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1. 贵州医科大学临床医学院
2. 贵州医科大学附属医院
纸质出版日期:2019
移动端阅览
王钰, 侯珣瑞, 李丽红, 等. 穴位注射对变应性鼻炎大鼠Th17/Treg相关转录因子及细胞因子表达的影响[J]. 针刺研究, 2019,44(4):276-281.
WANG Yu, HOU Xun-rui, LI Li-hong, et al. Acupoint injection improves allergic rhinitis by balancing Th17/Treg in allergic rhinitis rats[J]. Acupuncture research, 2019, 44(4): 276-281.
王钰, 侯珣瑞, 李丽红, 等. 穴位注射对变应性鼻炎大鼠Th17/Treg相关转录因子及细胞因子表达的影响[J]. 针刺研究, 2019,44(4):276-281. DOI: 10.13702/j.1000-0607.180695.
WANG Yu, HOU Xun-rui, LI Li-hong, et al. Acupoint injection improves allergic rhinitis by balancing Th17/Treg in allergic rhinitis rats[J]. Acupuncture research, 2019, 44(4): 276-281. DOI: 10.13702/j.1000-0607.180695.
目的:观察穴位注射对变应性鼻炎(AR)大鼠鼻黏膜叉头状转录因子p3(Foxp3)和维甲酸相关孤儿受体γt(RORγt)、血清白细胞介素-17(IL-17)表达的影响
从Th17/Treg平衡角度探讨穴位注射治疗AR的作用机制。方法:SD大鼠随机分为正常组、模型组、穴位注射组、非经非穴组
每组8只。采用卵清蛋白致敏法复制AR模型。穴位注射组每隔3d于"印堂"和双侧"迎香"注射地塞米松、转移因子和利多卡因混合液各0.1mL
共4次。非经非穴组同样方法于大鼠左右臀部"后海"与"环跳"连线中点和左(或右)前肢腋窝直下5cm处注射。采用叠加量化记分法进行行为学评分
采用免疫组织化学法检测鼻黏膜中Foxp3和RORγt的表达
酶联免疫吸附法检测血清中IL-17的表达。结果:模型组症状评分高于正常组(P<0.05)
穴位注射组症状评分低于模型组和非经非穴组(P<0.05)
非经非穴组症状评分略低于模型组
但差异无具统计学意义(P>0.05)。模型组较正常组鼻黏膜Foxp3阳性细胞率降低(P<0.05)
鼻黏膜RORγt阳性细胞率增高、血清IL-17表达升高(P<0.05)
Foxp3/RORγt比值下降(P<0.05)。与模型组和非经非穴组比较
穴位注射组鼻黏膜Foxp3阳性细胞率增高(P<0.05)
鼻黏膜RORγt阳性细胞率、血清IL-17表达降低(P<0.05)
Foxp3/RORγt比值升高(P<0.05)。大鼠鼻黏膜Foxp3表达与症状评分呈负相关(P<0.05)
鼻黏膜RORγt表达和血清IL-17表达与症状评分呈正相关(P<0.05)
鼻黏膜Foxp3/RORγt与症状评分呈负相关(P<0.05)。结论:穴位注射可通过上调鼻黏膜Foxp3表达水平
下调鼻黏膜RORγt表达水平
纠正其失衡
并抑制IL-17产生
从而缓解鼻部炎性反应。
Objective To observe the effect of acupoint injection on expression of fork head/winged helix protein 3(Foxp3)
retinoic acid-related orphan receptorγt(RORγt)in nasal mucosa and serum interleukin-17(IL-17)level in allergic rhinitis(AR)rats
so as to explore its mechanism underlying improvement of AR in terms of balancing Th17/Treg.Methods Thirty-two SD rats(half male and half female)were randomized into normal control
AR model
acupoint injection and non-acupoint injection groups(n=8 in each group).The AR model was established by ovalbumin sensitization.In the acupoint injection group
"Yintang"(EX-HN3)and bilateral"Yingxiang"(LI20)were selected for injection of mixture solution of dexamethasone(DEX)and transfer factor and lidocaine(0.1 mL/acupoint)
once every 3 days for a total of 4 times.The non-acupoints
located at the midpoint between the"Houhai"(GV1)and"Huantiao"(GB30)on the bilateral hips and the sites 5 cm inferior to the axillary were injected with the same dose of mixture solution as that in the acupoint injection.The AR severity was assessed by cumulative quantification scoring methods(including the numbers of nose-catching and sneezes
and the amount of nasal secretions in 30 min).The expressions of Foxp3 and RORγt in the nasal mucosa were detected by immunohistochemistry.The serum IL-17 content was detected by enzyme linked immunosorbent assay(ELISA).Results The AR symptom score and serum IL-17 content were significantly higher in the AR model group than those in the normal control group(P<0.05)
and significantly down-regulated in the acupoint injection group(not in the non-acupoint group)relevant to the AR model group(P<0.05).Following modeling
the expression levels of nasal Foxp3 protein was significantly down-regulated while that of RORγt protein markedly up-regulated in the AR model group relevant to the normal control group(P<0.05)
indicating an imbalance between Foxp3 and RORγt activity(P<0.05).After EA intervention
the increased expression of Foxp3 and the down-regulated expression of RORγt were revised in the acupoint injection group(P<0.05)but not in the non-acupoint group(P>0.05).The percentage of the Foxp3 positive cells and the ratio of Foxp3/RORγt were negatively correlated with the AR symptom score(P<0.05)
the expression of RORγt and the content of IL-17 were positively correlated with the symptom score(P<0.05).Conclusion Acupoint injection is able to improve symptoms of RA rats
which may be related with its function in up-regulating the level of nasal mucosal Foxp3 and suppressing the levels of nasal RORγt and serum IL-17 to correct the imbalance of Th17/Treg.
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