Effects of ICI 182780 on estrogen receptor expression, fluid absorption and sperm motility in the epididymis of the bonnet monkey
© Deshpande et al; licensee BioMed Central Ltd. 2005
Received: 15 December 2004
Accepted: 02 March 2005
Published: 02 March 2005
The importance of estrogen in regulation of fluid absorption and sperm maturation in the rodent epididymis has been established from studies on estrogen receptor-alpha knockout mice. However, functional studies on the role of estrogen in primate epididymis have been few. The main objective of this study was therefore to extend these observations and systematically analyze the presence and function of estrogen receptors in modulating the function of the primate epididymis, using the bonnet monkey (Macaca radiata) as a model system.
A steroidal estrogen receptor (ER) antagonist, ICI 182780 (ICI), was administered to adult male bonnet monkeys via mini-osmotic pumps for a duration of 30 to 180 days. The expression of key estrogen-regulated genes (ER-alpha, Na-K ATPase alpha-1 and Aquaporin-1) was examined at specific time points. Further, the effect of ICI in modulating fluid reabsorption in efferent ductules was monitored, and critical sperm-maturation parameters were also analyzed.
Our studies in the bonnet monkey revealed that both ER-alpha and ER-beta were expressed in all the three regions of the epididymis. We observed an increase in ER-alpha mRNA and protein in the caput of ICI-treated monkeys. Steady state mRNA levels of the water-channel protein, Aquaporin-1, was significantly lower in the caput of ICI-treated monkeys compared to controls, whereas the mRNA levels of Na-K ATPase alpha-1 remained unchanged. In vitro incubation of efferent ductules with ICI resulted in two-fold increase in tubular diameter, indicating affected fluid reabsorption capacity. Furthermore, sperm from ICI-treated monkeys were immotile.
Taken together, our results point to an integral role for estrogen in modulating the functions of the bonnet monkey epididymis. This study also demonstrates possible differences in the epididymal physiology of rodents and non-human primates, and thus underscores the significance of reports such as these, that examine the physiology of non-human primates (as opposed to rodents), in an attempt to understand similar events in the human.
Mammalian testicular spermatozoa are incapable of fertilizing ova. The metamorphosis of immature spermatozoa into mature, functional units capable of progressive motility and fertility, is thought to be the result of a highly regulated and complex series of events that occurs during their transit through the efferent ductules and the epididymis. The epididymis consists of tubules which form a conduit for spermatozoa traversing from the efferent ductules to the vas deferens. It is anatomically divided into three parts- the caput (the head), a narrow central portion- the corpus (the body) and the cauda (the tail). The epithelium lining of these tubules secretes ions and proteins, reabsorbs testicular fluid and creates a specialized luminal environment for the maturation of testicular spermatozoa . These important functions of the efferent ductules and the epididymis are regulated by a complex interplay of growth factors and hormones.
Recent studies point to the involvement of the steroid hormone estrogen, in the regulation of fluid reabsorption in the efferent ductules [2, 3]. The action of estrogen is classically mediated via estrogen receptors α and -β (ERα and ERβ), which are present in the male reproductive tract of several species . ERα and ERβ knockouts (αERKO and βERKO) in mice have provided valuable insights into the role of estrogen in male reproductive physiology. The male αERKO mice were infertile [5, 6] with gross morphological changes, disrupted spermatogenesis, and dilated efferent ductules due to increased fluid accumulation . In contrast, the male βERKO mice were fertile and had a reproductive tract that appeared normal , whereas the male double (α and β) knockout mice were infertile, and their reproductive tract had a αERKO-like morphology. Collectively, these observations suggested that, at least in rodents, functional ERα was necessary to maintain fertility and normal morphology of the efferent ductules. In support of this view, recent studies in mice have shown that estrogen might regulate the expression of key molecules involved in ion transport, resulting in modulation of fluid reabsorption in the efferent ductules .
The role of estrogen in the epididymis is, however, less clear. While a high level of ERα expression has been found in the efferent ductules of humans and non-human primates, the expression of ERα in the epididymis of the same species has been sporadic . The expression of ERβ, however, has been detected throughout the male reproductive tract . Now, it is well established that sperm maturation is not intrinsic to sperm cells themselves, but instead requires the interaction of spermatozoa with proteins that are synthesized and secreted by the epididymal epithelium in a highly regionalized manner. Given the potential importance of estrogen during development of the male reproductive system, and the growing possibility that the regional expression of each gene in the epididymis may actually reflect functional differences, the significance of analyzing region-restricted expression patterns of estrogen receptors is obvious. Such a detailed analysis of ERα and ERβ expression pattern, all along the epididymis, will provide valuable information in the quest to determine region-specific functions necessary for sperm maturation. Also, comparative elucidation of the ERα and ERβ expression profiles in the different epididymal segments is a crucial step toward uncovering the regulatory and functional differences (if any) between them.
Studies, in rodents have suggested a possible role for estrogen in modulating epididymal function . Now, although the general organization and functions of the non-human primate epididymis are similar to that of other mammals such as rodents , there are obvious limitations in extrapolating results from these models to the primate epididymis. A few studies performed using macaque and baboon tissues have suggested the presence of specific receptors for estrogen in the primate epididymis [12, 13]. However, detailed functional studies of primate epididymal expression patterns coupled with mechanistic correlations at the molecular level, have been sparse. Hence, with a view to better understand the role of estrogen in the epididymis of the non-human primate, we initiated studies using the bonnet monkey (Macaca radiata) as a model system. Because of its close similarity to the human system, this study using bonnet monkey epididymis, permits meaningful extrapolation to humans. This is all the more important, considering the fact that it is extremely difficult to obtain human epididymal samples (at a reproductively suitable age) for research purpose.
We analyzed the distribution of ERα and ERβ, in all three regions of the bonnet monkey epididymis, using Reverse-Transcription-Polymerase-Chain-Reaction (RT-PCR), Western blot analyses and immunohistochemistry. We next studied the effect of estrogen blockade on the expression pattern of key proteins known to be involved in fluid reabsorption. Estrogen action was blocked using the well-established estrogen receptor antagonist, ICI 182780 (ICI), which can bind both ERα and ERβ. It is important to note that this compound does not cross the blood-brain barrier [14, 15] and hence, the levels of gonadotropins and testosterone remain unchanged during this treatment . This allows us to examine authentic estrogen effects. Bonnet monkeys were implanted with mini-osmotic pumps containing ICI for varied durations, the longest being for a period of 180 days, which is greater than the duration of three rounds of spermatogenesis in the monkey [17, 18]. The effect of the treatment was studied at the molecular level by analyzing the expression of ERα, Aquaporin-1 (AQP-1) and Na+-K+ ATPase-α1, genes that are known to play a key role in modulating fluid reabsorption. It is important to note that among the different regions of the epididymis, the caput is most active in protein synthesis and secretion . Many of the reproductive and somatic genes studied, are either exclusively expressed or exhibit the highest level of expression in this region. Moreover, the caput region of the epididymis has been demonstrated to be extremely sensitive to estrogen action [20, 21]. Considering the above facts, our studies were restricted to analysis of the caput region.
Interestingly, in addition to the impaired fluid reabsorption observed in αERKO mice, Eddy et al, noticed that majority of the epididymal sperms collected, showed decreased motility and that even the small fraction of sperms with normal motility were unable to fertilize wild-type oocytes , indicating, for the first time, that estrogen was probably essential for sperm function per se, in rodents. Our own earlier studies  in which Tamoxifen (another Estrogen Receptor antagonist) was chronically administered via Alzet pumps to adult male bonnet monkeys, revealed that these monkeys were infertile and had a very high percentage of abnormal sperms, which exhibited poor motility, although there was no adverse effect on serum testosterone levels. These results suggested the possibility that estrogen may have a role in sperm maturation in non-human primates also.
In an attempt to evaluate the role of estrogen in the regulation of sperm maturation during their transit down the epididymis, we monitored sperm count in all the ICI-treated bonnet monkeys, upto 180 days. Also, in the 180-day ICI treated monkeys, motility of the sperms was analyzed. In this connection, it is pertinent to note that sperm motility is often used as a crucial parameter to assess sperm maturation .
Materials and Methods
Animals and treatment
Adult male bonnet monkeys (Macaca radiata; weighing 6–8 kg) of proven fertility, that exhibited a clear nocturnal surge of serum testosterone, were recruited into the study. The significance of nocturnal surge of serum testosterone as an index of male reproductive function has been described earlier [24, 25]. All animals chosen for the study, exhibited sperm counts in the range of 150–500 million/ejaculate. The maintenance of animals has been described previously . All procedures involving use of animals were approved by the Ethics Committee of Indian Institute of Science (Protocol No. 21).
Animals (3 per group) were administered estrogen receptor antagonist ICI 182780 (a pure anti-estrogen; a kind gift from Dr. A. E. Wakeling, Zeneca Pharmaceuticals, U.K.) in propylene glycol (250 μg ICI/day/animal) via Alzet pumps (model 2ML4; Alza Corporation, Palo Alto, CA), which were changed every 28 days. As a control, one set of animals was vehicle (propylene glycol)-treated. At the end of the treatment period (i.e. 30 or 60 days), the animals were subjected to unilateral castration under aseptic conditions, using standard surgical procedures. The epididymal tissue was dissected free of fat, separated into caput, corpus and cauda regions, washed extensively in PBS (pH 7.4) to remove sperms, and processed for immunohistochemistry and RT-PCR analyses. The separation of distinct epididymal regions was performed as follows: regions of one cm from the anterior and posterior ends were dissected out as caput and cauda respectively. One cm region at the center of the epididymis, approximately equidistant from the caput and cauda was delineated as corpus. The tissues were stored in Bouin's fluid for immunohistochemistry or flash frozen in liquid nitrogen and stored at -70°C until required for subsequent RNA extraction. Analysis of sperm motility was carried out with ejaculates of 180-day ICI treated bonnet monkeys.
Radioimmunoassay methods were based on the procedure standardized in the laboratory . The antiserum to testosterone was raised in rabbits against testosterone 3-carboxy methyloxime BSA conjugate and the cross reactivities with other related steroids were found to be negligible. The intra and inter assay variation was 4.8% and 7.6% respectively. Values reported are uncorrected for recovery.
Semi-quantitative RT-PCR analysis
Total RNA from epididymal tissue was isolated using TRI reagent (Sigma Chemicals Co., St. Louis, MO) according to manufacturer's instructions. The integrity of the isolated RNA was checked on 1% MOPS-HCHO agarose gel and the quantity of RNA estimated spectrophotometrically. Reverse transcription was carried out as described earlier [27, 28] with appropriate controls.
List of primers and conditions employed for PCR
Annealing Temp (°C)
Product size (base pairs)
FP 5' gag aca tga gag ctg cca ac 3'
RP 5' cca aga gca agt tag gag ca 3'
FP 5' cag cat ctt ccg tgc cct cat gta 3'
RP 5' cat act cct cca cct ggc cgc tgg 3'
FP 5' aaa ctt agc ctt gat gag ctt 3'
RP 5' tcc atg atc ttt gaa ctt tta 3'
FP 5' gga gtc aac gga ttt ggt 3'
RP 5' gtg atg gga ttt cca ttg at 3'
The authenticity of all the RTPCR products described in this study was confirmed by sequencing, following their purification from low-melting agarose gels using the commercially available GFX™ PCR DNA/Gel Band Purification kit (Amersham Pharmacia Biotech., UK). Sequencing was performed at the DNA sequencing facility, IISc, using the ABI Prism 377 automated DNA sequencer.
Preparation of protein lysates
Tissue samples were washed extensively with PBS (pH 7.4) and homogenized in the presence of ice-cold lysis buffer (50 mM Tris pH 8.0,150 mM Sodium Chloride, 0.1% SDS, 0.02% Sodium Azide, 1% Nonidet-P40 and 0.5% Sodium Deoxycholate) containing 100 μg/ml PMSF and 1 μg/ml Aprotinin. Protein lysates were clarified by centrifugation at 15000 × g for 20 minutes at 4°C, and the protein content was determined by the Bradford's assay . Aliquots of protein lysate were stored at -70°C until analyzed. All the chemicals used for lysis were purchased from Sigma Chemical Co., St. Louis, Mo.
Western Blot analyses
Equal quantities of protein (100 μg) were electrophoresed on 10% SDS-polyacrylamide gels and transferred onto nitrocellulose (Sartorius AG, Germany) membranes, using a semi-dry transfer apparatus. Western blot analysis was performed as described earlier . Following hybridization, the blot was stripped and re-probed (using the protocol recommended by the manufacturers, Amersham Pharmacia Biotech, UK) for actin which served as the internal control for assessing equality of protein-loading. ERα antibody was used at a dilution of 1:200. ERβ and actin primary antibodies were used at a dilution of 1:400. All antibodies were purchased from Santa Cruz Biotechnology Inc., CA. Each figure is representative of at least 3 independent experiments.
Monkey epididymal tissue was fixed in Bouin's fluid, dehydrated, embedded in paraffin using standard procedures  and sectioned at 8 μm thickness. Following deparaffinization and rehydration, the sections were pre-treated with methanol-hydrogen peroxide to quench endogenous peroxidase activity, followed by a microwave treatment in 0.01 M (pH 6.0) citrate buffer . The sections were stained according to the double PAP (peroxidase-anti-peroxidase) technique  with diaminobenzidine (Sigma Chemicals Co., St. Louis, MO, USA) as the chromogen. The sections were then counter-stained with toluidine blue, dehydrated with graded concentrations of ethanol and xylene and analyzed by microscopy. Goat anti-rabbit IgG serum and rabbit anti-goat IgG serum, adsorbed against human proteins was obtained from Antibodies Inc., Davis, CA. The rabbit and goat peroxidase-anti-peroxidase complexes were obtained from Jackson ImmunoResearch laboratories, West Grove PA and diaminobenzidine was obtained from Aldrich, Inc., Milwaukee, WI. Anti-ERα and -ERβ antibodies, purchased from SantaCruz Biotechnology Inc., CA, were used at an optimum dilution of 1:200.
As a positive control for ERα immuno-peroxidase staining, we used mouse uterus tissue . As a positive control for ERβ staining we used rat ventral prostate tissue . Pre-incubation of the ERα antibody with the corresponding blocking peptide (SantaCruz Biotechnology Inc., CA) prior to staining, served as an appropriate negative control. As a negative control for absence of ERβ staining, we used rat liver tissue . Omission of the primary antibody from the experiment served as another negative control.
Analyzing the effect of ICI on tubular diameter of efferent ductules
Following castration of untreated monkeys, the efferent ductules were identified and separated out by micro-dissection, minced and placed in the medium of the composition given below, for 24 hours. Both the ends were ligated with sterile 4-0 cat gut (Johnson, India), to prevent the in-flow of medium. The ligated efferent ductules were incubated in M-199 medium (Sigma Chemical Co., St. Louis, MO) containing Bovine Serum Albumin (500 μg/ml; Sigma Chemical Co., St. Louis, MO), 17β-estradiol (1 nM; Steraloids Inc., Wilton, NH, USA) and dihydrotestosterone (1 nM; Steraloids Inc., Wilton, NH, USA), at 34°C, in humidified 95% air/5% CO2, for 24 hours, with (test) or without (control) ICI (1 μM). At the end of the total incubation period, the samples were rapidly fixed in Bouin's and subsequently embedded in paraffin using standard procedures . 5 μm sections were cut, stained in hematoxylin and eosin, and analyzed by light microscopy. The diameters of both control and ICI-treated efferent tubules were measured at the minimum point and tabulated.
Sperm count and motility analysis
The details of electroejaculation and sperm analysis have been described earlier . Semen from the monkeys was collected by electroejaculation by the penile method . Ejaculates were kept at 37°C throughout the period of examination, which did not exceed a total of 90 minutes. Sperm count was determined using Neubauer hemacytometer following 1:200 dilution of the semen in saline. The number of live spermatozoa was determined using eosin-nigrosin stain. Motility of the semen was analyzed using a computer-assisted semen analysis system (CASA, Hamilton-Thorne Research, MA). Semen sample was diluted 20 times with Tris buffer pH 7.4 and employed for analysis. One drop of the diluted semen sample was added to the Makler chamber (10 μM) and inserted into the feeding chamber of CASA. The sperm from each monkey were analyzed for the following motion parameters: percentage of motile sperm, percentage of progressively motile sperm, average path velocity, curvilinear velocity, lateral head displacement, straightness ([straight line velocity/average path velocity] × 100) and linearity ([straight line velocity/curvilinear velocity] × 100). The analysis was carried out with the following instrument settings: 30 frames at a rate of 60 Hz; minimum cell size, 5 pixels; minimum contrast, 80. All these procedures were performed at 37°C.
Statistical analysis of data (where applicable)
Data are represented as mean ± S.E. of at least three independent experiments performed with the same treatment protocol. For comparison among groups involving two columns significance was evaluated using the unpaired two-tailed t-test. For comparison of data involving three columns, statistical significance was obtained using the Kruskal-Wallis ANOVA followed by Neuman-Keuls test. In both instances a P value less than or equal to 0.05 was considered to be statistically significant.
1. RT-PCR analysis for ERα, AQP-1 and Na+-K+ ATPase-α1 in the three regions of the epididymis
Western blot analyses for ERα and ERβ in the three regions of the bonnet monkey epididymis
We observed specific signals for ERα (65 kDa) and ERβ (a prominent band of 56 kDa) in the caput, corpus and cauda regions (Fig 1b). Comparative analysis revealed no significant difference in the intensity of expression of the two receptor subtypes (at the protein level) in the three regions of the monkey epididymis.
2. Immunolocalization of ERα and ERβ in the three regions of the bonnet monkey epididymis
The three regions of the epididymis stained intensely for ERβ (Fig 2b). Intense staining was observed in the peri-tubular and vascular smooth muscle nuclei. Staining was also observed in the tubular epithelial cell nuclei of caput, corpus and cauda regions. The cytoplasm in these cells was also weakly stained. This staining is in sharp contrast to the ERα staining which was mostly restricted to the tubular epithelial cell nuclei. As a positive control for ERβ staining, we used rat ventral prostate tissue, in which intense nuclear staining could be observed. We did not observe any staining with rat liver tissue, which was used as negative control.
3. Effect of ICI treatment on the bonnet monkey serum testosterone levels
4. Expression profile of ERα, AQP-1 and Na+-K+ ATPase-α1 in the caput region of 30-day and 60-day ICI treated monkey: RT-PCR analysis
5. ERα expression in the caput region of vehicle and ICI-treated bonnet monkey epididymis: Immunohistochemistry
6. Effect of ICI on the fluid reabsorption capacity of efferent ductules
7. Effect of ICI on sperm count and motility
Effect of ICI on sperm motility parameters: CASA (compiled in Table 2)
Effect of ICI on sperm motility parameters by Computer-Assisted Semen Analysis (CASA)
Path velocity (μm/s)
Progressive velocity (μm/s)
Track speed (μm/s)
Lateral amplitude (μm)
Beat frequency (Hz)
For this experiment, since only a small group of monkeys could be analyzed, the data could not be statistically evaluated. Nevertheless, it is pertinent to note that in both the 180-day ICI-treated monkeys tested, a drastic reduction in progressive motility was observed. A decrease in the beat frequency and lateral amplitude of the sperms was also observed in the same animals.
To our knowledge, this is the first study demonstrating the presence of both the estrogen receptors, ERα and -β, in the three regions of the bonnet monkey epididymis. In contrast to previous studies [9, 37], which were unable to detect ERα in the marmoset monkey epididymis, our results show the unequivocal expression of ERα at both the mRNA and protein level in all three regions of the bonnet monkey epididymis. Localization of ERα protein was prominent in the nuclei of the tubular epithelial cells lining the lumen while ERβ was expressed abundantly both in the epithelium and the stroma. The physiological significance of this differential staining pattern of the two receptor subtypes in Macaca radiata epididymis is at present, unclear. The presence of ERβ in the stromal cells, in addition to the epithelium, is interesting as stromal-epithelial cell interactions have been shown to modulate the response to estrogen . Although there is considerable regional overlap in the expression of both ER-α and -β, further specific studies are needed to assess the relative abundance and co-expression of the two receptors. Nevertheless, the presence of both the receptors indicates a plausible role for estrogen in the physiology of the bonnet monkey epididymis.
ER antagonists provide a good tool to study the effect of lack of estrogen action on the target tissue. ICI 182780, an ER antagonist, when administered to mice for 35 days produced an α ERKO-effect . In the current study, the effect of ICI treatment on the caput region of the bonnet monkey epididymis was examined. ERα mRNA expression was increased in the caput region of both 30- and 60-day ICI-treated monkeys. An appreciable increase in ERα protein expression was also noted in the caput of 60-day ICI-treated group. At this juncture, it is important to note that, most studies in rodents have actually reported a decrease in the receptor level with ICI treatment [40–42], with the exception of the endometrium where no change in the receptor level was seen with ICI treatment. Interestingly, results from our lab also showed decreased ERα expression in the caput of ICI-treated rodents (unpublished data). It is therefore possible that the increased expression of the receptor in the ICI-treated caput of the bonnet monkey could be a species-specific effect. This difference underscores the significance of studies such as these, that examine the physiology of non-human primates (as opposed to rodents), in an attempt to understand similar events in the human.
Impaired sperm production in male αERKO mice has been suggested to be due to disruption of estrogen action within the somatic cells of the testis and the excurrent duct system wherein fluid absorption fails to occur. Fluid transport is predominantly facilitated by a family of water channel proteins called aquaporins. This movement of water across the cell membrane is dependent on the concentration gradient, which is maintained by ion exchangers like the Na+-K+-ATPase pump, Na+-H+ exchangers, chloride channels, etc. Studies in rodent efferent ductules suggested that estrogen may be involved in the regulation of aquaporin-1 (AQP-1) and Na+-K+ ATPase-α1 expression [39, 44], although the precise mechanism is still unclear.
Our experiments in the bonnet monkey revealed robust expression of AQP-1 and Na+-K+-ATPase-α1 in all the three regions of the epididymis. This is in accordance with previous studies in rodent efferent ductules that also showed high expression of AQP-1 and Na+-K+-ATPase-α1, two proteins important for maintenance of fluid and ion balance . The effect of ICI treatment on the expression of these proteins was similar for both the 30-day and 60-day treatments. A significant decrease was observed in AQP-1 mRNA levels with ICI treatment, while Na+-K+-ATPase-α1 levels did not vary appreciably. These results are consistent with earlier findings, which showed that AQP-1 expression was modulated by estrogen in the efferent ductules of both rodents and monkeys [44, 45]. In view of all these observations, it is surprising that there was apparently no adverse effect on the efferent ductules in AQP1-knockout mice . As suggested, this could be attributed to the existence of compensatory mechanisms like paracellular movement of water or involvement of other isoforms of AQP.
Additionally, our results showed that incubation of efferent ductules with ICI in vitro, led to an increase in lumen diameter indicating absence of involvement of testicular factors in regulating fluid absorption. Although the increase in ERα expression upon ICI treatment was in sharp contrast to the observations made earlier, the downstream effects of ICI treatment, i.e., decease in AQP-1 expression and increase in lumen diameter, were similar to those observed in the rodent model. Taken together, these results indicate that fluid absorption in the bonnet monkey excurrent ducts is affected by ICI treatment, suggesting a role for estrogen in this process.
As a final read-out of ICI-treatment, we analyzed critical sperm-maturation parameters in the ICI-treated monkeys. Studies have shown that administration of aromatase-inhibitors reduced the transit time of spermatozoa and that such spermatozoa were not capable of fertilization [46, 47]. Sperm from the αERKO mouse also showed decreased motility . In our study too, we observed that sperm from the 180-day ICI-treated monkeys, revealed a precipitous drop in motility. The treatment affected the beat-frequency and progressive motility of sperms, which is indicative of a loss in their fertilization potential. Interestingly, these treatment-induced effects occurred in the absence of any obvious alteration in sperm morphology or sperm production, as sperm count in the treated monkeys was normal. This indicated that the treatment was probably affecting the maturation process and not so much the production process. It is known that sperm proteins and the membrane undergo several modifications during maturation in the epididymis. It is therefore reasonable to predict that some of the processes involved in maturation may be altered, leading to decreased sperm motility. These effects were observed in the absence of any detectable change in testosterone levels, and hence it is reasonable to conclude that the observed defects in motility could be due to blockade of estrogen action. In support of this view, a recent report suggested that aromatase expression in human spermatozoa was important for sperm motility . Understanding the role of ER-α and -β in fluid reabsorption and sperm motility, is thus of high physiological relevance for normal fertility. Further studies are required to assess if the observed reduction in sperm motility also results in decreased fertility. Future studies are aimed at identifying candidate sperm maturation factors that are subject to estrogen regulation in the bonnet monkey epididymis.
In conclusion, this study, for the first time, provides evidence for the presence of estrogen receptors in the bonnet monkey epididymis. The results obtained so far clearly establish that the bonnet monkey epididymis is also a target for estrogen action and that several genes reported to be involved in the regulation of fluid absorption in the rodents, are also regulated by estrogen in the monkey epididymis. We show that ICI-treatment alters epididymal and sperm-maturation functions. This study also demonstrates possible differences in the epididymal physiology of rodents and non-human primates, and thus underscores the significance of reports such as these, that examine the physiology of non-human primates (as opposed to rodents), in an attempt to understand similar events in the human.
List of abbreviations used
- ER :
- ERα :
- ERβ :
- αERKO :
α-Estrogen Receptor Knockout mouse
- βERKO :
β-Estrogen Receptor Knockout mouse
- Na + -K + ATPase-α1 :
- AQP-1 :
- RTPCR :
- GAPDH :
- CASA :
Computer-Assisted Semen Analysis
The authors wish to thank Dr. Ramachandra, Mr. Ramesh, Mr. Krishnamoorthy, Dr. Anbalagan, and Dr. Ravi Kumar for their technical assistance, and Mrs. Shailaja and Chitralekha for help in preparation of this manuscript. The authors are grateful to Dr. M.P. Hardy, Population Council, New York, for his keen interest and advice at various stages of this project. Financial assistance from DBT (Indo-U.S. programme- 'Identification of estrogen-regulated epididymal factors involved in sperm maturation'), Mellon Foundation, CONRAD U.S.A., CSIR (Emeritus Scientist Fellowship to AJR), CSIR, DST, ICMR Government of India, is gratefully acknowledged.
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