Effect of protein kinase Cbeta inhibition on renal hemodynamic function and urinary biomarkers in humans with type 1 diabetes: a pilot study

Diabetes Care. 2009 Jan;32(1):91-3. doi: 10.2337/dc08-1609. Epub 2008 Oct 22.

Abstract

Objective: The aim of this study was to examine the effect of protein kinase Cbeta inhibition with ruboxistaurin on renal hemodynamic function and urinary biomarkers (monocyte chemoattractant protein-1 [MCP-1] and epidermal growth factor) in renin angiotensin system blockade-treated type 1 diabetic subjects.

Research design and methods: Albuminuric subjects were randomized (2:1) to ruboxistaurin (32 mg daily; n = 13) or placebo (n = 7) for 8 weeks. Renal hemodynamic function was measured during clamped euglycemia or hyperglycemia and before and after ruboxistaurin or placebo.

Results: Ruboxistaurin was not associated with between-group differences during clamped euglycemia or hyperglycemia. In a post hoc analysis comparing hyperfilterers with normofilterers during euglycemia, glomerular filtration rate and MCP-1 decreased, whereas the epidermal growth factor-to-MCP-1 ratio increased in hyperfilterers versus normofilterers (all P < 0.05).

Conclusions: The effect of ruboxistaurin is modest and dependent, at least in part, on the level of ambient glycemia and baseline glomerular filtration rate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albuminuria / drug therapy
  • Blood Pressure / drug effects
  • Chemokine CCL2 / drug effects
  • Chemokine CCL2 / urine
  • Diabetes Mellitus, Type 1 / drug therapy
  • Diabetes Mellitus, Type 1 / physiopathology*
  • Diabetic Nephropathies / drug therapy
  • Diabetic Nephropathies / urine
  • Enzyme Inhibitors / therapeutic use*
  • Epidermal Growth Factor / urine
  • Glomerular Filtration Rate / drug effects*
  • Hemodynamics
  • Humans
  • Indoles / therapeutic use*
  • Kidney / drug effects
  • Kidney / physiopathology*
  • Maleimides / therapeutic use*
  • Protein Kinase C / antagonists & inhibitors*
  • Protein Kinase C beta

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Enzyme Inhibitors
  • Indoles
  • Maleimides
  • Epidermal Growth Factor
  • ruboxistaurin
  • Protein Kinase C
  • Protein Kinase C beta