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Telmisartan prevents high-fat diet-induced neurovascular impairments and reduces anxiety-like behavior

Gianna Huber, Mikolaj Ogrodnik, Jan Wenzel, Ines Stölting, Lukas Huber, Olga Will, Eva Peschke, Urte Matschl, Jan Bernd Hövener, Markus Schwaninger, Diana Jurk, Walter Raasch*

*Corresponding author for this work

Abstract

Angiotensin II receptor blockers (telmisartan) prevent rodents from diet-induced obesity and improve their metabolic status. Hyperglycemia and obesity are associated with reduced cerebral blood flow and neurovascular uncoupling which may lead to behavioral deficits. We wanted to know whether a treatment with telmisartan prevents these changes in obesity. We put young mice on high-fat diet and simultaneously treated them with telmisartan. At the end of treatment, we performed laser speckle imaging and magnetic resonance imaging to assess the effect on neurovascular coupling and cerebral blood flow. Different behavioral tests were used to investigate cognitive function. Mice developed diet-induced obesity and after 16, not 8 weeks of high-fat diet, however, the response to whisker pad stimulation was about 30% lower in obese compared to lean mice. Simultaneous telmisartan treatment increased the response again by 10% compared to obese mice. Moreover, telmisartan treatment normalized high-fat diet-induced reduction of cerebral blood flow and prevented a diet-induced anxiety-like behavior. In addition to that, telmisartan affects cellular senescence and string vessel formation in obesity. We conclude, that telmisartan protects against neurovascular unit impairments in a diet-induced obesity setting and may play a role in preventing obesity related cognitive deficits in Alzheimer’s disease.

Original languageEnglish
JournalJournal of Cerebral Blood Flow and Metabolism
Volume41
Issue number9
Pages (from-to)2356-2369
Number of pages14
ISSN0271-678X
DOIs
Publication statusPublished - 09.2021

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by research grants from the German Research Foundation to the GRK 1957 “Adipocyte-Brain Crosstalk”, University of Lübeck and GRK 2154 “Materials for Brain”, University of Kiel, a grant of the German Centre for Cardiovascular Research (DZHK) and by the Cluster of Excellence PMI 1267. Acknowledgments

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Areas and Centers

  • Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)

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