Yamaguchi S, Midorikawa Y, Okuda Y, Kitajima T
Department of Anesthesiology, Dokkyo University School of Medicine, Mibu, Tochigi, Japan.
Can J Anaesth. 1999 Jun;46(6):593-8. doi: 10.1007/BF03013553.
This study was conducted to ascertain whether propofol may protect against delayed neuronal death in the hippocampal CA1 subfield in gerbils.
Thirty-five gerbils were randomly assigned to five groups: Group I, the control group, a sham operation treated with physiological saline solution (PSS); Group II, ischemia/reperfusion treated with PSS; Group III, ischemia/reperfusion treated with 50 mg x kg(-1) propofol; Group IV, ischemia/reperfusion treated with 100 mg x kg(-1) propofol; Group V ischemia/reperfusion treated with 150 mg x kg(-1) propofol. Transient forebrain ischemia was induced by occluding the bilateral common carotid arteries for four minutes under N2O/O2/halothane anesthesia after administration of propofol or PSS. Five days later, histopathological changes in the hippocampal CA1 subfield were examined using a light microscope and degenerative ratio of the pyramidal cells were measured according to the following formula: (number of degenerative pyramidal cell/total number of pyramidal cells per 1 mm of hippocampal CA1 subfield) x 100.
In group II, the pyramidal cells were atrophic and pycnotic; vacuolation and structural disruption of the radial striated zone was observed. In the other four groups, these changes were not observed. The degenerative ratios of pyramidal cells were as follows; group I: 5.9 +/- 1.9%, group II: 94.6 +/- 2.5% (P < 0.01), group III: 10.7 +/- 1.7%, group IV: 9.7 +/- 1.8%, group V: 9.2 +/- 1.9%.
This study suggests that propofol may prevent delayed neuronal death in the hippocampal CA1 subfield after cerebral ischemia/reperfusion in gerbils.
本研究旨在确定丙泊酚是否可预防沙鼠海马CA1亚区延迟性神经元死亡。
35只沙鼠随机分为五组:第一组为对照组,接受生理盐水(PSS)假手术治疗;第二组为缺血/再灌注组,接受PSS治疗;第三组为缺血/再灌注组,接受50mg·kg⁻¹丙泊酚治疗;第四组为缺血/再灌注组,接受100mg·kg⁻¹丙泊酚治疗;第五组为缺血/再灌注组,接受150mg·kg⁻¹丙泊酚治疗。在给予丙泊酚或PSS后,于N₂O/O₂/氟烷麻醉下阻断双侧颈总动脉4分钟诱导短暂性前脑缺血。五天后,使用光学显微镜检查海马CA1亚区的组织病理学变化,并根据以下公式测量锥体细胞的退变率:(每1mm海马CA1亚区退变锥体细胞数/锥体细胞总数)×100。
第二组中,锥体细胞萎缩、固缩;观察到放射状条纹区有空泡形成和结构破坏。在其他四组中未观察到这些变化。锥体细胞的退变率如下:第一组:5.9±1.9%,第二组:94.6±2.5%(P<0.01),第三组:10.7±1.7%,第四组:9.7±1.8%,第五组:9.2±1.9%。
本研究表明丙泊酚可能预防沙鼠脑缺血/再灌注后海马CA1亚区延迟性神经元死亡。