创伤与急危重病医学
創傷與急危重病醫學
창상여급위중병의학
Trauma and Critical Care Medicine
2014年
2期
85-88
,共4页
王洋%陈克研%张铁铮%刁玉刚
王洋%陳剋研%張鐵錚%刁玉剛
왕양%진극연%장철쟁%조옥강
右美托咪定%α2 受体激动药%神经保护作用%抗交感神经活性%炎性反应
右美託咪定%α2 受體激動藥%神經保護作用%抗交感神經活性%炎性反應
우미탁미정%α2 수체격동약%신경보호작용%항교감신경활성%염성반응
Dexmedetomidine%α2 adrenoreceptor agonist%neuroprotective effects%sympatholytic properties%inflammatory re-sponse
右美托咪定是一高选择性α2受体激动剂,具有镇静、镇痛、抗焦虑和抑制交感活性等作用,现作为一种崭新的麻醉辅助药应用于手术和ICU镇静。近期诸多动物试验研究发现,右美托咪定具有神经保护作用,如调节脑血流与脑氧供,这可能与抑制中枢的交感活性,降低心率、增加氧供、降低氧耗有关。此外,其通过与α2A亚型受体结合产生的神经保护作用一方面可能与降低谷氨酸对神经元细胞的兴奋性毒性有关,另一方面通过抑制儿茶酚胺释放,从而改善缺血区域的血流灌注,并在调节神经元细胞凋亡等方面产生保护作用。同时,右美托咪定可能参与了调节其它细胞功能,如减少炎性因子的释放等。总而言之,其神经保护作用的确切机制尚不十分明确,并大多限于动物试验,故将来需在临床研究中深入到分子及基因水平。
右美託咪定是一高選擇性α2受體激動劑,具有鎮靜、鎮痛、抗焦慮和抑製交感活性等作用,現作為一種嶄新的痳醉輔助藥應用于手術和ICU鎮靜。近期諸多動物試驗研究髮現,右美託咪定具有神經保護作用,如調節腦血流與腦氧供,這可能與抑製中樞的交感活性,降低心率、增加氧供、降低氧耗有關。此外,其通過與α2A亞型受體結閤產生的神經保護作用一方麵可能與降低穀氨痠對神經元細胞的興奮性毒性有關,另一方麵通過抑製兒茶酚胺釋放,從而改善缺血區域的血流灌註,併在調節神經元細胞凋亡等方麵產生保護作用。同時,右美託咪定可能參與瞭調節其它細胞功能,如減少炎性因子的釋放等。總而言之,其神經保護作用的確切機製尚不十分明確,併大多限于動物試驗,故將來需在臨床研究中深入到分子及基因水平。
우미탁미정시일고선택성α2수체격동제,구유진정、진통、항초필화억제교감활성등작용,현작위일충참신적마취보조약응용우수술화ICU진정。근기제다동물시험연구발현,우미탁미정구유신경보호작용,여조절뇌혈류여뇌양공,저가능여억제중추적교감활성,강저심솔、증가양공、강저양모유관。차외,기통과여α2A아형수체결합산생적신경보호작용일방면가능여강저곡안산대신경원세포적흥강성독성유관,령일방면통과억제인다분알석방,종이개선결혈구역적혈류관주,병재조절신경원세포조망등방면산생보호작용。동시,우미탁미정가능삼여료조절기타세포공능,여감소염성인자적석방등。총이언지,기신경보호작용적학절궤제상불십분명학,병대다한우동물시험,고장래수재림상연구중심입도분자급기인수평。
Dexmedetomidine is a highly selective α2 adrenoreceptor agonist,which exhibits a wide range of effects,including sedation,analgesia,antianxiety and sympatholytic properties.As an anaesthetic adjuvant,it is widely used in operative processes and ICU sedation.Recently,in a good deal of animal experiments,dexmedetomidine has been demonstrated that it has neuroprotective effects,such as the function of adjusting cerebral blood flow and cerebral oxygen supply.It may be relat-ed to attenuating sympathetic activation,dropping heart rate,increasing oxygen supply while decreasing the consumption,so that it can keep the myocardial oxygen balance complications.In addition,by the binding of dexmedetomidine andα2 A sub-type receptor,the neuroprotective effects might be related with receding the excitatory toxicity of glutamate.On the other hand,it can attenuate catecholamine release,improve the blood perfusion of ischemia area,and adjust the apoptosis of neu-ron cells,etc.In the mean time,dexmedetomidine may be involved in the other adjusting of cell function.In conclusion,the exact mechanisms of its neuroprotective effects are still unclear,and are confined to the animal experiments.Future clinical research need to aim at investigating the molecular and genetic mechanisms of its cardioprotective effects.