PERTUSSIS TOXIN AND 4-AMINOPYRIDINE DIFFERENTIALLY AFFECT THE HYPNOTIC ANESTHETIC ACTION OF DEXMEDETOMIDINE AND PENTOBARBITAL

被引:38
作者
DOZE, VA [1 ]
CHEN, BX [1 ]
TINKLENBERG, JA [1 ]
SEGAL, IS [1 ]
MAZE, M [1 ]
机构
[1] STANFORD UNIV,MED CTR,SCH MED,DEPT ANESTHESIA,STANFORD,CA 94305
关键词
anesthetics; hypnotics:; pentobarbital; G-proteins: pertussis toxin; potassium channels: 4-aminopyridine; receptors; adrenergic:; α[!sub]2[!/sub; sympathetic nervous system; α[!sub]2[!/sub]-adrenoceptor agonist: dexmedetomidine;
D O I
10.1097/00000542-199008000-00019
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Dexmedetomidine, a highly selective and potent agonist at alpha-2 adrenoceptors, produces a hypnotic-anesthetic action in rats. The mechanism for this response may involve an inhibitory G-protein and increased conductance through a potassium channel. To investigate this, the efects of pertussis toxin, a specific inactivator of inhibitory G-proteins, and 4-aminopyridine, a blocker of potassium channels, on the hypnotic-anesthetic response to dexmedetomidine were studied in rats. Pertussis toxin and 4-aminopyridine both decreased the hypnotic-anesthetic action of dexmedetomidine in a dose-dependent fashion. To preclude the possibility that pertussis toxin and 4-aminopyridine attenuated the hypnotic-anesthetic action of dexmedetomidine via indirect central nervous system excitation, the effects of pertussis toxin and 4-aminopyridine on the hypnotic-anesthetic action of pentobarbital also were assessed. Pentobarbital-induced hypnosis was not attenuated by either treatment. These results suggest that the receptor-effector mechanism for the hypnotic-anesthetic action of dexmedetomidine involves an inhibitory G-protein and increased conductance through a potassium channel.
引用
收藏
页码:304 / 307
页数:4
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