Effect of fasting on insulin receptor-related receptor messenger ribonucleic acid in rat kidney

Abstract

The insulin receptor-related receptor (IRR), a member of the insulin receptor tyrosine kinase family, has structural homology to the insulin receptor (IR) and the IGF-I receptor (IGF-IR). The ligand, gene regulation and biological function of the IRR are not known. Because mRNAs for both the IR and IGF-IR are increased by nutrient restriction, we used RNase protection assays to assess the effects of fasting 48 h on IRR mRNA in kidneys of rats. We compared the changes in IRR with those in IR and IGF-IR mRNAs. We observed a significant increase in steady state levels of IRR (ratio of IRR mRNA to β-actin in fed vs fasted animals, 0.59±0.1 and 1.25±0.14 respectively, P<0.01), suggesting that the ligand for IRR also might be regulated by nutrients.