Abstract | INTRODUCTION:
Hyperglycemia is a principal characteristic of diabetes and influences many cellular functions. Diabetic nephropathy is characterized by glomerular mesangial expansion which could result from increased mesangial cell extracellular matrix synthesis induced by hyperglycemia. METHODS: RESULTS: The exposure of mesangial cells to a high glucose concentration (30 mM) significantly reduced AVP-induced thymidine incorporation and hyperplasia compared with normal glucose (10 mM). By contrast, treatment of mesangial cells with AVP in the presence of high extracellular glucose significantly increased leucine incorporation, hypertrophy, and type IV collagen synthesis compared with those at normal glucose levels. The administration of staurosporine, a protein kinase C inhibitor, reversed these effects of high- glucose conditions. Furthermore, the nonpeptide AVP V(1A) receptor-selective antagonists potently inhibited these AVP-induced physiological responses in mesangial cells cultured in high- glucose conditions. CONCLUSIONS: These results demonstrate that high glucose suppresses mesangial cell proliferation but enhances hypertrophy and type IV collagen synthesis induced by AVP. This increased mesangial cell hypertrophy and extracellular matrix synthesis may play a crucial role in the glomerular mesangial expansion common to diabetic nephropathy.
|
Authors | Atsuo Tahara, Junko Tsukada, Yuichi Tomura, Takeyuki Yatsu, Masayuki Shibasaki |
Journal | Endocrine research
(Endocr Res)
Vol. 37
Issue 4
Pg. 216-27
( 2012)
ISSN: 1532-4206 [Electronic] England |
PMID | 22594926
(Publication Type: Journal Article)
|
Chemical References |
- Antidiuretic Agents
- Collagen Type IV
- Enzyme Inhibitors
- Arginine Vasopressin
- Staurosporine
|
Topics |
- Animals
- Antidiuretic Agents
(pharmacology)
- Arginine Vasopressin
(antagonists & inhibitors, pharmacology)
- Cells, Cultured
- Collagen Type IV
(biosynthesis)
- Diabetic Nephropathies
(drug therapy, metabolism, prevention & control)
- Enzyme Inhibitors
(pharmacology)
- Glomerular Mesangium
(metabolism)
- Hyperglycemia
(physiopathology)
- Hyperplasia
(drug therapy, physiopathology)
- Hypertrophy
(drug therapy, physiopathology)
- Mesangial Cells
(drug effects, pathology, physiology)
- Rats
- Rats, Wistar
- Staurosporine
(pharmacology)
|