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Shenkang VII Recipe Attenuates Unilateral Ureteral Obstruction-induced Renal Fibrosis via TGF-β/Smad, NF-κB and SHH Signaling Pathway

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This study aimed to explore the protective effects of the traditional Chinese Medicine formula Shenkang VII recipe (SK-7) on renal fibrosis and the mechanisms. Renal fibrosis was induced by unilateral ureteral obstruction (UUO) in rats. The rats were then divided into 5 groups: control group (Sham operation), UUO model group, UUO model plus low to high doses of SK-7 (0.5, 1.0, or 2.0 g/kg/day, for 14 days) groups. The animals were sacrificed on the 7th or 14th day. Kidney tissues were collected for histopathological examinations (hematoxylin and eosin and Masson’s trichrome staining). Immunohistochemistry was used to detect the expression of collagen type III (Col III), fibronectin (FN), α-smooth muscle actin (α-SMA), TIMP metallopeptidase inhibitor 2 (TIMP2), matrix metallopeptidase 2 (MMP2), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and monocyte chemotactic protein-1 (MCP-1). The TGF-β1/Smad, NF-kB and Sonic hedgehog signaling proteins were detected by Western blotting. Our results showed that SK-7 prevented UUO-induced renal injury and accumulation of collagen fibrils. Renal fibrosis biomarkers Col III, FN, α-SMA and TIMP2 were increased in the rats after UUO and decreased by SK-7, while MMP2 was upregulated after treatment. SK-7 also suppressed the levels of TNF-α, IL-1β and MCP-1 in UUO rats. In addition, SK-7 inhibited activation of the TGF-β/Smad, NF-κB and sonic hedgehog signaling (SHH) pathways. Taken together, these findings suggest that SK-7 may regulate the synthesis and degradation of extracellular matrix, reduce inflammation and suppress the proliferation of fibroblasts, by blocking the TGF-β1/Smad, NF-κB and SHH signaling pathways to exert its anti-renal fibrosis effect in UUO rats.

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References

  1. Liu JH, He L, Zou ZM, et al. A Novel Inhibitor of Homodimerization Targeting MyD88 Ameliorates Renal Interstitial Fibrosis by Counteracting TGF-βl-Induced EMT in Vivo and in Vitro. Kidney Blood Press Res, 2018,43(5):1677–1687

    CAS  Google Scholar 

  2. Humphreys BD.. Mechanisms of Renal Fibrosis. Annu Rev Physiol, 2018,80:309–326

    CAS  Google Scholar 

  3. Tang PM, Nikolic-Paterson DJ, Lan HY. Macrophages: versatile players in renal inflammation and fibrosis. Nat Rev Nephrol, 2019,15(3):144–158

    Google Scholar 

  4. Yu Y, Feng XH. TGF-β signaling in cell fate control and cancer. Curr Opin Cell Biol, 2019,61:56–63

    CAS  Google Scholar 

  5. Lan HY. Diverse roles of TGF-β/Smads in renal fibrosis and inflammation. Int J Biol Sci, 2011,7(7):1056–1067

    CAS  Google Scholar 

  6. Zhou D, Liu Y. Renal fibrosis in 2015: Understanding the mechanisms of kidney fibrosis. Nat Rev Nephrol, 2016,12(2):68–70

    CAS  Google Scholar 

  7. Kassiri Z, Defamie V, Hariri M, et al. Simultaneous transforming growth factor beta-tumor necrosis factor activation and cross-talk cause aberrant remodeling response and myocardial fibrosis in Timp3-deficient heart. J Biol Chem, 2009,284(43):29893–29904

    CAS  Google Scholar 

  8. Meng XM, Tang PM, Li J, et al.. TGF-β/Smad signaling in renal fibrosis. Front Physiol, 2015,6:82

    Google Scholar 

  9. Ka SM, Huang XR, Lan HY, et al. Smad7 gene therapy ameliorates an autoimmune crescentic glomerulonephritis in mice. J Am Soc Nephrol, 2007,18(6):1777–1788

    CAS  Google Scholar 

  10. Liu GX, Li YQ, Huang XR, et al. Disruption of Smad7 promotes ANG II-mediated renal inflammation and fibrosis via Sp1-TGF-β/Smad3-NF. κB-dependent mechanisms in mice. PLoS One, 2013,8(1):e53573

    CAS  Google Scholar 

  11. Meng XM.. Inflammatory Mediators and Renal Fibrosis. Adv Exp Med Biol, 2019,1165:381–406

    CAS  Google Scholar 

  12. Sutariya B, Jhonsa D, Saraf MN. TGF-β: the connecting link between nephropathy and fibrosis. Immunopharmacol Immunotoxicol, 2016,38(1):39–49

    CAS  Google Scholar 

  13. Dennis EA, Smythies LE, Grabski R, et al. Cytomegalovirus promotes intestinal macrophage-mediated mucosal inflammation through induction of Smad7. Mucosal Immunol, 2018,11(6):1694–1704

    CAS  Google Scholar 

  14. Huang J, Wan D, Li J, et al. Histone acetyltransferase PCAF regulates inflammatory molecules in the development of renal injury. Epigenetics, 2015,10(1):62–72

    Google Scholar 

  15. Hall ET, Cleverdon ER, Ogden SK. Dispatching Sonic Hedgehog: Molecular Mechanisms Controlling Deployment. Trends Cell Biol, 2019,29(5):385–395

    CAS  Google Scholar 

  16. Sasai N, Toriyama M, Kondo T.. Hedgehog Signal and Genetic Disorders. Front Genet, 2019,10:1103

    CAS  Google Scholar 

  17. Zhou D, Li Y, Zhou L, et al. Sonic hedgehog is a novel tubule-derived growth factor for interstitial fibroblasts after kidney injury. J Am Soc Nephrol, 2014,25(10):2187–2200

    CAS  Google Scholar 

  18. Hong D, Dong Z, Sha H, et al. Sonic hedgehog signaling mediates epithelial-mesenchymal communication and promotes renal fibrosis. J Am Soc Nephrol, 2012,23(5):801–813

    Google Scholar 

  19. Wang Y, Liu N, Su X, et al.. Epigallocatechin-3-gallate attenuates transforming growth factor-β1 induced epithelial-mesenchymal transition via Nrf2 regulation in renal tubular epithelial cells. Biomed Pharmacother, 2015,70:260–267

    CAS  Google Scholar 

  20. Zhao YY, Chen H, Tian T, et al. A pharmaco-metabonomic study on chronic kidney disease and therapeutic effect of ergone by UPLC-QTOF/HDMS. PLoS One, 2014,9(12):e115467

    Google Scholar 

  21. Li S, Xiao X, Han L, et al. Renoprotective effect of Zhenwu decoction against renal fibrosis by regulation of oxidative damage and energy metabolism disorder. Sci Rep, 2018,8(1):14627

    Google Scholar 

  22. Jin R, Lin ZJ, Xue CM, et al. An improved association-mining research for exploring Chinese herbal property theory: based on data of the Shennong’s Classic of Materia Medica. J Integr Med, 2013,11(5):352–365

    Google Scholar 

  23. Lin WB, Lin CF, Mei GQ. Analysis of Mei Guo-qiang’s experience in treating intractable diseases with “Situ Decoction”. Shanghai J TCM (Chinese), 2012,46(9):16–17

    Google Scholar 

  24. Martínez-Klimova E, Aparicio-Trejo OE, Tapia E, et al. Unilateral Ureteral Obstruction as a Model to Investigate Fibrosis-Attenuating Treatments. Biomolecules, 2019, 9(4):141

    Google Scholar 

  25. Li A, Zhang X, Shu M, et al.. Arctigenin suppresses renal interstitial fibrosis in a rat model of obstructive nephropathy. Phytomedicine, 2017,30:28–41

    CAS  Google Scholar 

  26. Zhao J, Wang L, Cao AL, et al. HuangQi Decoction Ameliorates Renal Fibrosis via TGF-β/Smad Signaling Pathway In Vivo and In Vitro. Cell Physiol Biochem, 2016,38(5):1761–1774

    CAS  Google Scholar 

  27. Sampieri CL, Orozco-Ortega RA. Matrix metallopro-teinases and tissue inhibitors of metalloproteinases in chronic kidney disease and acute kidney injury: a systematic review of the literature. Hippokratia, 2018,22(3):99–104

    CAS  Google Scholar 

  28. Wang Z, Famulski K, Lee J, et al. TIMP2 and TIMP3 have divergent roles in early renal tubulointerstitial injury. Kidney Int, 2014,85(1):82–93

    CAS  Google Scholar 

  29. N El Agha E, Kramann R, Schneider RK, et al. Mesenchymal Stem Cells in Fibrotic Disease. Cell Stem Cell, 2017,21(2):166–177

    Google Scholar 

  30. Li JH, Zhu HJ, Huang XR, et al. Smad7 inhibits fibrotic effect of TGF-Beta on renal tubular epithelial cells by blocking Smad2 activation [published correction appears in J Am Soc Nephrol. 2003 Sep;14(9):2417]. J Am Soc Nephrol, 2002,13(6):1464–1472

    CAS  Google Scholar 

  31. Zhang ZH, Li MH, Liu D, et al.. Rhubarb Protect Against Tubulointerstitial Fibrosis by Inhibiting TGF-β/Smad Pathway and Improving Abnormal Metabolome in Chronic Kidney Disease. Front Pharmacol, 2018,9:1029

    Google Scholar 

  32. Hu HH, Chen DQ, Wang YN, et al.. New insights into TGF-β/Smad signaling in tissue fibrosis. Chem Biol Interact, 2018,292:76–83

    CAS  Google Scholar 

  33. House CD, Grajales V, Ozaki M, et al. IKKε cooperates with either MEK or non-canonical NF-kB driving growth of triple-negative breast cancer cells in different contexts. BMC Cancer, 2018,18(1):595

    Google Scholar 

  34. Shih RH, Wang CY, Yang CM. NF-kappaB Signaling Pathways in Neurological Inflammation: A Mini Review. Front Mol Neurosci, 2015,8:77

    Google Scholar 

  35. Tornatore L, Thotakura AK, Bennett J, et al. The nuclear factor kappa B signaling pathway: integrating metabolism with inflammation. Trends Cell Biol, 2012,22(11):557–566

    CAS  Google Scholar 

  36. Morgan MJ, Liu ZG. Crosstalk of reactive oxygen species and NF-κB signaling. Cell Res, 2011,21(1):103–115

    CAS  Google Scholar 

  37. Sun SC. The non-canonical NF-κB pathway in immunity and inflammation. Nat Rev Immunol, 2017,17(9):545–558

    CAS  Google Scholar 

  38. Voges D, Zwickl P, Baumeister W.. The 26S proteasome: a molecular machine designed for controlled proteolysis. Annu Rev Biochem, 1999,68:1015–1068

    CAS  Google Scholar 

  39. Schütz E, Bochenek ML, Riehl DR, et al. Absence of transforming growth factor beta 1 in murine platelets reduces neointima formation without affecting arterial thrombosis. Thromb Haemost, 2017,117(9):1782–1797

    Google Scholar 

  40. Du J, Paz K, Flynn R, et al. Pirfenidone ameliorates murine chronic GVHD through inhibition of macrophage infiltration and TGF-β production. Blood, 2017,129(18):2570–2580

    CAS  Google Scholar 

  41. Chung AC, Huang XR, Zhou L, et al. Disruption of the Smad7 gene promotes renal fibrosis and inflammation in unilateral ureteral obstruction (UUO) in mice. Nephrol Dial Transplant, 2009,24(5):1443–1454

    CAS  Google Scholar 

  42. Lin N, Ji Z, Huang C. Smad7 alleviates glomerular mesangial cell proliferation via the ROS-NF-κB pathway. Exp Cell Res, 2017,361(2):210–216

    CAS  Google Scholar 

  43. Zhou D, Tan RJ, Liu Y. Sonic hedgehog signaling in kidney fibrosis: a master communicator. Sci China Life Sci, 2016,59(9):920–929

    CAS  Google Scholar 

  44. Liu X, Sun N, Mo N, et al. Quercetin inhibits kidney fibrosis and the epithelial to mesenchymal transition of the renal tubular system involving suppression of the Sonic Hedgehog signaling pathway. Food Funct, 2019,10(6):3782–3797

    CAS  Google Scholar 

  45. Lu H, Chen B, Hong W, et al. Transforming growth factor-β1 stimulates hedgehog signaling to promote epithelial-mesenchymal transition after kidney injury. FEBS J, 2016,283(20):3771–3790

    CAS  Google Scholar 

  46. Cruz-Solbes AS, Youker K.. Epithelial to Mesenchymal Transition (EMT) and Endothelial to Mesenchymal Transition (EndMT): Role and Implications in Kidney Fibrosis. Results Probl Cell Differ, 2017,60:345–372

    CAS  Google Scholar 

  47. Devocelle A, Lecru L, François H, et al. Inhibition of TGF-β1 Signaling by IL-15: A Novel Role for IL-15 in the Control of Renal Epithelial-Mesenchymal Transition: IL-15 Counteracts TGF-β1-Induced EMT in Renal Fibrosis. Int J Cell Biol, 2019:9151394

  48. Kramann R. Hedgehog Gli signalling in kidney fibrosis. Nephrol Dial Transplant, 2016,31(12):1989–1995

    CAS  Google Scholar 

  49. Ji GQ, Chen RQ, Wang L. Anti-inflammatory activity of atractylenolide III through inhibition of nuclear factor-κB and mitogen-activated protein kinase pathways in mouse macrophages. Immunopharmacol Immunotoxicol, 2016,38(2):98–102

    CAS  Google Scholar 

  50. Yang J, Zeng Z, Wu T, et al. Emodin attenuates high glucose-induced TGF-β1 and fibronectin expression in mesangial cells through inhibition of NF-κB pathway. Exp Cell Res, 2013,319(20):3182–3189

    CAS  Google Scholar 

  51. Chen F, Zhu X, Sun Z, et al.. Astilbin Inhibits High Glucose-Induced Inflammation and Extracellular Matrix Accumulation by Suppressing the TLR4/MyD88/NF-κB Pathway in Rat Glomerular Mesangial Cells. Front Pharmacol, 2018,9:1187

    CAS  Google Scholar 

  52. Chen JK, Guo MK, Bai XH, et al. Astragaloside IV ameliorates intermittent hypoxia-induced inflammatory dysfunction by suppressing MAPK/NF-κB signalling pathways in Beas-2B cells. Sleep Breath, 2020,24(3):1237–1245

    Google Scholar 

  53. Gao Y, Hou R, Liu F, et al. Obacunone causes sustained expression of MKP-1 thus inactivating p38 MAPK to suppress pro-inflammatory mediators through intracellular MIF. J Cell Biochem, 2018,119(1):837–849

    CAS  Google Scholar 

  54. Tsang SW, Zhang H, Lin C, et al. Rhein, a natural anthraquinone derivative, attenuates the activation of pancreatic stellate cells and ameliorates pancreatic fibrosis in mice with experimental chronic pancreatitis. PLoS One, 2013,8(12):e82201

    Google Scholar 

  55. Ma L, Li H, Zhang S, et al. Emodin ameliorates renal fibrosis in rats via TGF-β1/Smad signaling pathway and function study of Smurf 2. Int Urol Nephrol, 2018,50(2):373–382

    CAS  Google Scholar 

  56. Qu W, Wang Y, Wu Q, et al.. Emodin Impairs Radioresistance of Human Osteosarcoma Cells by Suppressing Sonic Hedgehog Signaling. Med Sci Monit, 2017,23:5767–5773

    CAS  Google Scholar 

  57. Chen L, Lan Z, Zhou Y, et al. Astilbin attenuates hyperuricemia and ameliorates nephropathy in fructose-induced hyperuricemic rats. Planta Med, 2011,77(16):1769–1773

    CAS  Google Scholar 

  58. Chen F, Zhu X, Sun Z, et al.. Astilbin Inhibits High Glucose-Induced Inflammation and Extracellular Matrix Accumulation by Suppressing the TLR4/MyD88/NF-κB Pathway in Rat Glomerular Mesangial Cells. Front Pharmacol, 2018,9:1187

    CAS  Google Scholar 

  59. Guo LH, Cao Y, Zhuang RT, et al. Astragaloside IV promotes the proliferation and migration of osteoblast-like cells through the hedgehog signaling pathway. Int J Mol Med, 2019,43(2):830–838

    CAS  Google Scholar 

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Correspondence to Yuan-ming Ba.

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This study was supported by Academic Experience Inheritance of the Sixth National Group of Old Chinese Medicine Experts of the State Administration of Traditional Chinese Medicine (No. 2017 [29]), and the key projects of Hubei Provincial Department of Health (No. JX6A09).

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The authors declare that there is no conflict of interest.

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Zhou, Ss., Ai, Zz., Li, Wn. et al. Shenkang VII Recipe Attenuates Unilateral Ureteral Obstruction-induced Renal Fibrosis via TGF-β/Smad, NF-κB and SHH Signaling Pathway. CURR MED SCI 40, 917–930 (2020). https://doi.org/10.1007/s11596-020-2255-4

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