Liu Zirui, Li Yalan, Li Na, Wang Yongan, Li Qiuyi, Ge Dongyu, Peng Guiying, Zhou Mengyu
School of Life Sciences, Beijing University of Chinese Medicine, Beijing, 102488, China.
School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 102488, China.
J Tradit Complement Med. 2023 Jan 6;13(2):183-192. doi: 10.1016/j.jtcme.2023.01.003. eCollection 2023 Mar.
Dachengqi Decoction (DCQD) as a classic traditional Chinese medicine has been reported to be effective in treating asthma, but its mechanism remains unknown. This study aimed to reveal the mechanisms of DCQD on the intestinal complications of asthma mediated by group 2 innate lymphoid cells (ILC2) and intestinal microbiota.
Ovalbumin (OVA) was used to construct asthmatic murine models. IgE, cytokines (e.g., IL-4, IL-5), fecal water content, colonic length, histopathologic appearance, and gut microbiota were evaluated in asthmatic mice treated with DCQD. Finally, we administered DCQD to antibiotic-treated asthmatic mice to measure the ILC2 in the small intestine and colon.
DCQD decreased pulmonary IgE, IL-4, and IL-5 levels in asthmatic mice. The fecal water content, the colonic length weight loss, and the epithelial damage of jejunum, ileum, and colon of asthmatic mice were ameliorated by DCQD. Meanwhile, DCQD greatly improved intestinal dysbiosis by enriching , and in the whole intestine, and only in the colon. However, DCQD caused less abundant and in the small intestine of asthmatic mice. A higher ILC2 proportion in different gut segments of asthmatic mice was reversed by DCQD. Finally, significant correlations appeared between DCQD-mediated specific bacteria and cytokines (e.g., IL-4, IL-5) or ILC2. These findings indicate that DCQD alleviated the concurrent intestinal inflammation in OVA-induced asthma by decreasing the excessive accumulation of intestinal ILC2 in a microbiota-dependent manner across different gut locations.
大承气汤(DCQD)作为一种经典的中药,已报道其对哮喘治疗有效,但其作用机制尚不清楚。本研究旨在揭示DCQD对由2型固有淋巴细胞(ILC2)和肠道微生物群介导的哮喘肠道并发症的作用机制。
用卵清蛋白(OVA)构建哮喘小鼠模型。对接受DCQD治疗的哮喘小鼠评估免疫球蛋白E、细胞因子(如白细胞介素-4、白细胞介素-5)、粪便含水量、结肠长度、组织病理学表现和肠道微生物群。最后,我们对用抗生素处理的哮喘小鼠给予DCQD,以测量小肠和结肠中的ILC2。
DCQD降低了哮喘小鼠肺部免疫球蛋白E、白细胞介素-4和白细胞介素-5水平。DCQD改善了哮喘小鼠的粪便含水量、结肠长度减轻以及空肠、回肠和结肠的上皮损伤。同时,DCQD通过在整个肠道中富集 、 和 ,以及仅在结肠中富集 ,极大地改善了肠道菌群失调。然而,DCQD使哮喘小鼠小肠中的 和 丰度降低。DCQD逆转了哮喘小鼠不同肠道段中较高的ILC2比例。最后,DCQD介导的特定细菌与细胞因子(如白细胞介素-4、白细胞介素-5)或ILC2之间出现显著相关性。这些发现表明,DCQD通过以微生物群依赖的方式减少不同肠道部位肠道ILC2的过度积累,减轻了OVA诱导的哮喘中并发的肠道炎症。