Early effects of high-fat diet on neurovascular function and focal ischemic brain injury

Author:

Li Weiguo12,Prakash Roshini13,Chawla Dhruv2,Du Wenting2,Didion Sean P.4,Filosa Jessica A.2,Zhang Quanguang5,Brann Darrell W.5,Lima Victor V.26,Tostes Rita C.26,Ergul Adviye123

Affiliation:

1. Charlie Norwood Department of Veterans Affairs Medical Center, Augusta, Georgia;

2. Department of Physiology, Medical College of Georgia, Georgia Regents University, Augusta, Georgia;

3. Program in Clinical and Experimental Therapeutics, Department of Clinical and Administrative Pharmacy, College of Pharmacy, University of Georgia, Augusta, Georgia; and

4. Vascular Biology Center, Medical College of Georgia, Georgia Regents University, Augusta, Georgia;

5. Institute of Molecular Medicine and Genetics, Medical College of Georgia, Georgia Regents University, Augusta, Georgia;

6. Department of Pharmacology, School of Medicine of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil

Abstract

Obesity is a risk factor for stroke, but the early effects of high-fat diet (HFD) on neurovascular function and ischemic stroke outcomes remain unclear. The goal of this study was to test the hypotheses that HFD beginning early in life 1) impairs neurovascular coupling, 2) causes cerebrovascular dysfunction, and 3) worsens short-term outcomes after cerebral ischemia. Functional hyperemia and parenchymal arteriole (PA) reactivity were measured in rats after 8 wk of HFD. The effect of HFD on basilar artery function after middle cerebral artery occlusion (MCAO) and associated O-GlcNAcylation were assessed. Neuronal cell death, infarct size, hemorrhagic transformation (HT) frequency/severity, and neurological deficit were evaluated after global ischemia and transient MCAO. HFD caused a 10% increase in body weight and doubled adiposity without a change in lipid profile, blood glucose, and blood pressure. Functional hyperemia and PA relaxation were decreased with HFD. Basilar arteries from stroked HFD rats were more sensitive to contractile factors, and acetylcholine-mediated relaxation was impaired. Vascular O-GlcNAcylated protein content was increased with HFD. This group also showed greater mortality rate, infarct volume, HT occurrence rate, and HT severity and poor functional outcome compared with the control diet group. These results indicate that HFD negatively affects neurovascular coupling and cerebrovascular function even in the absence of dyslipidemia. These early cerebrovascular changes may be the cause of greater cerebral injury and poor outcomes of stroke in these animals.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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