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纸质出版日期:2017
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刘杨, 高玉亭, 苗宇船. 丹参注射液对大鼠脊髓损伤后Olig-2和OX-42表达的影响[J]. 中国实验方剂学杂志, 2017,23(20):102-107.
LIU Yang, GAO Yu-ting, MIAO Yu-chuan. Effect of Danshen Injection on Expression of Oligodendrocyte Lineage Transcription Factor-2 and OX-42 in Rats After Spinal Cord Injury[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(20): 102-107.
刘杨, 高玉亭, 苗宇船. 丹参注射液对大鼠脊髓损伤后Olig-2和OX-42表达的影响[J]. 中国实验方剂学杂志, 2017,23(20):102-107. DOI: 10.13422/j.cnki.syfjx.2017200102.
LIU Yang, GAO Yu-ting, MIAO Yu-chuan. Effect of Danshen Injection on Expression of Oligodendrocyte Lineage Transcription Factor-2 and OX-42 in Rats After Spinal Cord Injury[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(20): 102-107. DOI: 10.13422/j.cnki.syfjx.2017200102.
目的: 通过检测丹参注射液对大鼠脊髓损伤(SCI)后少突胶质细胞(Olig-2)和Ⅲ型补体受体(OX-42)系转录因子-2表达的影响,探讨其促进脊髓神经功能恢复的机制。方法: SPF大鼠50只随机分为正常组、模型组、丹参治疗组、丹参加雷帕霉素组和甲泼尼龙琥珀酸钠组(n=10)。采用Allen's法建立SCI模型(正常组除外)后,模型组:腹腔注射生理盐水(1 mL ·kg-1),1次/d;丹参治疗组:腹腔注射丹参注射液(1 mL ·kg-1),1次/d;丹参加雷帕霉素组:腹腔注射同等剂量丹参注射液(含雷帕霉素 3 mg ·kg-1),1次/d;甲泼尼龙琥珀酸钠组:尾静脉推注甲泼尼龙琥珀酸钠(30 mg ·kg-1),1次/d。伤后1,3,7,14 d时采用联合行为评分法(CBS)评价大鼠脊髓神经功能恢复情况。伤后14 d处死动物,采用免疫荧光和蛋白免疫印迹法(Western blot)检测各组大鼠脊髓内Olig-2和OX-42的表达。结果: 至伤后14 d时,与模型组、丹参加雷帕霉素组比较,丹参治疗组和甲泼尼龙琥珀酸钠组大鼠CBS评分显著降低(P<0.05);与正常组比较,模型组大鼠Olig-2表达(免疫阳性细胞数及蛋白相对表达量)降低,而OX-42表达升高(P<0.05);与模型组比较,丹参治疗组和甲泼尼龙琥珀酸钠组Olig-2表达升高,而OX-42表达降低(P<0.05);与丹参治疗组和甲泼尼龙琥珀酸钠组比较,丹参加雷帕霉素组大鼠Olig-2表达降低,而OX-42表达升高(P<0.05);上述指标在丹参治疗组和甲泼尼龙琥珀酸钠组之间的差异不具有统计学意义。结论: 丹参注射液可通过升高磷脂酰肌醇3-激酶(PI3K)/蛋白激酶B(Akt)/mTOR信号转导通路的活性以调节Olig-2和OX-42的表达,从而表明其参与大鼠脊髓神经功能恢复的机制可能与通过参与少突胶质细胞和小胶质细胞增殖有关。
Objective: To observe the effect of Danshen injection on expression of oligodendrocyte lineage transcription factor-2 (Olig-2) and OX-42 (markers of proliferation of oligodendrocyte and microglia) in rats after spinal cord injury (SCI)
in order to explore its mechanism of promoting spinal cord functional recovery. Method: Fifty SPF SD rats were randomly divided into five groups (n=10)
namely normal control group
model group
Danshen injection treatment group
Danshen injection+rapamycin group and methylprednisolone sodium group.All of the rats
except for normal control group
were included in the weight-drop SCI model by the Allens' method.Then
normal saline (1 mL · kg-1)
Danshen injection (1 mL · kg-1) and Danshen injection (1 mL · kg-1
containing rapamycin 3 mg · kg-1) were intraperitoneally injected into model group
Danshen injection treatment group and Danshen injection+rapamycin group rats once a day
respectively
and methylprednisolone sodium solution (30 g · L-1) was injected into the methylprednisolone sodium group rats through tail vein at the dosage of 1 mL · kg-1 once a day.The rats in normal control group were fed with routine foods
with no injection.The combine behavioral score (CBS) of rats in all group were detected on 1
3
7
14 d after SCI.All of these rats were put to death on 14 d after SCI
and the expressions of Olig-2 and OX-42 were detected with immunofluorescence staining and Western blot technique. Result: Compared with the model group and the Danshen injection+rapamycin group
CBS significantly declined in treatment group on 14 d after SCI (P<0.05).Compared with the normal control group
the expressions (including relative content and immunes histochemistry positive cells number) of Olig-2 declined
and OX-42 elevated in model group (P<0.05).Compared with the model group
the expressions of Olig-2 elevated and OX-42 declined in Danshen injection treatment group and methylprednisolone sodium group(P<0.05). Compared with the Danshen injection treatment group
the expressions of Olig-2 declined and OX-42 elevated in Danshen injection+rapamycin group (P<0.05).There was no statistically significant difference in these indicators between Danshen injection treatment group and methylprednisolone sodium group. Conclusion: Danshen injection could promote the recovery of nerve function after SCI by elevating the proliferation of OLS and inhibiting the activation of microglia
and the mechanism may be related to the activity of the phosphatidyl inositol 3-kinase(PI3K)/Akt/mTOR signaling pathway.
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