Impairment of the autoregulation of renal hemodynamics and of the pressure-natriuresis relationship precedes the development of hypertension in Cyp1a1-Ren-2 transgenic rats
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- aldosteron krev MeSH
- angiotensin II metabolismus MeSH
- blokátory receptorů AT1 pro angiotensin II farmakologie MeSH
- časové faktory MeSH
- cytochrom P-450 CYP1A1 genetika MeSH
- hemodynamika účinky léků MeSH
- hodnoty glomerulární filtrace účinky léků MeSH
- homeostáza * MeSH
- hypertenze genetika patofyziologie MeSH
- indoly aplikace a dávkování MeSH
- krevní tlak účinky léků MeSH
- krysa rodu Rattus MeSH
- ledviny krevní zásobení účinky léků MeSH
- losartan farmakologie MeSH
- natriuréza * MeSH
- potkani transgenní MeSH
- receptor angiotensinu typ 1 metabolismus MeSH
- renální oběh účinky léků MeSH
- renin-angiotensin systém fyziologie MeSH
- renin genetika MeSH
- sodík metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aldosteron MeSH
- angiotensin II MeSH
- blokátory receptorů AT1 pro angiotensin II MeSH
- cytochrom P-450 CYP1A1 MeSH
- indole-3-carbinol MeSH Prohlížeč
- indoly MeSH
- losartan MeSH
- receptor angiotensinu typ 1 MeSH
- renin MeSH
- sodík MeSH
OBJECTIVE: The present study was performed to characterize the autoregulatory efficiency of renal blood flow and glomerular filtration rate and the pressure-natriuresis relationship in transgenic rats with inducible angiotensin II (ANG II)-dependent hypertension (Cyp1a1-Ren-2 rats). METHODS: The renin gene was induced in Cyp1a1-Ren-2 rats through dietary administration of the natural xenobiotic indole-3-carbinol (I3C, 0.3%) for 12 and 24 h, respectively. Noninduced rats served as controls. Anesthetized rats were prepared for renal function studies and an aortic clamp was placed above the junction of the left renal artery to regulate the level of renal arterial pressure. Plasma renin activity, ANG II and aldosterone levels were measured at the end of the experiment by radioimmunoassay. RESULTS: Administration of I3C resulted in progressive increases in plasma renin activity and plasma and kidney ANG II levels; however, it did not significantly alter aldosterone levels as compared with those in noninduced rats. I3C induction for 12 h did not cause significant changes in blood pressure as compared with those in noninduced rats. I3C induction for 24 h elicited a significant rise in blood pressure. Twelve-hour I3C induction caused an impairment of the autoregulatory efficiency of renal blood flow and glomerular filtration rate and of the pressure-natriuresis relationship as compared with that in noninduced rats. In addition, 24 h I3C induction of the renin gene resulted in a marked reduction in renal blood flow and glomerular filtration rate and a further impairment of the pressure-natriuresis mechanism as compared with that in noninduced rats. CONCLUSION: Our findings indicate that an impairment of the pressure-natriuresis mechanism precedes the development of ANG II-dependent hypertension in Cyp1a1-Ren-2 transgenic rats.
Citace poskytuje Crossref.org
Research on Experimental Hypertension in Prague (1966-2009)