Chen Jian-Feng, Fan Jian, Tian Xiao-Wu, Tang Tian-Si
Deptment of Orthopaedics, the First Hospital Affilited to Suzhou University, Suzhou 215006, China.
Afr J Tradit Complement Altern Med. 2011 Dec 29;9(2):234-41. doi: 10.4314/ajtcam.v9i2.8. eCollection 2012.
Neuroprotective agents are becoming significant tools in the repair of central nervous system injuries. In this study, we determined whether ginkgolides (Gin, extract of GinkgoBiloba) and Acanthopanax senticosus saponins (ASS, flavonoids extracted from Acanthopanax herbal preparations) have protective effects on rat spinal cords exposed to anoxia and we explored the mechanisms that underlie the protective effects. Spinal motor neurons (SMNs) from rat spinal cords were obtained and divided into five groups with 10 wells in each group. In control group, SMNs suffered no injury under normal oxygen; in hypoxia- inducible (HI) group, SMNs suffered injury from hypoxia; in Gin group, 37.5µg/ml Gin were used before 24 hrs of hypoxia; in ASS group, 50µg/ml ASS were used before 24 hrs of hypoxia;in glial cell-lined derived neurotrophic factor (GDNF) group, 0.1µg/ml GDNF were used before 24 hrs of hypoxia. Changes in morphology, neuron viability, and lactate dehydrogenase (LDH) release were observed. In addition, the expression of HIF-1α induced by hypoxia was measured. The neuronal viability in the Gin, ASS, and GDNF pretreated groups was higher than that in the HI group (P<0.05). The viability in the Gin group was better than that in the ASS group (P<0.05), but there was no significant difference between the ASS and GDNF groups (P>0.05). The quantity of LDH released in the three pretreated groups was lower than that in the HI group (P<0.05). The expression of HIF-1α in the HI group was greater than that in the control group (P<0.05), and the expression in the three pretreated groups was greater than that in the HI and the control groups (P<0.05). Our results indicate that Gin and ASS which was not as effective as Gin, but its effects were similar to those of GNDF could all enhance the viability of SMNs and have protective effects on hypoxic neurons.
神经保护剂正成为修复中枢神经系统损伤的重要工具。在本研究中,我们确定银杏内酯(Gin,银杏叶提取物)和刺五加皂苷(ASS,从刺五加草药制剂中提取的黄酮类化合物)对暴露于缺氧环境的大鼠脊髓是否具有保护作用,并探讨其保护作用的潜在机制。从大鼠脊髓中获取脊髓运动神经元(SMNs),并将其分为五组,每组10孔。对照组中,SMNs在正常氧气条件下未受损伤;缺氧诱导(HI)组中,SMNs因缺氧而受损;银杏内酯组在缺氧前24小时使用37.5μg/ml银杏内酯;刺五加皂苷组在缺氧前24小时使用50μg/ml刺五加皂苷;胶质细胞源性神经营养因子(GDNF)组在缺氧前24小时使用0.1μg/ml GDNF。观察形态学变化、神经元活力和乳酸脱氢酶(LDH)释放情况。此外,检测缺氧诱导的HIF-1α表达。银杏内酯、刺五加皂苷和GDNF预处理组的神经元活力高于HI组(P<0.05)。银杏内酯组的活力优于刺五加皂苷组(P<0.05),但刺五加皂苷组和GDNF组之间无显著差异(P>0.05)。三个预处理组中LDH释放量低于HI组(P<0.05)。HI组中HIF-1α的表达高于对照组(P<0.05),三个预处理组中的表达高于HI组和对照组(P<0.05)。我们的结果表明,银杏内酯和效果不如银杏内酯但作用与GDNF相似的刺五加皂苷均可提高SMNs的活力,并对缺氧神经元具有保护作用。