response associated with chronic pain...
Selective inhibition of the NOP receptor in the ventrolateral periaqueductal gray attenuates the development and the expression of tolerance to morphine-induced antinociception in ratsGiovanna M Scoto
Department of Pharmaceutical Sciences Pharmacology Section, University of Catania, Vle A Doria 6, 95125 Catania, Italy
Peptides 31:696-700. 2010..These data suggest that the N/OFQ in the vlPAG may play a key role in opioid-induced antinociceptive tolerance...
Antinociceptive profile of LP1, a non-peptide multitarget opioid ligandCarmela Parenti
Department of Drug Sciences, Pharmacology and Toxicology Section, University of Catania, Viale A Doria 6, 95125 Catania, Italy
Life Sci 90:957-61. 2012..The aim of this work was to determine whether the antinociceptive effect produced by LP1 was central or peripheral and to assess which opioid receptor subtypes are involved in its effects...
The benzomorphan-based LP1 ligand is a suitable MOR/DOR agonist for chronic pain treatmentLorella Pasquinucci
Department of Drug Sciences, Medicinal Chemistry Section, University of Catania, Viale A Doria 6, 95125 Catania, Italy
Life Sci 90:66-70. 2012..The aim of this work was to evaluate and compare the induction of tolerance to antinociceptive effects from treatment with LP1 and morphine...
Synthesis and resolution of cis-(+/-)-methyl (1R,2S/1S,2R)-2-[(4-hydroxy-4-phenylpiperidin-1-yl)methyl]-1-(4-methylphenyl)cyclopropanecarboxylate [(+/-)-PPCC)]: new sigma receptor ligands with neuroprotective effectOrazio Prezzavento
Department of Pharmaceutical Sciences, Medicinal Chemistry Section, University of Catania, Catania, Italy
J Med Chem 53:5881-5. 2010..They exhibited in vivo anti-opioid effects on kappa opioid (KOP) receptor-mediated analgesia. Our findings demonstrate that the enantiomers display mainly sigma(1) agonist activity and that they have neuroprotective effects...
Supraspinal injection of Substance P attenuates allodynia and hyperalgesia in a rat model of inflammatory painCarmela Parenti
Department of Drug Sciences Pharmacology and Toxicology Section, University of Catania, V le A Doria 6, 95125 Catania, Italy
Peptides 34:412-8. 2012..These results suggest a significant antinociceptive role for SP and the NK1 receptor in inflammatory pain at the supraspinal level, possibly through the release of endogenous opioids...
Evaluation of N-substitution in 6,7-benzomorphan compoundsLorella Pasquinucci
Department of Pharmaceutical Sciences, Medicinal Chemistry Section, University of Catania, Viale A Doria 6, 95125 Catania, Italy
Bioorg Med Chem 18:4975-82. 2010..LP1, possessing a mu/delta agonist profile, could represent a lead in further developing benzomorphan-based ligands with potent in vivo analgesic activity and a reduced tendency to induce side effects...
The functional antiopioid action of the ventrolateral periaqueductal gray nociceptin/orphanin FQ and nociceptin receptor system underlies DAMGO analgesic toleranceCarmela Parenti
Department of Pharmaceutical Sciences Pharmacology Section, University of Catania, Italy cparenti unict it
Pharmacology 86:138-44. 2010..Inhibition of N/OFQ signaling can reverse and prevent the development of DAMGO tolerance in the vlPAG. The results confirm that N/OFQ acts as a functional opioid antagonist...
Novel potent and selective σ ligands: evaluation of their agonist and antagonist propertiesAgostino Marrazzo
Department of Drug Sciences, Medicinal Chemistry Section, University of Catania, Viale A Doria 6, 95125 Catania, Italy
J Med Chem 54:3669-73. 2011..The σ(2) ligand (-)-9 displayed agonist properties in an in vitro isolated organ bath assay and antiproliferative effects on LNCaP and PC3 prostate cancer cell lines...
A new sigma ligand, (+/-)-PPCC, antagonizes kappa opioid receptor-mediated antinociceptive effectOrazio Prezzavento
Department of Pharmaceutical Sciences, University of Catania, Viale A Doria, 6, 95125 Catania, Italy
Life Sci 82:549-53. 2008..This study confirms that (+/-)-PPCC plays the role of sigma agonist in this model and strengthens the hypothesis of the sigma receptor modulatory role on KOP-mediated analgesia...
Antiproliferative activity of phenylbutyrate ester of haloperidol metabolite II [(±)-MRJF4] in prostate cancer cellsAgostino Marrazzo
Department of Pharmaceutical Sciences, University of Catania, Viale A Doria 6, 95125 Catania, Italy
Eur J Med Chem 46:433-8. 2011..MRJF4 was also used in combination with σ(1) agonist (+)-pentazocine and σ(2) antagonist AC927 in order to evaluate the role of σ receptor subtypes in prostate cancer cell death...
