α2-Adrenergic receptors are found on large and small cerebral vessels, but their role in control of cerebral blood flow (CBF) and cerebral vascular reactivity is unclear. We assessed the effects of dexmedetomidine (DEX), a highly selective α2-adrenergic agonist, on the cerebrovascular response to hypercapnia in dogs anesthetized with either pentobarbital (PENTO) or isoflurane (ISO), drugs which produce different levels of CBF at a similar level of cerebral oxygen consumption (CMRO2). Dogs were anesthetized with either PENTO, 30 mg/kg, n = 6, or ISO 1.4% end-tidal, n = 7. CBF (radiolabeled microspheres) was determined during normocapnia and hypercapnia at baseline (pre-DEX), after DEX (10 μg/kg, intravenous bolus, plus an additional 5 μg/kg during hypercapnia), and after administration of a selective α2-adrenergic receptor antagonist (atipamezole, 500 μg/kg, intravenous bolus). In the PENTO group, CBF increased from 31 ± 3 to 137 ± 24 mL · min-1 · 100 g-1 in response to hypercapnia (PCO2 approximately 90 mm Hg) at pre-DEX and there was no change in normocapnic CBF or hypercapnic blood flow after DEX or atipamezole. In the ISO group, at pre- DEX, CBF increased from 86 ± 8 to 166 ± 19 mL · min-1 · 100 g-1 in response to hypercapnia (PCO2 approximately 90 mm Hg). DEX administration was associated with a decrease in both normocapnic (57 ± 4 mL · min-1 · 100 g-1, P <0.05) and hypercapnic (108 ± 11 mL · min-1 · 100 g-1, P <0.05) CBF without a change in vascular reactivity (pre-DEX, -0.013 ± 0.002 mm Hg · mL-1 · min-1 · 100 g-1; post-DEX, -0.016 ± 0.003 mm Hg · mL-1 · min-1 · 100 g-1; postatipamezole, -0.012 ± 0.003 mm Hg · mL-1 · min-1 · 100 g-1 per mm Hg change in PCO2). In the ISO group, atipamezole restored both normocapnic and hypercapnic flow to pre-DEX level. Pre-DEX CMRO2 was 2.7 ± 0.4 and 3.1 ± 0.6 mL · min-1 · 100 g-1 in the PENTO and ISO groups, respectively, and was not changed by hypercapnia, DEX, or atipamezole. We conclude that although DEX decreases CBF in ISO- anesthetized dogs during both normocapnia and hypercapnia, it does not alter CBF reactivity to hypercapnia.
|Original language||English (US)|
|Number of pages||7|
|Journal||Anesthesia and Analgesia|
|Publication status||Published - 1994|
ASJC Scopus subject areas
- Anesthesiology and Pain Medicine