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当归补血汤对环磷酰胺诱导的免疫抑制小鼠的免疫功能和肠道微生物群具有调节作用。

Danggui Buxue decoction regulates the immune function and intestinal microbiota of cyclophosphamide induced immunosuppressed mice.

作者信息

Huang Huan, Xie Yufei, Li Xifeng, Gui Fuxing, Yang Pingrui, Li Yutao, Zhang Li, Du Hongxu, Bi Shicheng, Cao Liting

机构信息

Department of Traditional Chinese Veterinary Medicine, College of Veterinary Medicine, Southwest University, Chongqing, China.

Weifang Academy of Agricultural Sciences, Institute of Animal Husbandry, Shandong, China.

出版信息

Front Pharmacol. 2024 Aug 19;15:1420411. doi: 10.3389/fphar.2024.1420411. eCollection 2024.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Danggui Buxue decoction (DBD) is a traditional Chinese herbal formula. According to the theory of traditional Chinese medicine, the combination of (AR) and (AS) is a classic prescription of tonifying and enriching blood. DBD has the functions of hematopoietic, immune enhancement and inflammation inhibition, usually used to treat qi and blood deficiency symptoms.

AIM OF THE STUDY

Cyclophosphamide (CY) can inhibit humoral and cellular immunity, leading to the overall immune disorder of the body, resulting in immunosuppressive (IS). Pre-laboratory studies confirmed the immunomodulatory effects of DBD, but its mechanisms have not been thoroughly studied. In this study, the main purpose was to determine the effects of DBD on the immune function and intestinal mucosal barrier function of IS mice induced by CY, and initially explored the immunomodulatory mechanism of DBD.

MATERIALS AND METHODS

100 g of AR and 20 g of AS were accurately weighed and 0.5 g/mL of the DBD was obtained by boiling, filtration and rotary evaporation. Then, mice in the DBD group were administered 5 g/kg of DBD by gavage, positive group were administered 40 mg/kg of levamisole hydrochloride, whereas those in the control and model groups were given the corresponding volume of normal saline by gavage for 1 week. At the end of the experiment, blood, spleen, thymus, ileum and cecum contents of all the experimental mice were collected aseptically. IS mouse model induced by intraperitoneal injection of 80 mg/kg CY for three consecutive days. Pathomorphology was used to observe the physical barrier of the intestine, flow cytometry to detect splenic lymphocytes, immunohistochemistry to determine the content of intestinal barrier-associated proteins, ELISA to measure the secretion of ileal SIgA, qRT-PCR to detect the mRNA expression of immune-related genes in the intestine, and high-throughput sequencing and analysis of cecum contents.

RESULTS

DBD alleviated spleen tissue damage and restored impaired immune functions, such as increased thymus index and CD4+/CD8+ subsets of spleen lymphocytes. In addition, DBD could increase ileum villi length and the ratio of villi length to crypt depth (V/C), and decrease crypt depth. Moreover, DBD administration up-regulated the expression of ZO-1, Occludin, Claudin-1, MUC-2 mRNA in ileum. And the secretions of sIgA and ZO-1 in ileum were also significantly improved. Furthermore, the administration of DBD can increase the diversity of gut microbiota, improve the composition of intestinal flora and increase the relative abundance of beneficial genus, such as .

CONCLUSION

DBD alleviated CY-induced immune damage by decreasing the ratio of spleen index to CD4+/CD8+ of T lymphocyte subsets. And the intestinal barrier function of mice was by improves improving the intestinal morphology of the ileum and up-regulating the expression levels of ZO-1, MUC-2 and SIgA. DBD regulates CY-induced gut microbiota dysregulation in mice by increasing species diversity and richness, regulating the phylum, class and order levels of .

摘要

民族药理学相关性

当归补血汤(DBD)是一种传统的中药配方。根据中医理论,黄芪(AR)和当归(AS)的组合是益气养血的经典方剂。DBD具有造血、增强免疫和抑制炎症的作用,常用于治疗气血亏虚症状。

研究目的

环磷酰胺(CY)可抑制体液免疫和细胞免疫,导致机体整体免疫紊乱,产生免疫抑制(IS)。前期实验研究证实了DBD的免疫调节作用,但其机制尚未深入研究。本研究的主要目的是确定DBD对CY诱导的IS小鼠免疫功能和肠道黏膜屏障功能的影响,并初步探讨DBD的免疫调节机制。

材料与方法

精确称取100 g黄芪和20 g当归,经煮沸、过滤和旋转蒸发得到0.5 g/mL的DBD。然后,DBD组小鼠按5 g/kg的剂量灌胃给予DBD,阳性组按40 mg/kg的剂量灌胃给予盐酸左旋咪唑,而对照组和模型组小鼠按相应体积灌胃给予生理盐水,连续给药1周。实验结束时,无菌采集所有实验小鼠的血液、脾脏、胸腺、回肠和盲肠内容物。通过连续3天腹腔注射80 mg/kg CY诱导IS小鼠模型。采用病理形态学观察肠道物理屏障,流式细胞术检测脾脏淋巴细胞,免疫组织化学法测定肠道屏障相关蛋白含量,酶联免疫吸附测定法(ELISA)检测回肠分泌型免疫球蛋白A(SIgA)的分泌,实时荧光定量聚合酶链反应(qRT-PCR)检测肠道免疫相关基因的mRNA表达,并对盲肠内容物进行高通量测序和分析。

结果

DBD减轻了脾脏组织损伤,恢复了受损的免疫功能,如增加了胸腺指数和脾脏淋巴细胞CD4+/CD8+亚群。此外,DBD可增加回肠绒毛长度和绒毛长度与隐窝深度之比(V/C),并减小隐窝深度。而且,给予DBD上调了回肠中紧密连接蛋白1(ZO-1)、闭合蛋白(Occludin)、Claudin-1、黏蛋白2(MUC-2)mRNA的表达。回肠中SIgA和ZO-1的分泌也得到显著改善。此外,给予DBD可增加肠道微生物群的多样性,改善肠道菌群组成,并增加有益菌属的相对丰度,如……

结论

DBD通过降低脾脏指数与T淋巴细胞亚群CD4+/CD8+的比值减轻CY诱导的免疫损伤。通过改善回肠肠道形态并上调ZO-1、MUC-2和SIgA的表达水平来改善小鼠的肠道屏障功能。DBD通过增加物种多样性和丰富度,调节……的门、纲和目水平,来调节CY诱导的小鼠肠道微生物群失调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a70d/11366653/26dee08de19a/fphar-15-1420411-g001.jpg

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