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

Exp Neurol. 2011 Jun;229(2):440-9. doi: 10.1016/j.expneurol.2011.03.014. Epub 2011 Mar 31.

Abstract

Several lines of evidence imply early alterations in metabolic and endocannabinoid neurotransmission in Huntington disease (HD). Using [(18)F]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 [(18)F]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 [(18)F]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.

MeSH terms

  • Analysis of Variance
  • Animals
  • Brain / diagnostic imaging
  • Brain / metabolism*
  • Brain Mapping
  • Disease Models, Animal
  • Exploratory Behavior / physiology
  • Glucose / metabolism*
  • Huntington Disease / diagnostic imaging
  • Huntington Disease / metabolism*
  • Image Processing, Computer-Assisted
  • Male
  • Maze Learning / physiology
  • Memory / physiology
  • Motor Skills / physiology
  • Neurons / diagnostic imaging
  • Neurons / metabolism*
  • Positron-Emission Tomography
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Transgenic
  • Receptor, Cannabinoid, CB1 / metabolism*
  • Statistics, Nonparametric

Substances

  • Receptor, Cannabinoid, CB1
  • Glucose