Compound 511 ameliorates MRSA-induced lung injury by attenuating morphine-induced immunosuppression in mice via PI3K/AKT/mTOR pathway

被引:17
|
作者
Li, Zhonghao [1 ,3 ,4 ]
Sun, Qinmei [1 ,2 ]
Liu, Qingyang [1 ,3 ,4 ]
Mu, Xinru [1 ,3 ,4 ]
Wang, Hui [1 ,3 ,4 ]
Zhang, Han [1 ,2 ]
Qin, Fenfen [1 ,3 ,4 ]
Wang, Qisheng [1 ,3 ,4 ]
Nie, Dengyun [1 ,3 ,4 ]
Liu, Anlong [7 ]
Li, Qian [4 ]
Ji, Jianjian [6 ]
Jiang, Yongwei [4 ]
Lu, Shengfeng [4 ]
Wang, Qian [5 ]
Lu, Zhigang [1 ,2 ,3 ,4 ,8 ]
机构
[1] Nanjing Univ Chinese Med, Nanjing Hosp Chinese Med, Nanjing 210022, Peoples R China
[2] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Tradit Chinese Med, Nanjing 210023, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Pharm, Jiangsu Key Lab Pharmacol & Safety Evaluat Chinese, Nanjing 210023, Peoples R China
[4] Nanjing Univ Chinese Med, Key Lab Acupuncture & Med Res, Minist Educ, Nanjing 210023, Peoples R China
[5] Nanjing Univ Chinese Med, Coll Int Educ, Nanjing 210023, Peoples R China
[6] Nanjing Univ Chinese Med, Inst Pediat, Jiangsu Key Lab Pediat Resp Dis, Affiliated Hosp, Nanjing 210023, Peoples R China
[7] Nanjing Univ, Nanjing Drum Tower Hosp, Dept Sports Med & Adult Reconstruct Surg, State Key Lab Pharmaceut Biotechnol,Affiliated Hos, Nanjing 210008, Peoples R China
[8] 138 Xianlin Ave, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Compound; 511; Morphine; Immunosuppression; Th1/Th2; Th17/Treg; PI3K; /AKT/mTOR; MRSA pneumonia; MU-OPIOID RECEPTOR; IMMUNE-RESPONSES; CELLS; EXPRESSION; DIFFERENTIATION; INNATE; KINASE; RISK; SUPPRESSION; LYMPHOCYTES;
D O I
10.1016/j.phymed.2022.154475
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Opioids are widely used in clinical practice. However, their long-term administration causes respiratory depression, addiction, tolerance, and severe immunosuppression. Traditional Chinese medicine (TCM) can alleviate opioid-induced adverse effects. Compound 511 is particularly developed for treating opioid addiction, based on Jiumi Liangfang, an ancient Chinese drug treatment and rehabilitation monograph completed in 1833 A.D. It is an herbal formula containing eight plants, each of them contributing to the overall pharmacological effect of the product: Panax ginseng C. A. Meyer (8.8%), Astragalus membranaceus (Fisch.) (18.2%), Datura metel Linn. (10.95%), Corydalis yanhusuo W. T. Wang (14.6%), Acanthopanar gracilist mu lus W. W. Smith (10.95%), Ophiopogon japonicus (Linn. f.) Ker-Gawl. (10.95%), Gynostemma pentaphyllum (Thunb.) Makino (10.95%), Polygala arvensis Willd. (14.6%). This formula effectively ameliorates opioid-induced immunosup-pression. However, the underlying mechanism remains unclear. P urpose: To reveal the effects of Compound 511 on the immune response of morphine-induced immunosup-pressive mice and their potential underlying molecular mechanism. This study provides information for a better clinical approach and scientific use of opioids. Methods: Immunosuppression was induced in mice by repeated morphine administration. Th1/Th2/Th17/Treg cell levels were measured using flow cytometry. Splenic transcription factors of Th1/Th2/Th17/Treg and outputs of the regulatory PI3K/AKT/mTOR signaling pathway were determined. Subsequently, methicillin-resistant Staphylococcus aureus (MRSA) was administered intranasally to morphine-induced immunosuppressive mice pretreated with Compound 511. Their lung inflammatory status was assessed using micro-computer tomography (CT), hematoxylin and eosin (H&E) staining, and enzyme-linked immunosorbent assay (ELISA). Results: Compared to morphine, Compound 511 significantly decreased the immune organ indexes of mice, corrected the Th1/Th2 and Treg/Th17 imbalance in the immune organs and peripheral blood, reduced the mRNA levels of FOXP3 and GATA3, and increased those of STAT3 and T-bet in the spleen. It improved immune function and reduced MRSA-induced lung inflammation. Conclusion: Compound 511 ameliorates opioid-induced immunosuppression by regulating the balance of Th1/ Th2 and Th17/Treg via PI3K/AKT/mTOR signaling pathway. Thus, it effectively reduces susceptibility of morphine-induced immunosuppressive mice to MRSA infection.
引用
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页数:13
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