Traditional Patchouli essential oil modulates the host's immune responses and gut microbiota and exhibits potent anti-cancer effects in ApcMin /+mice

被引:31
作者
Leong, Waikit [1 ]
Huang, Guoxin [1 ]
Liao, Weilin [1 ]
Xia, Wenrui [1 ]
Li, Xiaoang [1 ]
Su, Ziren [2 ]
Liu, Liang [1 ]
Wu, Qiang [1 ]
Wong, Vincent Kam Wai [1 ,3 ]
Law, Betty Yuen Kwan [1 ,3 ]
Xia, Chenglai [1 ]
Guo, Xiaoling
Khan, Imran [1 ,4 ]
Hsiao, W. L. Wendy [1 ,3 ,4 ]
机构
[1] Macau Univ Sci & Technol, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Guangzhou Univ Chinese Med, Sch Pharmaceut Sci, Guangzhou, Peoples R China
[3] Southern Med Univ, Affiliated Foshan Matern & Child Healthcare Hosp, Foshan, Guangdong, Peoples R China
[4] Macau Univ Sci & Technol, Ave Wai Long, Macau, Peoples R China
关键词
Patchouli essential oil; Patchouli alcohol; Pogostone; Gut microbiota; Apc (Min/+)mice; T-CELLS; CANCER; OCCLUDIN; EXPRESSION; PROLIFERATION; PROGRESSION; PROMOTES; CADHERIN; PATHWAY; PROTEIN;
D O I
10.1016/j.phrs.2022.106082
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Patchouli Essential Oil (PEO) has been used as a scent for various healing purposes since the ancient Egyptian period. The primary source of the oil is Pogostemon cablin (PC), a medicinal plant for treating gastrointestinal symptoms. However, the pharmacological function has not been addressed. Here, we report the cancer prevention and gut microbiota (GM) modulating property of PEO and its derivatives patchouli alcohol (PA) and pogostone (PO) in the Apc(Min /+) colorectal cancer mice model. We found that PEO, PA, and PO significantly reduced the tumor burden. At the same time, it strengthened the epithelial barrier, evidenced by substantially increasing the number of the goblet and Paneth cells and upregulation of tight junction and adhesion molecules. In addition, PEO, PA, and PO shifted M1 to M2 macrophage phenotypes and remodeled the inflammatory milieu of Apc(Min /+) mice. We also found suppression of CD4(+)CD25(+) and stimulation CD4(+) CD8(+) cells in the spleen, blood, mesenteric lymph nodes (MLNs), and Peyer's patches (PPs) of the treated mice. The composition of the gut microbiome of the drug-treated mice was distinct from the control mice. The drugs stimulated the short-chain fatty acids (SCFAs)-producers and the key SCFA-sensing receptors (GPR41, GPR43, and GPR109a). The activation of SCFAs/GPSs also triggered the alterations of PPAR-gamma, PYY, and HSDCs signaling mediators in the treated mice. Our work showed that PEO and its derivatives exert potent anti-cancer effects by modulating gut micro biota and improving the intestinal microenvironment of the ApcM(min /+) mice.
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页数:14
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