PMID- 36215828 OWN - NLM STAT- MEDLINE DCOM- 20221128 LR - 20221202 IS - 1872-9142 (Electronic) IS - 0161-5890 (Linking) VI - 152 DP - 2022 Dec TI - Ephedrae Herba polysaccharides inhibit the inflammation of ovalbumin induced asthma by regulating Th1/Th2 and Th17/Treg cell immune imbalance. PG - 14-26 LID - S0161-5890(22)00431-X [pii] LID - 10.1016/j.molimm.2022.09.009 [doi] AB - AIMS: This study aimed to investigate the anti-asthma effects of Ephedrae Herba polysaccharides (PE) and possible mechanisms related to immune inflammatory response. METHODS: An asthma model was established in rats using ovalbumin (OVA). Seventy rats were randomly assigned to five groups: control, model, dexamethasone (DEX, 0.075 mg/kg), low dose polysaccharides (LPE, 137.71 mg/kg) and high dose polysaccharides (HPE, 275.42 mg/kg). The cough and asthma were used to evaluate the basic state of asthmatic rats. Histological studies were evaluated by hematoxylin and eosin (H&E), Masson, and periodic acid-schiff (PAS) staining. The levels of interferon-gamma (IFN-gamma), interleukin (IL)-4, immunoglobulin E (IgE), tumor necrosis factor alpha (TNF-alpha), and IL-17A in bronchoalveolar lavage fluid (BALF), and the levels of transforming growth factor beta1 (TGF-beta1), IL-6, and IL-10 in serum were detected by enzyme-linked immunosorbent assay (ELISA). The mRNA levels of Ifn-gamma, Il-4, Tgf-beta1, Il-6, Il-10, Tnf-alpha, Il-13, and Il-17a were evaluated by quantitative real-time reverse transcription (qRT)-PCR. The dendritic cell (DCs), T helper cell (Th), natural killer cell (NK), regulatory T cell (Treg), and Th17 cells in blood, the lymphocytes, macrophages and neutrophils in spleen, and cell apoptosis and reactive oxygen species (ROS) in lung were analysed by flow cytometry (FCM). Immunohistochemistry (IHC) was used to stain DCs (CD11c(+), CD86(+), and CD80(+)), macrophages (CD68(+)), and neutrophils (MPO(+)) in the spleen and lung. The protein levels of IL-17A, CD11c, CD86, and CD80 in lung were measured by western blot. RESULTS: Our study demonstrated that PE could effectively improve the symptoms of asthmatic rats, ameliorate the lung pathological injury, inhibit inflammation, apoptosis and oxidative stress, regulate the levels of macrophages, neutrophils, DCs, NK, Thc, Treg and Th17 cells. CONCLUSION: PE could collectively inhibit the inflammation, apoptosis and ROS in asthma rats induced by OVA via regulating Th1/Th2 and Th17/Treg cell immune imbalance. CI - Copyright (c) 2022 Elsevier Ltd. All rights reserved. FAU - Zhang, Beibei AU - Zhang B AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Zeng, Mengnan AU - Zeng M AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China; Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases co-constructed by Henan province and Education Ministry of P.R. China, Henan University of Chinese Medicine, Zhengzhou 450046, China. FAU - Zhang, Qinqin AU - Zhang Q AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Wang, Ru AU - Wang R AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Jia, Jufang AU - Jia J AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Cao, Bing AU - Cao B AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Liu, Meng AU - Liu M AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Guo, Pengli AU - Guo P AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Zhang, Yuhan AU - Zhang Y AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China. FAU - Zheng, Xiaoke AU - Zheng X AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China; Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases co-constructed by Henan province and Education Ministry of P.R. China, Henan University of Chinese Medicine, Zhengzhou 450046, China. Electronic address: zhengxk.2006@163.com. FAU - Feng, Weisheng AU - Feng W AD - Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China; Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases co-constructed by Henan province and Education Ministry of P.R. China, Henan University of Chinese Medicine, Zhengzhou 450046, China. Electronic address: fwsh@hactcm.edu.cn. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20221007 PL - England TA - Mol Immunol JT - Molecular immunology JID - 7905289 RN - 130068-27-8 (Interleukin-10) RN - 0 (Interleukin-17) RN - 0 (Interleukin-6) RN - 0 (Polysaccharides) RN - 0 (Reactive Oxygen Species) RN - 0 (Transforming Growth Factor beta1) RN - 0 (Tumor Necrosis Factor-alpha) RN - 0 (Phytochemicals) RN - 51QBA3IQ91 (Ephedrae herba) RN - 0 (Drugs, Chinese Herbal) SB - IM MH - Animals MH - Mice MH - Rats MH - *Asthma/chemically induced/drug therapy MH - Bronchoalveolar Lavage Fluid MH - Disease Models, Animal MH - Inflammation MH - Interleukin-10/metabolism MH - Interleukin-17/metabolism MH - Interleukin-6/metabolism MH - Lung/pathology MH - Mice, Inbred BALB C MH - *Polysaccharides/pharmacology MH - Reactive Oxygen Species/metabolism MH - *T-Lymphocytes, Regulatory MH - Th17 Cells MH - Transforming Growth Factor beta1/metabolism MH - Tumor Necrosis Factor-alpha/metabolism MH - Phytochemicals/pharmacology MH - *Drugs, Chinese Herbal/pharmacology OTO - NOTNLM OT - Allergic immune response OT - Asthma OT - Ephedrae Herba polysaccharides OT - Ovalbumin-induced airway inflammation COIS- Declaration of Competing Interest The authors declare no conflict of interest. EDAT- 2022/10/11 06:00 MHDA- 2022/11/26 06:00 CRDT- 2022/10/10 18:23 PHST- 2022/06/01 00:00 [received] PHST- 2022/09/18 00:00 [revised] PHST- 2022/09/19 00:00 [accepted] PHST- 2022/10/11 06:00 [pubmed] PHST- 2022/11/26 06:00 [medline] PHST- 2022/10/10 18:23 [entrez] AID - S0161-5890(22)00431-X [pii] AID - 10.1016/j.molimm.2022.09.009 [doi] PST - ppublish SO - Mol Immunol. 2022 Dec;152:14-26. doi: 10.1016/j.molimm.2022.09.009. Epub 2022 Oct 7.