Li Heng-Cong, Chen Wei, Yu Qing-Quan, Chen Li-Zhen, Su Yang-Shuai, Liu Yi-Han, Zhu Bing, He Wei, Jing Xiang-Hong
Center of Meridian Research, Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Zhongguo Zhen Jiu. 2022 Jul 12;42(7):785-93. doi: 10.13703/j.0255-2930.20210914-k0002.
To investigate the changes of skin temperature, blood infusion and inflammatory cytokines of cutaneous tissue in the sensitized area of colitis model rats, as well as the relationship between sensory and sympathetic nerves and the formation of sensitized area, and to initially reveal the partial physicalchemical characteristics of the sensitized area in the colitis model rats.
Thirty-five male SD rats were randomly divided into a control group (=10), a model group (=18) and a guanethidine group (=7). 5% dextran sulfate sodium (DSS) was adopted for 6-day free drinking to establish colitis model in the model group and the guanethidine group. On day 6 and 7, in the guanethidine group, guanethidine solution (30 mg/kg) was injected intraperitoneally for sympathetic block. On day 7, after injection of evans blue (EB) solution, the EB extravasation areas on the body surface were observed to investigate the distribution and physical-chemical characteristics of the sensitized area. The control area was set up, 0.5 cm away from the sensitized area, and with the same nerve segment innervation. Disease activity index (DAI) score of rats was compared between the normal group and the model group, and the morphological changes in the colon tissue were investigated with HE method. Using infrared thermal imaging technology and laser speckle flow imaging technology, skin temperature and blood infusion were determined in the sensitized area and the control area of the rats in the model group. Immunofluorescence technique was adopted to observe the expression levels of the positive nerve fibers of substance P (SP), calcitonin gene-related peptide (CGRP) and tyrosine hydroxylase (TH), and the correlation with blood vessels; as well as the expression levels of SP positive nerve fibers/tryptase mast cells, and tryptase mast cells/5-hydroxytryptamine (5-HT) in skin tissue in the sensitized area and the control area of the rats in the model group. MSD multi-level factorial method and ELISA were applied to determine the contents of pro-inflammatory and anti-inflammatory cytokines (e.g. TNF-α, IL-1β, IL-6, IL-4 and IL-10) and anti-inflammatory substance corticosterone (CORT).
Sensitization occurred at the T-S segments of the colitis model rats, especially at L-L segments. Compared with the normal group, DAI score was increased in the rats of the model group (<0.05), and the colonic mucosal damage was obvious, with the epithelial cells disordered, even disappeared, crypt destructed, submucosal edema and a large number of inflammatory cells infiltrated. In comparison with the control area, the skin temperature and blood infusion were increased in the sensitized area of the model group (<0.05, <0.01); as well as the expression levels of the positive nerve fibers of SP, CGRP and TH of skin tissue (<0.05), which was specially distributed in peripheral vessels, the expression levels of SP positive nerve fibers/tryptase mast cells, and tryptase mast cells/5-HT of the skin tissue were all expanded (<0.05) in the sensitized area of the model group. Compared with the model group, the number of sensitized areas was reduced in the guanethidine group (<0.05). In comparison with the control area of the model group, in the sensitized area, the contents of pro-inflammatory cytokines, e.g. TNF-α, IL-1β and IL-6, and the anti-inflammatory substance CORT of skin tissue were all increased (<0.05); and the contents of IL-6 and TNF-α were negatively correlated with CORT (<0.05).
The sensitized areas on the body surface of colitis rats are mainly distributed in the L-L segments. Sensory and sympathetic nerves are involved in the acupoint sensitization, and the sensitized areas may have the dynamic changes in pro-inflammatory and anti-inflammatory substances.
探讨结肠炎模型大鼠致敏区皮肤温度、血液灌注及皮肤组织炎性细胞因子的变化,以及感觉神经和交感神经与致敏区形成的关系,初步揭示结肠炎模型大鼠致敏区的部分理化特性。
将35只雄性SD大鼠随机分为对照组(n = 10)、模型组(n = 18)和胍乙啶组(n = 7)。模型组和胍乙啶组采用5%葡聚糖硫酸钠(DSS)自由饮用6天建立结肠炎模型。第6天和第7天,胍乙啶组腹腔注射胍乙啶溶液(30 mg/kg)进行交感神经阻滞。第7天,注射伊文思蓝(EB)溶液后,观察体表EB外渗区域,以研究致敏区的分布及理化特性。设置对照区,距致敏区0.5 cm,且神经节段支配相同。比较正常组和模型组大鼠的疾病活动指数(DAI)评分,并用苏木精-伊红(HE)染色法观察结肠组织的形态学变化。采用红外热成像技术和激光散斑血流成像技术,测定模型组大鼠致敏区和对照区的皮肤温度和血液灌注。采用免疫荧光技术观察P物质(SP)、降钙素基因相关肽(CGRP)和酪氨酸羟化酶(TH)阳性神经纤维的表达水平及其与血管的相关性;以及模型组大鼠致敏区和对照区皮肤组织中SP阳性神经纤维/类胰蛋白酶肥大细胞、类胰蛋白酶肥大细胞/5-羟色胺(5-HT)的表达水平。采用多信号检测(MSD)多级因子法和酶联免疫吸附测定(ELISA)法测定促炎和抗炎细胞因子(如肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-6、白细胞介素-4和白细胞介素-10)及抗炎物质皮质酮(CORT)的含量。
结肠炎模型大鼠在胸11-骶1(T-S)节段出现致敏,尤其在腰1-腰5(L-L)节段。与正常组相比,模型组大鼠DAI评分升高(P < 0.05),结肠黏膜损伤明显,上皮细胞排列紊乱甚至消失,隐窝破坏,黏膜下层水肿,大量炎性细胞浸润。与对照区相比,模型组致敏区皮肤温度和血液灌注增加(P < 0.05,P < 0.01);皮肤组织中SP、CGRP和TH阳性神经纤维的表达水平也增加(P < 0.05),且特别分布于外周血管,模型组致敏区皮肤组织中SP阳性神经纤维/类胰蛋白酶肥大细胞、类胰蛋白酶肥大细胞/5-HT的表达水平均升高(P < 0.05)。与模型组相比,胍乙啶组致敏区数量减少(P < 0.05)。与模型组对照区相比,致敏区皮肤组织中促炎细胞因子如肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6以及抗炎物质CORT的含量均增加(P < 0.05);白细胞介素-6和肿瘤坏死因子-α的含量与CORT呈负相关(P < 0.05)。
结肠炎大鼠体表致敏区主要分布在L-L节段。感觉神经和交感神经参与穴位致敏,且致敏区促炎和抗炎物质可能存在动态变化。