Cytokine gene expression in Adriamycin nephropathy: effects of antioxidant nuclear factor kappaB inhibitors in established disease

Nephron. 2000 Dec;86(4):482-90. doi: 10.1159/000045838.

Abstract

Background/aim: Inhibition of nuclear factor kappaB with the antioxidant pyrrolidine dithiocarbamate (PDTC) reduced tubulointerstitial injury in Adriamycin nephropathy (AN), whereas N-acetylcysteine (NAC) was ineffective. Here we hypothesize that PDTC reduces the renal cortical expression of nuclear factor kappaB dependent cytokines in AN.

Methods: Male Wistar rats received a single intravenous injection of doxorubicin hydrochloride (7.5 mg/kg). NAC (150 mg/kg twice daily i.p.), PDTC (50 mg/kg twice daily i.p.), or vehicle were commenced on day 14 and continued until day 30.

Results: On day 30, mRNAs of selected cytokines were increased in AN (TNF-alpha 3.4-fold, MCP-1 5.1-fold, IL-10 2.7-fold, TGF-beta1 3.5-fold, all p < 0.05) as determined by RT-PCR. PDTC reduced IL-10 and TGF-beta1 mRNAs (p < 0.05), whereas the upregulation of MCP-1 and TNF-alpha mRNAs was not affected. In contrast, NAC increased TNF-alpha and IL-10 mRNAs (p < 0.05). Nuclear protein levels of activator protein-1 were increased in AN (4.4-fold, p < 0.01) and not significantly altered by PDTC (3.0-fold, p = 0.13) or NAC (5. 2-fold, p = 0.18).

Conclusions: The protective effects of PDTC in AN are not associated with a local reduction in TNF-alpha and MCP-1 gene expression. The latter may be due to continued transactivation by activator protein-1. These data also suggest that IL-10 and TGF-beta1 mRNA expressions are PDTC dependent and have a role in mediating tubulointerstitial injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / pharmacology
  • Animals
  • Antibiotics, Antineoplastic / toxicity*
  • Antioxidants / pharmacology*
  • Cytokines / biosynthesis*
  • Cytokines / genetics
  • Doxorubicin / toxicity*
  • Free Radical Scavengers / pharmacology
  • Kidney Diseases / chemically induced
  • Kidney Diseases / metabolism*
  • Male
  • NF-kappa B / antagonists & inhibitors*
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / isolation & purification
  • Pyrrolidines / pharmacology
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thiocarbamates / pharmacology

Substances

  • Antibiotics, Antineoplastic
  • Antioxidants
  • Cytokines
  • Free Radical Scavengers
  • NF-kappa B
  • Nuclear Proteins
  • Pyrrolidines
  • RNA, Messenger
  • Thiocarbamates
  • pyrrolidine dithiocarbamic acid
  • Doxorubicin
  • Acetylcysteine