1. 贵州中医药大学研究生院
2. 贵州中医药大学第二附属医院
纸质出版:2021
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陈方园, 张燕平, 杨荣刚, 等. 复方肿节风雾化剂对慢性咽炎模型大鼠咽部黏膜组织炎症因子的影响[J]. 中医杂志, 2021,62(17):1533-1539.
CHEN Fangyuan, ZHANG Yanping, YANG Ronggang, et al. Effect of Compound Zhongjiefeng Nebulizer(复方肿节风雾化剂) on Inflammatory Factors of Pharyngeal Mucosa in Chronic Pharyngitis Model Rats[J]. Journal of Traditional Chinese Medicine2021, 62(17): 1533-1539.
陈方园, 张燕平, 杨荣刚, 等. 复方肿节风雾化剂对慢性咽炎模型大鼠咽部黏膜组织炎症因子的影响[J]. 中医杂志, 2021,62(17):1533-1539. DOI: 10.13288/j.11-2166/r.2021.17.013.
CHEN Fangyuan, ZHANG Yanping, YANG Ronggang, et al. Effect of Compound Zhongjiefeng Nebulizer(复方肿节风雾化剂) on Inflammatory Factors of Pharyngeal Mucosa in Chronic Pharyngitis Model Rats[J]. Journal of Traditional Chinese Medicine2021, 62(17): 1533-1539. DOI: 10.13288/j.11-2166/r.2021.17.013.
目的探讨复方肿节风雾化剂治疗慢性咽炎的可能作用机制。方法将60只SD大鼠随机分为正常组10只和造模组50只。造模组大鼠采用A族乙型溶血性链球菌注射液咽部注射构建慢性咽炎大鼠模型
将造模成功的42只大鼠随机分为模型组10只
氨苄西林钠组及复方肿节风低、中、高剂量组
每组8只。复方肿节风低、中、高剂量组分别给予20ml含有复方肿节风雾化剂2.33、4.66、9.32g/(kg·d)的氯化钠溶液进行超声雾化
正常组、模型组给予等体积生理盐水雾化
氨苄西林钠组腹腔注射氨苄西林钠0.93g/(kg·d)。在造模开始后第4、14天观察各组大鼠毛发、精神状态、口腔分泌物、咽部黏膜等情况
14天后HE染色观察咽部黏膜组织病理;ELISA法检测咽部黏膜组织肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β)、白细胞介素6(IL-6)含量。采用RT-qPCR和免疫组化法检测咽部黏膜组织中肿瘤坏死因子受体相关因子6(TRAF6)、核因子κB p65(NF-κB p65)蛋白及mRNA表达。结果与正常组比较
模型组大鼠咽部黏膜结构不完整
破坏明显
上皮脱落、坏死
见大量炎性细胞浸润
咽部黏膜组织TNF-α、IL-1β、IL-6水平
TRAF-6、NF-κB p65蛋白及mRNA表达量均升高(P<0.05)。与模型组比较
复方肿节风高、中剂量组及氨苄西林钠组咽部黏膜上皮未见明显角质化
复合鳞状上皮未见明显增生
可见少量炎症细胞浸润
肌层纤维排列整齐;复方肿节风低剂量组咽部黏膜组织复层鳞状上皮角质化、增生、脱落
黏膜下层水肿
大量炎症细胞浸润
肌层纤维排列欠规则。与模型组比较
复方肿节风高、中剂量组及氨苄西林钠组大鼠咽部黏膜组织中TNF-α、IL-1β、IL-6含量
TRAF-6、NF-κB p65蛋白及mRNA表达均降低(P<0.05)。结论复方肿节风雾化剂能有效改善慢性咽炎模型大鼠咽部黏膜炎性状态
其中高、中剂量效果更好
其作用机制可能与调控咽部黏膜组织TRAF6/NF-κB p65通路有关。
Objective To explore the possible mechanism of Compound Zhongjiefeng Nebulizer(复方肿节风雾化剂
CZN) in the treatment of chronic pharyngitis. Methods Sixty SD rats were randomly divided into normal group(n=10) and model group(n=50). The rats in the model group were injected with group A beta hemolytic streptococcus into the pharynx to develop the model of chronic pharyngitis. The 42 successfully modeled rats were further randomly divided into model group(n=10)
ampicillin sodium group(n=8) and CZN low
medium
and high-dose groups(each with 8 rats). The CZN low
medium
and high-dose groups were given ultrasonic atomization of 20 ml solution containing 2.33
4.66
and 9.32 g/(kg·d) of CZN
respectively; the normal group and the model group received atomization of the same volume of normal saline; the ampicillin sodium group was injected intraperitoneally with 0.93 g/(kg·d) of ampicillin sodium. The hair
mental state
oral secretions
and pharyngeal mucosa of rats in each group were assessed on the 4 th and 14 th day after modeling. After 14 days
the pathology of the pharyngeal mucosa was observed through HE staining; ELISA method was used to detect the content of the tumor necrosis factor α(TNF-α)
interleukin 1β(IL-1β) and interleukin 6(IL-6) in the pharyngeal mucosal tissue; RT-qPCR and immunohistochemistry were used to detect tumor necrosis factor receptor-associated factor 6(TRAF6)
nuclear factor κB p65(NF-κB p65) protein and mRNA expression. Results Compared to those of the normal group
the pharyngeal mucosal structure of the model group was incomplete and damaged heavily; epithelial shedding
necrosis and massive inflammatory cell infiltrations were seen; the levels of TNF-α
IL-1β and IL-6 in the pharyngeal mucosa significantly increased
as well as the TRAF-6 and NF-κB p65 protein and mRNA expression(P<0.05). Compared to the model group
there was no obvious keratinization in the pharyngeal mucosal epithelium in the high-dose and middle-dose CZN group and the ampicillin sodium group; no obvious hyperplasia of the compound squamous epithelium and a small amount of inflammatory cell infiltration were seen
and the muscle fibers were arranged neatly; the compound squamous epithelium in the pharyngeal mucosal tissue of the CZN low-dose group was keratinized
proliferated and shed
with submucosal edema
massive inflammatory cell infiltration and irregularly arranged muscular fibers. Compared to the model group
the high-dose and middle-dose CZN group and the ampicillin sodium group had decreased levels of TNF-α
IL-1β and IL-6 in the pharyngeal mucosal tissue
as well as decreased TRAF-6 and NF-κB p65 protein and mRNA expression(P<0.05). Conclusion Compound Zhongjiefeng Nebulizer can effectively improve the inflammatory status of the pharyngeal mucosa in rats model of chronic pharyngitis; and the high and medium doses are more effective. The mechanism of action may be related to the regulation of the TRAF6/NF-κB p65 pathway in the pharyngeal mucosa tissue.
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