Fig. 5. Concentration-dependent effect of halothane, sevoflurane, and isoflurane on acetylcholine (ACh)–promoted exchange of the radioactive, nonhydrolyzable form of guanosine-5′-triphosphate (GTP), [35S]GTPγS, for guanosine-5′-diphosphate (GDP) ([35S]GTPγS–GDP exchange) at the α subunit of the Gqheterotrimeric G protein (Gαq). Assays were performed using crude membranes prepared from COS-7 cells expressing the human M3muscarinic receptor and human Gαq. The ACh-promoted increase in Gαq[35S]GTPγS–GDP exchange was expressed as the percentage of the difference between the values measured in the absence of acetylcholine or halothane, and the values measured in the presence of ACh (% ACh-promoted). The  dashed lines identify the values measured at anesthetic concentrations equivalent to 2 minimum alveolar concentration. Data are mean ± SD; n = 9. 

Fig. 5. Concentration-dependent effect of halothane, sevoflurane, and isoflurane on acetylcholine (ACh)–promoted exchange of the radioactive, nonhydrolyzable form of guanosine-5′-triphosphate (GTP), [35S]GTPγS, for guanosine-5′-diphosphate (GDP) ([35S]GTPγS–GDP exchange) at the α subunit of the Gqheterotrimeric G protein (Gαq). Assays were performed using crude membranes prepared from COS-7 cells expressing the human M3muscarinic receptor and human Gαq. The ACh-promoted increase in Gαq[35S]GTPγS–GDP exchange was expressed as the percentage of the difference between the values measured in the absence of acetylcholine or halothane, and the values measured in the presence of ACh (% ACh-promoted). The  dashed lines identify the values measured at anesthetic concentrations equivalent to 2 minimum alveolar concentration. Data are mean ± SD; n = 9. 

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