ONINTZA
SAGREDO EZQUIOGA
Profesora titular de universidad
Publicaciones (33) Publicaciones de ONINTZA SAGREDO EZQUIOGA
2023
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Disease-modifying effects of cannabidiol, β-caryophyllene and their combination in Syn1-Cre/Scn1aWT/A1783V mice, a preclinical model of Dravet syndrome
Neuropharmacology, Vol. 237
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Participación y género en las facultades de ciencias de la salud de la UCM
Miradas a la participación y al género en las aulas universitarias: una guía para docentes (Los Libros de la Catarata), pp. 104-116
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Retinal Tissue Shows Glial Changes in a Dravet Syndrome Knock-in Mouse Model
International Journal of Molecular Sciences, Vol. 24, Núm. 3
2022
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Editorial: Cannabinoids as potential treatment for neurological diseases
Frontiers in Neuroscience
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Preclinical investigation of β-caryophyllene as a therapeutic agent in an experimental murine model of Dravet syndrome
Neuropharmacology, Vol. 205
2021
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Chapter 2: Phytocannabinoids Versus Endocannabinoids. A Modern View of the Endocannabinoid System
RSC Drug Discovery Series (Royal Society of Chemistry), pp. 10-47
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Neuropathological Characterization of a Dravet Syndrome Knock-In Mouse Model Useful for Investigating Cannabinoid Treatments
Frontiers in Molecular Neuroscience, Vol. 13
2020
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Possible therapeutic applications of cannabis in the neuropsychopharmacology field
European Neuropsychopharmacology, Vol. 36, pp. 217-234
2018
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Cannabinoid signalling in the immature brain: Encephalopathies and neurodevelopmental disorders
Biochemical Pharmacology, Vol. 157, pp. 85-96
2017
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Effects of a sativex-like combination of phytocannabinoids on disease progression in R6/2 mice, an experimental model of huntington’s disease
International Journal of Molecular Sciences, Vol. 18, Núm. 4
2016
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A double-blind, randomized, cross-over, placebo-controlled, pilot trial with Sativex in Huntington’s disease
Journal of Neurology, Vol. 263, Núm. 7, pp. 1390-1400
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Analysis of endocannabinoid signaling elements and related proteins in lymphocytes of patients with Dravet syndrome
Pharmacology Research and Perspectives, Vol. 4, Núm. 2
2015
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Neuroprotective Properties of Cannabigerol in Huntington’s Disease: Studies in R6/2 Mice and 3-Nitropropionate-lesioned Mice
Neurotherapeutics, Vol. 12, Núm. 1, pp. 185-199
2014
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A restricted population of CB1 cannabinoid receptors with neuroprotective activity
Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Núm. 22, pp. 8257-8262
2013
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Cannabidiol for neurodegenerative disorders: Important new clinical applications for this phytocannabinoid?
British Journal of Clinical Pharmacology, Vol. 75, Núm. 2, pp. 323-333
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Natural cannabinoids improve dopamine neurotransmission and tau and amyloid pathology in a mouse model of tauopathy
Journal of Alzheimer's Disease, Vol. 35, Núm. 3, pp. 525-539
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The inhibition of 2-arachidonoyl-glycerol (2-AG) biosynthesis, rather than enhancing striatal damage, protects striatal neurons from malonate-induced death: A potential role of cyclooxygenase-2-dependent metabolism of 2-AG
Cell Death and Disease, Vol. 4, Núm. 10
2012
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Cannabinoids: Novel medicines for the treatment of Huntington's disease
Recent Patents on CNS Drug Discovery, Vol. 7, Núm. 1, pp. 41-48
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Sativex-like combination of phytocannabinoids is neuroprotective in malonate-lesioned rats, an inflammatory model of Huntington's disease: Role of CB1 and CB2 receptors
ACS Chemical Neuroscience
2011
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Loss of striatal type 1 cannabinoid receptors is a key pathogenic factor in Huntington's disease
Brain, Vol. 134, Núm. 1, pp. 119-136