We. Johnston et al., PHENYLEPHRINE DOES NOT REDUCE CEREBRAL PERFUSION DURING CANINE CARDIOPULMONARY BYPASS, Anesthesia and analgesia, 79(1), 1994, pp. 14-18
Gaseous microemboli during cardiopulmonary bypass (CPB) could injure t
he blood-brain barrier so that cerebral vasoconstriction would result
from infusing alpha-agonist drugs, such as phenylephrine. Cerebral blo
od flow (radioactive microspheres) and metabolism were measured in sev
en dogs after rewarming from 150 min hypothermic CPB with bubble oxyge
nators used to produce gaseous microemboli. Phenylephrine (40 mu g/min
) was infused directly into the brachiocephalic artery so that aortic
pressure before (80 +/- 2 mm Hg) and during (79 +/- 3 mm Hg) the infus
ion did not change. Neither blood flow to the cerebral hemispheres (P
= 0.960), cerebellum (P = 0.854), and brainstem (P = 0.694) nor the ce
rebral metabolic rate for oxygen (P = 0.862) differed when values obta
ined before and after 30 min of phenylephrine infusion were compared.
Cerebral vascular resistance was also unchanged by phenylephrine, bein
g 1.22 +/- 0.10 mm Hg . mL(-1) . min(-1) . 100 g(-1) before infusion a
nd 1.25 +/- 0.17 mm Hg . mL(-1) . min(-1) . 100 g(-1) during infusion
(P = 0.849). Phenylephrine does not cause cerebral vasoconstriction af
ter rewarming from hypothermic CPB, a finding which suggests that the
blood-brain barrier is preserved during bypass.