【羊肠线植入对大鼠足三里(ST36)巨噬细胞CD68、肿瘤坏死因子-α和白细胞介素-1β的影响】。

Qian Zhang, Li-Hong Li, Xun-Rui Hou, Xin Liang, Yu-Wei Lu, Hong-Fang Nie, Yu-Jia Wang, Ling Cheng, Ting-Ting Ye
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Rats of the CE group were uniformly subjected into catgut embedding at ST36 once, and those of the sham CE group received embedding needle puncture at ST36 without catgut retention, and the blank control group was only grasped and fixed without other treatments. Tissues from the ST36 area in each group were collected at the corresponding time points, and the expression of CD68 in macrophages in the acupoint area was detected by immunofluorescence, the contents of TNF-α and IL-1β in the acupoint area were detected by ELISA.</p><p><strong>Results: </strong>Following catgut embedment at ST36, the contents of TNF-α and IL-1β, and macrophage CD68 expression level began to increase at 8 h, peaked at 3 d, and then gradually decreased at 7, 14, and 21 d, being still higher in the CE group than in the blank control group at 21 d (<i>P</i><0.05). 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引用次数: 0

摘要

目的:观察“足三里”猫肠线植入大鼠后局部巨噬细胞及相关细胞因子肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)的表达,探讨其诱导治疗作用的潜在机制。方法:将110只雄性SD大鼠随机分为空白对照组(n=10)、肠线包埋(CE)组(n=50)和假CE组(n=5 0)。CE组和假CE组在干预后随机分为8h、3d、7d、14d和21d亚组(每个时间点组n=10)。CE组大鼠于ST36均匀包埋肠线1次,假CE组于ST36包埋针穿刺,无肠线滞留,空白对照组仅抓握固定,无其他处理。在相应时间点采集各组ST36区组织,免疫荧光法检测穴位巨噬细胞CD68的表达,ELISA法检测穴位区TNF-α和IL-1β的含量,巨噬细胞CD68表达水平在8h开始升高,在3d达到峰值,然后在7、14和21d逐渐降低,在21 d时,CE组仍高于空白对照组(PPPPC结论:ST36肠线包埋可诱导大鼠局部微环境中炎性细胞因子TNF-α、IL-1β和巨噬细胞CD68水平升高,这可能有助于其启动治疗作用。
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[Effect of catgut implantation on macrophage CD68, tumor necrosis factor-α and interleukin-1β in "Zusanli" (ST 36) region of rats].

Objective: To observe the expression of local macrophages and related cytokines tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) after catgut implantation in "Zusanli"(ST 36) in rats, so as to explore its underlying mechanisms in inducing therapeutic effect.

Methods: A total of 110 male SD rats were randomly divided into blank control group (n=10), catgut embedding (CE) group (n=50), and sham CE group (n=50). The CE and sham CE groups were randomly divided into 8 h, 3 d, 7 d, 14 d and 21 d subgroups after the intervention (n=10 in each time point group). Rats of the CE group were uniformly subjected into catgut embedding at ST36 once, and those of the sham CE group received embedding needle puncture at ST36 without catgut retention, and the blank control group was only grasped and fixed without other treatments. Tissues from the ST36 area in each group were collected at the corresponding time points, and the expression of CD68 in macrophages in the acupoint area was detected by immunofluorescence, the contents of TNF-α and IL-1β in the acupoint area were detected by ELISA.

Results: Following catgut embedment at ST36, the contents of TNF-α and IL-1β, and macrophage CD68 expression level began to increase at 8 h, peaked at 3 d, and then gradually decreased at 7, 14, and 21 d, being still higher in the CE group than in the blank control group at 21 d (P<0.05). Compared with the blank control group, the contents of TNF-α and IL-1β, and macrophage CD68 expression were significantly increased at 8 h, and 3, 7, 14 and 21 d in the CE group (P<0.05). Following sham CE at ST36, the content of TNF-α at 8 h and 3 d, IL-1β at 8 h and 3, 7 and 14 d, and expression of CD68 at 8 h were significantly increased in comparison with the blank control group (P<0.05). Comparison between the CE and sham CE groups showed that the contents of IL-1β at 3, 7, 14 and 21 d, and contents of TNF-α,CD68 expression at 8 h, and 3, 7, 14 and 21 d were significantly higher in the CE group than in the sham CE group (P<0.05).

Conclusion: Catgut embedding at ST36 can induce an increase levels of inflammatory cytokines TNF-α, IL-1β and macrophage CD68 in the local microenvironment in rats, which may contribute to its functions in initiating therapeutic effect.

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