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Sativex-like Combination of Phytocannabinoids is Neuroprotective in Malonate-Lesioned Rats, an Inflammatory Model of Huntington’s Disease: Role of CB<sub>1</sub> and CB<sub>2</sub> Receptors
27/27 checkable references clean · checked 2026-07-22
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
The 27 checked references that resolve
resolves10.1152/physrev.00041.2009
Molecular Mechanisms and Potential Therapeutical Targets in Huntington's Disease
resolves10.1093/hmg/ddq148
Huntington's disease: progress toward effective disease-modifying treatments and a cure
resolves10.1517/14728221003709792
The endocannabinoid system as a target for the treatment of neuronal damage
resolves10.1097/00001756-200410250-00015
Potential involvement of cannabinoid receptors in 3-nitropropionic acid toxicity in vivo
resolves10.1111/j.1460-9568.2007.05717.x
Cannabidiol reduced the striatal atrophy caused 3‐nitropropionic acid<i>in vivo</i>by mechanisms independent of the activation of cannabinoid, vanilloid TRPV<sub>1</sub>and adenosine A<sub>2A</sub>receptors
resolves10.1093/brain/awq278
Loss of striatal type 1 cannabinoid receptors is a key pathogenic factor in Huntington’s disease
resolves10.1093/brain/awp239
Microglial CB2 cannabinoid receptors are neuroprotective in Huntington's disease excitotoxicity
resolves10.1002/glia.20838
Cannabinoid CB<sub>2</sub>receptor agonists protect the striatum against malonate toxicity: Relevance for Huntington's disease
resolves10.1016/j.neuropharm.2006.06.013
The cannabinoid receptor agonist WIN 55,212-2 attenuates the effects induced by quinolinic acid in the rat striatum
resolves10.1016/j.neuroscience.2010.06.056
Behavioural and molecular consequences of chronic cannabinoid treatment in Huntington's disease transgenic mice
resolves10.1586/ern.11.47
THC and CBD oromucosal spray (Sativex<sup>®</sup>) in the management of spasticity associated with multiple sclerosis
resolves10.1111/j.1476-5381.2008.00048.x
Emerging strategies for exploiting cannabinoid receptor agonists as medicines
resolves10.1002/jnr.22682
Neuroprotective effects of phytocannabinoid‐based medicines in experimental models of Huntington's disease
resolves10.1093/hmg/ddq026
Full-length huntingtin levels modulate body weight by influencing insulin-like growth factor 1 expression
resolves10.1016/0091-3057(91)90386-G
Controlled clinical trial of cannabidiol in Huntington's disease
resolves10.1176/jnp.2006.18.4.553
Nabilone Could Treat Chorea and Irritability in Huntington’s Disease
resolves10.1002/mds.22809
A pilot study using nabilone for symptomatic treatment in Huntington's disease
resolves10.1002/1531-8257(199911)14:6<1038::AID-MDS1024>3.0.CO;2-7
Nabilone increases choreatic movements in Huntington's disease
resolves10.1212/WNL.0b013e3181e62076
High insulinlike growth factor I is associated with cognitive decline in Huntington disease
resolves10.1212/01.wnl.0000222734.56412.17
Microglial activation correlates with severity in Huntington disease
resolves10.1016/j.mehy.2005.08.026
A tale of two cannabinoids: The therapeutic rationale for combining tetrahydrocannabinol and cannabidiol
resolves10.1097/00001756-200305060-00007
Effects of cannabinoids in the rat model of Huntington’s disease generated by an intrastriatal injection of malonate
resolves10.1016/j.tips.2006.11.001
Cannabinoid CB2 receptor: a new target for controlling neural cell survival?
resolves10.1203/PDR.0b013e318186e5dd
Neuroprotective Effects of the Nonpsychoactive Cannabinoid Cannabidiol in Hypoxic-Ischemic Newborn Piglets
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