Background: Several types of renal disease progress at a faster rate in men compared with women, but the reasons for this sex difference are not well understood. Chronic renal disease is associated with elevated levels of toxic reactive oxygen species (ROS). Superoxide, the major ROS in the kidney, is generated by nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. Objective: To determine if female protection from renal disease progression is consistent with 17 beta-estradiol (E-2) attenuation of superoxide production, this study was conducted to assess superoxide production in the renal cortex of male and female control and renal wrap (RW) rats, as well as in ovariectomized rats treated with vehicle or E-2. Methods: Sprague-Dawley rats were divided into 2 sham operation male (Sham-M) and female (Sham-F) control groups, and 4 RW hypertensive groups: RW-M; RW-F; RW ovariectomized females treated with vehicle (RW-OVX); and RW ovariectomized females treated with E-2, supplied as a 0.24 mg/60-day release pellet (RW-OVX+E-2). All groups were maintained on a high-sodium (4% NaCl) diet for 6 weeks. Results: Mean (SEM) markers of renal injury and oxidative stress, including urinary protein (mg/24 h: RW-M, 298 [31] vs RW-F, 169 [22]; P < 0.001), microalbuminuria (RW/Sham arbitrary units [AU]/24 h: M, 8.78 [0.58] vs F, 4.31 [1.0]; P < 0.005), and malondialdehyde (nmol/24 h: RW-M, 167 [23] vs RW-F, 117 [8.5]; P < 0.05) levels, as well as mean glomerular volume (mu m(3) x 10(6): RW-M, 2.25 [0.16] vs RW-F, 1.25 [0.04]; P < 0.001) and the glomerulosclerotic index (AU: RW-M, 2.64 [0.19] vs RW-F, 1.10 [0.09]; P < 0.001) were greater in both control and RW males compared with females in the same treatment groups. Though RW surgery increased mean arterial pressure in both male and female rats, no sex difference was observed. Under these conditions, mean (SEM) renal cortical NADPH oxidase activity was 1.3-fold higher in RW males compared with RW females (relative light units [RLU]/180 sec: RW-M, 4080 [240] vs RW-F, 3200 [260]; P < 0.05). Ovariectomy increased NADPH oxidase activity by 1.4-fold (RLU/180 sec: RW-OVX, 4520 [184]; P < 0.01) under conditions in which the mean glomerular volume and glomerulosclerotic index were both increased by 1.5-fold, whereas E-2 replacement (RLU/180 sec: RW-OVX+E-2, 2745 [440]) prevented these effects. Furthermore, the effects on NADPH oxidase activity were mirrored by changes in the protein abundance of NADPH oxidase subunit p22(phox). Conclusion: These results suggest that E-2 protects the female kidney in part by attenuating injury-induced increases in renal superoxide production. (Gend Med. 2007;4:5 6-71) Copyright (c) 2007 Excerpta Medica, Inc.

Female protection in progressive renal disease is associated with estradiol attenuation of superoxide production / Hong, Ji; Wei, Zheng; Menini, Stefano; Carlo, Pesce; James, Kim; Xie, Wu; Susan E., Mulroney; Kathryn, Sandberg. - In: GENDER MEDICINE. - ISSN 1550-8579. - 4:1(2007), pp. 56-71. [10.1016/s1550-8579(07)80009-x]

Female protection in progressive renal disease is associated with estradiol attenuation of superoxide production

MENINI, Stefano;
2007

Abstract

Background: Several types of renal disease progress at a faster rate in men compared with women, but the reasons for this sex difference are not well understood. Chronic renal disease is associated with elevated levels of toxic reactive oxygen species (ROS). Superoxide, the major ROS in the kidney, is generated by nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. Objective: To determine if female protection from renal disease progression is consistent with 17 beta-estradiol (E-2) attenuation of superoxide production, this study was conducted to assess superoxide production in the renal cortex of male and female control and renal wrap (RW) rats, as well as in ovariectomized rats treated with vehicle or E-2. Methods: Sprague-Dawley rats were divided into 2 sham operation male (Sham-M) and female (Sham-F) control groups, and 4 RW hypertensive groups: RW-M; RW-F; RW ovariectomized females treated with vehicle (RW-OVX); and RW ovariectomized females treated with E-2, supplied as a 0.24 mg/60-day release pellet (RW-OVX+E-2). All groups were maintained on a high-sodium (4% NaCl) diet for 6 weeks. Results: Mean (SEM) markers of renal injury and oxidative stress, including urinary protein (mg/24 h: RW-M, 298 [31] vs RW-F, 169 [22]; P < 0.001), microalbuminuria (RW/Sham arbitrary units [AU]/24 h: M, 8.78 [0.58] vs F, 4.31 [1.0]; P < 0.005), and malondialdehyde (nmol/24 h: RW-M, 167 [23] vs RW-F, 117 [8.5]; P < 0.05) levels, as well as mean glomerular volume (mu m(3) x 10(6): RW-M, 2.25 [0.16] vs RW-F, 1.25 [0.04]; P < 0.001) and the glomerulosclerotic index (AU: RW-M, 2.64 [0.19] vs RW-F, 1.10 [0.09]; P < 0.001) were greater in both control and RW males compared with females in the same treatment groups. Though RW surgery increased mean arterial pressure in both male and female rats, no sex difference was observed. Under these conditions, mean (SEM) renal cortical NADPH oxidase activity was 1.3-fold higher in RW males compared with RW females (relative light units [RLU]/180 sec: RW-M, 4080 [240] vs RW-F, 3200 [260]; P < 0.05). Ovariectomy increased NADPH oxidase activity by 1.4-fold (RLU/180 sec: RW-OVX, 4520 [184]; P < 0.01) under conditions in which the mean glomerular volume and glomerulosclerotic index were both increased by 1.5-fold, whereas E-2 replacement (RLU/180 sec: RW-OVX+E-2, 2745 [440]) prevented these effects. Furthermore, the effects on NADPH oxidase activity were mirrored by changes in the protein abundance of NADPH oxidase subunit p22(phox). Conclusion: These results suggest that E-2 protects the female kidney in part by attenuating injury-induced increases in renal superoxide production. (Gend Med. 2007;4:5 6-71) Copyright (c) 2007 Excerpta Medica, Inc.
2007
17 beta-estradiol; 17β-estradiol; chronic renal disease; nadph oxidase; renal wrap hypertension; sex/gender differences; superoxide
01 Pubblicazione su rivista::01a Articolo in rivista
Female protection in progressive renal disease is associated with estradiol attenuation of superoxide production / Hong, Ji; Wei, Zheng; Menini, Stefano; Carlo, Pesce; James, Kim; Xie, Wu; Susan E., Mulroney; Kathryn, Sandberg. - In: GENDER MEDICINE. - ISSN 1550-8579. - 4:1(2007), pp. 56-71. [10.1016/s1550-8579(07)80009-x]
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/343502
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 25
  • Scopus 60
  • ???jsp.display-item.citation.isi??? 59
social impact