1. 江苏省中医药研究院肿瘤科
2. 江苏省中医药研究院细胞与分子生物学实验室
纸质出版:2012
移动端阅览
[1]霍介格,胡莹,杨杰,蔡雪婷,胡春萍,王小宁,曹鹏.黄芪桂枝五物汤对化疗致大鼠周围神经损伤的作用[J].中医杂志,2012,53(23):2031-2034.
HUO Jiege, HU Ying, YANG Jie, et al. Effect of Huangqi Guizhi Wuwu Decoction on Chemotherapy-induced Peripheral Never Injury in Rats[J]. Journal of Traditional Chinese Medicine2012, 53(23): 2031-2034.
[1]霍介格,胡莹,杨杰,蔡雪婷,胡春萍,王小宁,曹鹏.黄芪桂枝五物汤对化疗致大鼠周围神经损伤的作用[J].中医杂志,2012,53(23):2031-2034. DOI: 10.13288/j.11-2166/r.2012.23.025.
HUO Jiege, HU Ying, YANG Jie, et al. Effect of Huangqi Guizhi Wuwu Decoction on Chemotherapy-induced Peripheral Never Injury in Rats[J]. Journal of Traditional Chinese Medicine2012, 53(23): 2031-2034. DOI: 10.13288/j.11-2166/r.2012.23.025.
目的评价黄芪桂枝五物汤对化疗致大鼠周围神经损伤的保护作用。方法将55只Wistar大鼠随机分为空白组、模型组、甲钴胺组、黄芪桂枝五物汤低、高剂量组
每组11只。除空白组
其余各组采用多次腹腔注射奥沙利铂的方式建立大鼠周围神经损伤模型
黄芪桂枝五物汤高、低剂量组分别采用黄芪桂枝五物汤19.40g/kg·d、4.85g/kg·d灌胃
连续50天;甲钴胺组腹腔注射甲钴胺注射液104μg/kg
每周2次;模型组给予黄芪桂枝五物汤低、高剂量组等体积的生理盐水灌胃
连续50天;空白组每周2次等体积腹腔注射5%葡萄糖及灌胃等体积生理盐水。分别于给药第1、10、13、20、27、34、42、48天进行大鼠机械性缩足阈值及大鼠尾部热痛觉潜伏期测试。给药结束后
处死大鼠
荧光定量PCR(qRT-PCR)检测L4-6脊髓NR2B mRNA水平的影响
免疫组织化学法检测L5背根神经节(DRG)中pNF-H的表达。结果第13天后各时间点
模型组的大鼠机械性缩足阈值与空白组比较明显下降(P<0.05);黄芪桂枝五物汤低、高剂量组、甲钴胺组与模型组比较明显增高(P<0.05);第42、48天
黄芪桂枝五物汤低、高剂量组与甲钴胺组比较机械性缩足阈值差异有统计学意义(P<0.05);各组大鼠不同时间点热辐射甩尾反应时间比较差异均无统计学意义(P>0.05);与空白组比较
模型组NR2B mRNA水平升高(P<0.01)
黄芪桂枝五物汤低、高剂量组大鼠NR2B mRNA水平较模型组降低(P<0.01);黄芪桂枝五物汤低、高剂量组pNF-H阳性细胞数量较多
胞体肥大
染色加深
呈多角形或圆形。结论黄芪桂枝五物汤可改善化疗致大鼠周围神经毒性
其机制可能是通过下调大鼠L4-6脊髓中NR2B的表达以及上调DRG中pNF-H蛋白水平来介导。
Objective To study the protective effect of Huangqi Guizhi Wuwu Decoction ( Astragalus and Cinnamon Twig Five Agents Decoction ) on chemotherapy-induced peripheral never injury in rats.Methods Fifty-five adult female Wistar rats were randomized into five groups
i.e.blank group
model group
mecobalamin ( 104 μ g / kg ) group
Huangqi Guizhi Wuwu Decoction small-dose ( 4.85g / kg · d ) group and Huangqi Guizhi Wuwu Decoction large-dose ( 19.40g / kg · d ) group
with 11in each.Rat models with blood arthralgia syndrome were established with repeated intraperitoneal injection of oxaliplatin.The rats in Huangqi Guizhi Wuwu Decoction groups and mecobalamin group were preventively administered from 7days before modeling and lasted for 50days.The rat mechanical paw withdrawal threshold and rat tail thermal hyperalgesia latency were recorded on the 1st
10th
13th
20th
27th
34th
42nd
and 48th day during the administration.The rats were sacrificed after administration and the L4-6lumbar spinal segments and L5dorsal root ganglion ( DRG ) were resected.The level of NR2B mRNA in L4-6lumbar spinal segments was detected with the real-time quantitative reverse transcriptase polymerase chain reaction ( qRT-PCR ) method.The expression of pNF-H in L5DRG was detected with immunohistochemistry assay.Results Comparing with the blank group
rat mechanical paw withdrawal threshold decreased obviously in the model group after the 13th day of experiment ( P<0.05 ) .Rat mechanical paw withdrawal threshold increased obviously in Huangqi Guizhi Wuwu Decoction groups and mecobalamin group as compared with the model group ( P<0.05 ) .There was a significant difference between Huangqi Guizhi Wuwu Decoction groups and mecobalamin group in rat mechanical paw withdrawal threshold after the 42nd day of experiment ( P<0.05 ) .There was no significant difference in tail thermal pain incubation period between groups ( P>0.05 ) .The level of NR2BmRNA in the model group was significantly higher than that in the blank group ( P<0.05 ) . The levels of NR2BmRNA significantly decreased in Huangqi Guizhi Wuwu Decoction groups ( P<0.05 )
but the decrement in the mecobalamin group was not significant ( P>0.05 ) .A large number of pNF-H positive cells and deeply stained cell body could be seen in the normal group.A small number of pNF-H positive cells could be seen in the model group.A large number of pNF-H positive cells
cell hypertrophy and deeply stained cell body could be seen in Huangqi Guizhi Wuwu Decoction groups.Conclusion Huangqi Guizhi Wuwu Decoction could relieve pain of the blood arthralgia syndrome induced by chemo-therapy and its mechanism may be relevant to down-regulating the expression of NR2Bin the L4-6lumbar spinal segments and up-regulating the level of pNF-H protein in DRG.
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