Huaiqihuang (HQH) granule alleviates cyclophosphamide-induced nephrotoxicity via suppressing the MAPK/NF-κB pathway and NLRP3 inflammasome activation

Pharm Biol. 2021 Dec;59(1):1425-1431. doi: 10.1080/13880209.2021.1990356.

Abstract

Context: Severe nephrotoxicity greatly limits the clinical use of the common effective chemotherapeutic agent cyclophosphamide (CYP). Huaiqihuang (HQH) is a Chinese herbal complex with various pharmacological activities, widely used for treating kidney disease.

Objective: This study estimates the protective effect of HQH against CYP-induced nephrotoxicity in rats.

Materials and methods: Four groups of 10 Sprague-Dawley rats were pre-treated with once-daily oral gavage of 3 and 6 mg/kg HQH for 5 days before receiving a single dose of CYP (200 mg/kg i.p.) on the 5th day; the control group received equivalent dose of saline. Renal function indices, morphological changes, oxidative stress, apoptosis and inflammatory mediators were measured. In addition, phosphorylation of the NF-κB/MAPK pathway and the activation of the NLRP3 inflammasome were analysed.

Results: Both doses of HQH reduced the levels of serum creatinine (31.27%, 43.61%), urea nitrogen (22.66%, 32.27%) and urine protein (12.87%, 15.98%) in the CYP-treated rats, and improved histopathological aberrations. Additionally, HQH decreased the production of MDA (37.02%, 46.18%) and increased the activities of antioxidant enzyme CAT (59.18%, 112.25%) and SOD (67.10%, 308.34%) after CYP treatment. HQH protected against CYP-induced nephrotoxicity by modulating apoptosis-related protein and suppressing the inflammatory responses. Furthermore, the phosphorylation of the NF-κB/MAPK pathway and the activation of the NLRP3 inflammasome were significantly boosted in CYP-treated rats, which was also abrogated by HQH treatment.

Conclusions: HQH effectively protected against CYP-induced nephrotoxicity, which was associated with regulating oxidative stress, apoptosis and inflammation, and so HQH may be a useful agent for treating nephrotoxicity caused by CYP.

Keywords: Chinese medicine; apoptosis; chemotherapeutic agent; inflammation; oxidative stress.

MeSH terms

  • Animals
  • Antineoplastic Agents, Alkylating / toxicity
  • Apoptosis / drug effects
  • Cyclophosphamide / toxicity*
  • Drugs, Chinese Herbal / pharmacology*
  • Inflammasomes / drug effects
  • Inflammasomes / metabolism
  • Inflammation / chemically induced
  • Inflammation / prevention & control
  • Kidney Diseases / chemically induced
  • Kidney Diseases / prevention & control*
  • MAP Kinase Signaling System / drug effects
  • Male
  • NF-kappa B / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism
  • Oxidative Stress / drug effects*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Antineoplastic Agents, Alkylating
  • Drugs, Chinese Herbal
  • Inflammasomes
  • NF-kappa B
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Nlrp3 protein, rat
  • huai qi huang
  • Cyclophosphamide

Grants and funding

This study was supported by the National Natural Science Foundation of China under Grant number 81803608 and 81903712 and 9th Youth Foundation of the First Hospital Jilin University under Grant number JDYY92018037.