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Valeriana jatamansi Jones Inhibits Rotavirus-Induced Diarrhea via Phosphatidylinositol 3-Kinase/Protein Kinase B Signaling Pathway

  • Zhang, Bin (Jiangsu Agri-Animal Husbandry Vocational College) ;
  • Wang, Yan (Food, Animal and Plant Inspection and Quarantine Technical Center of Shanghai Customs) ;
  • Jiang, Chunmao (Jiangsu Agri-Animal Husbandry Vocational College) ;
  • Wu, Caihong (Jiangsu Agri-Animal Husbandry Vocational College) ;
  • Guo, Guangfu (Jiangsu Agri-Animal Husbandry Vocational College) ;
  • Chen, Xiaolan (Jiangsu Agri-Animal Husbandry Vocational College) ;
  • Qiu, Shulei (Jiangsu Agri-Animal Husbandry Vocational College)
  • Received : 2020.03.05
  • Accepted : 2020.05.18
  • Published : 2021.08.28

Abstract

Rotavirus (RV), as the main cause of diarrhea in children under 5 years, contributes to various childhood diseases. Valeriana jatamansi Jones is a traditional Chinese herb and possesses antiviral effects. In this study we investigated the potential mechanisms of V. jatamansi Jones in RV-induced diarrhea. MTT assay was performed to evaluate cell proliferation and the diarrhea mice model was constructed using SA11 infection. Mice were administered V. jatamansi Jones and ribavirin. Diarrhea score was used to evaluate the treatment effect. The enzyme-linked immunosorbent assay was performed to detect the level of cytokines. Western blot and quantitative reverse transcription-PCR were used to determine protein and mRNA levels, respectively. Hematoxylin-eosin staining was applied to detect the pathological change of the small intestine. TdT-mediated dUTP nick-end labeling was conducted to determine the apoptosis rate. The results showed V. jatamansi Jones promoted MA104 proliferation. V. jatamansi Jones downregulated phosphatidylinositol 3-kinase (PI3K) and protein kinase B (AKT) in protein level, which was consistent with the immunohistochemistry results. Moreover, V. jatamansi Jones combined with ribavirin regulated interleukin-1β (IL-1β), interferon γ, IL-6, tumor necrosis factor α, and IL-10, and suppressed secretory immunoglobulin A secretion to remove viruses and inhibit dehydration. V. jatamansi Jones + ribavirin facilitated the apoptosis of small intestine cells. In conclusion, V. jatamansi Jones may inhibit RV-induced diarrhea through PI3K/AKT signaling pathway, and could therefore be a potential therapy for diarrhea.

Keywords

Acknowledgement

This study was suported by Jiangsu Province Agricultural Three New Projects (SXGC[2017]249), Jiangsu Province Agri-animal Husbandry Vocational Project (NSF201901), and Qing Lan Project of Jiangsu.

References

  1. Chiappini E, Azzari C, Moriondo M, Galli L, de Martino M. 2005. Viraemia is a common finding in immunocompetent children with rotavirus infection. J. Med. Virol. 76: 265-267. https://doi.org/10.1002/jmv.20351
  2. Dennehy PH. 2000. Transmission of rotavirus and other enteric pathogens in the home. Pediatr. Infect. Dis. J. 19: S103-S105. https://doi.org/10.1097/00006454-200010001-00003
  3. Clarke P, Tyler KL. 2003. Reovirus-induced apoptosis: a minireview. Apoptosis 8: 141-150. https://doi.org/10.1023/A:1022966508671
  4. Lepage P, Vergison A. 2007. Prevention of childhood rotavirus disease through the use of Rotarix (TM) and Rota Teq vaccines. Expert Opin. Biol. Ther. 7: 1881-1892. https://doi.org/10.1517/14712598.7.12.1881
  5. Kochhar S, Rath B, Seeber LD, Rundblad G, Khamesipour A, Ali M. et al. 2013. Introducing new vaccines in developing countries. Expert Rev. Vaccines 12: 1465-1478. https://doi.org/10.1586/14760584.2013.855612
  6. Mathela CS, Chanotiya CS, Sammal SS, Pant AK, Pandey S. 2005. Compositional diversity of terpenoids in the Himalayan Valeriana genera. Chem. Biodivers. 2: 1174-1182. https://doi.org/10.1002/cbdv.200590087
  7. Wang C, Xiao Y, Yang B, Wang Z, Wu L, Su X, et al. 2014. Isolation and screened neuroprotective active constituents from the roots and rhizomes of Valeriana amurensis. Fitoterapia 96: 48-55. https://doi.org/10.1016/j.fitote.2014.04.007
  8. Li YD, Wu ZY, Li HM, Li H, Li RT. 2013. Iridoids from the roots of Valeriana jatamansi. Helvetica Chimica Acta 96: 424-430. https://doi.org/10.1002/hlca.201100465
  9. Xu J, Guo P, Guo Y, Fang L, Li Y, Sun Z, Gui L. 2013. Iridoids from the roots of Valeriana jatamansi and their biological activities. Nat. Prod. Res. 26: 1996-2001. https://doi.org/10.1080/14786419.2011.636747
  10. Wang RJ, Chen HM, Yang F, Deng Y, Ao H, Xie XF, et al. 2017. Iridoids from the roots of Valeriana jatamansi Jones. Phytochemistry 141: 156-161. https://doi.org/10.1016/j.phytochem.2017.05.010
  11. Bhatt, ID, Preeti R, Sandeep G, Kailash SJ, Arun R, Ranbeer SD, et al. 2012. Characterization of essential oil composition, phenolic content, and antioxidant properties in wild and planted individuals of Valeriana jatamansi Jones. Sci. Hortic. 136: 61-68. https://doi.org/10.1016/j.scienta.2011.12.032
  12. Dong FW, Liu Y, Wu ZK, Wei G, Zi CT, Yang D, et al. 2015. Iridoids and sesquiterpenoids from the roots of Valeriana jatamansi Jones. Fitoterapia 102: 27-34. https://doi.org/10.1016/j.fitote.2015.01.021
  13. Simpson E, Wittet S, Bonilla J, Gamazina K, Cooley L, Winkler JL. 2007. Use of formative research in developing a knowledge translation approach to rotavirus vaccine introduction in developing countries. BMC Public Health 7: 281. https://doi.org/10.1186/1471-2458-7-281
  14. Lopez S, Arias CF. 1992. Simian rotavirus SA11 strains. J. Virol. 66: 1832-1832. https://doi.org/10.1128/jvi.66.3.1832-.1992
  15. Liu YH, Wu PQ, Hu QL, Pei YJ, Qi FM, Zhang ZX, et al. 2017. Cytotoxic and antibacterial activities of iridoids and sesquiterpenoids from Valeriana jatamansi. Fitoterapia 123: 73-78. https://doi.org/10.1016/j.fitote.2017.09.011
  16. Sun Y, Zhang Y, Chi P. 2018. Pirfenidone suppresses TGF-β1-induced human intestinal fibroblasts activities by regulating proliferation and apoptosis via the inhibition of the Smad and PI3K/AKT signaling pathway. Mol. Med. Rep. 18: 3907-3913. https://doi.org/10.3892/mmr.2018.9423
  17. Khedr RM, Ahmed AAE, Kamel R, Raafat EM. 2018. Sitagliptin attenuates intestinal ischemia/reperfusion injury via cAMP/PKA, PI3K/Akt pathway in a glucagon-like peptide 1 receptor-dependent manner. Life Sci. 211: 31-39. https://doi.org/10.1016/j.lfs.2018.09.013
  18. Shao Y, Wolf PG, Guo S, Guo Y, Gaskins HR, Zhang B. 2017. Zinc enhances intestinal epithelial barrier function through the PI3K/AKT/mTOR signaling pathway in Caco-2 cells. J. Nutr. Biochem. 43: 18-26. https://doi.org/10.1016/j.jnutbio.2017.01.013
  19. Liu X, Cohen JI. 2015. The role of PI3K/Akt in human herpesvirus infection: from the bench to the bedside. Virology 479-480: 568-577. https://doi.org/10.1016/j.virol.2015.02.040
  20. Zhang X, Wu H, Liu C, Tian J, Qu L. 2015. PI3K/Akt/p53 pathway inhibits reovirus infection. Infect. Genet. Evol. 34: 415-422. https://doi.org/10.1016/j.meegid.2015.06.008
  21. Kong N, Wu Y, Meng Q, Wang Z, Zuo Y, Pan X, et al. 2016. Suppression of virulent porcine epidemic diarrhea virus proliferation by the PI3K/Akt/GSK-3α/β pathway. PLoS One 11: e0161508. https://doi.org/10.1371/journal.pone.0161508
  22. Ding S, Zhu S, Ren L, Feng N, Song Y, Ge X. et al. 2018. Rotavirus VP3 targets MAVS for degradation to inhibit type III interferon expression in intestinal epithelial cells. Elife 7: e39494. https://doi.org/10.7554/eLife.39494
  23. Yin Y, Dang W, Zhou X, Xu L, Wang W, Cao W, et al. 2018. PI3K-Akt-mTOR axis sustains rotavirus infection via the 4E-BP1 mediated autophagy pathway and represents an antiviral target. Virulence 9: 83-98. https://doi.org/10.1080/21505594.2017.1326443
  24. Murray JL, McDonald NJ, Sheng J, Shaw MW, Hodge TW, Rubin DH, et al. 2012. Inhibition of influenza A virus replication by antagonism of a PI3K-AKT-mTOR pathway member identified by gene-trap insertional mutagenesis. Antivir. Chem. Chemother. 22: 205-215. https://doi.org/10.3851/IMP2080
  25. Liu J, Gao R, Shi H, Cong G, Chen J, Zhang X, et al. 2020. Development of a rapid immunochromatographic strip test for the detection of porcine epidemic diarrhea virus specific SIgA in colostrum. J. Virol. Methods 279: 113855. https://doi.org/10.1016/j.jviromet.2020.113855