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[靶向阻断大麻素受体1对慢性间歇性缺氧小鼠脾脏免疫功能及炎症反应的调控作用]

[Regulation of targeted blocking cannabinoid receptor 1 on spleen immune function and inflammatory response in mice under chronic intermittent hypoxia].

作者信息

Cheng X Q, Shi Y X, Gong Y P, Han J X, Wang B

机构信息

The Second Clinical School of Medicine, Shanxi Medical University, Taiyuan 030001, China.

Department of Stomatology, the Second Hospital of Shanxi Medical University, Taiyuan 030001, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2024 Sep 12;47(9):827-833. doi: 10.3760/cma.j.cn112147-20240115-00031.

Abstract

To observe the effects of targeting and blocking cannabinoid receptor 1 (CB1R) on mouse spleen immune function and inflammatory response under chronic intermittent hypoxia (CIH) conditions, and to explore its regulatory effort. Forty SPF male C57BL/6 mice aged 4 to 5 weeks,from May 2021 to August 2021 in Experimental Animal Center of the Second Hospital of Shanxi Medical University, were randomly divided into normal oxygen control group (NC), 6-week CIH group (6w CIH), 10-week CIH group (10w CIH), 6-week CIH+CB1R group (6w CIH+AM251) and 10-week CIH+CB1R group (10w CIH+AM251) according to the method of random number table. The advanced programmable intermittent low oxygen chamber was used to prepare the CIH mouse model. The morphological structure of spleen tissue of CIH mice was stained by hematoxylin-eosin (HE) staining. The expression levels of M1 and M2 macrophage surface markers CD86, CD206 were determined by immunofluorescence. The mRNA expression levels of CB1R, CD86, CD206 and the relative expression levels of RORγt and Foxp3,which are characteristic transcriptional regulators of T helper 17(Th17) and Treg cells were detected by quantitative reverse transcriptase PCR(qRT-PCR). The expression of inflammatory factors IL-6 and IL-10 was determined by ELISA. SPSS 26.0 and Graphpad prism 8.3 were used to analyze the data. (1) Compared with NC group, spleen tissue structure was disordered, fibrous tissue hyperplasia, lymphocyte proliferation and disordered arrangement in periarteriole lymphatic sheath in CIH group. The expression of CB1R in CIH group was higher than that in NC group (<0.05), and with the prolongation of CIH time, the expression of 10w CIH group was higher than that in 6w CIH group(<0.05). The expression of CB1R in CIH+AM251 group was lower than that in the corresponding CIH group(all <0.05). (2) Compared with NC group, the expression level of CD86 in macrophages in CIH group was higher than that in NC group(all <0.05). The relative expression of RORγt in 6w and 10w CIH groups was 0.76±0.03 and 0.91±0.04, respectively, which was higher than that in NC group (0.65±0.06)(all <0.05). The relative expression levels of inflammatory factor IL-6 were 10.80±1.73 and 14.86±0.01, respectively, which were higher than 6.69±0.23 in the NC group (all <0.05). The expression level of CD206 in macrophages in the CIH+AM251 group was higher than that in the CIH group(all <0.05). The relative expression levels of Foxp3 in 6w and 10w CIH+AM251 groups were 0.62±0.05 and 0.32±0.21, respectively, which were higher than those in 6w CIH group (0.28±0.02) and 10w CIH group (0.02±0.01)(<0.05). The relative expression levels of anti-inflammatory factor IL-10 were 668.45±15.71 and 379.15±56.84, respectively, which were higher than those in CIH group (all <0.05). Targeted sealing of CB1R may alleviate inflammatory response of mouse spleen under CIH conditions by regulating macrophage polarization and the expression of inflammatory factors, and may have some protective effect.

摘要

观察靶向阻断大麻素受体1(CB1R)对慢性间歇性缺氧(CIH)条件下小鼠脾脏免疫功能和炎症反应的影响,并探讨其调节作用。选取2021年5月至2021年8月在山西医科大学第二医院实验动物中心的40只4至5周龄的SPF级雄性C57BL/6小鼠,按照随机数字表法将其随机分为常氧对照组(NC)、6周CIH组(6w CIH)\(10\)周CIH组(\(10\)w CIH)、6周CIH+CB1R组(6w CIH+AM251)和\(10\)周CIH+CB1R组(\(10\)w CIH+AM251)。采用先进的可编程间歇性低氧舱制备CIH小鼠模型。用苏木精-伊红(HE)染色法对CIH小鼠脾脏组织的形态结构进行染色。通过免疫荧光法测定M1和M2巨噬细胞表面标志物CD86、CD206的表达水平。采用定量逆转录聚合酶链反应(qRT-PCR)检测CB1R、CD86、CD206的mRNA表达水平以及辅助性T细胞17(Th17)和调节性T细胞(Treg)特征性转录调节因子RORγt和Foxp3的相对表达水平。用酶联免疫吸附测定(ELISA)法测定炎症因子白细胞介素-6(IL-6)和白细胞介素-10(IL-10)的表达。采用SPSS 26.0和Graphpad prism 8.3软件进行数据分析。(1)与NC组相比,CIH组脾脏组织结构紊乱,纤维组织增生,淋巴细胞增殖且动脉周围淋巴鞘排列紊乱。CIH组CB1R的表达高于NC组(\(P<0.05\)),且随着CIH时间延长,\(10\)w CIH组的表达高于6w CIH组(\(P<0.05\))。CIH+AM251组CB1R的表达低于相应的CIH组(均\(P<0.05\))。(2)与NC组相比,CIH组巨噬细胞中CD86的表达水平高于NC组(均\(P<0.05\))。6w和\(10\)w CIH组RORγt的相对表达分别为\(0.76±0.03\)和\(0.91±0.04\),高于NC组的\(0.65±0.06\)(均\(P<0.05\))。炎症因子IL-6的相对表达水平分别为\(10.80±1.73\)和\(14.86±0.01\),高于NC组的\(6.69±0.23\)(均\(P<0.05\))。CIH+AM251组巨噬细胞中CD206的表达水平高于CIH组(均\(P<0.05\))。6w和\(10\)w CIH+AM251组Foxp3的相对表达分别为\(0.62±0.05\)和\(0.32±0.21\),高于6w CIH组的\(0.28±0.02\)和\(10\)w CIH组的\(0.02±0.01\)(\(P<0.05\))。抗炎因子IL-10的相对表达水平分别为\(668.45±15.71\)和\(379.15±56.84\),高于CIH组(均\(P<0.05\))。靶向封闭CB1R可能通过调节巨噬细胞极化和炎症因子表达减轻CIH条件下小鼠脾脏的炎症反应,可能具有一定保护作用。

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