Zobrazeno 1 - 10 of 10 pro vyhledávání: '"M. G. Cascio"'
1
Cannabidiol, a non-psychotropic component of cannabis, attenuates vomiting and nausea-like behaviour via indirect agonism of 5-HT(1A) somatodendritic autoreceptors in the dorsal raphe nucleus
Autor: E M, Rock, D, Bolognini, C L, Limebeer, M G, Cascio, S, Anavi-Goffer, P J, Fletcher, R, Mechoulam, R G, Pertwee, L A, Parker
Publikováno v: British journal of pharmacology. 165(8)
To evaluate the hypothesis that activation of somatodendritic 5-HT(1A) autoreceptors in the dorsal raphe nucleus (DRN) produces the anti-emetic/anti-nausea effects of cannabidiol (CBD), a primary non-psychoactive cannabinoid found in cannabis.The pot
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3aa5ebffc7483da280988c1aa4ffe7b7
https://pubmed.ncbi.nlm.nih.gov/21827451
Zobrazit plný text záznamu
2
Inhibitory effect of salvinorin A, from Salvia divinorum, on ileitis-induced hypermotility: cross-talk between kappa-opioid and cannabinoid CB(1) receptors
Autor: CAPASSO, RAFFAELE, BORRELLI, FRANCESCA, M. G. Cascio, G. Aviello, K. Huben, J. K. Zjawiony, P. Marini, ROMANO, BARBARA, V. Di Marzo, CAPASSO, FRANCESCO, IZZO, ANGELO ANTONIO
BACKGROUND AND PURPOSE: Salvinorin A, the active component of the hallucinogenic herb Salvia divinorum, inhibits intestinal motility through activation of kappa-opioid receptors (KORs). However, this compound may have target(s) other than the KORs in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::e4263338447bedcf5da798f1c55ae2fa
http://hdl.handle.net/11588/333247
Zobrazit plný text záznamu
3
In vitro and in vivo pharmacology of synthetic olivetol-derived cannabinoid receptor ligands
Autor: M. G. Cascio, T. Bisogno, E. Palazzo, A. Thomas, M. van der Stelt, A. Brizzi, V. de Novellis, I. Marabese, R. Ross, T. van de Doelen, V. Brizzi, R. Pertwee, S. Maione, V. Di Marzo
Publikováno v: British journal of pharmacology 149 (2006): 431–440.
info:cnr-pdr/source/autori:M. G. Cascio, T. Bisogno, E. Palazzo, A. Thomas, M. van der Stelt, A. Brizzi, V. de Novellis, I. Marabese, R. Ross, T. van de Doelen, V. Brizzi, R. Pertwee, S. Maione and V. Di Marzo/titolo:In vitro and in vivo pharmacology of synthetic olivetol-derived cannabinoid receptor ligands/doi:/rivista:British journal of pharmacology/anno:2006/pagina_da:431/pagina_a:440/intervallo_pagine:431–440/volume:149
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::af0b0c8eace37cdd1519b7d689785318
http://www.cnr.it/prodotto/i/15481
Zobrazit plný text záznamu
4
New potent and selective inhibitors of anandamide re-uptake with anti-spastic activity in a mouse model of multiple sclerosis
Autor: A. Ligresti, M. G. Cascio, G. Pryce, S. Kulasegram, I. Beletskaya, L. De Petrocellis, B. Saha, A. Mahadevan, C. Visintin, J. L. Wiley, D. Baker, B. R. Martin, R. K. Razdan, V. Di Marzo
Publikováno v: British journal of pharmacology 147 (2006): 138–141.
info:cnr-pdr/source/autori:A. Ligresti, M. G. Cascio, G. Pryce, S. Kulasegram, I. Beletskaya, L. De Petrocellis, B. Saha, A. Mahadevan, C. Visintin, J. L. Wiley, D. Baker, B. R. Martin, R. K. Razdan and V. Di Marzo/titolo:New potent and selective inhibitors of anandamide re-uptake with anti-spastic activity in a mouse model of multiple sclerosis/doi:/rivista:British journal of pharmacology/anno:2006/pagina_da:138/pagina_a:141/intervallo_pagine:138–141/volume:147
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::9673fe4e78012ec65d5afcd856008c91
http://www.cnr.it/prodotto/i/15305
Zobrazit plný text záznamu
5
Analysis of behavioral and molecular changes elicited by an acute administration of SR141716 to D9-tetrahydrocannabinol-tolerant rats, an experimental model of cannabinoid abstinence
Autor: S. González, J. Fernández-Ruiz, V. Di Marzo, M. Hernández, C. Arévalo, C. Nicanor, M. G. Cascio, E. Ambrosio, J. A. Ramos
Publikováno v: 74 (2004): 159–170.
info:cnr-pdr/source/autori:S. González, J. Fernández-Ruiz, V. Di Marzo, M. Hernández, C. Arévalo, C. Nicanor, M. G. Cascio, E. Ambrosio and J. A. Ramos/titolo:Analysis of behavioral and molecular changes elicited by an acute administration of SR141716 to D9-tetrahydrocannabinol-tolerant rats, an experimental model of cannabinoid abstinence/doi:/rivista:/anno:2004/pagina_da:159/pagina_a:170/intervallo_pagine:159–170/volume:74
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::0dd56ef78eafed9f8e7aa523b0033b65
http://www.cnr.it/prodotto/i/15017
Zobrazit plný text záznamu
6
Comparative evaluation of four different infusion rates of ropivacaine (2 mg/mL) for epidural labor analgesia
Autor: M G, Cascio, R R, Gaiser, W R, Camann, P, Venkateswaran, J, Hawkins, D, McCarthy
Publikováno v: Regional anesthesia and pain medicine. 23(6)
Previous studies have reported comparable efficacy for ropivacaine and bupivacaine when used for labor analgesia at concentrations of 2.5 mg/mL. In this multicenter study, we assessed ropivacaine at the commercially available concentration of 2 mg/mL
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a02fa84bf0f0c0a351198018ba0bd6d1
https://pubmed.ncbi.nlm.nih.gov/9840848
Zobrazit plný text záznamu
7
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
9
Synthesis, cannabinoid receptor affinity, and molecular modeling studies of substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides
Autor: Maurizio Botta, Antonio Lavecchia, Maria Grazia Cascio, Romano Silvestri, Giuseppe La Regina, Serena Pasquini, Francesco Piscitelli, Antonella Brizzi, Vincenzo Di Marzo, Federico Corelli, Ettore Novellino
Publikováno v: Journal of medicinal chemistry 51 (2008): 1560–1576.
info:cnr-pdr/source/autori:Silvestri R, Cascio MG, La Regina G, Piscitelli F, Lavecchia A, Brizzi A, Pasquini S, Botta M, Novellino E, Di Marzo V, Corelli F./titolo:Synthesis, cannabinoid receptor affinity, and molecular modeling studies of substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides/doi:/rivista:Journal of medicinal chemistry/anno:2008/pagina_da:1560/pagina_a:1576/intervallo_pagine:1560–1576/volume:51
The new 1-phenyl-5-(1 H-pyrrol-1-yl)pyrazole-3-carboxamides were compared with the reference compounds AM251 and SR144528 for cannabinoid hCB 1 and hCB 2 receptor affinity. Compounds bearing 2,4-dichlorophenyl or 2,4-difluorophenyl groups at position
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc6676ed56013f75c262dac654e96cf1
https://pubmed.ncbi.nlm.nih.gov/18293908
Zobrazit plný text záznamu
10
Endocannabinoids as physiological regulators of colonic propulsion in mice
Autor: Luisa Pinto, Nicola Mascolo, Vincenzo Di Marzo, Karen Hospodar-Scott, Angelo A. Izzo, Maria Grazia Cascio, Tiziana Bisogno, David R. Brown, Francesco Capasso
Publikováno v: Gastroenterology (N.Y.N.Y., 1943) 123 (2002): 227–234.
info:cnr-pdr/source/autori:Pinto L., Izzo A., Cascio M.G., Bisogno T., Hospodar-Scott K., Brown D.R., Mascolo N., Di Marzo V., Capasso F./titolo:Endocannabinoids as physiological regulators of colonic propulsion in mice/doi:/rivista:Gastroenterology (N.Y.N.Y., 1943)/anno:2002/pagina_da:227/pagina_a:234/intervallo_pagine:227–234/volume:123
Background & Aims: Activation of enteric cannabinoid CB 1 receptors inhibits motility in the small intestine; however, it is not known whether endogenous cannabinoids (anandamide and 2-arachidonylglycerol) play a physiologic role in regulating intest
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ae18b9aaad2f8f3d430656b0539db5
https://publications.cnr.it/doc/14671
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje