Fig. 7.
Coadministration of the adenosine A1 receptor agonist N6-sulfophenyl adenosine (SPA) and antagonist 1,3-dipropyl-8-cyclopentylxanthine (DPCPX) to the pontine reticular formation (A) blocked the SPA-induced decrease in acetylcholine (ACh) release, and (B) increased time to resumption of righting after isoflurane anesthesia. Data for SPA (solid bars) are from figure 6A and B (0.1 mm SPA). Asterisks indicate a significant (P < 0.05) difference from SPA.

Coadministration of the adenosine A1 receptor agonist N6-sulfophenyl adenosine (SPA) and antagonist 1,3-dipropyl-8-cyclopentylxanthine (DPCPX) to the pontine reticular formation (A) blocked the SPA-induced decrease in acetylcholine (ACh) release, and (B) increased time to resumption of righting after isoflurane anesthesia. Data for SPA (solid bars) are from figure 6A and B (0.1 mm SPA). Asterisks indicate a significant (P < 0.05) difference from SPA.

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