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1. 广西中医药大学第一临床医学院
2. 广西中医药大学第一附属医院针灸科
纸质出版日期:2020
移动端阅览
蔡慧倩, 粟胜勇, 张熙, 等. 温和灸对神经根型颈椎病大鼠脊髓Beclin-1/Bcl-2表达的影响[J]. 针刺研究, 2020,45(10):799-805.
CAI Hui-qian, SU Sheng-yong, ZHANG Xi, et al. Effects of mild moxibustion on Beclin-1/Bcl-2 expression in spinal cord of rats with cervical spondylotic radiculopathy[J]. Acupuncture research, 2020, 45(10): 799-805.
蔡慧倩, 粟胜勇, 张熙, 等. 温和灸对神经根型颈椎病大鼠脊髓Beclin-1/Bcl-2表达的影响[J]. 针刺研究, 2020,45(10):799-805. DOI: 10.13702/j.1000-0607.191004.
CAI Hui-qian, SU Sheng-yong, ZHANG Xi, et al. Effects of mild moxibustion on Beclin-1/Bcl-2 expression in spinal cord of rats with cervical spondylotic radiculopathy[J]. Acupuncture research, 2020, 45(10): 799-805. DOI: 10.13702/j.1000-0607.191004.
目的:观察温和灸对神经根型颈椎病(CSR)大鼠脊髓(包括神经根组织)自噬和凋亡因子Beclin-1、Bcl-2 mRNA及蛋白表达的影响
探讨温和灸"大椎"对CSR大鼠的镇痛机制。方法:将SD大鼠随机分为空白组、模型组、温和灸组、温和灸+3-methyladenine(3-MA)组
每组10只。除空白组外
其他3组大鼠均采用插线入颈神经根的方法制备CSR模型。空白组大鼠仅正常饲养
不做任何干预;模型组只注射0.9%氯化钠溶液干预;温和灸组予温和灸"大椎"
10 min/次
并腹腔注射0.9%氯化钠溶液;温和灸+3-MA组予温和灸"大椎"并注射3-MA干预。3组均从造模后第3天开始连续干预7 d
1次/d。观察各组大鼠步态评分;用疼痛分析仪测量各组大鼠的痛阈值;用荧光定量PCR法检测各组大鼠脊髓(包括神经根)组织中Beclin-1、 Bcl-2 mRNA的表达;用免疫组织化学法检测脊髓(包括神经根)组织中Beclin-1、Bcl-2蛋白的表达水平;用透射电镜观察脊髓神经根组织自噬小体及超微结构。结果:与空白组比较
造模后模型组大鼠步态评分升高(P<0.01)
机械痛阈值降低(P<0.01)。干预后
与模型组比较
温和灸组及温和灸+3-MA组大鼠的步态评分明显降低(P<0.01)
痛阈值及大鼠脊髓组织Beclin-1、Bcl-2 mRNA与蛋白表达均明显升高(P<0.01
P<0.05)
且温和灸组较温和灸+3-MA组上述指标的改善更显著(P<0.05)。与空白组比较
模型组大鼠脊髓神经根组织细胞内的细胞器出现破损
有少量的自噬小体;与模型组比较
温和灸组大鼠脊髓神经根组织细胞的细胞器超微结构较为完整
自噬小体数量增多。结论:温和灸"大椎"对CSR大鼠具有良好的镇痛效应
其机制可能与上调Beclin-1、Bcl-2表达
激活细胞的自噬、抑制细胞凋亡有关。
Objective To observe the effects of mild moxibustion on the expression of autophagy and apoptosis factors Beclin-1
Bcl-2 mRNA and protein in spinal cord(including nerve root tissues) of cervical spondylotic radiculopathy(CSR) rats
so as to explore the analgesic mechanism of mild moxibustion at "Dazhui"(GV14) on CSR. Methods SD rats were randomly divided into blank group
model group
mild moxibustion group and mild moxibustion+3-methyladenine(3-MA) group
with 10 rats in each group. CSR model was established by inserting the wire into the cervical nerve root. The rats in the blank group were only fed normally without any intervention.The rats in the mild moxibustion group and mild moxibustion+3-MA group were given mild moxibustion at GV14 for 10 min each time
and intraperitoneal injection of 1 mL 0.9% normal saline and 1 mL 3-MA(15 mg/kg)separately. Rats in the model group were given 0.9% normal saline every day. All the three interventions were started from the 3 rd day after modeling for 7 days. The rat's behavioral reaction of gait was scored and the pain threshold of rat was measured with a pain analyzer; the expressions of Beclin-1 and Bcl-2 mRNA and protein in the spinal cord(including nerve root) were detected by fluorescence quantitative PCR and immunohistochemistry
separately. The autophagosome and ultrastructure of the spinal nerve root tissue were observed by transmission electron microscope. Results After modeling
the gait score was significantly increased(P<0.01) and the pain threshold significantly decreased(P<0.01) in the model group in comparison with the blank group. There was no statistical difference in Beclin-1 and Bcl-2 mRNA and protein expression between the blank and the model groups. After intervention
compared with the model group
the gait scores were significantly reduced(P<0.01)
the pain threshold and the expressions of Beclin-1 and Bcl-2 mRNA and protein were significantly increased(P<0.01
P<0.05) in the mild moxibustion and mild moxibustion+3-MA groups. The improvement of the above indicators as more significant in the mild moxibustion group than that in the mild moxibustion+3-MA group(P<0.05). After modeling
the organelles in the spinal nerve root tissue cells of the model group were damaged and there were a small amount of autophagosomes. Compared with the model group
the ultrastructure of the spinal nerve root tissue cells in the mild moxibustion group were relatively complete
and the number of autophagosomes increased. Conclusion Mild moxibustion at GV14 has a good analgesic effect on CSR rats
which may be related to its effects in up-regulation of Beclin-1 and Bcl-2 expressions and activation of autophagy and inhibition of apoptosis.
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