The intrarenal angiotensin system and inflammation in Dahl salt‐sensitive hypertension
TL;DRAbstract
Dahl salt‐sensitive (S) hypertension is characterized by renal damage, renal immune cell infiltration and low plasma renin activity. Recent studies have shown that the intrarenal angiotensin (ANGII) system may be activated in these rats and along with the immune system may play important roles in the development of renal injury and hypertension. However, the roles of intrarenal ANGII/immune systems in the Dahl salt‐sensitive hypertension are not clear. Dahl S rats were equipped arterial catheters and subjected to a 5‐week diet of high Na (8% NaCl) or high Na+ARB (ANGII AT1 receptor blocker, candesartan cilexetil, 15 mg/kg/day). By the end of week 5 in the high Na+ARB group: mean arterial pressure (MAP) was 145 ± 1 mmHg compared to the high Na group value of 168 ± 7 mmHg*; kidney tissue ANGII concentration, macrophages, TNFα, and MCP‐1 and urinary protein excretion were 3.2 ± 1.4 pg/mg, 7.1 ± 0.6 cells/mm 2 , 0.38 ± 0.01 pg/mg, 21.7 ± 1.4 pg/mg, and 168 ± 20 mg/day in ARB rats compared
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Dahl salt‐sensitive (S) hypertension is characterized by renal damage, renal immune cell infiltration and low plasma renin activity. Recent studies have shown that the intrarenal angiotensin (ANGII) system may be activated in these rats and along with the immune system may play important roles in the development of renal injury and hypertension. However, the roles of intrarenal ANGII/immune systems in the Dahl salt‐sensitive hypertension are not clear. Dahl S rats were equipped arterial catheters and subjected to a 5‐week diet of high Na (8% NaCl) or high Na+ARB (ANGII AT1 receptor blocker, candesartan cilexetil, 15 mg/kg/day). By the end of week 5 in the high Na+ARB group: mean arterial pressure (MAP) was 145 ± 1 mmHg compared to the high Na group value of 168 ± 7 mmHg*; kidney tissue ANGII concentration, macrophages, TNFα, and MCP‐1 and urinary protein excretion were 3.2 ± 1.4 pg/mg, 7.1 ± 0.6 cells/mm 2 , 0.38 ± 0.01 pg/mg, 21.7 ± 1.4 pg/mg, and 168 ± 20 mg/day in ARB rats compared
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