Details

Autor(en) / Beteiligte

• Casteels, C.
• Vandeputte, C.
• Rangarajan, J.R.
• Dresselaers, T.
• Riess, O.
• Bormans, G.
• Maes, F.
• Himmelreich, U.
• Nguyen, H.
• Van Laere, K.

Titel

Metabolic and Type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of Huntington disease

Ist Teil von

• Experimental neurology, 2011-06, Vol.229 (2), p.440-449

Ort / Verlag

Amsterdam: Elsevier Inc

Erscheinungsjahr

2011

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Several lines of evidence imply early alterations in metabolic and endocannabinoid neurotransmission in Huntington disease (HD). Using [ 18F]MK-9470 and small animal PET, we investigated for the first time cerebral changes in type 1 cannabinoid (CB1) receptor binding in vivo in pre-symptomatic and early symptomatic rats of HD (tgHD), in relation to glucose metabolism, morphology and behavioral testing for motor and cognitive function. Twenty-three Sprague–Dawley rats (14 tgHD and 9 wild-types) were investigated between the age of 2 and 11 months. Relative glucose metabolism and parametric CB1 receptor images were anatomically standardized to Paxinos space and analyzed voxel-wise. Volumetric microMRI imaging was performed to assess HD neuropathology. Within the first 10 months, bilateral volumes of caudate–putamen and lateral ventricles did not significantly differ between genotypes. Longitudinal- and genotype evolution showed that relative [ 18F]MK-9470 binding progressively decreased in the caudate–putamen and lateral globus pallidus of tgHD rats (− 8.3%, p ≤ 1.1 × 10 − 5 at 5 months vs. − 10.9%, p < 1.5 × 10 − 5 at 10 months). In addition, relative glucose metabolism increased in the bilateral sensorimotor cortex of 2-month-old tgHD rats (+ 8.1%, p ≤ 1.5 × 10 − 5 ), where it was positively correlated to motor function at that time point. TgHD rats developed cognitive deficits at 6 and 11 months of age. Our findings point to early regional dysfunctions in endocannabinoid signalling, involving the lateral globus pallidus and caudate–putamen. In vivo CB1 receptor measurements using [ 18F]MK-9470 may thus be a useful early biomarker for HD. Our results also provide evidence of subtle motor and cognitive deficits at earlier stages than previously described. ►We characterized brain CB1 receptor alterations in Huntington disease in vivo. ►Transgenic rats were investigated in pre-symptomatic and early symptomatic phase. ►CB1 receptor binding decreased in basal ganglia areas upon disease progression. ►We suggest that [ 18F]MK-9470 may be useful as early biomarker of HD.