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Open Access

Reveal the pharmacodynamic substances and mechanism of an edible medicinal plant Rhodiola crenulate in DSS-induced colitis through plasma pharmacochemistry and metabolomics

Yu PengaXiaoao XiaoaTingting JiaXinyuan WangaYixuan XuaJianbo Xiaob,c,d( )Hui Caoc,dZhiyong CheneHuifan LiufYuanqing Gaoa( )Hongxun Taob,g( )
Key Laboratory of Cardiovascular and Cerebrovascular Medicine, School of Pharmacy, Nanjing Medical University, Nanjing 211166, China
School of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013, China
Department of Analytical Chemistry and Food Science, Faculty of Science, University of Vigo, Vigo 36310, Spain
CISPAC, Fontan Building, City of Culture, Santiago de Compostela 15707, Spain
Shaanxi Academy of Traditional Chinese Medicine, Xi'an 710003, China
Guangdong Key Laboratory of Science and Technology of Lingnan Specialty Food, Zhongkai University of Agriculture and Engineering, Guangzhou 510550, China
State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu 610075, China

Peer review under responsibility of Tsinghua University Press.

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Highlights

• 88 compounds were identified in RCE, among which 29 compounds could be absorbed into blood, following by the identification of 8 metabolites.

• A total of 111 characteristic endogenous metabolites were identified.

• Colitis caused the alternation of fatty acid metabolism, steroid hormone biosynthesis and bile acid metabolism.

• The body disposes of the active components in RCE differently under DSS pathological conditions and physiological conditions.

• RCE could prevent colitis by improving fatty acid metabolism and bile acid metabolism.

Abstract

Rhodiola crenulate is the edible medicinal herbal medicine widely used for altitude sickness in China. Interestingly, our previous work has found that R. crenulate extract (RCE) could significantly improve the pathology associated with dextran sulfate sodium-induced colitis. Thus, the current research aims to reveal the pharmacodynamic material basis of RCE, as well as its mechanism against colitis. The chemical characterization of RCE was performed by UHPLC-HR-MS, through which a total of 88 constituents were identified. Meanwhile, our results also found 29 constituents absorbed into blood and 8 metabolized absorbable compounds. The decreased flavonoids prototype and the elevated sulfated products of phenols were observed under pathophysiological conditions of colitis. The metabolomics study revealed that colitis caused the alternation of fatty acid metabolism, steroid hormone biosynthesis and bile acid metabolism. Correspondingly, RCE could prevent colitis by improving fatty acid metabolism and secondary bile acid metabolism.

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References

[1]

H. Tao, X. Wu, J. Cao, et al., Rhodiola species: A comprehensive review of traditional use, phytochemistry, pharmacology, toxicity, and clinical study, Med. Res. Rev. 39(5) (2019) 1779-1850. https://doi.org/10.1002/med.21564.

[2]

J.D. Amsterdam, A.G. Panossian, Rhodiola rosea L. as a putative botanical antidepressant, Phytomedicine 23(7) (2016) 770-783. https://doi.org/10.1016/j.phymed.2016.02.009.

[3]

S.Y. Lee, M.H. Li, L.S. Shi, et al., Rhodiola crenulata extract alleviates hypoxic pulmonary edema in rats, Evid. Based Complement Alternat. Med. 2013 (2013) 718739. https://doi.org/10.1155/2013/718739.

[4]

V. Darbinyan, A. Kteyan, A. Panossian, et al., Rhodiola rosea in stress induced fatigue: a double blind cross-over study of a standardized extract SHR-5 with a repeated low-dose regimen on the mental performance of healthy physicians during night duty, Phytomedicine 7(5) (2000) 365-371. https://doi.org/10.1016/S0944-7113(00)80055-0.

[5]

W. Zhuang, L. Yue, X. Dang, et al., Rosenroot (Rhodiola): potential applications in aging-related diseases, Aging Dis. 10(1) (2019) 134-146. https://doi.org/10.14336/AD.2018.0511.

[6]

Q. Zhou, X. Han, R. Li, et al., Anti-atherosclerosis of oligomeric proanthocyanidins from Rhodiola rosea on rat model via hypolipemic, antioxidant, anti-inflammatory activities together with regulation of endothelial function, Phytomedicine 51 (2018) 171-180. https://doi.org/10.1016/j.phymed.2018.10.002.

[7]

S. Burdach, The granulocyte/macrophage-colony stimulating factor (GM-CSF): basic science and clinical application, Klin. Padiatr. 203(4) (1991) 302-310. https://doi.org/10.1055/s-2007-1025445.

[8]

A.K. Pandurangan, N. Mohebali, N.M. Esa, et al., Gallic acid suppresses inflammation in dextran sodium sulfate-induced colitis in mice: possible mechanisms, Int. Immunopharmacol. 28(2) (2015) 1034-1043. https://doi.org/10.1016/j.intimp.2015.08.019.

[9]

Y. Qu, X. Li, F. Xu, et al., Kaempferol alleviates murine experimental colitis by restoring gut microbiota and inhibiting the LPS-TLR4-NF-κB axis, Front Immunol 12 (2021) 679897. https://doi.org/10.3389/fimmu.2021.679897.

[10]

Y. Wang, H. Tao, H. Huang, et al., The dietary supplement Rhodiola crenulata extract alleviates dextran sulfate sodium-induced colitis in mice through anti-inflammation, mediating gut barrier integrity and reshaping the gut microbiome, Food Funct. 12(7) (2021) 3142-3158. https://doi.org/10.1039/D0FO03061A.

[11]

G. Yan, H. Sun, A. Zhang, et al., Progress of serum pharmacochemistry of traditional Chinese medicine and further development of its theory and method, China Journal of Chinese Materia Medica 40(17) (2015) 3406-3412. https://doi.org/10.4268/cjcmm20151715.

[12]

K. Zhang, T. Li, X.C. Gong, et al., Online energy-resolved MS boosts the potential of LC-MS towards metabolite characterization of salidroside and tyrosol, Anal. Methods 12(42) (2020) 5120-5127. https://doi.org/10.1039/D0AY01639J.

[13]

T. Farrell, L. Poquet, F. Dionisi, et al., Characterization of hydroxycinnamic acid glucuronide and sulfate conjugates by HPLC-DAD-MS2: enhancing chromatographic quantification and application in Caco-2 cell metabolism, J. Pharm. Biomed. Anal. 55(5) (2011) 1245-1254. https://doi.org/10.1016/j.jpba.2011.03.023.

[14]

L. Poquet, M.N. Clifford, G. Williamson, Investigation of the metabolic fate of dihydrocaffeic acid, Biochem. Pharmacol. 75(5) (2008) 1218-1229. https://doi.org/10.1016/j.bcp.2007.11.009.

[15]

M. Imran, B. Salehi, J. Sharifi-Rad, et al., Kaempferol: a key emphasis to its anticancer potential, Molecules 24(12) (2019) 2277. https://doi.org/10.3390/molecules24122277.

[16]

Y. Li, Y. Zhao, X. Li, et al., Characterization of global metabolic profile of Rhodiola crenulata after oral administration in rat plasma, urine, bile and feces based on UHPLC-FT-ICR MS, J Pharm Biomed Anal 149 (2018) 318-328. https://doi.org/10.1016/j.jpba.2017.10.032.

[17]

A. Gandhi, B. Moorthy, R. Ghose, Drug disposition in pathophysiological conditions, Curr. Drug Metab. 13(9) (2012) 1327-1344. https://doi.org/10.2174/138920012803341302.

[18]

Y. Ma, M. Zeng, R. Sun, et al., Disposition of flavonoids impacts their efficacy and safety, Curr. Drug Metab. 15(9) (2014) 841-864. https://doi.org/10.2174/1389200216666150206123719.

[19]

T. Nishida, H. Miwa, M. Yamamoto, et al., Bile acid absorption kinetics in Crohn’s disease on elemental diet after oral administration of a stable-isotope tracer with chenodeoxycholic-11,12-d2 acid, Gut 23(9) (1982) 751-757. http://dx.doi.org/10.1136/gut.23.9.751.

[20]

E. Mizoguchi, R.J. Xavier, H.C. Reinecker, et al., Colonic epithelial functional phenotype varies with type and phase of experimental colitis, Gastroenterology 125(1) (2003) 148-161. https://doi.org/10.1016/S0016-5085(03)00665-6.

[21]

P.S. Gromski, H. Muhamadali, D.I. Ellis, et al., A tutorial review: metabolomics and partial least squares-discriminant analysis: a marriage of convenience or a shotgun wedding, Anal. Chim. Acta 879 (2015) 10-23. https://doi.org/10.1016/j.aca.2015.02.012.

[22]

F.A. Kuehl, Jr., R.W. Egan, Prostaglandins, arachidonic acid, and inflammation, Science 210 (1980) 978-984. https://doi.org/10.1126/science.6254151.

[23]

N. Nemani, Z. Dong, C.C. Daw, et al., Mitochondrial pyruvate and fatty acid flux modulate MICU1-dependent control of MCU activity, Sci. Signal. 13(628) (2020). https://doi.org/10.1126/scisignal.aaz6206.

[24]

D.Q. Shih, M. Bussen, E. Sehayek, et al., Hepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolism, Nat. Genet. 27(4) (2001) 375-382. https://doi.org/10.1038/86871.

[25]

L. Chen, T. Jiao, W. Liu, et al., Hepatic cytochrome P450 8B1 and cholic acid potentiate intestinal epithelial injury in colitis by suppressing intestinal stem cell renewal, Cell Stem. Cell 29(9) (2022) 1366-1381.e9. https://doi.org/10.1016/j.stem.2022.08.008.

[26]

O. Ramirez-Perez, V. Cruz-Ramon, P. Chinchilla-Lopez, et al., The role of the gut microbiota in bile acid metabolism, Ann. Hepatol. 16 (2017) s15-s20. https://doi.org/10.5604/01.3001.0010.5494.

[27]

G.W. Tannock, A. Tangerman, A. Van Schaik, et al., Deconjugation of bile acids by Lactobacilli in the mouse small bowel, Appl. Environ. Microbiol. 60(9) (1994) 3419-3420. https://doi.org/10.1128/aem.60.9.3419-3420.1994.

[28]

W. Jia, G. Xie, W. Jia, Bile acid-microbiota crosstalk in gastrointestinal inflammation and carcinogenesis, Nat. Rev. Gastroenterol. Hepatol. 15(2) (2018) 111-128. https://doi.org/10.1038/nrgastro.2017.119.

Food Science and Human Wellness
Pages 2116-2131
Cite this article:
Peng Y, Xiao X, Ji T, et al. Reveal the pharmacodynamic substances and mechanism of an edible medicinal plant Rhodiola crenulate in DSS-induced colitis through plasma pharmacochemistry and metabolomics. Food Science and Human Wellness, 2024, 13(4): 2116-2131. https://doi.org/10.26599/FSHW.2022.9250176

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Received: 22 November 2022
Revised: 26 December 2022
Accepted: 24 January 2023
Published: 20 May 2024
© 2024 Beijing Academy of Food Sciences. Publishing services by Tsinghua University Press.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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