Zhang Qian, Li Li-Hong, Hou Xun-Rui, Liang Xin, Lu Yu-Wei, Nie Hong-Fang, Wang Yu-Jia, Cheng Ling, Ye Ting-Ting
Affiliated Hospital of Guizhou Medical University, Guiyang 550004, China.
Affiliated Hospital of Guizhou Medical University, Guiyang 550004, China; Clinical Medicine School, Guizhou Medical University, Guiyang 550004.
Zhen Ci Yan Jiu. 2023 Jul 25;48(7):681-5. doi: 10.13702/j.1000-0607.20220177.
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.
A total of 110 male SD rats were randomly divided into blank control group (=10), catgut embedding (CE) group (=50), and sham CE group (=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 (=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.
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 (<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 (<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 (<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 (<0.05).
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.
观察大鼠“足三里”(ST 36)穴位埋线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,探讨其产生治疗效应的潜在机制。
将110只雄性SD大鼠随机分为空白对照组(n = 10)、埋线组(n = 50)和假埋线组(n = 50)。埋线组和假埋线组在干预后再随机分为8 h、3 d、7 d、14 d和21 d亚组(每个时间点组n = 10)。埋线组大鼠于ST36穴位统一埋线1次,假埋线组大鼠于ST36穴位行埋线针穿刺但不埋线,空白对照组仅抓取固定,不做其他处理。在相应时间点采集各组ST36区域组织,采用免疫荧光法检测穴位局部巨噬细胞中CD68的表达,采用酶联免疫吸附测定法检测穴位局部TNF-α和IL-1β的含量。
ST36穴位埋线后,TNF-α和IL-1β的含量以及巨噬细胞CD68表达水平在8 h开始升高,3 d达到峰值,然后在7 d、14 d和21 d逐渐下降,21 d时埋线组仍高于空白对照组(P<0.05)。与空白对照组比较,埋线组在8 h、3 d、7 d、14 d和21 d时TNF-α和IL-1β的含量以及巨噬细胞CD68表达均显著升高(P<0.05)。ST36穴位假埋线后,与空白对照组比较,8 h和3 d时TNF-α的含量、8 h、3 d、7 d和14 d时IL-1β的含量以及8 h时CD68的表达均显著升高(P<0.05)。埋线组与假埋线组比较,3 d、7 d、14 d和21 d时IL-1β的含量、8 h、3 d、7 d、14 d和21 d时TNF-α的含量以及CD68的表达,埋线组均显著高于假埋线组(P<0.05)。
ST36穴位埋线可诱导大鼠局部微环境中炎症细胞因子TNF-α、IL-1β水平及巨噬细胞CD68表达升高,这可能是其发挥治疗作用的机制之一。