Summary: Previously, it has been observed that fL-opioid receptors contribute to while K-opioid receptors oppose pial artery dilation in response to hypoxia. The present study was designed to investigate the contribution of 5 1-and 52-opioid receptor activation to hypoxia-induced pial vasodilation. Newborn pigs equipped with a closed cra nial window were used to measure pial artery diameter and collect cortical periarachnoid CSF for assay of opio ids. Hypoxia increased CSF leucine enkephalin (a 5-ago nist) from 36 ± 6 to 113 ± 17 pg/ml (n = 5). Hypoxia induced pial artery vasodilation was attenuated during moderate hypoxia (Pa02 = 35 mm Hg), while this re sponse was blunted during severe hypoxia (P a02 = 25 mm Hg), by the 5 1-opioid receptor antagonist 7-benzylidenen altrexone (BNTX; 10-8 M) (23 ± 2 vs. 13 ± 2 and 34 ± 6 vs. 10 ± 3% for moderate and severe hypoxia in the absence and presence of BNTX, respectively; n = 5). In contrast, the 52-opioid receptor antagonist naltrindole (10-9 M) blunted pial vasodilation during moderate hypSeveral mechanisms have been proposed to ac count for hypoxia-induced cerebral vasodilation. These possibilities include adenosine, prostaglan dins, and nitric oxide (Winn et ai., 1981; Iwamoto et ai., 1992; Coyle et ai., 1993
539oxia, but only attenuated the vasodilator response during severe hypoxia (22 ± 2 vs. 8 ± 2 and 33 ± 4 vs. 23 ± 4% for moderate and severe hypoxia in the absence and pres ence of naltrindole, respectively; n = 5). Receptor selec tivity experiments show that BNTX blocked responses to the 5 1-agonist DPDPE, whereas responses to the 52-agonist deltorphin II were unchanged (12 ± 3 vs. 2 ± 1% and 14 ± 4 vs. 14 ± 3% for DPDPE at 10-6 M and del torphin II at 10-6 M in the absence and presence of BNTX; n = 5). Similarly, naltrindole blocked responses to deltorphin II, but responses to DPDPE were un changed. These data indicate that 5 1-receptor activation contributes to both moderate and severe hypoxia-induced vasodilation, but the 5 1-receptors appear to be more im portant during severe hypoxia relative to 52-receptors. Additionally, these data show that 52-receptors primarily contribute to dilation during moderate hypoxia.