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作 者:向秋玲[1] 陈健文[2] 马仁强[2] 李靖[2] 李承[2] 朱建铭[2] 曹伟伟[2]
机构地区:[1]中山大学中山医学院,广东广州510080 [2]中山大学药学院,广东广州510080
出 处:《中山大学学报(医学科学版)》2008年第6期705-709,共5页Journal of Sun Yat-Sen University:Medical Sciences
基 金:广东省重点攻关基金(2003C30113);中山大学实验室开放基金(KF200727)
摘 要:【目的】研究三七中人参三醇皂苷(PTS)对脑缺血的保护作用。【方法】将48只SD大鼠随机分为:假手术组、大脑中动脉栓线法局灶性脑缺血(MCAO)模型组、PTS低(25mg/kg)、中(50mg/kg)、高(100mg/kg)剂量组和血栓通注射液(0.45mL/kg)组,通过行为学评分、脑含水量、脑梗塞范围和组织病理学检查等指标观察PTS对局灶性脑缺血的保护作用。同样将60只昆明小鼠随机分为:假手术组、不完全全脑缺血模型组、PTS低(25mg/kg)、中(60mg/kg)、高(120mg/kg)剂量组和血栓通注射液(0.45mL/kg)组,通过检测脑指数和脑伊文思蓝含量观察PTS对不完全全脑缺血的保护作用。【结果】对于大鼠,与模型组比较,PTS中、高剂量组均明显降低术后24h大鼠行为学评分,减轻缺血侧脑半球水肿程度(P<0.01);PTS低、中、高剂量组的缺血脑梗塞范围(19.0%±4.5%、16.4%±3.9%、16.4%±3.7%)明显低于模型组(23.5%±3.4%,P<0.05),缺血脑组织的病理改变也得到明显的改善,提示PTS对大鼠局灶性脑缺血有明显的保护作用。对于小鼠,PTS各剂量组的脑指数和脑伊文思蓝含量较模型组显著降低(P<0.05),提示PTS可通过抑制脑血管通透性的增加,从而降低脑指数,减轻脑水肿。【结论】PTS对大鼠大脑中动脉栓线法局灶性脑缺血(MCAO)损伤、小鼠不完全全脑缺血损伤均具有明显的保护作用。[Objective] To observe the anti-cerebral ischemia effects of Panaxatriol Saponins (PTS). [Methods] SD rats (n = 48) were derided into six groups: sham group, MCAO (middle cerebral artery occlusion) model group, low-dose-PTS (25mg/kg), middle-dose-PTS (50mg/kg), high-dose-PTS (100mg/kg) groups or Xueshuantong injection (0.45 mL/kg) group. We observed the anti-cerebral ischemia effects of PTS in MCAO rats through ethology scores, brain water content, cerebral infarction scope and histopathology examination. Similarly, Kunming mice (n = 60) were divided into sham group, imcompleted global brain ischemia model group, low-dose- PTS (25 mg/kg), middle-dose-PTS (50 mg/kg), high-dose-PTS (100 mg/kg) group or Xueshuantong injection (0.45 mL/kg) group. We observed the protection effects of PTS to imcompleted global brain ischemia through cerebral index and Evans blue content of brain. [Results] To the rats, ethology scores and degrees of encephaledema significantly decreased in middle-dose-PTS and high-dose-PTS group (P 〈 0.01). Cerebral infarction scopes of low- dose-PTS, middle-dose-PTS, and high-dose-PTS group (19.0% ± 4.5%, 16.4% ± 3.9%, 16.4% ± 3.7%) were signifancantly lower than the model group (23.5% ± 3.4%, P 〈 0.05). PTS improved the pathological changes of cerebral ischemia of MACO rats. To the imcompleted global brain ischemia mice, PTS reduced cerebral index by down-regulating the increase of vasopermeability (P 〈 0.05). [Conclusion] PTS have protective effects on the focal cerebral ischemia of MACO rats or incompleted global brain ischemia mice.
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