国际麻醉学与复苏杂志
國際痳醉學與複囌雜誌
국제마취학여복소잡지
INTERNATIONAL JOURNAL OF ANESTHESIOLOGY AND RESUSCITATION
2015年
5期
463-466
,共4页
分子靶点%受体%γ-氨基丁酸%甘氨酸%乙酰胆碱%谷氨酸%钾通道%钠通道
分子靶點%受體%γ-氨基丁痠%甘氨痠%乙酰膽堿%穀氨痠%鉀通道%鈉通道
분자파점%수체%γ-안기정산%감안산%을선담감%곡안산%갑통도%납통도
Molecular targets%Receptor%γ-aminobutyric acid%Glycine%Acetylcholine%Glutamate%Potassium channels%Sodium channels
背景 全身麻醉药物通过增强抑制性神经传递和减弱兴奋性神经传递在中枢神经系统中发挥作用.兴奋性神经递质如谷氨酸和乙酰胆碱(acetylcholine,ACh)引起去极化,而抑制性神经递质如γ-氨基丁酸(γ-aminobutyric acid,GABA)和甘氨酸通过超极化或分流兴奋性电流来降低突触后活性.目的 探讨药物分子靶点在全身麻醉中的作用机制.内容 就全身麻醉药物主要分子靶点作简要介绍.趋向 针对麻醉药物分子靶点对全身麻醉的促进作用所进行的研究可能有助于研发出更有效且更安全的麻醉药.
揹景 全身痳醉藥物通過增彊抑製性神經傳遞和減弱興奮性神經傳遞在中樞神經繫統中髮揮作用.興奮性神經遞質如穀氨痠和乙酰膽堿(acetylcholine,ACh)引起去極化,而抑製性神經遞質如γ-氨基丁痠(γ-aminobutyric acid,GABA)和甘氨痠通過超極化或分流興奮性電流來降低突觸後活性.目的 探討藥物分子靶點在全身痳醉中的作用機製.內容 就全身痳醉藥物主要分子靶點作簡要介紹.趨嚮 針對痳醉藥物分子靶點對全身痳醉的促進作用所進行的研究可能有助于研髮齣更有效且更安全的痳醉藥.
배경 전신마취약물통과증강억제성신경전체화감약흥강성신경전체재중추신경계통중발휘작용.흥강성신경체질여곡안산화을선담감(acetylcholine,ACh)인기거겁화,이억제성신경체질여γ-안기정산(γ-aminobutyric acid,GABA)화감안산통과초겁화혹분류흥강성전류래강저돌촉후활성.목적 탐토약물분자파점재전신마취중적작용궤제.내용 취전신마취약물주요분자파점작간요개소.추향 침대마취약물분자파점대전신마취적촉진작용소진행적연구가능유조우연발출경유효차경안전적마취약.
Background General anesthetics produce widespread depression in the central nervous system by enhancing inhibitory neurotransmission and reducing excitatory neurotransmission.Excitatory neurotransmitters induce depolarization,such as glutamate and acetylcholine(ACh).Whereas inhibitory neurotransmitters reduce postsynaptic activity by hyperpolarization or shunting excitatory currents,such as γ-aminobutyric acid(GABA) and glycine.Objective To investigate the mechanisms of drug molecular targets in general anesthesia.Content In this review,we briefly introduce the research progress of drug molecular targets of general anesthesia.Trend Studies on the contributions of anesthetic targets to general anesthesia may facilitate the development of more effective and safer anesthetics.