Carlo Cifani

Prof. Dr. Carlo Cifani

University of Camerino - School of Pharmacy
orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 February 2011 in Nature Neuroscience
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Journal Article
Open access
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JBJennifer M Bossert
Jennifer M Bossert
ASAnna L Stern
Anna L Stern
FTFlorence R M Theberge
Florence R M Theberge
CCCarlo Cifani
Carlo Cifani
EKEisuke Koya
Eisuke Koya
YSYavin Shaham
Yavin Shaham
Using a pharmacogenetic method of Daun02 to selectively inhibit activated neurons, Bossert et al. find that neurons in the ventral medial prefrontal cortex mediate context-induced drug relapse in a rat model of drug reinstatement. In a rat model of context-induced relapse to heroin, we identified sparsely distributed ventral medial prefrontal cortex (mPFC) neurons that were activated by the heroin-associated context. Selective pharmacogenetic inactivation of these neurons inhibited context-induced drug relapse. A small subset of ventral mPFC neurons formed neuronal ensembles that encode the learned associations between heroin reward and heroin-associated contexts; re-activation of these neuronal ensembles by drug-associated contexts during abstinence provoked drug relapse.

1 October 2017 in Neuron
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Journal Article
Closed access
MVMarco Venniro
Marco Venniro
DCDaniele Caprioli
Daniele Caprioli
MZMichelle Zhang
Michelle Zhang
LWLeslie R. Whitaker
Leslie R. Whitaker
SZShiliang Zhang
Shiliang Zhang
YSYavin Shaham
Yavin Shaham

1 November 2005 in Psychopharmacology
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Journal Article
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DEDaina Economidou
Daina Economidou
LMLaura Mattioli
Laura Mattioli
CCCarlo Cifani
Carlo Cifani
MPMarina Perfumi
Marina Perfumi
MMMaurizio Massi
Maurizio Massi
RCRoberto Ciccocioppo
Roberto Ciccocioppo

9 May 2012 in Neuropsychopharmacology
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Journal Article
Closed access
LPLaura Piccoli
Laura Piccoli
Maria Vittoria Micioni Di BonaventuraMaria Vittoria Micioni Di Bonaventura
Maria Vittoria Micioni Di Bonaventura
CCCarlo Cifani
Carlo Cifani
VCVivian J A Costantini
Vivian J A Costantini
MMMario Massagrande
Mario Massagrande
MCMauro Corsi
Mauro Corsi

12 February 2011 in Psychopharmacology
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Journal Article
Closed access
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ALA. D. Lê
A. D. Lê
DFDouglas Funk
Douglas Funk
WJWalter Juzytsch
Walter Juzytsch
KCKathleen Coen
Kathleen Coen
BNBrittany M. Navarre
Brittany M. Navarre
YSYavin Shaham
Yavin Shaham

Verified
Journal Article
Open access
PDF file
PMPhilippe A. Melas
Philippe A. Melas
MSMaria Scherma
Maria Scherma
WFWalter Fratta
Walter Fratta
CCCarlo Cifani
Carlo Cifani
PFPaola Fadda
Paola Fadda
Cannabidiol (CBD) is the most abundant non-psychoactive component of cannabis; it displays a very low affinity for cannabinoid receptors, facilitates endocannabinoid signaling by inhibiting the hydrolysis of anandamide, and stimulates both transient receptor potential vanilloid 1 and 2 and serotonin type 1A receptors. Since CBD interacts with a wide variety of molecular targets in the brain, its therapeutic potential has been investigated in a number of neuropsychiatric diseases, including anxiety and mood disorders. Specifically, CBD has received growing attention due to its anxiolytic and antidepressant properties. As a consequence, and given its safety profile, CBD is considered a promising new agent in the treatment of anxiety and mood disorders. However, the exact molecular mechanism of action of CBD still remains unknown. In the present preclinical review, we provide a summary of animal-based studies that support the use of CBD as an anxiolytic- and antidepressant-like compound. Next, we describe neuropharmacological evidence that links the molecular pharmacology of CBD to its behavioral effects. Finally, by taking into consideration the effects of CBD on DNA methylation, histone modifications, and microRNAs, we elaborate on the putative role of epigenetic mechanisms in mediating CBD’s therapeutic outcomes.