4.3 Article

Plasma brain-derived neurotrophic factor and dynamic cerebral autoregulation in acute response to glycemic control following breakfast in young men

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00059.2020

Keywords

cerebral circulation; glucose; insulin; neurotrophin; transfer function analysis

Categories

Funding

  1. Japanese Ministry of Education, Culture, Sports, Science, and Technology [17H07244, 18H03200]
  2. Japan Society for the Promotion of Science [201960215]
  3. Royal Society Wolfson Research Fellowship [WM170007]
  4. Royal Society International Exchanges Award [IES\R2\192137]
  5. Japan Society for the Promotion of Science Research Fellowship [JSPS/OF317]
  6. Grants-in-Aid for Scientific Research [17H07244, 18H03200] Funding Source: KAKEN

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The study found that breakfast consumption enhanced dynamic cerebral autoregulation in the low frequency range, but a high glycemic index breakfast reduced the brain's ability to regulate blood flow against slow changes in blood pressure. Therefore, breakfast and glycemic control may be important strategies for optimizing cerebrovascular health.
We examined the acute impact of both lowand high-glycemic index (GI) breakfasts on plasma brain-derived neurotrophic factor (BDNF) and dynamic cerebral autoregulation (dCA) compared with breakfast omission. Ten healthy men (age 24 +/- 1 yr) performed three trials in a randomized crossover order; omission and Low-GI (GI = 40) and High-GI (GI = 71) breakfast conditions. Middle cerebral artery velocity (transcranial Doppler ultrasonography) and arterial pressure (finger photoplethysmography) were continuously measured for 5 min before and 120 min following breakfast consumption to determine dCA using transfer function analysis. After these measurements of dCA, venous blood samples for the assessment of plasma BDNF were obtained. Moreover, blood glucose was measured before breakfast and every 30 min thereafter. The area under the curve of 2 h postprandial blood glucose in the High-GI trial was higher than the Low-GI trial (P < 0.01). The GI of the breakfast did not affect BDNF. In addition, both very-low (VLF) and low-frequency (LF) transfer function phase or gains were not changed during the omission trial. In contrast, LF gain (High-GI P < 0.05) and normalized gain (Low-GI P < 0.05) were decreased by both GI trials, while a decrease in VLF phase was observed in only the High-GI trial (P < 0.05). These findings indicate that breakfast consumption augmented dCA in the LF range but High-GI breakfast attenuated cerebral blood flow regulation against slow change (i.e., the VLF range) in arterial pressure. Thus we propose that breakfast and glycemic control may be an important strategy to optimize cerebrovascular health.

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