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Cerebral blood flow is regulated by changes in blood pressure and in blood viscosity alike

Stroke
|January 1, 1986
PubMed

Insights

Blood viscosity significantly impacts cerebral blood flow (CBF) when autoregulation is impaired. Changes in blood viscosity, particularly in defective autoregulation zones, necessitate compensatory vessel adjustments, suggesting a shared mechanism with pressure autoregulation.

Area of Science:

  • Neuroscience
  • Physiology
  • Cerebrovascular Research

Background:

  • Cerebral blood flow (CBF) regulation is complex, with ongoing debate on blood viscosity's role.
  • Autoregulation mechanisms normally maintain stable CBF despite pressure fluctuations.
  • The caudate nucleus and ectosylvian cortex are key areas for studying cerebrovascular dynamics.

Purpose of the Study:

  • To investigate the influence of blood viscosity on CBF in cats.
  • To determine if blood viscosity changes affect CBF differently in areas with intact versus impaired autoregulation.
  • To explore the potential link between blood viscosity autoregulation and pressure autoregulation.

Main Methods:

  • CBF was measured using microspheres in 23 cats.
  • Autoregulation was intentionally disrupted in the left caudate nucleus via microsurgical occlusion.
  • Intravenous mannitol was administered to induce changes in blood viscosity, alongside induced hypertension or hypotension.

Main Results:

  • Mannitol administration caused significant, albeit temporary, decreases in blood viscosity.
  • CBF in the left caudate nucleus (impaired autoregulation) showed greater sensitivity to viscosity and pressure changes compared to the right caudate nucleus (intact autoregulation).
  • Specific findings include: CBF decreased 18% with higher viscosity and 21% with hypotension in the left caudate; CBF increased 47% with lower viscosity and 56% with hypertension in the left caudate.

Conclusions:

  • Changes in blood viscosity necessitate compensatory adjustments in cerebral vessel diameter.
  • These viscosity-induced adjustments are impaired in brain regions with defective pressure autoregulation.
  • The study proposes 'blood viscosity autoregulation' and hypothesizes a shared regulatory mechanism with pressure autoregulation.

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