Investigation of Crucial Affected Proteins in Rat Liver in the Presence of Scrophularia

Document Type : Original paper

Authors

1 Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

2 Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

3 Traditional Medicine and Materia Medica Research Center, Department of Traditional Medicine, School of Traditional Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

4 Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

5 Department of Surgery, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Abstract

Background and objectives: Radix Scropholaria is dried root Scrophularia ningpoensis Hemsl. which is used uses as a drug against several diseases. In the present study, the crucial affected proteins of rat liver in the presence of radix Scrophularia have been investigated. Methods: The differentially expressed proteins (DEPs) were downloaded from literature. The significant DEPs plus 100 added first neighbors were determined and included in “protein query” of STRING database via Cytoscape software. The network was analyzed and the central nodes among the queried DEPs were identified. The 10 first neighbors of the central DEPs were determined. Results: RT1-CE12, Gfer, Serpina3c, Rab13, Rbm14, Ighg Psmb8, COX2, Olr796, Mga, Ugt1a6, Ugt2b, Ebpl, Ugt2b, Igf2r, and Amacr as significant DEPs were analyzed via protein-protein interaction (PPI) network analysis, Ugt1a1 and Ugt2b the two up-regulated proteins were highlighted as the crucial proteins in response to the radix Scrophularia. Conclusion: Two members of UDP glucuronosyltransferase family; Ugt1a1 and Ugt2b, were pointed as the critical liver enzyme which are dysregulated under effect of radix Scrophulariae. Due to crucial role of Ugt1a1 in the liver function, it is suggested that consumption of Scrophularia ningpoensis Hemsl. as a traditional medicine required more investigation.
 

Keywords

Main Subjects


  • Ren D, Shen ZY, Qin LP, Zhu B. Pharmacology, phytochemistry, and traditional uses of Scrophularia ningpoensis J Ethnopharmacol. 2021; Article ID 113688.
  • Lee HJ, Kim HL, Lee DR, Choi BK, Yang SH. Scrophulariae radix: an overview of its biological activities and nutraceutical and pharmaceutical applications. Molecules. 2021; 26(17): 1–11.
  • Zhang Q, Liu A, Wang Y. Scrophularia ningpoensis Hemsl: a review of its phytochemistry, pharmacology, quality control and pharmacokinetics. J Pharm Pharmacol. 2021; 73(5): 573–600.
  • Li HW, Liu P, Zhang HQ, Feng WM, Yan H, Guo S, Qian DW, Duan Determination of bioactive compounds in the nonmedicinal parts of Scrophularia ningpoensis using ultra‐high‐performance liquid chromatography coupled with tandem mass spectrometry and chemometric analysis. J Sep Sci. 2020; 43(22): 4191–4201.
  • Lu F, Zhang N, Yu D, Zhao H, Pang M, Fan Y, Liu An integrated metabolomics and 16S rRNA gene sequencing approach exploring the molecular pathways and potential targets behind the effects of radix Scrophulariae. RSC Adv. 2019; 9(57): 33354–33367.
  • Chao HH, Chen PY, Hsu WF. Long-term traditional Chinese medicine–induced liver cirrhosis: a case report. Med Case Rep Study Protoc. 2022; 3(10): 1–4.
  • Vella D, Marini S, Vitali F, Di Silvestre D, Mauri G, Bellazzi R. MTGO: PPI network analysis via topological and functional module identification. Sci Rep. 2018; 8(1): 1–13.
  • Zhu Z, Jin Z, Deng Y, Wei L, Yuan X, Zhang M, Sun Co-expression network analysis identifies four hub genes associated with prognosis in soft tissue sarcoma. Front Genet. 2019; 10: 1–10.
  • Zito A, Lualdi M, Granata P, Cocciadiferro D, Novelli A, Alberio T, Casalone R, Fasano Gene set enrichment analysis of interaction networks weighted by node centrality. Front Genet. 2021; 12: 1–10.
  • Rezaei Tavirani M, Rezaei Tavirani M, Akbari Z, Hajimehdipoor H. Prediction of coffee effects in rats with healthy and NAFLD conditions based on protein-protein interaction network analysis. Res J Pharmacogn. 2019; 6(4): 7–15.
  • Xu Z, Lin S, Gong J, Feng P, Cao Y, Li Q, Jiang Y, You Y, Tong Y, Wang Exploring the protective effects and mechanism of crocetin from saffron against NAFLD by network pharmacology and experimental validation. Fronti Med. 2021; 8: 1–15.
  • Zhang MM, Wang D, Lu F, Zhao R, Ye X, He L, Ai L, Wu Identification of the active substances and mechanisms of ginger for the treatment of colon cancer based on network pharmacology and molecular docking. BioData Min. 2021; 14(1): 1–16.
  • Li ZH, Yu D, Huang NN, Wu JK, Du XW, Wang XJ. Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking. Sci Rep. 2021; 11(1): 1–13.
  • Lu F, Zhang N, Ye T, Zhao H, Pang M, Liu SM. High throughput metabolomics-proteomics investigation on metabolic phenotype changes in rats caused by radix Scrophulariae using ultra-performance liquid chromatography with mass spectrometry. RSC Adv. 2019; 9(31): 17791–17800.
  • Shen X, Eichhorn T, Greten HJ, Efferth T. Effects of Scrophularia ningpoensis on inhibition of proliferation, apoptosis induction and NF-κB signaling of immortalized and cancer cell lines. Pharmaceuticals (Basel). 2012; 5(2): 189–208.
  • Burchell B, Nebert DW, Nelson DR, Bock KW, Iyanagi T, Jansen PL, Lancet D, Mulder GJ, Chowdhury JR, Siest G, Tephly TR, Mackenzie PI. The UDP glucuronosyltransferase gene super family: suggested nomenclature based on evolutionary divergence. DNA Cell Biol. 1991; 10(7): 487–494.
  • Uno Y, Takahira R, Murayama N, Onozeki S, Kawamura S, Uehara S, Ikenaka Y, Ishizuka M, Ikushiro S, Yamazaki Functional and molecular characterization of UDP-glucuronosyltransferase 2 family in Cynomolgus macaques. Biochem Pharmacol. 2019; 163: 335–344.
  • Li Z, Jiang Y, Guengerich FP, Ma L, Li S, Zhang W. Engineering cytochrome P450 enzyme systems for biomedical and biotechnological applications. J Biol Chem. 2020; 295(3): 833–849.
  • Kwon SS, Kim JH, Jeong HU, Ahn KS, Oh SR, Lee HS. Role of cytochrome P450 and UDP-glucuronosyltransferases in metabolic pathway of homoegonol in human liver microsomes. Drug Metab Pharmacokinet. 2015; 30(4): 305–313.
  • Shin IS, Ahn KS, Shin NR, Jeon CM, Kwon OK, Chin YW, Lee K, Oh Homoegonol attenuates the asthmatic responses induced by ovalbumin challenge. Arch Pharm Res. 2014; 37(9): 1201–1210.
  • Kurita A, Miyauchi Y, Ikushiro Si, Mackenzie PI, Yamada H, Ishii Y. Comprehensive characterization of mouse UDP-glucuronosyltransferase (Ugt) belonging to the Ugt2b subfamily: identification of Ugt2b36 as the predominant isoform involved in morphine glucuronidation. J Pharmacol Exp Ther. 2017; 361(2): 199–208.