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Inflammopharmacology

, Volume 24, Issue 5, pp 233–251 | Cite as

Chemomodulatory effect Melastoma Malabathricum Linn against chemically induced renal carcinogenesis rats via attenuation of inflammation, oxidative stress, and early markers of tumor expansion

  • Amita Verma
  • Prakash Chandra Bhatt
  • Gaurav kaithwas
  • Nikunj Sethi
  • Mohd Rashid
  • Yashwant Singh
  • Mahfoozur Rahman
  • Fahad Al-Abbasi
  • Firoz Anwar
  • Vikas Kumar
Original Article

Abstract

Melastoma malabathricum Linn (MM) has high valued for its commercial significance. Indian market (northeast) has great demand for the plants, which extended, its use as a traditional home remedy due to its anti-inflammatory effects. In this study, we scrutinize the therapeutic and protective effect of MM against diethylnitrosamine (DEN) and ferric nitrilotriacetate (Fe-NTA)-induced renal carcinogenesis, renal hyperproliferation, and oxidative stress in rats. Liquid chromatography mass spectroscopy (LC–MS) was used for identification of phytoconstituents. Administration of DEN confirmed the initiation the renal carcinogenesis via enhancing the expansion of tumor incidence. Intraperitoneally, administration of Fe-NTA boost the antioxidant enzymes (phase I), viz., superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR), glutathione peroxidase (GPx) and phase II, viz., quinone reductase (QR) and glutathione-S-transferase (GST). It also increased the content of renal lipid peroxidation (LPO), hydrogen peroxidase (H2O2) with decrease content in glutathione content (GSH). It also increased the renal biochemical and non-biochemical parameter. It also confirmed the augment the level of thymidine [3H] incorporation into renal DNA, ornithine decarboxylase (ODC) activity and increased the generation of proinflammatory (TNF-α, IL-6 and IL-β) and inflammatory mediator (PGE2). We also analyzed the macroscopic and histologic of renal tissue. In addition, the effect of phytoconstituent of MM extract was evaluated in silico and free radical scavenging activity against the DPPH and ABTS free radicals. LC–MS confirmed the presence of quercetin >gallic acid in MM extract. Renal carcinogenesis rats treated with MM (100, 250, and 500 mg/kg) confirmed the significantly (P < 0.001) protective effect via reduction the antioxidant (phase I and phase II) enzymes, biochemical parameter and restore the proinflammatory and inflammatory mediator at dose dependent manner. MM altered the ODC and thymidine activity in renal DNA. The chemoprotective effect of MM was confirmed via decreased the renal tumor incidence, which was confirmed by the macroscopic and histopathological observation. Consequently, our result suggests that MM is a potent chemoprotective agent and suppresses DEN+ Fe-NTA-induced renal carcinogenesis, inflammatory reaction, and oxidative stress injury in Wister rats.

Keywords

Melastoma malabathricum Inflammatory cytokines DEN Fe-NTA 

Notes

Acknowledgments

The current research was partially funded by the Department of Pharmaceutical Sciences, Faculty of Health Sciences, Sam Higginbottom Institute of Agriculture, Technology & Sciences (Deemed University), Allahabad, 211007.

Compliance with Ethical Standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer International Publishing 2016

Authors and Affiliations

  • Amita Verma
    • 1
  • Prakash Chandra Bhatt
    • 2
  • Gaurav kaithwas
    • 3
  • Nikunj Sethi
    • 4
  • Mohd Rashid
    • 1
  • Yashwant Singh
    • 5
  • Mahfoozur Rahman
    • 1
  • Fahad Al-Abbasi
    • 6
  • Firoz Anwar
    • 6
  • Vikas Kumar
    • 1
  1. 1.Natural Product Drug Discovery Laboratory, Department of Pharmaceutical Sciences, Faculty of Health SciencesSam Higginbottom Institute of Agriculture, Technology and Sciences (Deemed to be University)AllahabadIndia
  2. 2.Microbial and Pharmaceutical Biotechnology Laboratory, Faculty of PharmacyCenter for Advanced Research in Pharmaceutical Sciences, Jamia HamdardNew DelhiIndia
  3. 3.Department of Pharmaceutical Sciences, School of Biosciences and BiotechnologyBabasaheb Bhimrao Ambedkar University (A Central University)LucknowIndia
  4. 4.University Institute of Pharmacy, Chhatrapati Shahu Ji Maharaj UniversityKanpurIndia
  5. 5.Pharmacokinetics & Metabolism DivisionCSIR-Central Drug Research InstituteLucknowIndia
  6. 6.Department of Biochemistry, Faculty of ScienceKing Abdulaziz UniversityJeddahSaudi Arabia

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