INTRODUCTION: The upregulation of cyclooxygenase (COX) expression by aldosterone (ALDO) or high salt diet intake is very interesting and complex in the light of what is known about the role of COX in renal function. Thus, in this study, we hypothesize that apocynin (APC) and/or eplerenone (EPL) inhibit ALDO/salt-induced kidney damage by preventing the production of prostaglandin E₂ (PGE₂). METHODS: Dahl salt-sensitive rats on either a low-salt or high-salt diet were treated with ALDO (0.2 mg pellet) in the presence of EPL (100 mg/kg/day) or APC (1.5 mM). Indirect blood pressure, prostaglandins and ALDO levels and histological changes were measured. RESULTS: Cyclooxygenase-2 (COX-2) levels were upregulated in the renal tubules and peritubular vessels after high-salt intake, and APC attenuated renal tubular COX-2 protein expression induced by ALDO. Plasma PGE₂ levels were significantly reduced by ALDO in the rats fed a low-salt diet when compared to rats fed a high-salt diet. PGE₂ was blocked by EPL but increased in the presence of APC. CONCLUSIONS: The beneficial effects of EPL may be associated with an inhibition of PGE₂. The mechanism underlying the protective effects of EPL is clearly distinct from that of APC and suggests that these agents can have differential roles in cardiovascular disease.
INTRODUCTION: The upregulation of cyclooxygenase (COX) expression by aldosterone (ALDO) or high salt diet intake is very interesting and complex in the light of what is known about the role of COX in renal function. Thus, in this study, we hypothesize that apocynin (APC) and/or eplerenone (EPL) inhibit ALDO/salt-induced kidney damage by preventing the production of prostaglandin E₂ (PGE₂). METHODS:Dahl salt-sensitive rats on either a low-salt or high-salt diet were treated with ALDO (0.2 mg pellet) in the presence of EPL (100 mg/kg/day) or APC (1.5 mM). Indirect blood pressure, prostaglandins and ALDO levels and histological changes were measured. RESULTS:Cyclooxygenase-2 (COX-2) levels were upregulated in the renal tubules and peritubular vessels after high-salt intake, and APC attenuated renal tubularCOX-2 protein expression induced by ALDO. Plasma PGE₂ levels were significantly reduced by ALDO in the rats fed a low-salt diet when compared to rats fed a high-salt diet. PGE₂ was blocked by EPL but increased in the presence of APC. CONCLUSIONS: The beneficial effects of EPL may be associated with an inhibition of PGE₂. The mechanism underlying the protective effects of EPL is clearly distinct from that of APC and suggests that these agents can have differential roles in cardiovascular disease.
Authors: G G Neri Serneri; G F Gensini; R Abbate; S Castellani; F Bonechi; M Carnovali; C Rostagno; R P Dabizzi; A Dagianti; L Arata Journal: Am Heart J Date: 1990-07 Impact factor: 4.749
Authors: A Paliege; A Pasumarthy; A Parsumathy; D Mizel; T Yang; J Schnermann; S Bachmann Journal: Am J Physiol Regul Integr Comp Physiol Date: 2006-03 Impact factor: 3.619
Authors: Yong Chia Tan; Munavvar Abdul Sattar; Ahmad F Ahmeda; Nurzalina Abdul Karim Khan; Vikneswaran Murugaiyah; Ashfaq Ahmad; Zurina Hassan; Gurjeet Kaur; Mohammed Hadi Abdulla; Edward James Johns Journal: PLoS One Date: 2020-04-16 Impact factor: 3.240