Skip to main navigation Skip to search Skip to main content

Pharmacodynamic/pharmacogenomic modeling of insulin resistance genes in rat muscle after methylprednisolone treatment: Exploring regulatory signaling cascades

  • SUNY Buffalo
  • Children's National Medical Center

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Corticosteroids (CS) effects on insulin resistance related genes in rat skeletal muscle were studied. In our acute study, adrenalectomized (ADX) rats were given single doses of 50 mg/kg methylprednisolone (MPL) intravenously. In our chronic study, ADX rats were implanted with Alzet mini-pumps giving zero-order release rates of 0.3 mg/kg/h MPL and sacrificed at various times up to 7 days. Total RNA was extracted from gastrocnemius muscles and hybridized to Affymetrix GeneChips. Data mining and literature searches identified 6 insulin resistance related genes which exhibited complex regulatory pathways. Insulin receptor substrate-1 (IRS-1), uncoupling protein 3 (UCP3), pyruvate dehydrogenase kinase isoenzyme 4 (PDK4), fatty acid translocase (FAT) and glycerol-3-phosphate acyltransferase (GPAT) dynamic profiles were modeled with mutual effects by calculated nuclear drug-receptor complex (DR(N)) and transcription factors. The oscillatory feature of endothelin-1 (ET-1) expression was depicted by a negative feedback loop. These integrated models provide testable quantitative hypotheses for these regulatory cascades.

Original languageEnglish
Pages (from-to)141-161
Number of pages21
JournalGene Regulation and Systems Biology
Volume2008
Issue number2
DOIs
StatePublished - 2008

Keywords

  • Corticosteroid
  • Glucocorticoid
  • Insulin resistance
  • Mathematical modeling
  • Microarrays

Fingerprint

Dive into the research topics of 'Pharmacodynamic/pharmacogenomic modeling of insulin resistance genes in rat muscle after methylprednisolone treatment: Exploring regulatory signaling cascades'. Together they form a unique fingerprint.

Cite this