Dietary nitrate facilitates an acetazolamide-induced increase in cerebral blood flow during visual stimulation
Aamand R, Ho YC, Dalsgaard T, Roepstorff A, Lund TE
Journal of applied physiology (Bethesda, Md. : 1985) · 9 citations
How it was studied
- Design
- Randomized controlled trial (indexed by PubMed)
- Studied in
- People
- Main outcome
- Health markers and function
- Intake measured by
- Not stated
Who paid for it
- Funding
- Independent funding
- Government
- Ministério da Ciência, Tecnologia e Inovação
- Nonprofit
- Augustinus Fonden
- Nonprofit
- Frimodt-Heineke Fonden
Based on 3 listed funder(s).
Publication
- Published
- 2013-12-13 · J Appl Physiol (1985) · vol. 116 · issue 3 · pp. 267–273
- Publisher
- American Physiological Society
- Cited
- 14 citations · more than 78% of similar papers · 1.1× the field average
- References
- 35 works
- Access
- Paywalled
- Research areas
- Eicosanoids and Hypertension Pharmacology · Nitric Oxide and Endothelin Effects · Traumatic Brain Injury and Neurovascular Disturbances
- Keywords
- Acetazolamide, Stimulation, Cerebral blood flow, Blood flow, Nitrate, Medicine, Anesthesia, Internal medicine, Chemistry, Endocrinology
- MeSH
- humans, nitrates, nitrites, nitric oxide, acetazolamide, blood flow velocity, cross-over studies, double-blind method, photic stimulation, cerebrovascular circulation, drug synergism, adult, male, young adult
5 authors
From DK
- Rasmus Aamand · correspondingAarhus University
- Yi-Ching Lynn HoAarhus University
- Thomas DalsgaardAarhus University
- Andreas RoepstorffAarhus University
- Torben E. LundAarhus University
Abstract
The carbonic anhydrase (CA) inhibitor acetazolamide (AZ) is used routinely to estimate cerebrovascular reserve capacity in patients, as it reliably increases cerebral blood flow (CBF). However, the mechanism by which AZ accomplishes this CBF increase is not entirely understood. We recently discovered that CA can produce nitric oxide (NO) from nitrite, and that AZ enhances this NO production in vitro. In fact, this interaction between AZ and CA accounted for a large part of AZ's vasodilatory action, which fits well with the known vasodilatory potency of NO. The present study aimed to assess whether AZ acts similarly in vivo in the human cerebrovascular system. Hence, we increased or minimized the dietary intake of nitrate in 20 healthy male participants, showed them a full-field flickering dartboard, and measured their CBF response to this visual stimulus with arterial spin labeling. Doing so, we found a significant positive interaction between the dietary intake of nitrate and the CBF modulation afforded by AZ during visual stimulation. In addition, but contrary to studies conducted in elderly participants, we report no effect of nitrate intake on resting CBF in healthy human participants. The present study provides in vivo support for an enhancing effect of AZ on the NO production from nitrite catalyzed by CA in the cerebrovascular system. Furthermore, our results, in combination with the results of other groups, indicate that nitrate may have significant importance to vascular function when the cerebrovascular system is challenged by age or disease.
Abstract via Europe PMC. Copyright remains with the authors or publisher.
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