Gut microbiota and metabonomics used to explore the mechanism of Qing'e Pills in alleviating osteoporosis

被引:50
作者
Xie, Hui [1 ,2 ]
Hua, Zhengying [1 ,2 ]
Guo, Mengyu [1 ,2 ]
Lin, Shangyang [1 ,2 ]
Zhou, Yaqian [1 ,2 ]
Weng, Zebin [3 ]
Wu, Li [1 ]
Chen, Zhipeng [1 ,2 ]
Xu, Zisheng [4 ]
Li, Weidong [1 ,2 ]
机构
[1] Nanjing Univ Chinese Med, Sch Pharm, Nanjing, Peoples R China
[2] Nanjing Univ Chinese Med, Jiangsu Key Lab Chinese Med Proc, Engn Ctr State Minist Educ Standardizat Chinese M, Nanjing, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Chinese Med, Nanjing, Peoples R China
[4] Wuhu Pure Sunshine Nat Med Co Ltd, Wuhu, Peoples R China
基金
中国国家自然科学基金;
关键词
Traditional Chinese medicine; intestinal flora; mass spectrometry; postmenopausal; BONE; EXPRESSION; CELLS; HOST;
D O I
10.1080/13880209.2022.2056208
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Context The traditional Chinese medicine Qing'e Pills (QEP) has been used to treat postmenopausal osteoporosis (PMO). Objective We evaluated the regulatory effects of QEP on gut microbiota in osteoporosis. Materials and methods Eighteen female SD rats were divided into three groups: sham surgery (SHAM), ovariectomized (OVX) and ovariectomized treated with QEP (OVX + QEP). Six weeks after ovariectomy, QEP was administered to OVX + QEP rats for eight weeks (4.5 g/kg/day, i.g.). After 14 weeks, the bone microstructure was evaluated. Differences in gut microbiota were analysed via 16S rRNA gene sequencing. Changes in endogenous metabolites were studied using UHPLC-Q-TOF/MS technology. GC-MS was used to detect short-chain fatty acids. Furthermore, we measured serum inflammatory factors, such as IL-6, TNF-alpha and IFN-gamma, which may be related to gut microbiota. Results OVX + QEP exhibited increased bone mineral density (0.11 +/- 0.03 vs. 0.21 +/- 0.02, p< 0.001) compared to that of OVX. QEP altered the composition of gut microbiota. We identified 19 potential biomarkers related to osteoporosis. QEP inhibited the elevation of TNF-alpha (38.86 +/- 3.19 vs. 29.43 +/- 3.65, p< 0.05) and IL-6 (83.38 +/- 16.92 vs. 45.26 +/- 3.94, p< 0.05) levels, while it increased the concentrations of acetic acid (271.95 +/- 52.41 vs. 447.73 +/- 46.54, p< 0.001), propionic acid (28.96 +/- 5.73 vs. 53.41 +/- 14.26, p< 0.01) and butyric acid (24.92 +/- 18.97 vs. 67.78 +/- 35.68, p< 0.05). Conclusions These results indicate that QEP has potential of regulating intestinal flora and improving osteoporosis. The combination of anti-osteoporosis drugs and intestinal flora could become a new treatment for osteoporosis.
引用
收藏
页码:785 / 800
页数:16
相关论文
共 43 条
[1]
Akkermansia muciniphila-derived extracellular vesicles influence gut permeability through the regulation of tight junctions [J].
Chelakkot, Chaithanya ;
Choi, Youngwoo ;
Kim, Dae-Kyum ;
Park, Hyun T. ;
Ghim, Jaewang ;
Kwon, Yonghoon ;
Jeon, Jinseong ;
Kim, Min-Seon ;
Jee, Young-Koo ;
Gho, Yong S. ;
Park, Hae-Sim ;
Kim, Yoon-Keun ;
Ryu, Sung H. .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2018, 50 :e450-e450
[2]
Akkermansia muciniphila and improved metabolic health during a dietary intervention in obesity: relationship with gut microbiome richness and ecology [J].
Dao, Maria Carlota ;
Everard, Amandine ;
Aron-Wisnewsky, Judith ;
Sokolovska, Nataliya ;
Prifti, Edi ;
Verger, Eric O. ;
Kayser, Brandon D. ;
Levenez, Florence ;
Chilloux, Julien ;
Hoyles, Lesley ;
Dumas, Marc-Emmanuel ;
Rizkalla, Salwa W. ;
Dore, Joel ;
Cani, Patrice D. ;
Clement, Karine .
GUT, 2016, 65 (03) :426-436
[3]
Pharmacological Management of Osteoporosis in Postmenopausal Women: An Endocrine Society Clinical Practice Guideline [J].
Eastell, Richard ;
Rosen, Clifford J. ;
Black, Dennis M. ;
Cheung, Angela M. ;
Murad, M. Hassan ;
Shoback, Dolores .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2019, 104 (05) :1595-1622
[4]
Gut microbiota and diet in patients with different glucose tolerance [J].
Egshatyan, Lilit ;
Kashtanova, Daria ;
Popenko, Anna ;
Tkacheva, Olga ;
Tyakht, Alexander ;
Alexeev, Dmitry ;
Karamnova, Natalia ;
Kostryukova, Elena ;
Babenko, Vladislav ;
Vakhitova, Maria ;
Boytsov, Sergey .
ENDOCRINE CONNECTIONS, 2016, 5 (01) :1-9
[5]
Gut Microbiota as a Target in the Pathogenesis of Metabolic Disorders: A New Approach to Novel Therapeutic Agents [J].
Ejtahed, H. -S. ;
Soroush, A. -R. ;
Angoorani, P. ;
Larijani, B. ;
Hasani-Ranjbar, S. .
HORMONE AND METABOLIC RESEARCH, 2016, 48 (06) :349-358
[6]
Feng WC, 2014, HEILONGJIANG J TRADI, V43, P90
[7]
Finlayson A, 2015, WORLD J GASTRO ENDOS, V7, P1103, DOI [10.4291/wjgp.v6.i4.110, 10.4291/wjgp.v6.i4.110, 10.4253/wjge.v7.i13.1103]
[8]
The Effect of Hops (Humulus lupulus L.) Extract Supplementation on Weight Gain, Adiposity and Intestinal Function in Ovariectomized Mice [J].
Hamm, Alison K. ;
Manter, Daniel K. ;
Kirkwood, Jay S. ;
Wolfe, Lisa M. ;
Cox-York, Kimberly ;
Weir, Tiffany L. .
NUTRIENTS, 2019, 11 (12)
[9]
Gut Microbiota in Patients with Different Metabolic Statuses: Moscow Study [J].
Kashtanova, Dania A. ;
Tkacheva, Olga N. ;
Doudinskaya, Ekaterina N. ;
Strazhesko, Irina D. ;
Kotovskaya, Yulia, V ;
Popenko, Anna S. ;
Tyakht, Alexander, V ;
Alexeev, Dmitry G. .
MICROORGANISMS, 2018, 6 (04)
[10]
Mechanisms Underlying Bone Loss Associated with Gut Inflammation [J].
Ke, Ke ;
Arra, Manoj ;
Abu-Amer, Yousef .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (24)