Enhanced kidney damage induced by increasing nonylphenol doses: impact on autophagy-related proteins and proinflammatory cytokines in rats

Toxicol Mech Methods. 2024 Oct;34(8):867-876. doi: 10.1080/15376516.2024.2358348. Epub 2024 Jul 15.

Abstract

Nonylphenol (NP) is an organic pollutant and endocrine disruptor chemical that has harmful effects on the environment and living organisms. This study looked at whether kidney tissues subjected to increasing doses of nonylphenol generated alterations in histopathologic, pro-inflammatory, and autophagic markers. Fifty rats were divided into five groups of ten each: group I: healthy group, II: control (corn oil), group III: 25 μl/kg NP, group IV: 50 μl/kg NP, group V: 75 μl/kg NP. The kidney tissue samples were obtained for histopathological, immunohistochemical, and biochemical analyses. The histological deteriorations observed in all NP groups included tubular epithelial cell degeneration, inflammation areas, and hemorrhage. The immunohistochemical investigations showed that NP significantly elevated the autophagy markers (Beclin-1, LC3A/B, p62), pro-inflammatory cytokines (TNF-α, IL-6), HIF-1α, and eNOS in group III, IV and V compared with group I and II. The biochemical analysis also revealed that pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6) increased in correlation with the NP doses, but only IL-1β reached statistical significance in NP treated rats kidney tissue. The biochemical findings have been confirmed by the histological studies. The damage to renal tissue caused by NP exposure may worsen it by increasing inflammatory and autophagic markers.

Keywords: Nonylphenol; autophagy; inflammation; kidney damage.

MeSH terms

  • Animals
  • Autophagy* / drug effects
  • Autophagy-Related Proteins / metabolism
  • Cytokines* / metabolism
  • Dose-Response Relationship, Drug
  • Endocrine Disruptors / toxicity
  • Inflammation Mediators / metabolism
  • Kidney Diseases / chemically induced
  • Kidney Diseases / pathology
  • Kidney* / drug effects
  • Kidney* / metabolism
  • Kidney* / pathology
  • Male
  • Phenols* / toxicity
  • Rats
  • Rats, Wistar

Substances

  • nonylphenol
  • Cytokines
  • Phenols
  • Autophagy-Related Proteins
  • Endocrine Disruptors
  • Inflammation Mediators