Oxygen delivery at high blood viscosity and decreased arterial oxygen content to brains of conscious rats

Am J Physiol Heart Circ Physiol. 2001 Jun;280(6):H2591-7. doi: 10.1152/ajpheart.2001.280.6.H2591.

Abstract

We addressed the question to which extent cerebral blood flow (CBF) is maintained when, in addition to a high blood viscosity (Bvis) arterial oxygen content (CaO2) is gradually decreased. CaO2) was decreased by hemodilution to hematocrits (Hct) of 30, 22, 19, and 15% in two groups. One group received blood replacement (BR) only and served as the control. The second group received an additional high viscosity solution of polyvinylpyrrolidone (BR/PVP). Bvis was reduced in the BR group and was doubled in the BR/PVP. Despite different Bvis, CBF did not differ between BR and BR/PVP rats at Hct values of 30 and 22%, indicating a complete vascular compensation of the increased Bvis at decreased CaO2. At an Hct of 19%, local cerebral blood flow (LCBF) in some brain structures was lower in BR/PVP rats than in BR rats. At the lowest Hct of 15%, LCBF of 15 brain structures and mean CBF were reduced in BR/PVP. The resulting decrease in cerebral oxygen delivery in the BR/PVP group indicates a global loss of vascular compensation. We concluded that vasodilating mechanisms compensated for Bvis increases thereby maintaining constant cerebral oxygen delivery. Compensatory mechanisms were exhausted at a Hct of 19% and lower as indicated by the reduction of CBF and cerebral oxygen delivery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antipyrine / analogs & derivatives*
  • Biological Transport / drug effects
  • Biological Transport / physiology
  • Blood Flow Velocity / drug effects
  • Blood Flow Velocity / physiology
  • Blood Viscosity / drug effects
  • Blood Viscosity / physiology*
  • Brain / blood supply*
  • Brain / drug effects
  • Brain / metabolism*
  • Cerebral Arteries / metabolism*
  • Cerebrovascular Circulation / drug effects
  • Cerebrovascular Circulation / physiology
  • Hematocrit
  • Male
  • Oxygen / metabolism*
  • Povidone / analogs & derivatives*
  • Povidone / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Vasodilation / drug effects
  • Vasodilation / physiology
  • Wakefulness

Substances

  • polyvinylpolypyrrolidone
  • Povidone
  • Oxygen
  • Antipyrine
  • iodoantipyrine