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Am J Physiol Renal Physiol 288: F399-F405, 2005. First published September 28, 2004; doi:10.1152/ajprenal.00195.2004
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17{beta}-Estradiol replacement improves renal function and pathology associated with diabetic nephropathy

Richard W. Mankhey,1 Faizah Bhatti,1 and Christine Maric1,2

Department of 1Medicine and 2Center for the Study of Sex Differences: in Health, Aging and Disease, Georgetown University Medical Center, Washington, District of Columbia

Submitted 27 May 2004 ; accepted in final form 23 September 2004


   ABSTRACT
TOP
 ABSTRACT
MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
The protective factor of female gender appears to be lost in diabetes; the incidence of diabetes and its complications, including diabetic nephropathy, are equal in women and men. This study examined the effects of estrogen deficiency by ovariectomy (OVX) and replacement with 17{beta}-estradiol (OVX+E2) on renal function and pathology in the nondiabetic (ND) and streptozotocin (STZ)-induced diabetic (D) rat kidneys for 12 wk. Diabetes was associated with an increase in urine albumin excretion (UAE; ND, 0.39 ± 0.03; D, 5.9 ± 0.8 mg/day; P < 0.001), decrease in creatinine clearance (CrCl; ND, 0.69 ± 0.03; D, 0.43 ± 0.09 mg·min–1·100 g body wt–1; P < 0.05), increase in the index of glomerulosclerosis [GSI; ND, 0.01 ± 0.01; D, 0.15 ± 0.04 arbitrary units (AU); P < 0.01], tubulointerstitial fibrosis (TIFI; ND, 0.04 ± 0.04; D, 0.68 ± 0.2 AU; P < 0.01), and transforming growth factor-{beta} (TGF-{beta}) protein expression (ND, 0.61 ± 0.02; D, 1.25 ± 0.07 AU; P < 0.01). In the D group, the severity of these changes was augmented with OVX (UAE, 8.1 ± 0.6 mg/day; CrCl, 0.40 ± 0.04 mg·min–1·100 g body wt–1; GSI, 0.29 ± 0.04 AU; TIFI, 0.90 ± 0.06 AU; TGF-{beta}, 1.26 ± 0.10 AU), whereas E2 replacement attenuated these changes (UAE, 6.3 ± 0.8 mg/day; CrCl, 0.66 ± 0.03 mg·min–1·100 g body wt–1; GSI, 0.06 ± 0.02 AU; TIFI, 0.36 ± 0.08 AU; TGF-{beta}, 0.57 ± 0.08 AU). We conclude that E2 deficiency increases the severity of renal disease in a diabetic animal model and that E2 replacement is renoprotective by attenuating the decline in renal function and pathology associated with diabetes.

diabetes; kidney; estrogen; extracellular matrix; fibrosis

UNLIKE MOST CHRONIC RENAL diseases, in which the female gender is a protective factor, this "female advantage" appears to be lost in diabetes; the prevalence of both type 1 and 2 diabetes and its associated end-organ complications, including diabetic nephropathy, are equal in both premenopausal women and age-matched men (20, 31). Furthermore, diabetes dramatically increases the risk of cardiovascular disease in women compared with age-matched men (5, 19). The contribution of gender in diabetic renal disease is still unclear. Although some studies indicate that females progress at a faster rate (15), others studies indicate the opposite (21). In fact, most available data are insufficient to assess whether gender does play a role in the progression of diabetic renal complications. Similarly, there is a serious lack of data on whether the progression of diabetic renal complications changes after menopause. However, the observation that gender is no longer a protective factor in diabetes remains undisputed, but little is known about the mechanisms underlying this phenomenon. One possible explanation may be that female sex hormones are differentially regulated in diabetes and that this abnormal activity/regulation of female sex hormones may contribute to the pathogenesis of diabetic renal complications. To date, however, very little is known about the role of female sex hormones in diabetic nephropathy.

Estrogen and its major metabolites have been reported to exert renoprotective actions under both physiological and pathophysiological conditions. In cultured mesangial cells, 17{beta}-estradiol (E2) inhibits apoptosis and transforming growth factor-{beta} (TGF-{beta}) activity and expression (10, 26), increases the expression of extracellular matrix (ECM)-degrading metalloproteinases (24, 30), and reduces synthesis of ECM proteins, including collagen type I and type IV (29, 35). In the kidney of the diabetic Otsuka-Long-Evans-Tokushima-Fatty (OLETF) rat, E2 attenuates mesangial expansion and glomerular basement membrane thickening (40). Findings from this study support the concept that estrogen replacement may be beneficial in attenuating cellular processes that are adversely affected in diabetic renal complications. Some, but not all, studies report that the incidence of diabetes is lower in postmenopausal women on hormone replacement therapy (14, 43). Evidence also suggests that short-term administration of estradiol and norgestrel (a synthetic progestin) reduces proteinuria and improves creatinine clearance (CrCl) in diabetic and hypertensive postmenopausal women (39). However, no studies have addressed the contribution of estrogen in the pathophysiology of diabetic nephropathy in the female animal model and the potential benefits of E2 replacement on attenuating the disease process. Thus we examined the effects of E2 replacement in the kidney of streptozotocin (STZ)-induced diabetic rats on albuminuria, CrCl, glomerulosclerosis, and tubulointerstitial fibrosis (TIF).


   MATERIALS AND METHODS
TOP
 ABSTRACT
 MATERIALS AND METHODS
RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
Animal model. Female Sprague-Dawley rats (Harlan, Madison, WI) were purchased at 6–7 wk of age and maintained on a phytoestrogen-free rat chow (Harlan) and allowed free access to tap water. The animals were randomly divided into three treatment groups: intact (control), ovariectomized (OVX), and ovariectomized with E2 replacement (OVX+E2). After an overnight fast, each group of animals was further divided to receive either a single intraperitoneal injection of 0.1 M citrate buffer [pH 4.5, nondiabetic (ND)] or 55 mg/kg STZ (Sigma, St. Louis, MO) in 0.1 M citrate buffer [diabetic (D)]. All the diabetic animals were given daily injections of insulin (2–4 U, Lantus, Aventis Pharmaceuticals, Kansas City, MO) to maintain blood glucose levels between 250 and 400 mg/dl. During the treatment period (12 wk), the animals (n = 6–8 per group) were placed in metabolic cages every 4 wk and urine samples were collected for measurement of urine albumin excretion (UAE) and CrCl. At the end of the treatment period, the animals were weighed, anesthetized with pentobarbital sodium (40 mg/kg ip), and blood samples were collected, by cardiac puncture, for measurement of plasma levels of E2 and creatinine. Body length was measured for determination of body surface area and body mass index according to the DuBois formula (12). After an abdominal incision was made, the right kidney was removed, and the cortex and medulla were separated and snap-frozen in liquid nitrogen for protein analysis. The left kidney was perfusion fixed with 4% paraformaldehyde for morphological and immunohistochemical analysis. The experiments were performed according to the guidelines recommended by the National Institutes of Health and approved by the Georgetown University Animal Care and Use Committee.

Ovariectomy, estrogen replacement, and plasma estradiol levels. Under gas anesthesia (2% isofluorane), the ovaries were exposed via bilateral flank incisions and excised. At the time of OVX, the animals receiving E2 were implanted with E2 pellets (10 µg/day continuous release, Innovative Research, Sarasota, FL). This dose of E2 results in circulating estradiol levels that are in the peak physiological range (36). Plasma E2 levels were measured from samples obtained by cardiac puncture by a radioimmunoassay (Hypertension and Vascular Disease Center Core Facility, Wake Forest University Health Science, Winston-Salem, NC).

Urine albumin and plasma creatinine. Urine albumin concentration was determined using a Nephrat II albumin kit (Exocell, Philadelphia, PA), according to the manufacturer's protocol. Plasma and urine creatinine concentrations were determined using Beckman Creatinine Analyzer II (Brea, CA) with the modified Jaffe rate method (33).

Morphology. After fixation with 4% paraformaldehyde, the kidneys were routinely processed to paraffin, sectioned at 4 µm, and stained with periodic acid-Schiff's (PAS; for demonstration of glycogen deposition) or Masson's trichrome (for demonstration of collagen deposition) (41).

Glomerulosclerotic index. Glomerulosclerosis was defined as thickening of the basement membrane and mesangial expansion (3a). The glomerulosclerotic index (GSI) was determined in PAS-stained sections using a light microscope. Eighty randomly selected glomeruli in 10 sections were assessed and the degree of sclerosis was graded using a semiquantitative scoring method as previously described (34).

Index of tubulointerstitial fibrosis. Tubulointerstitial fibrosis was defined as tubular atrophy or dilatation, deposition of ECM, and interstitial fibroblast proliferation (3a). The index of tubulointerstitial fibrosis (TIFI) was assessed in 10 different Masson's trichrome-stained sections using a light microscope on a scale of 0 to 4 (grade 0, normal; grade 1, affected area <10%; grade 2, affected area 10–25%; grade 3, affected area 25–75%; grade 4, affected area greater than 75%).

Immunohistochemistry. Paraffin sections (4 µm) were incubated with 10% nonimmune goat serum for blocking of nonspecific immunoreactivity. The sections were then incubated with antisera against TGF-{beta} (rabbit polyclonal, R&D Systems, Minneapolis, MN) at 4°C overnight. The positive immunoreaction was detected using the Envision Plus peroxidase kit (Dako, Carpentaria, CA) and by counterstaining with Mayer's hematoxylin. Sections incubated with 10% nonimmune goat serum instead of the primary antiserum were used as negative controls.

Western blot analysis. Homogenized samples from the renal cortex and medulla were loaded on a 18% SDS-PAGE gel, and the proteins were transferred to a nitrocellulose membrane. The membranes were incubated with 5% nonfat milk, 0.05% Tween 20 in TBS [10 mM Tris·HCl (pH 7.4), 150 mM NaCl], then with the primary antiserum as described for immunohistochemistry at 4°C overnight. The membranes were washed and incubated with goat anti-rabbit IgG conjugated to horseradish peroxidase, and proteins were visualized by enhanced chemiluminescence (KPL, Gaithersburg, MD). The densities of specific bands were normalized to the total amount of protein loaded in each well following densitometric analysis of gels stained with Coomassie blue. The densities of specific bands were quantitated by densitometry using Scion Image beta (version 4.02) software.

Statistical analysis. Data are expressed as means ± SE and were analyzed with a two-way ANOVA followed by a Bonferroni posttest, using Sigma Stat software. Differences were considered significant at P < 0.05.


   RESULTS
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
DISCUSSION
 GRANTS
 REFERENCES
 
Body and kidney weight, body mass index, and food intake. In the ND group, OVX was associated with a 20% increase in body weight, 36% increase in kidney weight, and 14% increase in body mass index (BMI), compared with the intact group, whereas replacement with E2 completely prevented the increases in all three of these parameters; in fact, all three parameters were lower in the OVX+E2 group compared with the intact rats (Table 1). No differences in food intake were observed between the intact, OVX, or OVX+E2 in the ND (Table 1). In the D group, OVX was associated with a more modest (9%) increase in body weight, which was similar to the ND group, whereas E2 replacement decreased body weight to levels similar to the intact animals (Table 1). However, no significant differences in kidney weight or BMI were observed in the D group between the intact and OVX or OVX+E2 animals. Similar to the ND group, no differences in food intake were observed between the intact, OVX, or OVX+E2 in the D (Table 1).


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  		Table 1. Effects of OVX and E2 replacement on metabolic parameters in diabetic rats

 
Blood glucose and plasma E2 levels. In the intact D rats, a 390% increase in blood glucose levels was observed compared with the intact ND rats (Table 1). A similar increase in blood glucose was observed in the D group with OVX and OVX+E2 compared with the respective ND group. Plasma estradiol levels were reduced by 53% in the intact D compared with intact ND animals (Table 1). In both the ND and D animals, OVX reduced and OVX+E2 increased plasma estradiol levels to a similar extent.

UAE, CrCl, and mean arterial pressure. In the intact D rats, a 1,400% increase in UAE was observed compared with the intact ND rats (Table 2). A similar increase in UAE was observed in the D group with OVX and OVX+E2 compared with the respective ND group. In both the ND and D groups, the increase in UAE was greatest in the OVX groups compared with intact, whereas E2 replacement attenuated this increase. In the intact D rats, a 61% decrease in CrCl was observed compared with the intact ND rats (Table 2). Although a similar decrease in CrCl was observed in the D group with OVX compared with the ND OVX group, in the ND group, OVX+E2 increased CrCl to 53% above that of the D intact group. No differences in mean arterial pressure (MAP) were observed between any of the treatment groups (Table 2).


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  		Table 2. Effects of OVX and E2 replacement on renal and systemic function in diabetic rats

 
GSI and TIFI. In the ND group, OVX was associated with a ninefold increase in the GSI (Figs. 1 and 2A) compared with the intact group. These kidneys were characterized by glomerular basement thickening and mesangial expansion. Replacement with E2 attenuated glomerulosclerosis associated with OVX in the ND group and, as observed in the intact group, these kidneys exhibited normal renal morphology (Figs. 1 and 2A). In the D group, the kidneys of intact animals exhibited a 14.5-fold increase in the GSI compared with ND intact animals. As in the ND group, E2 replacement attenuated these changes (Figs. 1 and 2A). In the ND group, OVX was associated with a ninefold increase in the degree of medullary TIFI (Figs. 1 and 2B) compared with the intact group. These kidneys were characterized by accumulation of ECM deposits in the tubulovascular bundles. Replacement with E2 attenuated the TIFI associated with OVX in the ND group and as observed in the intact group, these kidneys exhibited normal medullary morphology (Figs. 1 and 2B). In both the renal cortex and medulla in the D group, the kidneys of intact animals exhibited a 6.0- and 17.0-fold increase in the TIFI compared with ND intact animals (Figs. 1 and 2B). As in the ND group, E2 replacement attenuated these changes (Figs. 1 and 2B).



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  		Fig. 1. Morphology of the nondiabetic (ND) and diabetic (D) rat kidney. A: periodic acid-Schiff-stained sections of the renal cortex. The diabetic kidneys are characterized by moderate glomerulosclerosis (g) with thickening of glomerular basement membrane and mesangium expansion (arrows). The severity of lesions was most pronounced in the ovariectomy (OVX) group, whereas replacement with E2 attenuated these changes. B: Masson's trichrome-stained sections of the renal medulla. The diabetic kidneys are characterized by moderate tubulointerstitial fibrosis (TIF), characterized by the presence of extracellular matrix deposits within and surrounding the tubulovascular bundles (outlined). The severity of lesions was most pronounced in the OVX group, whereas replacement with E2 attenuated these changes. Original magnification x400.

 


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  		Fig. 2. Indexes of glomerulosclerosis (GSI) and TIF (TIFI) in the ND and D rat kidney. A: intact animals in the diabetic group exhibited a 14.5-fold increase in the degree of GSI compared with the intact ND group. OVX exacerbated, whereas E2 replacement attenuated these changes. B: intact animals in the diabetic cortex and medulla exhibited a 6.4- and 17-fold increase, respectively, in the degree of TIFI compared with the renal cortex and medulla in the intact ND group. OVX exacerbated, whereas E2 replacement attenuated these changes. Data are expressed as means ± SE; n = 6. aP < 0.05, aaP < 0.0, aaaP < 0.001 vs. ND in the same treatment group. bP < 0.05, bbP < 0.01 vs. intact in the same metabolic group. cP < 0.05, ccP < 0.01 vs. OVX in the same metabolic group.

 
TGF-{beta} localization and expression. In the kidneys of ND rats, no immunostaining for TGF-{beta} could be detected (Fig. 3). In the renal cortex of intact D rats, TGF-{beta} immunostaining was confined to the glomerular mesangium (Fig. 3), whereas in the OVX D group, staining was also prominent in the tubulointerstitium, most noticeably in the proximal tubules. Replacement with E2 in the D group reduced the intensity of immunostaining and was detectable only in a few glomeruli. Western analysis showed a twofold increase in TGF-{beta} protein expression in the renal cortex of D intact and OVX rats (Fig. 4). E2 replacement completely prevented the D-induced increase in TGF-{beta} protein expression; the levels of TGF-{beta} protein expression were indistinguishable from the intact ND and D groups.



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  		Fig. 3. Immunohistochemical localization of transforming growth factor (TGF)-{beta} in the ND and D rat kidney. In the kidneys of ND animals, no immunolocalization of TGF-{beta} was detected. In the intact animals of the D group, TGF-{beta} (brown staining) was immunolocalized to the glomeruli (g) mainly in the mesangium (arrowhead). In the OVX animals, in addition to staining in the mesangium, TGF-{beta} was also found in the proximal tubules (pt), whereas very little TGF-{beta} immunostaining was observed with E2 replacement. Original magnification x400.

 


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  		Fig. 4. Western blot analysis of TGF-{beta} expression in the ND and D rat kidney. In the renal cortex of the ND kidneys, very low levels of TGF-{beta} were detected. In the intact and OVX kidneys in the D group, TGF-{beta} protein expression was increased by 2-fold compared with the ND compared. This increase was attenuated with E2 replacement. Top: SDS gels of TGF-{beta} protein expression. Bottom: densitometric scans in arbitrary units (AU) of TGF-{beta} protein from top. Data are expressed as means ± SE; n = 6. aaP < 0.0 vs. ND in the same treatment group. bP < 0.05, bbP < 0.01 vs. intact in the same metabolic group. ccP < 0.01 vs. OVX in the same metabolic group.

 

   DISCUSSION
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
GRANTS
 REFERENCES
 
In the present study, we demonstrate that in the STZ-induced D rat, replacement with E2 for 12 wk is renoprotective, by reducing albuminuria, improving CrCl, attenuating glomerulosclerosis and tubulointerstitial fibrosis, and reducing TGF-{beta} protein expression.

Increased UAE and a decline in CrCl are hallmarks of diabetic renal disease (2, 38, 42a). In our study, increased UAE and decreased CrCl were observed after 12 wk of diabetes. The changes in UAE were most pronounced in the OVX group and attenuated by E2 replacement, whereas changes in CrCl were not as consistent with different treatments within the same metabolic group. Variable effects of E2 replacement on UAE and CrCl have been reported in other studies. Although in the OLETF diabetic rat E2 had no effect on albuminuria (40), previous studies from this and other laboratories reported that replacement with E2 attenuates the decline in CrCl associated with aging in the Dahl salt-sensitive rat (25) and attenuates albuminuria in the uninephrectomized spontaneously hypertensive rat (18). Furthermore, in type II diabetic patients, replacement with E2 reduced proteinuria and improved CrCl (39). These findings indicate that E2 may prevent as well as reverse the decline in renal function associated with diabetic nephropathy.

At 12 wk of age, the STZ-D rat exhibited moderate glomerulosclerosis, characterized by mild thickening of glomerular basement membrane and mesangial expansion. The degree of glomerulosclerosis was worsened in the absence of ovarian hormones in both the nondiabetic and the diabetic kidney, whereas the damage was attenuated by E2 replacement. These changes in glomerulosclerosis correlated with the changes in UAE. Previous studies reported variable effects of estrogen deficiency and modulation of estrogen effects in experimental models of diabetic nephropathy. In the glomerulosclerosis-prone mouse model with a mutation in oligosyndactyly (ROP Os/+), estrogen deficiency accelerates the progression of glomerulosclerosis (13). In contrast, in the Cohen diabetic rat, estrogen deficiency and treatment with tamoxifen, a selective estrogen receptor modulator, decrease glomerulosclerosis (9, 32). These variable findings are most likely due to different models of diabetic nephropathy, the type of diet fed, as well as the duration of treatments.

Our study suggests that changes in TGF-{beta} protein expression correlate with the degree of glomerular structural damage. Numerous studies have demonstrated that TGF-{beta} promotes renal cell growth and ECM accumulation, the two hallmarks of diabetic nephropathy (8, 17). Although our study did not directly examine the effects of E2 replacement on TGF-{beta} expression, the fact that TGF-{beta} expression decreased in animals replaced with E2 suggests that one of the mechanisms by which E2 is renoprotective may be through regulating TGF-{beta} expression. Estradiol and its metabolites have been shown to inhibit TGF-{beta} protein expression under hyperglycemic conditions (26, 28). Further studies are needed to examine the effects of E2 on regulating TGF-{beta} expression in our experimental model.

In addition to glomerulosclerosis, the STZ-D rat also exhibited moderate TIF in both the cortex and medulla, characterized by accumulation of ECM deposits in the tubulovascular bundles, presence of inflammatory infiltrates and tubular casts. Most recent studies have suggested that the degree of tubulointerstitial fibrosis is the most reliable marker of the progression of renal disease (16). The mechanisms leading to these changes have not been explored in the current study, but numerous other studies demonstrate local activation of growth factors and cytokines, including angiotensin, endothelin, and TGF-{beta} in response to hyperglycemia (8, 16, 42). Similar to glomerulosclerosis, we found that the degree of tubulointerstitial fibrosis correlated with the changes in albuminuria and that E2 replacement attenuated these changes. A similar renoprotective effect of E2 has been observed in the 5/6 remnant kidney model, in which E2 replacement inhibited tubulointerstitial fibrosis via reducing TGF-{beta} expression (4, 22). In the ROP Os/+ mice, E2 also prevented tubulointerstitial fibrosis by decreasing synthesis of interstitial and basement membrane collagens (13), whereas in cultured mesangial cells, E2 increases the activity of ECM-degrading enzymes, matrix metalloproteinases (30), and inhibits TGF-{beta}-induced apoptosis (27). Similar mechanisms may underlie the renoprotective effect of E2 in our model, and further studies are underway to more specifically examine these mechanisms.

Although several studies suggest that the renoprotective effects of E2 are mediated via its blood pressure-lowering effects (11, 39), our studies show that E2 is renoprotective irrespective of its effect on blood pressure. No differences in MAP were observed in any of the treatment groups, suggesting that the renoprotective effects of E2 may indeed be direct, most likely via mediating cellular process such as cell proliferation and ECM metabolism.

Estrogen-deficient animals, in both D and ND states, exhibited an increase in body weight and BMI. These findings are in concert with the previously reported studies on the increase in body weight and BMI associated with menopause and decline in ovarian function. Although the mechanisms for the increase in body weight and BMI in the absence of ovarian hormones are not completely understood, a recent study showed that the increase is not due to an increase in food intake but rather due to altered levels of luteinizing hormone and leptin (1, 23). Similar mechanisms may be responsible for the prevention of body weight gain after E2 replacement in the STZ-D rat, as no differences in food intake were observed between intact, OVX, and OVX+E2 rats.

An interesting observation from our studies is that the STZ-induced D rat has lower circulating estradiol levels compared with its ND counterpart. Although very few studies in fact report the hormone levels in patients with diabetic nephropathy, there are some reports that suggest that diabetic women also have lower circulating levels of estradiol (31). These studies point to a relationship between ovarian hormones and diabetes and this interaction may contribute to the mechanisms underlying why women with diabetes "lose" the protective effect of the female gender and exhibit prevalence and progression of disease that are similar to men. Our findings suggest that E2 replacement may be beneficial in preventing or retarding the development of diabetic renal complications. Interestingly, however, our studies also indicate that despite the similar levels of E2 in the intact and E2-replaced group with diabetes, the E2-replaced group is characterized by higher CrCl and lower markers of renal pathology compared with the intact. These findings suggest that the presence of progesterone in the intact rats (the E2-replaced animals are deficient of progesterone as a result of ovariectomy) may have adverse effects in the face of hyperglycemia. Although no studies to date have addressed the effects of progesterone in diabetic nephropathy, a study examining the effects of E2 alone and combined E2 and progesterone in type II diabetic women reported beneficial effects of E2 alone, but not the combined study (37). These findings suggest that the presence of progesterone may attenuate the beneficial effects of E2 in diabetes. Further studies are warranted to examine the specific effects of progesterone in diabetic renal complications.

Despite the early termination of the E2 alone arm of the Women's Health Initiative (WHI) trial due to adverse effects of conjugated equine estrogen on stroke and hip fractures, this study did not show adverse effects on cardiovascular, whereas the renal effects have not even been examined in this study (3). Furthermore, the WHI trial was performed on average in woman who had been postmenopausal for at least 10 years, that is women who have experienced low levels of ovarian hormones for an extended period of time. Our animal studies were performed in young, premenopausal animals to examine if E2 replacement attenuates the development of diabetic nephropathy in animals that have not experienced an age-related decline in circulating estradiol. Whether E2 is also beneficial in attenuating or reversing the disease process once it has advanced or after the animals have been estrogen depleted for an extended period of time, such as with aging, remains to be elucidated.

In summary, our study demonstrates that E2 in the STZ-induced D rat is renoprotective by preventing the decline in renal function and pathological changes associated with diabetic nephropathy. These findings suggest that E2 replacement may be beneficial in preventing diabetic renal complications, but most importantly, stress the importance of examining the contribution of gender and sex hormones in the incidence and progression of cardiovascular disease, renal disease, and diabetes.


   GRANTS
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 GRANTS
REFERENCES
 
This work was supported by the Carl W. Gottschalk Award from the American Society of Nephrology, the Research Award from the American Diabetes Association, and the Junior Faculty Research Award from Georgetown University to C. Maric.


   ACKNOWLEDGMENTS
 
The authors acknowledge the technical expertise of Dr. L. Asico, S. Afridi, and G. Fitzgerald, Dr. D. Roesch for valuable discussions, and Dr. K. Sandberg for the critical evaluation of the manuscript.


   FOOTNOTES
 

Address for reprint requests and other correspondence: C. Maric, Center for the Study of Sex Differences: in Health, Aging and Disease, Georgetown Univ. Medical Center, 394 Bldg D, 4000 Reservoir Road NW, Washington, DC 20057 (E-mail: cm255{at}georgetown.edu)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.


   REFERENCES
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 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 

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