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Subpressor dose of angiotensin II increases susceptibility to the haemodynamic injury of blood pressure in Dahl salt-sensitive rats
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1995
Year
HypertensionHeart FailureRenal PathologyCardiovascular PharmacologyRenal InflammationAng IiBlood PressureRenal FunctionAcute Kidney InjuryChronic Kidney DiseaseRenal PharmacologyEndocrine HypertensionCardiorenal SyndromesSodium HomeostasisAntihypertensive TherapyVascular BiologyRenal PathophysiologyDiuretic ResistancePharmacologySubpressor DosePotassium HomeostasisUrologyAngiotensin IiCardiovascular DiseasePhysiologyMedicineNephrologyKidney Research
Objective To investigate the effects of subpressor doses of angiotensin II (Ang II) on the progression of renal injuries in Dahl salt-sensitive (Dahl-S) rats with hypertension. Methods Rats were fed a high-salt (4% NaCI) diet and given an Ang II infusion (10 or 50 ng/kg per min, subcutaneously) for 4 weeks. Results The plasma Ang II concentration achieved in the high-dose Ang II infusion was lower than that in low-salt (0.3% NaCI) normotensive rats. The Ang II infusion did not affect systolic blood pressure, cardiac hypertrophy or weight of thoracic aorta. However, the high-dose Ang II infusion increased proteinuria by 58%, enhanced the urinary N-acetyl-β-D-glucosaminase index by 77% and reduced the glomerular filtration rate by 37%. The impaired renal function was associated with a progression of glomerulosclerotic lesions. Neither tubular nor arterial lesions were exacerbated. The infusion did not influence prostacyclin production or urinary cyclic GMP excretion. Conclusion A subpressor dose of Ang II infusion impairs renal function with progression of glomerulosclerosis, and these alterations may be due to increased susceptibility of the glomerulus in Dahl-S rats to Ang II-induced injuries. Such a mechanism might underlie a predisposition to hypertension-induced organ damage seen in Dahl-S rats with salt-induced hypertension.