4.5 Article

Prior head-down tilt does not impair the cerebrovascular response to head-up tilt

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 118, Issue 11, Pages 1356-1363

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00871.2014

Keywords

push-pull effect; transcranial Doppler ultrasound; cerebrovascular autoregulation

Funding

  1. Defense Medical Fund of China [CWS11J146]
  2. Military Science Foundation of China [13QNP126]
  3. Natural Sciences and Engineering Research Council [RGPIN-6473]

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The hypothesis that cerebrovascular autoregulation was not impaired during head-up tilt (HUT) that followed brief exposures to varying degrees of prior head-down tilt (HDT) was tested in 10 healthy young men and women. Cerebral mean flow velocity (MFV) and cardiovascular responses were measured in transitions to a 60-s period of 75 degrees HUT that followed supine rest (control) or 15 s HDT at -10 degrees, -25 degrees, and -55 degrees. During HDT, heart rate (HR) was reduced for -25 degrees and -55 degrees, and cardiac output was lower at -55 degrees HDT. MFV increased during -10 degrees HDT, but not in the other conditions even though blood pressure at the middle cerebral artery (BPMCA) increased. On the transition to HUT, HR increased only for -55 degrees condition, but stroke volume and cardiac output transiently increased for -25 degrees and -55 degrees. Total peripheral resistance index decreased in proportion to the magnitude of HDT and recovered over the first 20 s of HUT. MFV was significantly less in all HDT conditions compared with the control in the first 5-s period of HUT, but it recovered quickly. An autoregulation correction index derived from MFV recovery relative to BPMCA decline revealed a delay in the first 5 s for prior HDT compared with control but then a rapid increase to briefly exceed control after -55 degrees HDT. This study showed that cerebrovascular autoregulation is modified by but not impaired by brief HDT prior to HUT and that cerebral MFV recovered quickly and more rapidly than arterial blood pressure to protect against cerebral hypoperfusion and potential syncope.

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