Evidence for G-Protein-Coupled Estrogen Receptor as a Pronatriuretic Factor.

Background The novel estrogen receptor, G-protein-coupled estrogen receptor (GPER), is responsible for rapid estrogen signaling. GPER activation elicits cardiovascular and nephroprotective effects against salt-induced complications, yet there is no direct evidence for GPER control of renal Na+ handling. We hypothesized that GPER activation in the renal medulla facilitates Na+ excretion. Methods and Results Herein, we show that infusion of the GPER agonist, G1, to the renal medulla increased Na+ excretion in female Sprague Dawley rats, but not male rats. We found that GPER mRNA expression and protein abundance were markedly higher in outer medullary tissues from females relative to males. Blockade of GPER in the renal medulla attenuated Na+ excretion in females. Given that medullary endothelin 1 is a well-established natriuretic factor that is regulated by sex and sex steroids, we hypothesized that GPER activation promotes natriuresis via an endothelin 1-dependent pathway. To test this mechanism, we determined the effect of medullary infusion of G1 after blockade of endothelin receptors. Dual endothelin receptor subtype A and endothelin receptor subtype B antagonism attenuated G1-induced natriuresis in females. Unlike males, female mice with genetic deletion of GPER had reduced endothelin 1, endothelin receptor subtype A, and endothelin receptor subtype B mRNA expression compared with wild-type controls. More important, we found that systemic GPER activation ameliorates the increase in mean arterial pressure induced by ovariectomy. Conclusions Our data uncover a novel role for renal medullary GPER in promoting Na+ excretion via an endothelin 1-dependent pathway in female rats, but not in males. These results highlight GPER as a potential therapeutic target for salt-sensitive hypertension in postmenopausal women.

estrogen receptors

endothelin 1

endothelin receptor subtype A

endothelin receptor subtype B

G protein‐coupled estrogen receptor

mean arterial pressure

urinary K+ excretion

Urinary Na+ excretion

urine flow

Clinical Perspective

What Is New?

This study identifies a novel mechanism by which females efficiently excrete sodium and maintain blood pressure.

We also report that the G‐protein–coupled estrogen receptor facilitates sodium excretion, at least in part, through activation of the renal medullary endothelin system.

What Are the Clinical Implications?

This study highlights the importance of the G‐protein–coupled estrogen receptor in regulating blood pressure and sodium excretion in females.

G‐protein–coupled estrogen receptor activation is a potential therapeutic target for salt‐sensitive hypertension in postmenopausal women.

Premenopausal women have a lower risk of cardiovascular and renal diseases compared with age‐matched men. This female advantage is lost when women reach menopause, pointing to a fundamental role for ovarian hormones, particularly estradiol, in protecting the cardiovascular and renal health in premenopausal women. In addition to the well‐established classic genomic effects of this sex steroid, rapid nongenomic responses to estradiol have also been reported. The G‐protein–coupled estrogen receptor (GPER) is a membrane‐associated receptor linked to short‐term estrogenic signaling pathways.1, 2, 3, 4, 5, 6 More important, GPER is widely expressed throughout the body, including the kidney.7, 8, 9 However, the physiological and pathophysiological role of renal GPER is poorly understood.

Similar to classic steroid receptors, estrogen receptors α and β, GPER is implicated as a protective pathway in cardiovascular and kidney disease.8, 10, 11, 12 Activation of GPER acutely lowers blood pressure in normotensive rats13 and ameliorates renal and salt‐induced injury.8, 10, 12 GPER activation reduces oxidative stress and proteinuria as well as attenuates aortic remodeling in the salt‐sensitive female mRen2.Lewis rats.8, 10 Activation of GPER blunts diastolic dysfunction induced by a high salt diet in intact female mRen2 rats.14 In addition, the GPER locus in the human genome has been associated with hypertension.15

A series of recent studies have reported sex‐dependent discrepancies in mechanisms that regulate Na+ handling within the renal medulla.16, 17, 18, 19, 20, 21 Given the critical role of the renal medulla in fine‐tuning of Na+ excretion and blood pressure, we designed experiments to identify the effect of GPER on Na+ handling within the renal medulla. We hypothesized that GPER within the renal medulla promotes natriuresis. We tested our hypothesis by determining the excretory response to intramedullary infusion of the GPER agonist, G1, in age‐matched male and female Sprague Dawley rats. To provide further mechanistic insight, we explored a possible relationship between GPER and the renal endothelin 1 (ET‐1) system because of its importance in Na+ handling in the renal medulla. To elucidate the role of the endogenous ligand, estradiol, on GPER pronatriuretic effects, we determined the effect of ovariectomy on GPER activation within the renal medulla. Additional experiments determined whether GPER has long‐term effects on blood pressure in ovariectomized rats.

Methods

The data that support the findings of this study are available from the corresponding author on reasonable request.

Animals

Male and female (16–20 weeks of age) Sprague Dawley rats from Envigo (Indianapolis, IN) were used. Rats used in intramedullary infusion experiments were maintained on our standard 7917 Irradiated NIH‐31 Mouse/Rat diet (0.8% NaCl; Envigo). Rats used in telemetry experiments were maintained on TD 96208 (0.49% NaCl [Envigo], matched control diet for our high salt diet, TD 92034, 4% NaCl [Envigo]). Male and female wild‐type and GPER knockout mice (18–25 weeks of age) were generated and genotyped as previously described.22, 23 Mice were maintained on 5053 Picolab Rodent diet 20 (0.82% NaCl; LabDiet, St. Louis, MO). Animals were conventionally housed in a temperature (18°C–23°C) controlled room with a 12:12‐hour light‐dark cycle with free access to food and water. All protocols were in accordance with the Guide for the Care and Use of Laboratory Animals and were approved in advance by the University of Alabama at Birmingham or Tulane University Institutional Animal Care and Use Committee.

Short‐Term Intramedullary Infusion

Rats were anesthetized using thiobutabarbitone (Inactin, hydrate, 100 mg/kg, IP, T133; Sigma‐Aldrich Co, St. Louis, MO) at 8 to 11 am and surgically prepared, as detailed in our previous studies.17 Animals were then allowed to equilibrate for 60 to 80 minutes, before a 20‐minute baseline urine collection, during which the vehicle (0.02% dimethyl sulfoxide in saline) was infused into the renal medulla. This was followed by intramedullary infusion of the GPER agonist, G1 (5 pmol/kg per minute, 41004001, purity ≥98%; Sandia Biotec Inc, Albuquerque, NM; n=8 female rats, n=9 male rats, n=8 ovariectomized rats) and/or GPER antagonist, G15 (5 pmol/kg per minutes, 41004003, purity ≥99%; Sandia Biotec Inc; n=4 and 9 female rats, respectively) for an additional 20‐minute period (Figure 1A). In an additional group of female rats (n=6), we continued to infuse the vehicle for the second 20‐minute urine collection period to serve as a time control. At the end of each experiment, the kidney was dissected to confirm correct positioning of the catheter. Urinary Na+ and K+ concentrations were measured using an atomic absorption spectrometer (iCE 3000 series paired with a CETAC ASX‐520 AutoSampler; Thermo Fisher Scientific, Waltham, MA).

Figure 1

Activation of G‐protein–coupled estrogen receptor (GPER) in the renal medulla facilitates urinary Na+ excretion in female rats.

Schematic presentation of the surgical procedure and experimental time line employed (A). Urinary Na+ excretion (U aV) (B), urine flow (UV) (C), urinary K+ excretion (U) (D), and mean arterial pressure (MAP) (E) in anesthetized intact female Sprague Dawley rats receiving renal medullary interstitial infusions of vehicle (Veh), G1 (GPER agonist, 5 pmol/kg per minute), G1+G15 (GPER antagonist, 5 pmol/kg per minute), or G15 alone, respectively. n=4 to 9 in each group. Statistical comparisons performed by paired Student t test.

A separate group of female rats (n=5) was used to determine the role of endothelin receptor subtype A (ETA) and endothelin receptor subtype B (ETB) in response to medullary GPER activation. Rats received an IV bolus injection (0.5 mL/kg via femoral vein catheter) of a combination of the ABT‐627 (selective ETA receptor antagonist, 5 mg/kg; AbbVie Inc, Abbott Park, IL) simultaneously with the selective ETB receptor antagonist A‐192621 (10 mg/kg; PepTech Corp, Bedford, MA) 30 minutes before the end of the equilibration period. These doses are known to maintain efficient blockade of ETA and ETB receptors, respectively, in male rats for the duration of our experimental protocol, as previously demonstrated.17 After the equilibration period and the 20‐minute baseline urine collection during which vehicle was infused, G1 was infused for an additional 20‐minute urine collection period.

RNA Extraction and Gene Expression Assessment by Reverse Transcription–Polymerase Chain Reaction

Tissue RNA was isolated using Purelink Mini RNA extraction kit (12183018A; Thermo Fischer Scientific), according to manufacturer's instructions. The isolated RNA was reverse transcribed using QuantiTect Reverse Transcription kit (Qiagen, Hilden, Germany). The resulting cDNA was used to quantify mRNA by reverse transcription–polymerase chain reaction (CFX96 Real‐Time System; BIORAD) using TaqMan primer gene expression assays with rat GPER (Rn00592091_s1), mouse ET‐1 (Mm00438656_m1), mouse ETA receptor (Mm01243722_m1), mouse ETB receptor (Mm00432989_m1), mouse β‐actin (Mm02619580_g1), and rat β‐actin (Rn00667869_m1) primers. Gene expression was quantified relative to β‐actin using 2−ΔΔCt method.

Western Blotting

Samples were processed as previously described.24 Briefly, 20 μg of renal outer and inner medulla was separated, transferred, and incubated in goat GPER primary antibody (AF5534; R&D, Minneapolis, MN) at 1:500 dilution or Na+/K+ ATPase α‐subunit primary antibody (Developmental Studies Hybridoma Bank at the University of Iowa) at 1:1000 dilution. Donkey anti‐goat (H+L) cross‐adsorbed secondary antibody, Alexa Fluor 680 (A‐21109; Invitrogen, Waltham, MA) at 1:500 dilution, and goat anti‐mouse IgG (H+L) secondary antibody DyLight 680 (35518; Thermo Fisher Scientific) at 1:1000 were used for GPER and Na+/K+ ATPase α‐subunit, respectively. Coomassie Blue staining was performed to ensure equal loading.

Na+/K+ ATPase Activity

Renal outer medullary Na+/K+ ATPase activity was measured using Na+/K+ ATPase Microplate Assay Kit (MBS8243226; MyBioSource, San Diego, CA), according to manufacturer's instructions.

Telemetry

Blood pressure measurements were made using HD‐S10 transmitters (Data Sciences International, Duluth, MN), as previously described.25 Rats were allowed to recover for 7 to 10 days postsurgically before baseline blood pressure and heart rate recording.

Ovariectomy

Female rats were subjected to bilateral ovariectomy, as described previously.19 Three weeks after ovariectomy, rats were used in short‐term intramedullary infusion experiments.

Osmotic Mini Pump Implantation

At the same time of ovariectomy, rats underwent subcutaneous implantation of an Alzet osmotic pump (model 2ML4; Cupertino, CA) that infused G1, a GPER agonist (400 μg/kg per day, 41004003; Sandia Biotec Inc; n=6) or vehicle (75% dimethyl sulfoxide in saline; n=6). This dose of G1 has been shown in previous studies to elicit cardiovascular protection in rats.26, 27 More important, G1 is a potent and selective GPER agonist. Even at high concentrations, G1 (1–10 μmol/L) displays no activity toward classic estrogen receptors.28, 29 G1 showed no activity toward a panel of 25 other important G‐protein–coupled receptors,30 and elicited no activity in GPER knockout mice.13, 23, 31

Metabolic Cages

Rats were placed into metabolic cages, allowing daily quantitative urine collections and measurements of intake on day 14 after performing ovariectomy and pump implantation surgeries. The 24‐hour urine samples were collected at 8 am.

Statistical Analysis

Data are presented as mean±SEM. Statistical tests used for each data set are specified in each figure legend. This includes analysis by paired and unpaired Student t test. Two‐way ANOVA followed by Sidak's post hoc tests were also used for data analysis, where indicated. A probability of P<0.05 was considered statistically significant. Statistical analysis was performed using GraphPad Prism version 8.

Results

GPER‐Induced Natriuresis in Female Rats

Medullary infusion of G1 significantly increased Na+ excretion in female Sprague Dawley rats by 70±22% relative to baseline (Figure 1B). Urine flow also significantly increased at commencing intramedullary infusion of G1 (Figure 1C). In time control experiments where vehicle was infused, urine flow and electrolyte excretion were not significantly changed (Figure 1B and 1C). Medullary infusion of the GPER antagonist, G15, simultaneously with G1 prevented G1‐evoked natriuretic and diuretic effects (Figure 1B and 1C). Urinary K+ excretion (Figure 1D) and mean arterial pressure (MAP) (Figure 1E) were not significantly changed during intramedullary infusions of vehicle, G1 alone, or when combined with G15. Of note, many females elicited a small increase in urinary K+ in response to G1 infusion; however, this effect did not reach statistical significance (Figure 1D). G1 infusion slightly decreased medullary blood flow, 7±2%, relative to baseline (n=5). This was not significantly different compared with the change observed during vehicle infusion, 14±5% (n=5).

To determine the contribution of GPER activation by its endogenous ligand, estradiol, in facilitating basal Na+ excretion in females, we performed experiments with intramedullary infusion of G15. G15 significantly decreased urinary Na+ excretion by 30±9% relative to baseline (Figure 1B). Urine flow did not significantly change during medullary blockade of GPER (Figure 1C). Urinary K+ excretion and MAP were not significantly altered by G15 (Figure 1D and 1E).

In contrast to data from female rats, medullary activation of GPER did not significantly increase urinary Na+ excretion or urine flow in male rats (Figure 2A and 2B). Urinary K+ excretion and MAP also remained unchanged during G1 infusion in males (Figure 2C and 2D). GPER mRNA expression was 5‐fold higher in outer medulla from female rats, compared with males (Figure 2E). Similarly, outer medullary GPER protein abundance was higher in females relative to males (Figure 2E). We did not observe a significant sex‐related difference in inner medullary GPER mRNA expression or protein abundance; however, there was a trend toward lower abundance in males that did not reach statistical significance (Figure 2F).

Figure 2

Activation of G‐protein–coupled estrogen receptor (GPER) in the renal medulla did not change urinary Na+ excretion in male rats.

Effect of renal medullary interstitial infusions of the GPER agonist, G1 (5 pmol/kg per minute) on urinary Na+ excretion (U aV) (A), urine flow (UV) (B), urinary K+ excretion (U) (C), and mean arterial pressure (MAP) (D) in anesthetized male Sprague Dawley rats. Relative mRNA expression and protein abundance of GPER in outer medulla (E) and inner medulla (F) from male and female rats (representative Western blots are presented). Gene expression values represent fold change from corresponding female levels. Protein abundance is presented relative to female levels. n=5 to 10 rats in each group. Statistical comparisons performed by paired Student t test (A through D) and unpaired Student t test (E and F).

GPER and ET‐1 Pathway Interactions

Dual blockade of ETA and ETB receptors completely abolished the natriuretic and diuretic response to medullary GPER activation (Figure 3A and 3B). Urinary K+ excretion and MAP remained unchanged during these experiments (Figure 3C and 3D). We also determined the effect of genetic ablation of GPER on mRNA expression of renal ET‐1, ETA, and ETB. GPER knockout resulted in significant reductions in the expression of ET‐1, ETA, and ETB receptors only in female mice, but not in males (Figure 3E). ETB receptor expression in wild‐type mice was significantly lower in males relative to females (Figure 3E).

Figure 3

Pharmacologic and genetic evidence for the interaction between G‐protein–coupled estrogen receptor (GPER) and renal endothelin 1 (ET‐1) system in females.

Effect of renal medullary interstitial infusions of the GPER agonist, G1 (5 pmol/kg per minute), after a bolus injection of the selective endothelin receptor subtype A (ETA) receptor blocker (ABT‐627) and the selective endothelin receptor subtype B (ETB) receptor blocker (A‐192621) on urinary Na+ excretion (U aV) (A), urine flow (UV) (B), urinary K+ excretion (U) (C), and mean arterial pressure (MAP) (D) in anesthetized intact female Sprague Dawley rats. mRNA expression of renal ET‐1, ET and ET receptors (E) in male and female wild‐type (WT) and GPER knockout (KO) mice. n=5 to 12 animals in each group. Statistical comparisons performed by paired Student t test (A through D) and 2‐way ANOVA with Sidak's post hoc test for multiple comparisons (E).

Na+/K+ ATPase

Given that ET receptor activation mediates GPER pronatriuretic effects and ET‐1 has been previously shown to inhibit Na+/K+ ATPase activity,32 we tested whether GPER activation reduces Na+/K+ ATPase activity and protein abundance. Specifically, we determined the effect of medullary GPER activation on the activity of Na+/K+ ATPase and the protein abundance of its α‐subunit in the outer medulla, where we have observed a significant sex difference in GPER expression and protein abundance. We found that infusion of G1 to the renal medulla in females significantly reduced Na+/K+ ATPase activity in the outer medulla, in comparison to the contralateral kidneys (0.45±0.02 versus 0.53±0.02 U/100 mg; n=5 each; Figure S1). However, the protein abundance was not different between G1‐infused and contralateral kidneys (Figure S1).

Medullary GPER in Ovariectomized Rats

To test whether the loss of estradiol, endogenous GPER ligand, exaggerates the natriuretic response to exogenous GPER activation, ovariectomized rats were subjected to the same experimental protocol depicted in Figure 1A. In ovariectomized rats, medullary activation of GPER significantly increased urinary Na+ excretion by 64±16% relative to baseline (Figure 4A). No significant changes in urinary K+ or MAP were observed (Figure 4C and 4D). No significant differences in G1‐induced natriuresis or diuresis between intact female rats and ovariectomized rats were observed (Figure 4A and 4B). GPER mRNA expression in the outer medulla from ovariectomized rats was increased relative to intact females (Figure 4E). In contrast, ovariectomy resulted in a decrease in GPER mRNA expression within the inner medulla (Figure 4F). However, ovriectomy did not have significant impact on GPER protein abundance in either the outer medulla or the inner medulla (Figure 4E and 4F).

Figure 4

Ovariectomy (OVX) does not impact the natriuretic response to medullary G‐protein–coupled estrogen receptor (GPER) activation.

Urinary Na+ excretion (U aV) and percentage change in U aV (A), urine flow (UV) and percentage change in UV (B), urinary K+ excretion (U) (C), and mean arterial pressure (MAP) (D) in anesthetized OVX Sprague Dawley rats receiving renal medullary interstitial infusions of G1 (GPER agonist, 5 pmol/kg per minute). Percentage change in U aV and UV in response to intramedullary infusion of G1 in intact females, and OVX is represented relative to baseline values. Relative mRNA expression and protein abundance of GPER in outer medulla (E) and inner medulla (F) from intact female and OVX rats (representative Western blots are presented). Gene expression values represent fold change from corresponding female levels. Protein abundance is presented relative to female levels. n=6 to 12 rats in each group. Statistical comparisons performed by Student t test (A through F).

Long‐Term Systemic Activation of GPER

To determine whether GPER activation contributes to long‐term blood pressure regulation, we determined the effect of systemic activation of GPER on blood pressure elevation in ovariectomized rats (Figure 5A). Ovariectomy significantly increased MAP in vehicle‐treated rats, compared with their baseline before ovariectomy (Figure 5B). This increase in MAP was prevented by G1 (Figure 5B). Similar hypertensive responses to ovariectomy were observed in both systolic and diastolic blood pressure in vehicle‐treated rats (Figure 5C and 5D). G1 abolished ovariectomy‐induced increase in systolic blood pressure, but not diastolic blood pressure (Figure 5C and 5D). Heart rate was increased in both vehicle‐ and G1‐treated rats in response to ovariectomy (Figure 5E). After day 11 postovariectomy, the increase in heart rate was normalized in vehicle‐treated rats only; however, heart rate remained increased in G1‐treated animals relative to baseline (Figure 5E). G1 supplementation to ovariectomized rats did not have a significant impact on body weight or food or water intake (Figure 6A through 6C). Urine volume and excretion of Na+ and K+ remained unchanged in G1‐treated rats, relative to vehicle‐treated ovariectomized rats (Figure 6D through 6F).

Figure 5

Systemic activation of G‐protein–coupled estrogen receptor prevents the ovariectomy (OVX)–induced increase in blood pressure.

Experimental time line (A). The 24‐hour mean arterial pressure (MAP) (B), systolic blood pressure (SBP) (C), diastolic blood pressure (DBP) (D), and heart rate (HR) (E) along the experimental time line in conscious female rats subjected to OVX and vehicle (Veh) or G1 (400 μg/kg per day, osmotic minipump). Panels on the right‐hand side show MAP, SBP, DBP, and HR at baseline (before OVX, average of blood pressure at days ‐1 and ‐2) and 2 weeks after OVX (average of blood pressure at days 13 and 14). Data are means±SE of 6 rats in each group. Statistical comparisons performed by repeated measures 2‐way ANOVA with Sidak's post hoc test for multiple comparisons. *P<0.05 vs corresponding baseline values.

Figure 6

Effect of systemic activation of G protein–coupled estrogen receptor on body weight and basal metabolic cage parameters.

Body weight at baseline and 2 weeks after ovariectomy (OVX) (A), food intake (B), water intake (C), urinary Na+ excretion (U aV) (D), urine flow (UV) (E), and urinary K+ excretion (U) (F) in OVX Sprague Dawley rats supplemented with vehicle (Veh) or G1 (400 g/kg per day, osmotic minipump) for 2 weeks. Data are mean±SE of 5 to 6 rats in each group. Statistical comparisons performed by repeated measures 2‐way ANOVA with Sidak's post hoc test for multiple comparisons (A) and unpaired Student t test (B through F).

Discussion

The current study shows that activation of GPER within the renal medulla provoked a natriuretic response via the ET‐1 pathway in female but not male rats. In addition, we observed that systemic GPER activation ameliorated the ovariectomy‐induced increase in mean and systolic blood pressure but not diastolic blood pressure. Together, these findings indicate an interaction between renal GPER and ET‐1 systems in females to efficiently excrete Na+ and maintain blood pressure. Furthermore, these findings provide in vivo evidence for estradiol‐dependent GPER activation as a novel female‐specific natriuretic pathway accounting for more efficient Na+ excretion in females.33, 34

Estradiol plays an integral role in the maintenance of cardiovascular and renal health.35, 36, 37, 38 However, the impact of estradiol on renal Na+ handling, which plays a central role in blood pressure regulation, is not totally clear. Sexual dimorphism in the abundance of Na+ transporters along the nephron has been recently described.33 Renal Na+ excretion was higher in women compared with men during short‐term hypertonic saline infusion,34 presumably attributable to estradiol actions along the nephron, but the evidence is limited.

Previous evidence suggests a potential contribution of GPER to the maintenance of Na+ homeostasis. Our study demonstrated that exogenous GPER activation by G1 provoked natriuresis that was abolished by simultaneous infusion of the GPER antagonist, G15. Infusion of G15 alone reduced basal Na+ excretion, indicating that endogenous activation of medullary GPER exerts an inhibitory tone on tubular reabsorption of Na+. The effects of estradiol on renal Na+ handling may not be mediated solely through GPER, especially under long‐term conditions. Future studies are needed to determine the role of estrogen receptors α and β in regulating Na+ excretion.

The renal medullary ET‐1 system, which plays a central role in the regulation of blood pressure and Na+ excretion, contributes to sex‐related differences in blood pressure control.39, 40, 41 Previous evidence indicates that GPER regulates ET‐1–dependent effects on the cardiovascular system. GPER agonists inhibit ET‐1–dependent vasoconstriction5, 42, 43 and ET‐1–dependent vascular tone in carotid arteries.44 In addition, GPER facilitates the age‐dependent increase in myocardial ETB expression45 and antagonizes ET‐1–induced hypertrophy in cultured neonatal cardiomyocytes.46 Taken together, a link between GPER and ET‐1 signaling has been demonstrated in the cardiovascular system; however, the renal interaction between these 2 systems has not been established.

In the current study, a sex‐specific regulatory role of GPER on ET‐1 signaling was supported by use of both pharmacological and genetic approaches. Specifically, dual blockade of ETA and ETB abolished the natriuretic and diuretic response to G1 infusion in female rats. More important, previously published studies from our laboratory showed no time‐dependent effect of ETA and ETB blockers on the response to intramedullary infusion of isosmotic NaCl.47 In addition, genetic deletion of GPER diminishes ET‐1, ETA, and ETB mRNA expression in female but not male mice. The influence of GPER in provoking ET‐1–induced natriuresis introduces a novel pathway by which estradiol maintains Na+ homeostasis in females. Previous studies showed the existence of GPER mRNA and protein in the kidney.7, 8, 9 Early studies demonstrated smooth muscle cells in renal pelvis and to a lesser extent the renal medulla.9 However, multiple studies reported that GPER expression is mainly in tubular epithelial cells.8, 48, 49 Cheng and colleagues demonstrated that GPER is within or in close proximity to the basolateral membrane of epithelia within proximal and distal convoluted tubules and the loop of Henle and in the renal medullary, cortical, and pelvic areas.48, 49 However, Lindsey et al8 observed that GPER is localized to the apical aspect of the renal epithelium in the hypertensive mRen2.Lewis females. Whether the differences in cellular localization of GPER within renal tubular epithelia are based on sex or physiological versus pathophysiological conditions remain to be determined.

Interestingly, it has been demonstrated that GPER expression in the kidney and brain is modulated during the estrus cycle.48, 50 Experiments involving intact cycling female rats in the current study were conducted in a periodic manner by performing experiments with cohoused rats over 4 consecutive days to maximize use across the estrus cycle. Modulation of GPER expression by estrus cycle may contribute to the observed variability in the mRNA of ET‐1, ETA, and ETB receptors in wild‐type animals. Future studies are needed to identify the impact of estrus cycle on the renal GPER function and its interaction with ET‐1.

The nature of the interaction between GPER and ET‐1 signaling at the cellular level is not clear yet. It is possible that GPER activation in a short‐term setting directly triggers ET‐1 release to activate ETA and ETB receptors. As G‐protein–coupled receptors, GPER, ETA, and ETB are capable of forming dimers or even higher‐order oligomers that might contribute to functional synergy. Despite the fact that GPER deletion resulted in changes in ETA and ETB receptor mRNA expression, we do not anticipate that the short‐term response to G1 involves changes in ETA and ETB receptors at the mRNA level. We cannot exclude the possibility of changes in protein expression or localization, so future experiments are required to identify the nature of the interaction between GPER, ETA, and ETB receptors. Experiments directed toward assessing potential posttranslational modifications in response to short‐term GPER activation will advance our understanding of rapid estrogenic signaling in the kidney.

Na+/K+ ATPase plays a key role in Na+ reabsorption. Enhanced activity of Na+/K+ ATPase results in Na+ retention.51, 52 Early studies have shown that ET‐1 reduces Na+/K+ ATPase activity in inner medullary collecting duct.32 Of note, our data demonstrate that intramedullary infusion of G1 resulted in decreased Na+/K+ ATPase activity in the renal outer medulla, which may contribute to G1‐induced natriuretic effect. Ovariectomy decreased the expression and activity of Na+/K+ ATPase in the renal cortex, which was normalized by supplementation of estradiol to ovariectomized rats.53 Similarly, estradiol induces the expression and activity of Na+/K+ ATPase in rat arterioles.54 Contrasting effects of estradiol may relate to stimulating different subtypes of ER. Future studies directed toward identifying the effect of specific activation of ER on Na+ channels and transporters are needed.

Multiple studies have established a vasodilatory role for GPER.44, 55, 56, 57, 58, 59, 60 Thus, we tested whether the natriuretic response to G1 resulted from an increase in medullary blood flow. Our finding that GPER activation did not increase medullary blood flow excludes a role for GPER‐induced renal medullary vasodilatation in mediating G1 natriuretic effects.

The current study did not show a difference in renal medullary GPER abundance or short‐term G1‐pronatriuretic effects in response to ovariectomy. It was also reported that mesenteric and aortic relaxation responses to G1 were not different in vessels from ovariectomized versus intact female rats,61, 62 suggesting that ovariectomy does not alter renal medullary or vascular responsiveness to GPER activation. However, ovariectomy appears to elicit differential effects on brain GPER expression based on the region of interest.50, 63

More important, our data also showed that systemic GPER activation ameliorated the increase in blood pressure induced by ovariectomy, suggesting that GPER contributes to the antihypertensive effect of ovarian hormones. Short‐term intrarenal GPER activation was used in the current study to specifically identify the role of renal medullary GPER on Na+ excretion, whereas systemic infusion established an overall effect of GPER on blood pressure control. It is known that GPER triggers vasodilation,57, 62, 64, 65 a potential underlying mechanism that may have contributed to the antihypertensive actions of GPER demonstrated in the current study. Despite the relatively high abundance of GPER in the brain,66 the contribution of central GPER to blood pressure regulation is not defined yet. Thus, it is possible that the antihypertensive effect of GPER in the current study may involve multiple systems, including peripheral vascular and central mechanisms, and not solely a kidney‐specific mechanism. Additional studies are needed to identify the contribution of intrarenal versus extrarenal GPER in the control of Na+ homeostasis and blood pressure.

Sources of Funding

This project was supported by an American Heart Association 18CDA34110010 and 15POST25090329 to Dr Gohar; a STRIDE fellowship from the American Physiological Society to Aceves; and grants from the National Institutes of Health: K99DK119413 to Dr Gohar; R25 DK115353 Kidney Undergraduate Research Experience to Daugherty; F31 DK111067 to Sedaka; K01 HL145324 to Dr De Miguel; T32 HL007918 to Dr Obi; R01 HL133619 to Dr Lindsey; and P01 HL 069999 and P01 HL136267 to David M. Pollock and Jennifer S. Pollock.

Disclosures

Dr Gohar is affiliated with Department of Pharmacology and Toxicology, Faculty of Pharmacy, Alexandria University, Egypt. The remaining authors have no disclosures to report.

Figure S1

Click here for additional data file.