Natural Cannabinoids Improve Dopamine Neurotransmission and Tau and Amyloid Pathology in a Mouse Model of Tauopathy

作者:Casarejos Maria J; Perucho Juan; Gomez Ana; Munoz Maria P; Fernandez Estevez Marian; Sagredo Onintza; Fernandez Ruiz Javier; Guzman Manuel; Garcia de Yebenes Justo; Mena Maria A*
来源:Journal of Alzheimer's Disease, 2013, 35(3): 525-539.
DOI:10.3233/JAD-130050

摘要

Cannabinoids are neuroprotective in models of neurodegenerative dementias. Their effects are mostly mediated through CB1 and CB2 receptor-dependent modulation of excitotoxicity, inflammation, oxidative stress, and other processes. We tested the effects of Sativex (R), a mixture of Delta(9)-tetrahydrocannabinol and cannabidiol, acting on both CB1 and CB2 receptors, in parkin-null, human tau overexpressing (PK-/-/Tau(VLW)) mice, a model of complex frontotemporal dementia, parkinsonism, and lower motor neuron disease. The animals received Sativex (R), 4.63 mg/kg, ip, daily, for one month, at six months of age, at the onset of the clinical symptoms. We evaluated the effects of Sativex (R) on behavior, dopamine neurotransmission, glial activation, redox state, mitochondrial activity, and deposition of abnormal proteins. PK-/-/Tau(VLW) mice developed the neurological deficits, but those treated with Sativex (R) showed less abnormal behaviors related to stress, less auto and hetero-aggression, and less stereotypy. Sativex (R) significantly reduced the intraneuronal, MAO-related free radicals produced during dopamine metabolism in the limbic system. Sativex (R) also decreased gliosis in cortex and hippocampus, increased the ratio reduced/oxidized glutathione in the limbic system, reduced the levels of iNOS, and increased those of complex IV in the cerebral cortex. With regard to tau and amyloid pathology, Sativex (R) reduced the deposition of both in the hippocampus and cerebral cortex of PK-/-/Tau(VLW) mice and increased autophagy. Sativex (R), even after a short administration in animals with present behavioral and pathological abnormalities, improves the phenotype, the oxidative stress, and the deposition of proteins in PK-/-/Tau(VLW) mice, a model of complex neurodegenerative disorders.

  • 出版日期2013