4.7 Article

Nootkatone confers antifibrotic effect by regulating the TGF-β/Smad signaling pathway in mouse model of unilateral ureteral obstruction

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 910, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ejphar.2021.174479

Keywords

Nootkatone; Unilateral ureteral obstruction; Oxidative stress; Renal fibrosis; TGF-beta/Smad signaling

Funding

  1. Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Government of India
  2. Epidemiology Data Analytics (EDA) of Interdisciplinary Cyber Physical Systems (ICPS) Programme, Department of Science and Technology (DST), Government of India [DST/ICPS/EDA/2018/General]

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The study revealed that NTK has a protective effect against renal fibrosis, significantly reducing renal tubular injury and fibrosis area. Additionally, it restores endogenous antioxidants, reduces oxidative stress and inflammation response in the kidneys.
Chronic kidney disease (CKD) with underlying interstitial fibrosis is often associated with end-stage renal disease (ESRD). In the present study, we investigated the renoprotective and antifibrotic potential of nootkatone (NTK), a bioactive sesquiterpene, in an experimental model of renal fibrosis. Unilateral ureteral obstruction (UUO) model was performed to induce renal fibrosis in Balb/C mice. The animals were randomly assigned into 5 groups: sham, NTK control, UUO control, UUO and NTK 5 mg/kg, and UUO and NTK 10 mg/kg. Animals received NTK at a dose of 5 mg/kg and 10 mg/kg orally for the next 14 consecutive days. UUO induced histological alterations, accumulation of extracellular matrix (ECM) components including collagens, fibronectin, and alpha-smooth muscle actin (alpha-SMA), activation of the transforming growth factor-beta (TGF-beta)/Smad signaling and oxidative damage in the obstructed kidneys. Our study revealed that NTK (10 mg/kg) inhibits UUO mediated kidney fibrosis in vivo. Administration of NTK (10 mg/kg) prevented the activation of the TGF-beta/Smad signaling, expression of ECM components, markedly attenuated the renal tubular injury and fibrosis area (% area: 6.66 +/- 1.45% vs UUO: 26.33 +/- 2.90%). Administration of NTK at 10 mg/kg significantly restored the endogenous antioxidants and prevented the reactive oxygen species generation (25.31 +/- 1.65% vs UUO: 45.01 +/- 4.85%) and reduced the level of tumor necrosis factor (TNF)-alpha (95.22 +/- 12.39 vs UUO: 215.57 +/- 60.45 pg/mg protein) in the kidneys. Altogether, our findings suggest that NTK might be a budding therapeutic candidate for renal fibrosis.

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