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Fatty acid amide hydrolase controls mouse intestinal motility in vivo

Autor: CAPASSO, RAFFAELE, BORRELLI, FRANCESCA, CAPASSO, FRANCESCO, MASCOLO, NICOLA DOMENICO, IZZO, ANGELO ANTONIO, I. MATIAS, B. LUTZ, G. MARSICANO, S. PETROSINO, K. MONORY, M. VALENTI, V. DI MARZO

Publikováno v: Gastroenterology (N.Y.N.Y., 1943) 129 (2005): 941–951.
info:cnr-pdr/source/autori:R. Capasso, I. Matias, B. Lutz, F. Borrelli, F. Capasso, G. Marsicano, N. Mascolo, S. Petrosino, K. Monory, M. Valenti, V. Di Marzo and A.A. Izzo,/titolo:Fatty acid amide hydrolase controls mouse intestinal motility in vivo/doi:/rivista:Gastroenterology (N.Y.N.Y., 1943)/anno:2005/pagina_da:941/pagina_a:951/intervallo_pagine:941–951/volume:129

BACKGROUND & AIMS: Fatty acid amide hydrolase (FAAH) catalyzes the hydrolysis both of the endocannabinoids (which are known to inhibit intestinal motility) and other bioactive amides (palmitoylethanolamide, oleamide, and oleoylethanolamide), which mi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e958b461810e33c9392531b83c5a7608
http://www.cnr.it/prodotto/i/15291

Cannabinoid CB₁ receptor in the modulation of stress coping behavior in mice: the role of serotonin and different forebrain neuronal subpopulations

Autor: M, Häring, M, Grieb, K, Monory, B, Lutz, F A, Moreira

Publikováno v: Neuropharmacology. 65

The endocannabinoid system (ECS) may either enhance or inhibit responses to aversive stimuli, possibly caused by its modulatory activity on diverse neurotransmitters. The aim of this work was to investigate the involvement of serotonin (5-HT) and cat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5dd05e80050ac834dfa8833c86efe356
https://pubmed.ncbi.nlm.nih.gov/23000076

The roles of the endogenous cannabinoid system in learning and memory in mice

Autor: Carsten T. Wotjak, Giovanni Marsicano, Kornelia Kamprath, Beat Lutz, K. Monory, Heike Hermann, A. Cannich

Publikováno v: Pharmacopsychiatry. 36

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::45710518a6b13cbeb7f10ab55f2ff21d
https://doi.org/10.1055/s-2003-825430

Specific activation of the mu opioid receptor (MOR) by endomorphin 1 and endomorphin 2

Autor: K, Monory, M C, Bourin, M, Spetea, C, Tömböly, G, Tóth, H W, Matthes, B L, Kieffer, J, Hanoune, A, Borsodi

Publikováno v: The European journal of neuroscience. 12(2)

The recently discovered endomorphin 1 (Tyr-Pro-Trp-Phe-NH2) and endomorphin 2 (Tyr-Pro-Phe-Phe-NH2) were investigated with respect to their direct receptor-binding properties, and to their ability to activate G proteins and to inhibit adenylyl cyclas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::41bc102f3e66a0660c8b1af25e1f85de
https://pubmed.ncbi.nlm.nih.gov/10712637