Chronic activation of vasopressin V2 receptor signalling lowers renal medullary oxygen levels in rats

• Published in: Acta Physiologica 2013-04, Vol.207 (4), p.721-731
• Main Authors: Dietrich, A., Mathia, S., Kaminski, H., Mutig, K., Rosenberger, C., Mrowka, R., Bachmann, S., Paliege, A.
• Format: Article
• Language: English
• Subjects: Animals; Deamino Arginine Vasopressin - pharmacology; Disease Models, Animal; gene expression analysis; gene ontology analysis; Hypoxia - metabolism; hypoxia-inducible factor; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism; Kidney Medulla - drug effects; Kidney Medulla - metabolism; Nitroimidazoles - metabolism; Oxygen - metabolism; pimonidazole; Rats; Rats, Brattleboro; Rats, Sprague-Dawley; Receptors, Vasopressin - agonists; Receptors, Vasopressin - drug effects; Receptors, Vasopressin - physiology; Signal Transduction - physiology; urine concentrating; Vasopressins - deficiency; Vasopressins - genetics; Vasopressins - metabolism
• ISSN: 1748-1708; 1748-1716
• DOI: 10.1111/apha.12067

Aim In the present study, we aimed to elucidate the effects of chronic vasopressin administration on renal medullary oxygen levels. Methods Adult Sprague Dawley or vasopressin‐deficient Brattleboro rats were treated with the vasopressin V2 receptor agonist, desmopressin (5 ng/h; 3d), or its vehicle via osmotic minipumps. Immunostaining for pimonidazole and the transcription factor HIF‐1α (hypoxia‐inducible factor‐1α) were used to identify hypoxic areas. Activation of HIF‐target gene expression following desmopressin treatment was studied by microarray analysis. Results Pimonidazole staining was detected in the outer and inner medulla of desmopressin‐treated rats, whereas staining in control animals was weak or absent. HIF‐1α immunostaining demonstrated nuclear accumulation in the papilla of desmopressin‐treated animals, whereas no staining was observed in the controls. Gene expression analysis revealed significant enrichment of HIF‐target genes in the group of desmopressin‐regulated gene products (P = 2.6*10−21). Regulated products included insulin‐like growth factor binding proteins 1 and 3, angiopoietin 2, fibronectin, cathepsin D, hexokinase 2 and cyclooxygenase 2. Conclusion Our results demonstrate that an activation of the renal urine concentrating mechanism by desmopressin causes renal medullary hypoxia and an upregulation of hypoxia‐inducible gene expression.