Cargando…

Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study

OBJECTIVE—The aim of this study was to examine the effect of protein kinase Cβ 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 subj...

Descripción completa

Detalles Bibliográficos
Autores principales: Cherney, David Z.I., Konvalinka, Ana, Zinman, Bernard, Diamandis, Eleftherios P., Soosaipillai, Anton, Reich, Heather, Lorraine, Joanne, Lai, Vesta, Scholey, James W., Miller, Judith A.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2606837/
https://www.ncbi.nlm.nih.gov/pubmed/18945921
http://dx.doi.org/10.2337/dc08-1609
_version_ 1782162992767434752
author Cherney, David Z.I.
Konvalinka, Ana
Zinman, Bernard
Diamandis, Eleftherios P.
Soosaipillai, Anton
Reich, Heather
Lorraine, Joanne
Lai, Vesta
Scholey, James W.
Miller, Judith A.
author_facet Cherney, David Z.I.
Konvalinka, Ana
Zinman, Bernard
Diamandis, Eleftherios P.
Soosaipillai, Anton
Reich, Heather
Lorraine, Joanne
Lai, Vesta
Scholey, James W.
Miller, Judith A.
author_sort Cherney, David Z.I.
collection PubMed
description OBJECTIVE—The aim of this study was to examine the effect of protein kinase Cβ 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.
format Text
id pubmed-2606837
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher American Diabetes Association
record_format MEDLINE/PubMed
spelling pubmed-26068372010-01-01 Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study Cherney, David Z.I. Konvalinka, Ana Zinman, Bernard Diamandis, Eleftherios P. Soosaipillai, Anton Reich, Heather Lorraine, Joanne Lai, Vesta Scholey, James W. Miller, Judith A. Diabetes Care Emerging Treatments and Technologies OBJECTIVE—The aim of this study was to examine the effect of protein kinase Cβ 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. American Diabetes Association 2009-01 /pmc/articles/PMC2606837/ /pubmed/18945921 http://dx.doi.org/10.2337/dc08-1609 Text en Copyright © 2009, American Diabetes Association https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Emerging Treatments and Technologies
Cherney, David Z.I.
Konvalinka, Ana
Zinman, Bernard
Diamandis, Eleftherios P.
Soosaipillai, Anton
Reich, Heather
Lorraine, Joanne
Lai, Vesta
Scholey, James W.
Miller, Judith A.
Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study
title Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study
title_full Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study
title_fullStr Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study
title_full_unstemmed Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study
title_short Effect of Protein Kinase Cβ Inhibition on Renal Hemodynamic Function and Urinary Biomarkers in Humans With Type 1 Diabetes: A Pilot Study
title_sort effect of protein kinase cβ inhibition on renal hemodynamic function and urinary biomarkers in humans with type 1 diabetes: a pilot study
topic Emerging Treatments and Technologies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2606837/
https://www.ncbi.nlm.nih.gov/pubmed/18945921
http://dx.doi.org/10.2337/dc08-1609
work_keys_str_mv AT cherneydavidzi effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT konvalinkaana effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT zinmanbernard effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT diamandiseleftheriosp effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT soosaipillaianton effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT reichheather effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT lorrainejoanne effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT laivesta effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT scholeyjamesw effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy
AT millerjuditha effectofproteinkinasecbinhibitiononrenalhemodynamicfunctionandurinarybiomarkersinhumanswithtype1diabetesapilotstudy