[The role of protein kinase C in the pathophysiology of diabetic retinopathy].

Abstract

Hyperglycemic control in diabetes mellitus is a major key to prevent the development and progression of diabetic retinopathy. One important pathomechanism in the development of diabetic complications is the activation of protein kinase C (PKC) induced by high glucose due to an increased diacylglycerol (DAG) level. Resulting vascular dysfunctions are increased vascular permeability and contractility, increased production of extracellular matrix and cell proliferation. The PKC isoenzyme family plays a fundamental role in the cellular signal transduction via phosphorylation and modification of enzymes, receptors, transcription factors and kinases. The PKC activation influences the gene transcription and ion transport. Different PKC isoenzymes function as mediators but also as inhibitors of the insulin effects. The hyperglycemia induced DAG production seems to predominantly activate PKC-beta in retinal vascular endothelial cells. The development of selective PKC-beta inhibitors enables new pharmacological therapeutical approaches for treatment of diabetic retinopathy. Ongoing clinical studies investigate if the treatment with specific PKC-beta inhibitors can prevent the progression of diabetic retinopathy and diabetic macular edema.

• Authors: Gabriele E Lang, Jürgen Kampmeier
• Journal: Klinische Monatsblatter fur Augenheilkunde (Klin Monbl Augenheilkd) Vol. 219 Issue 11 Pg. 769-76 (Nov 2002) ISSN: 0023-2165 [Print] Germany
• Vernacular Title: Die Bedeutung der Proteinkinase C in der Pathophysiologie der diabetischen Retinopathie.
• PMID: 12494366 (Publication Type: English Abstract, Journal Article, Review)

Chemical References

• Blood Glucose
• Isoenzymes
• Protein Kinase C

Topics

• Blood Glucose (metabolism)
• Diabetic Retinopathy (physiopathology)
• Enzyme Activation (physiology)
• Humans
• Isoenzymes (physiology)
• Protein Kinase C (physiology)