Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Clarissa Anna, Pisanò"'
Publikováno v:
Neurobiology of Disease, Vol 144, Iss , Pp 105044- (2020)
Acetylcholine muscarinic receptors (mAChRs) contribute to both the facilitation and inhibition of levodopa-induced dyskinesia operated by striatal cholinergic interneurons, although the receptor subtypes involved remain elusive. Cholinergic afferents
Externí odkaz:
https://doaj.org/article/baa2add88b2b4381b0a823f7bffc5faf
Autor:
Gerard W. O'Keeffe, Nurulain T. Zaveri, Ilaria Morella, Daniela Mercatelli, Martina Mazzocchi, Riccardo Brambilla, Michele Morari, Alberto Brugnoli, Stefania Fasano, Richard R. Neubig, Clarissa Anna Pisanò
Background and purpose Regulator of G-protein signal 4 (RGS4) is a signal transduction protein that accelerates intrinsic GTPase activity of Gαi/o and Gαq subunits, suppressing GPCR signaling. Here we investigate whether RGS4 modulates nociceptin/o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a564af83ffb46926abc647c19aea84b
https://hdl.handle.net/11392/2472868
https://hdl.handle.net/11392/2472868
Publikováno v:
Neurobiology of Disease, Vol 144, Iss, Pp 105044-(2020)
Acetylcholine muscarinic receptors (mAChRs) contribute to both the facilitation and inhibition of levodopa-induced dyskinesia operated by striatal cholinergic interneurons, although the receptor subtypes involved remain elusive. Cholinergic afferents
Autor:
Nurulain T. Zaveri, Michele Morari, Dennis Yasuda, Clarissa Anna Pisanò, Alberto Brugnoli, Matteo Marti, Uma Gayathri Kamakolanu, Michael E Meyer, Daniela Mercatelli, Willma E. Polgar
Publikováno v:
Journal of medicinal chemistry. 63(5)
A novel series of C(3)-substituted piperdinylindoles were developed as nociceptin opioid receptor (NOP) partial agonists to explore a pharmacological hypothesis that NOP partial agonists would afford a dual pharmacological action of attenuating Parki
Autor:
Clarissa Anna Pisanò, Harkaitz Bengoetxea, Catalina Requejo, Michele Morari, José Vicente Lafuente, Cristina Miguelez, Luisa Ugedo, Sergio Vegas-Suarez
Publikováno v:
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
British Journal of Pharmacology
Addi. Archivo Digital para la Docencia y la Investigación
instname
Universidad del País Vasco
British Journal of Pharmacology
Addi. Archivo Digital para la Docencia y la Investigación
instname
Background and Purpose l-DOPA-induced dyskinesia (LID) is considered a major complication in the treatment of Parkinson's disease (PD). Buspirone (5-HT(1A)partial agonist) have shown promising results in the treatment of PD and LID, however no 5-HT-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c62193f03edfecb32d5e9376e90812d4
http://hdl.handle.net/11392/2471960
http://hdl.handle.net/11392/2471960
Autor:
Stefania Fasano, Nurulain T. Zaveri, Martina Frassineti, Ludovico Arcuri, Clarissa Anna Pisanò, Michele Morari, Willma E. Polgar, Riccardo Brambilla, Michael E Meyer, Ilaria Morella, Daniela Mercatelli, V. Blair Journigan, Salvatore Novello
Publikováno v:
British Journal of Pharmacology. 175:782-796
Background and Purpose We previously showed that nociceptin/orphanin FQ opioid peptide (NOP) receptor agonists attenuate the expression of levodopa-induced dyskinesia in animal models of Parkinson's disease. We now investigate the efficacy of two nov
Autor:
Clarissa Anna Pisanò, Paolo Bolognesi, Michele Morari, Francesco Longo, Derya R. Shimshek, Martina Frassineti, Daniela Mercatelli
Publikováno v:
Pharmacology Research & Perspectives
Mutations in leucine‐rich repeat kinase 2 (LRRK2) gene have been pathogenically linked to Parkinson's disease, and pharmacological inhibition of LRRK2 is being pursued to tackle nigro‐striatal dopaminergic neurodegeneration. However, LRRK2 kinase
Publikováno v:
Handbook of experimental pharmacology. 254
Nociceptin/Orphanin FQ (N/OFQ) and its NOP receptor are highly expressed in motor areas of the rodent, nonhuman, and human primate brain, such as primary motor cortex, thalamus, globus pallidus, striatum, and substantia nigra. Endogenous N/OFQ negati
Publikováno v:
Handbook of Experimental Pharmacology ISBN: 9783030201852
Nociceptin/Orphanin FQ (N/OFQ) and its NOP receptor are highly expressed in motor areas of the rodent, nonhuman, and human primate brain, such as primary motor cortex, thalamus, globus pallidus, striatum, and substantia nigra. Endogenous N/OFQ negati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774cbb9bca92a7529d2adef95118c8a8
http://hdl.handle.net/11392/2411797
http://hdl.handle.net/11392/2411797
Autor:
Michele Morari, Elsa Melloni, Carla Caccia, Alberto Brugnoli, Salvatore Novello, Silvia Vailati, Charlotte Keywood, Gloria Padoani, Clarissa Anna Pisanò
Publikováno v:
Neuropharmacology. 167:108006
To investigate whether the reversible MAO-B inhibitor and sodium channel blocker safinamide impairs glutamate release under parkinsonian conditions in vivo, and this effect is dependent on MAO-B inhibition, safinamide (and rasagiline as a comparator)