Executive dysfunction and blockage of brain microvessels in a rat model of vascular cognitive impairment

Author:

Langdon Kristopher D12,Cordova Chris A1,Granter-Button Shirley1,Boyd Jamie D3,Peeling James45,Murphy Timothy H3678,Corbett Dale16910

Affiliation:

1. BioMedical Sciences, Memorial University, St. John’s, NL, Canada

2. Department of Pathology and Laboratory Medicine, Western University, London, ON, Canada

3. Department of Psychiatry, Brain Research Centre, University of British Columbia, Vancouver, BC, Canada

4. Department of Radiology, University of Manitoba, Winnipeg, MB, Canada

5. Department of Chemistry, University of Winnipeg, Winnipeg, MB, Canada

6. Canadian Partnership for Stroke Recovery, Ottawa, ON, Canada

7. Kinsmen Laboratory, Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada

8. Department of Cellular & Physiological Sciences, University of British Columbia, Vancouver, BC, Canada

9. Department of Cellular & Molecular Medicine, University of Ottawa, Ottawa, ON, Canada

10. Department of Medicine, University of Toronto, Toronto, ON, Canada

Abstract

Most research focuses on overt stroke caused by blockage of major blood vessels. Less attention has been paid to small vessel disease which gives rise to covert stroke that often leads to vascular cognitive impairment (VCI). One reason for this may be the relative lack of relevant animal models. Herein, we describe, a model of VCI induced in middle-aged Sprague-Dawley rats exposed to a diet high in saturated fats, salt and refined sugar (HFSS). In Experiment 1, rats were fed HFSS and subjected to a small mediodorsal (MD) thalamic stroke with or without concomitant permanent bilateral carotid artery occlusion. MD lesions produce significant executive dysfunction in an attention set-shift task ( p = 0.012). In Experiment 2, rats were exposed to either HFSS or control diet and functional effects assessed. We found significant hypertension ( p = 0.013), blockage of brain microvessels ( p = 0.018) and white matter atrophy ( p = 0.039) in HFSS diet animals. As in Experiment 1, profound, specific set-shifting executive dysfunction was noted ( p = 0.003) following both small MD infarcts (0.332 mm3) and the HFSS diet. In summary, these data describe a middle-aged animal model of VCI that includes clinically relevant metabolic disturbances and small vessel disease and as such may be helpful in developing new cognitive therapies.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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