Effect of long-term antihypertensive treatment on cerebrovascular structure and function in hypertensive rats

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作者
Daphne M. P. Naessens
Judith de Vos
Edo Richard
Micha M. M. Wilhelmus
Cornelis A. M. Jongenelen
Edwin R. Scholl
Nicole N. van der Wel
Johannes A. Heijst
Charlotte E. Teunissen
Gustav J. Strijkers
Bram F. Coolen
Ed VanBavel
Erik N. T. P. Bakker
机构
[1] Biomedical Engineering and Physics,Amsterdam UMC Location University of Amsterdam
[2] Microcirculation,Amsterdam Cardiovascular Sciences
[3] Neurovascular Disorders,Amsterdam Neuroscience
[4] Public and Occupational Health,Amsterdam UMC Location University of Amsterdam
[5] Radboud University Medical Center,Department of Neurology, Donders Institute for Brain, Cognition and Behaviour
[6] Anatomy and Neurosciences,Amsterdam UMC Location Vrije Universiteit Amsterdam
[7] Neurodegeneration,Amsterdam Neuroscience
[8] Medical Biology,Amsterdam UMC Location University of Amsterdam
[9] Electron Microscopy Center Amsterdam,Amsterdam UMC Location Vrije Universiteit Amsterdam
[10] Neurochemistry Laboratory,Amsterdam Neuroscience
[11] Clinical Chemistry,undefined
[12] Neuroinfection and -Inflammation,undefined
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Midlife hypertension is an important risk factor for cognitive impairment and dementia, including Alzheimer’s disease. We investigated the effects of long-term treatment with two classes of antihypertensive drugs to determine whether diverging mechanisms of blood pressure lowering impact the brain differently. Spontaneously hypertensive rats (SHR) were either left untreated or treated with a calcium channel blocker (amlodipine) or beta blocker (atenolol) until one year of age. The normotensive Wistar Kyoto rat (WKY) was used as a reference group. Both drugs lowered blood pressure equally, while only atenolol decreased heart rate. Cerebrovascular resistance was increased in SHR, which was prevented by amlodipine but not atenolol. SHR showed a larger carotid artery diameter with impaired pulsatility, which was prevented by atenolol. Cerebral arteries demonstrated inward remodelling, stiffening and endothelial dysfunction in SHR. Both treatments similarly improved these parameters. MRI revealed that SHR have smaller brains with enlarged ventricles. In addition, neurofilament light levels were increased in cerebrospinal fluid of SHR. However, neither treatment affected these parameters. In conclusion, amlodipine and atenolol both lower blood pressure, but elicit a different hemodynamic profile. Both medications improve cerebral artery structure and function, but neither drug prevented indices of brain damage in this model of hypertension.
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