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Belen Ferrer

Researcher at Complutense University of Madrid

Publications -  11
Citations -  1141

Belen Ferrer is an academic researcher from Complutense University of Madrid. The author has contributed to research in topics: Cannabinoid & Dopamine receptor. The author has an hindex of 9, co-authored 11 publications receiving 1096 citations. Previous affiliations of Belen Ferrer include University of California, Irvine.

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Journal ArticleDOI

A Peripheral Mechanism for CB1 Cannabinoid Receptor-Dependent Modulation of Feeding

TL;DR: An unexpected role for peripheral CB1 receptors in the regulation of feeding is revealed and Capsaicin deafferentation abolished the peripheral effects of both cannabinoid agonists and antagonists, suggesting that these agents modulate food intake by acting onCB1 receptors located on capsaicin-sensitive sensory terminals.
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Effects of levodopa on endocannabinoid levels in rat basal ganglia: implications for the treatment of levodopa‐induced dyskinesias

TL;DR: A deficiency in endocannabinoid transmission may contribute to levodopa‐induced dyskinesias and that these complications may be alleviated by activation of CB1 receptors.
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Expression and function of CB1 receptor in the rat striatum: Localization and effects on D1 and D2 dopamine receptor-mediated motor behaviors

TL;DR: This study indicates that the endocannabinoid system is a relevant negative modulator of both dopamine D1 and D2 receptor-mediated behaviors, a finding that may contribute to the understanding of basal ganglia motor disorders.
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Regulation of brain anandamide by acute administration of ethanol.

TL;DR: The results suggest that receptor-mediated release of acylethanolamide is inhibited by the acute administration of ethanol, and that this effect is not derived from increased fatty acid ethanolamide degradation.
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Cannabinoid CB1 antagonists possess antiparkinsonian efficacy only in rats with very severe nigral lesion in experimental parkinsonism.

TL;DR: The results suggest that CB1 receptor antagonists that lack psychoactive effects might be of therapeutic value in the control of very advanced stage of Parkinson's disease in humans.