Effects of oral adsorbent on gene expression profile in uremic rat kidney: cDNA array analysis

Am J Kidney Dis. 2003 Mar;41(3 Suppl 1):S8-14. doi: 10.1053/ajkd.2003.50075.

Abstract

Background: An oral adsorbent, AST-120, is effective in removing such uremic toxins as indoxyl sulfate and delays the progression of chronic renal failure. To elucidate the molecular mechanisms underlying the renoprotective effects of AST-120, the complementary DNA (cDNA) array method was used to survey the alteration in gene expression profiles of uremic rat kidneys in response to AST-120.

Methods: Six weeks after five-sixth nephrectomy, 10 uremic rats were divided into two groups: those administered AST-120 and control uremic rats. Rats subjected to sham operation also were included as normal rats. After administration of AST-120 for 18 weeks, renal tissues were analyzed by cDNA array.

Results: Among the 343 genes selected as expressed, control uremic rats showed significantly increased levels of 139 genes and significantly decreased levels of 45 genes compared with normal rats. AST-120 treatment attenuated expression levels of 43 of the 139 upregulated renal genes and 21 of the 45 downregulated renal genes in uremic rat kidney. Those genes could be subdivided into several functional categories, including cytokine (transforming growth factor-beta1 [TGF-beta1], etc), intracellular signaling, transcription, translation, channel and transporter (organic anion transporter 1 [OAT1], etc), metabolism, and protease and its inhibitor. Quantitative reverse-transcriptase polymerase chain reaction (RT-PCR) analysis showed that AST-120 significantly increased OAT1 renal expression and tended to decrease TGF-beta1, tissue inhibitor of metalloproteinase-1 (TIMP-1), and endothelin-1 renal expression in uremic rats. There were statistically significant positive correlations between cDNA array-based and RT-PCR-based gene expression levels of TGF-beta1, TIMP-1, and endothelin-1.

Conclusion: The cDNA array method determines changes in the gene expression profile in uremic rat kidney in response to AST-120 and provides new insights into elucidation of the molecular mechanism underlying the renoprotective effects of AST-120.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Oral
  • Adsorption
  • Animals
  • Carbon / administration & dosage
  • Carbon / pharmacology*
  • Carbon / therapeutic use
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Enzyme Induction / drug effects
  • Enzyme Induction / genetics
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation, Enzymologic / drug effects
  • Kidney Failure, Chronic / enzymology
  • Kidney Failure, Chronic / etiology
  • Kidney Failure, Chronic / prevention & control
  • MAP Kinase Signaling System / genetics
  • Male
  • Oligonucleotide Array Sequence Analysis / methods*
  • Oxides / administration & dosage
  • Oxides / pharmacology*
  • Oxides / therapeutic use
  • Protective Agents / administration & dosage
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Up-Regulation / drug effects
  • Up-Regulation / genetics
  • Uremia / complications
  • Uremia / enzymology
  • Uremia / genetics*

Substances

  • Oxides
  • Protective Agents
  • Carbon
  • AST 120