Establishment of Rat Models Mimicking Gender-affirming Hormone Therapies

Summary

The protocol describes the development of two rodent models mimicking gender-affirming hormone therapies through subcutaneous administration of testosterone or estradiol plus cyproterone acetate (used in human therapies for transgender people): setting of the doses, identification of relevant biomarkers, and evaluation of the effects.

Abstract

Transgender (TG) people are individuals whose gender identity and sex assigned at birth do not match. They often undergo gender-affirming hormone therapy (GAHT), a medical intervention that allows the acquisition of secondary sex characteristics more aligned with their individual gender identity, providing consistent results in the improvement of numerous socio-psychological variables. However, GAHT targets different body systems, and some side effects are recorded, although not yet fully identified and characterized. Therefore, TG people undergoing GAHT may be considered as a susceptible sub-group of population and specific attention should be paid in the frame of risk assessment, e.g., through the use of targeted animal models. The present work describes the procedures set to implement two rat models mimicking GAHT: the demasculinizing-feminizing model (dMF) mimicking the GAHT for TG women and the defeminizing-masculinizing model (dFM) mimicking the GAHT for TG men. The models have been implemented through the administration of the same hormones used for human GAHT, namely, β-estradiol plus cyproterone acetate for dMF and testosterone for dFM, by the same routes of exposure for a 2 week period. Rats are checked daily during the treatment to evaluate health status and potentially aggressive behaviors. At sacrifice, blood and target tissues have been sampled and stored for biochemical, molecular, and histopathological analysis. Sex-specific parameters, namely, sperm count and clitoral dimensions, have also been evaluated. In addition, CYP450 isoforms, exclusively and/or preferentially expressed in male and female rat liver, are identified and characterized as novel biomarkers to verify the success of GAHT and to set the model. Thyroid involvement has also been explored as a key target in the endocrine system.

Introduction

The individual's psychological perception of being male, female, neither, both, or somewhere in between¹ is called gender identity. It can match the biological sex (cisgender) or can be different (transgender - TG). A TG man is an individual born as a female but who identifies himself as a man. A TG woman is born as a male but identifies herself as a woman². It is estimated that, at present, there are 25 million TG people worldwide³, most of them suffering from gender dysphoria, a psychological condition characterized by incongruence between their gender and the one they were assigned at birth⁴, which can result in social discrimination and difficulties at work and in family, often leading to depression, anxiety, and stress⁵. For such reasons, TG people often go through gender-affirming hormone therapy (GAHT) and/or gender-affirming surgery. GAHT for TG men is characterized by the administration of testosterone (T) (Table 1), and for TG women, estrogens (E2) plus antiandrogens (Table 2)⁶.

GAHT usually lasts for the entire life of the individual, acting continuously on the endocrine system^7,8. So, it is important to analyze the GAHT's impact on the health of TG people and its potential long-lasting effects. Moreover, TG people are exposed, as the general population, to chemical contaminants -- in particular, the endocrine disrupters (ED) -- that target the endocrine system as the GAHT, resulting in overstimulation⁹.

ED are a group of chemicals affecting the organisms and/or their progeny by altering different hormonal and metabolic processes, such as the secretion, activation, synthesis, release, and binding of natural hormones. Since ED are widespread in the environment, food and products of everyday use (e.g., plastic bottles and containers, liners of metal food cans, detergents, flame retardants, food, toys, cosmetics and pesticides, etc.) general population is continuously exposed during the whole life¹⁰. In addition, even low-dose exposure to EDs can lead to tissue and organ damage, and a common phenomenon associated with ED exposure is the occurrence of sex-specific effects both in laboratory animals and in humans¹¹. As an example, exposure to the food contact material, bisphenol A (BPA), is linked to health risks such as endometriosis and polycystic ovary syndrome in women, as well as reduced fertility, due to its estrogenic effects¹². In men, BPA can lower levels and diminish sperm quality¹³. Additionally, pesticides are associated with a higher risk of breast cancer in women and significant fertility issues in men¹³. So far, no specific tools are available to study the toxicological effects of environmental contaminants, including ED, in TG people⁹.

The present study aims to describe methods and parameters selected for the development of two TG animal models: a demasculinizing-feminizing model (dMF) and a defeminizing-masculinizing model (dFM). In particular, the selection of suitable dose levels, time, and way of administration of the hormones on the basis of the current human therapies are assessed¹⁴. Moreover, tissue and functional biomarkers that define the models uniquely are identified and characterized. In addition, the efficacy and tolerability of therapy in animals as well as the selection of the most appropriate markers for use in long-term studies, are described in detail together with the techniques used for such purposes.

In order to characterize the models, the following endpoints are analyzed: testosterone (T) serum level (the best biomarker to evaluate the success of GAHT in both models^9,15); estradiol (E2) serum level (both models); thyroid stimulating hormone (TSH) and thyroxine (T4) (dMF model); sperm count (dMF model); clitoral dimension (dFM model); histopathological analysis of reproductive organs, liver and thyroid (for both models). In addition, gene expression of the following sex-specific liver cytochrome P450 isoforms (CYP450s, for both models) are also analyzed^16,17: CYP2C11 (specifically expressed in the male liver), CYP3A18 (expressed 25 times more in male liver than in female), CYP2C12 (specifically expressed in the female liver), and CYP2C6 (predominantly expressed in female liver, but present at lower levels, also in the male).

Protocol

The studies are performed following Directive 2010/63/EU, the Italian Legislative Decree n. 26 of 4 March 2014, and the OECD Principles of Good Laboratory Practice (GLP). The study protocol was approved by the Italian Ministry of Health (authorization no. 806/2021-PR). Here, 16 young sexually mature Sprague-Dawley rats of both sexes (304 ± 13 g male rats and 190 ± 7 g female rats, 8-9 weeks old) are purchased and housed in two/cage under standard laboratory conditions (22 ± 0.5 °C, 50%-60% relative humidity, 12 h of dark-light alternation with 12-14 air changes per hour) with water and food available ad libitum. In all the cages, for each animal's environmental enrichment, insert wood gnawing blocks and replace them weekly.

NOTE: The animals aged 8-9 weeks have been chosen since GAHT can start during adolescence (Tanner stages 2 to 3), corresponding to 8-9 weeks in rodents, and it lasts for a long time, potentially for the whole life of TG people⁹.

1. Group sizing and animal care

1. Use young adult male and female Sprague-Dawley rats (8-9 weeks old) as a model since rat is the preferred species indicated by OECD (e.g., Guideline 421 Reproductive/Developmental Toxicity Screening Test) and the only rodent species proposed and considered in OECD Guideline 407 (28-day oral toxicity study at a repeated dose in rodents, updated with the parameters for the detection of EIs).
2. Use the G*Power software for the group sizing. For both the dFM and the dMF models, select four test groups: one control group (C) and three groups of animals treated with different doses of GAHT. Do the sizing with reference to the comparison between two groups (treatment dose versus C) with the Mann-Whitney test, a two-tailed significance level alpha = 0.0167 (corresponding to alpha = 0.05 with Bonferroni correction applied to the 3 comparisons between each treatment dose and the C), and 1-beta power = 0.80.
   1. The calculated number of rats/groups is as follows:
      for dFM model, animals/group n=4, according to Kinnear et al.¹⁸ indicating after 2 weeks of treatment, the following levels: in the control group: 0.2 ± 0.3 ng/mL, in the hormone therapy group: 16 ± 5 ng/mL (mean ± standard deviation), corresponding to an effect dimension measured with Cohen's d = 4.46 (very large effect).
      ​for dMF model: animals/group n=3, according to Gómez et al.¹⁹ indicating after 2 weeks of treatment, the following levels: control group: 1.901 ± 0.413 ng/mL and hormone therapy group: 0.043 ± 0.023 ng/mL (mean ± standard error) corresponding to an effect dimension measured with Cohen's d = 6.35 (very large effect).
   2. To align the two models, choose n=4 animals per sex/group, for a total of N = 32 animals.
3. After 1 week of acclimatization, divide rats by sex into two experimental groups (dMF and dFM, 4 rats/group), each composed of one C (control male, CM and control female, CF) and three treatment groups of the selected GAHT.
4. Monitor all rats 2x a day (at 8:30 a.m. and 4:00 p.m.) to check general health conditions and potential aggressiveness due to GAHT administration. Record body weight (bw) and feed consumption 2x a week, using an analytical balance with the dynamic weighting function optimal for laboratory animals' weight.
5. In the dFM experimental model, measure the clitoral diameter of all rats immediately before the start of treatment (point 0) and at the end of treatment (point 13), using a digital gauge for precision readings.
6. Weigh all animals before the sacrifice and, in the dMF model, immediately after sacrifice remove the epididymis in order to perform the sperm count.

2. Dose selection and preparation

1. Use the following three doses of hormones to be administered to dFM rats: 5, 10.5 and 22.5 mg/kg per week, for the dMF model, use the following three selected dose levels (DL): DL1 E2 0.045 mg/kg + CPA 0.2 mg/kg, DL2 E2 0.09 mg/kg + CPA 0.2 mg/kg and DL3 E2 0.18 mg/kg + CPA 0.2 mg/kg.
   NOTE: All the doses are selected taking into account the main human clinical guidelines used for TG people¹⁵ and the limited data available in the literature.
2. Prepare all the stock solutions weekly using a chemical safety hood. Properly mix all the substances into the sesame oil as a vehicle, ensuring their complete solubilization.
   NOTE: For both models, use a dose conversion calculator (https://dosecal.cftri.res.in/) to enter the dose to convert, the species for which the dose has been set, the animal species, and the weight for which to convert the dose. For the dFM model (Table 3), human hormone therapy, a maximum dose of 100 mg of T per week²⁰. The dose calculated in rats is 10.5 mg/kg of T per week. The second dose is 22.5 mg/kg per week in rats¹⁸. The third dose is 5 mg/kg per week, identified by maintaining the factor of 2.1 between the two calculated doses. For the dMF model see Table 4, the dosages are based on recommended regimens for humans²¹ and data available through in vivo studies^14,19,22.

3. Animal treatment

1. Perform subcutaneous administration of T (for the dFM model) and E2 plus CPA (for the dMF model) by pinching and lifting the skin at the injection site, forming a kind of curtain. Then, insert the needle of a 1 mL syringe parallel to the animal's back. Once inside, slowly inject the required volume (100 µL for T; 200 µL for E2+CPA)²³.
   1. Treat the animals as follows: for the dFM model, administer T enanthate dissolved in sesame oil (vehicle) 2x/week for 2 weeks (100 µL for each subcutaneous injection of T). For the dMF model, administer E2 plus CPA acetate dissolved in sesame oil (vehicle) 5x/week for 2 weeks (200 µL for each subcutaneous injection). Treat the rats of C group in the same way with the vehicle only (sesame oil).

4. Blood sampling, sacrifice, and tissue sampling

1. After 2 weeks of treatment, just before the sacrifice, use a gaseous anesthesia system and anesthetize all animals. Induce anesthesia by dose varying from 2% to 3.5% isoflurane in 100% oxygen at a rate of 1.5 L/min till loss of the reflexes in a clear, polystyrene induction chamber. Place the rat in the prone position on the heating pad and regulate the dose of isoflurane at a maintenance dose varying from 1.5% to 3.5% administered by a standard rat nose mask throughout the intracardiac blood sampling procedure.
2. Prepare a 5 mL syringe with a 21G needle, eliminating the vacuum. Probing the heart with the fingers, carefully insert the needle into the lateral thoracic wall perpendicular to the body at approximately the point of flexed elbows, between ribs 5 and 6. Once inside the heart ventricle, the blood enters the syringe by capillarity. Retract the syringe piston slowly and continuously until blood draws.
3. After the blood sampling, place the rats into the CO₂ chamber in order to perform euthanasia using CO₂ asphyxiation with a fill rate of 30%-70% displacement of the chamber volume per minute. After 2-3 min, verify the animals' death by monitoring breathing and heartbeat²⁴.
4. After the sacrifice, place every animal on the dissection table in a supine position, with the front legs facing upwards and the hind legs facing down, and fix them with pins. Sprinkle the animal's abdomen with a disinfectant solution.
5. Excise the following organs: testes, epididymis, uterus, ovaries, liver, and thyroid. Weigh and store them in 50 mL tubes with 35 mL of 10% buffered formalin (all organs) or Bouin's solution (testis only) or collect them in cryogenic tubes (an organ/tube) and immediately freeze them in liquid nitrogen (for storing at -80 °C).
   1. Firstly, cut the skin with scissors on the midline, from the pubis to the upper abdomen. Make two lateral cuts on the rib cage and reflect the skin on both sides of the incision to expose the thoracic viscera.
   2. Remove the reproductive organs first; in male rats, remove the testes, oval-shaped paired organs located in the abdominal cavity, in the intra-abdominal position (scrotal sac). Cut and press the scrotal sac to ensure that the testes are sticking out, then grasp them gently. Hold the visceral fat with pliers, then cut the testes away from the viscera. After the excision, weigh and store the testes in Bouin's solution for histopathological analysis.
   3. In female rats, first grab the uterus delicately, then cut the ovaries (which are located at the end of both the uterine horns) from the visceral adipose tissue. After the excision, weigh the ovaries.
   4. In both female and male rats, move on to the right side of the abdominal cavity, where the liver is located. The liver is a multilobulated organ and it is possible to identify many parts: left medial (smaller), left lateral (major), right medial (smaller), right lateral (major), caudate, and square lobe²⁵. Grab the liver with forceps, taking care not to break it. Grasp the xiphoid process with pliers and completely cut the diaphragm with scissors.
   5. Use forceps to lift the xiphoid process and extract the liver from the abdominal cavity. Separate the liver from the diaphragm with scissors. After that, weigh the liver and store.
   6. For thyroid extraction, with the help of scissors, cut perpendicularly along the neck of the animal, remove the skin and musculature, and gently trim the ends of the trachea, in which the thyroid gland is located. Store the thyroid for further analysis²⁶.
6. Perform sperm count as described below.
   1. After testis removal, grab the epididymis, which is attached to the posterior margin of the respective testis and contained in the scrotum.
   2. In this experiment, semen samples are taken from the tail of the right epididymis. At the time of collection, clean the tail of fat and connective tissue using scissors, separate it from the remaining part, and place it in a Petri dish (35 mm x 10 mm) containing 1 mL of DMEM. Cut with scissors and flow with a Pasteur pipette to facilitate the release of the content.
   3. Transfer all the liquid obtained into a 15 mL tube and bring the volume to 10 mL with DMEM (dilution factor 1:10=0.1). Pipette the content to homogenize and create a suspension. After a slight shaking, take 10 µL of the suspension to load the Neubauer chamber. Load the camera and after 3 min of camera loading, start the counting.

5. Enzyme-linked immunosorbent assay (ELISA) assay

1. Collect blood samples (about 2-5 mL per animal) in 2 mL tubes and allow them to coagulate at room temperature for 1 h. Spin all blood samples in a centrifuge 2x for 15 min at 4 °C and 3000 x g.
2. Centrifuged blood has a multi-layered appearance with three layers of different colors. The top layer consists of plasma (usually yellow or transparent), the liquid portion of blood; the layer below the plasma may have a whitish or gray coloration and is the Buffy coat. The lowest layer contains red blood cells, and the color may appear dark red or bright red. To determine sex hormone levels, collect the serum of all samples with a pipette (without touching the buffy coat or the erythrocyte layers), divide them into aliquots (500 µL) and store them at -80 °C.
3. In both models, perform ELISA test to detect and/or measure the presence of proteins, antibodies or antigens in the sample for the determination of sex hormones. Use the direct method and follow the instructions of each ELISA kit. In this study, serum levels of the following hormones were determined in rats: E2, Rat Estradiol ELISA; T, Mouse/Rat Testosterone Elisa; TSH, Rat ELISA Kit and T4, Rat ELISA Kit.

6. Histopathological analysis

1. Prepare histological slides of tissues according to the following procedures.
2. Fix the samples of the uterus, ovary, thyroid and liver at the time of extraction in 10% buffered formalin for at least 48 h.
   CAUTION: Work under a chemical hood. Do not inhale the substance/mixture. Avoid generating vapor/aerosols.
3. Wash samples under running water for 1 h and then store in 80% ethyl alcohol (C₂H₅OH) until processing, to preserve the protoplasmic structure from alterations resulting from cellular death.
4. Fix the testis in Bouin's solution consisting of 15 mL of saturated solution of picric acid, 5 mL of concentrated formalin (33%-40%), and 1 mL of glacial acetic acid for 48 h. Wash samples with 80% ethyl alcohol.
   CAUTION: Work under a chemical hood.
5. Perform inclusion in solid paraffin using an automatic tissue processor. At the end of the inclusion process, place the samples in small metal containers in which melted paraffin has been poured and cool on a frozen plate, forming the blocks for the cut. Orient them depending on the desired cutting section.
6. After that, cut the samples using a rotating microtome. Collect 5-6 µm sections using small brushes, spread them into water at 37 °C for a few seconds, and place them on microscope glass slides. Leave the slides to drain perpendicularly for a few minutes and dry them in the oven at 36 °C for at least 1 h.
7. Perform hematoxylin and eosin staining as described below.
   1. Deparaffinize the slides by dipping them in clearing agent of terpene origin (xylene substitute) for 5 min.
   2. Rehydrate the slides by dipping them through the following series of graded ethanol. For each solution, 2 min per dip: 100% ethanol, 95% ethanol, 80% ethanol, 50% ethanol, and distilled water.
      NOTE: The can be a stop point for the protocol, and the slides can be left at RT in water for several hours. Optionally, the slides can also be stored at 4 °C in water.
   3. Place the slides in Mayer's hematoxylin for 5 min. Immediately transfer them back to the container with tap water for 5 min. Run tap water into the back corner of the container farthest away from the sections. Periodically empty the container until the purple coloring in the water is no longer present.
      NOTE: To prevent sections from peeling off from the slides, do not run water directly onto the slides.
   4. Place the slides into the eosin Y 1% aqueous solution for 2 min. Transfer the slides to distilled water for 15 s. Dehydrate the slides by dipping them through the following series of graded ethanol. For each solution, 15 s per dip: 50% ethanol, 80% ethanol, 95% ethanol.
   5. Place the slides in 100% ethanol for 1 min and change it to fresh 100% ethanol for another 1 min. Place the slides in a clearing agent of terpene origin (xylene substitute) for 2 min and change it to a fresh clearing agent of terpene origin (xylene substitute) for another 2 min. Remove one slide at a time and place a coverslip.
   6. Cover the sections with mounting medium and place a coverslip on the bottom of the slide.
      NOTE: Ensure the mounting medium pulls the slide into position. If the coverslip is not flat, gently tap it into place. Blot any excess mounting medium using a paper towel.
   7. Dip a cleaning wipe into the clearing agent of terpene origin (xylene substitute) and wipe the back of the slide to remove any dripped medium. Place the slide flat on a mobile solid surface, like a piece of cardboard. Add coverslip to all the remaining slides as described in step 6.7.6. Allow the slides to dry and the mounting medium to harden at RT in the hood.
      CAUTION: Work under a chemical hood.
8. After the staining, cover the samples with a cover slip and evaluate them using an optical microscope. Histopathological changes have been described based on distribution, severity, and morphological characteristics.
9. Perform injury scoring semi-quantitatively, using a 5-point assessment scale (0 to 4), considering the severity of the changes based on criteria explained by Shackelford et al.²⁷ and summarized as follows:
   Grade 0: no change
   Grade 1: minimum change. The effect is barely visible on the tissue; small and infrequent. Affects a portion of tissue less than or equal to 10%.
   Grade 2: light change. Represents a small histological change. This grade is used when the tissue, or its structure, has shown a change in volume between 11% and 20%.
   Grade 3: moderate change. The change is evident in the tissue. The degree indicates the presence of variations between 21%-40% of the tissue or its structure
   ​Grade 4: marked change. Overwhelming histological change of tissue or its structure. Variations affect 41%-100% of the tissue.
10. Perform quantitative histomorphometrical analysis on uterus, ovary, testis and thyroid. Examine tissue sections using an image analysis system applied to an optical microscope and follow the steps described below.
    1. Uterus: Using a 2x objective measure the total area of each transverse section of the right uterine horn, the external and internal myometrium, and the uterine lumen. Calculate the area of the endometrium and myometrium and the ratio between the area of the endometrium and the myometrium²⁸.
    2. Ovary: Use one of the whole-section in the central position of the ovary to reveal follicles in various stages of development; count the primary, secondary, corpus luteum, Graaf, and atresic follicles using a 4x objective. Perform classification of follicles according to Fortune²⁹. In addition, measure the area of the ovary for each sample and its follicular density (number of follicles/ovary area x 100)³⁰.
    3. Testis: Using the 10x objective, measure 20 tubules/sample; in addition, measure total lumen area, total area, longitudinal diameter, and transverse diameter²⁸.
    4. Thyroid: Measure the following parameters: follicular density (ratio between the number of follicles and a given area, 10x objective); indirect follicular cell height (mean ratio of follicle area and colloid area in five randomly selected follicles/sample 40x objective); the mean ratio of follicular epithelium areas and the nuclei number (in the same follicle to ascertain follicular maturation); follicular cell height (mean of five cell height in five randomly selected follicles/sample, 64x objective)³¹.

7. Gene expression

1. For both models, perform the gene expression analysis using liver samples stored at -80 °C. Follow the protocol of total RNA purification using a kit, starting from a lysate of animal tissue.
   1. To obtain the liver lysate, grind the tissue sample (10 mg) with a minipinner, add 600 µL of RL BUFFER (provided with the kit) to the tissue sample, and continue to grind until the sample has been homogenized.
2. Immediately after the extraction, quantify the RNA obtained and evaluate its quality (for denaturation or the presence of any protein residues) using a fluorospectrometer. Perform spectrophotometric absorbance readings at wavelengths of 260 nm and 280 nm, where nucleic acids and proteins respectively absorb.
3. After the evaluation of the total RNA concentration, using a cDNA Synthesis Kit following the manufacturer's instructions, reverse transcribe the appropriate volume containing 1 µg of total RNA from each sample to cDNA.
4. Analyze the obtained cDNA by RT-PCR.
   1. To analyze gene expressions of genes of interest, specific forward and reverse primers have been designed for each target gene, as well as for the reference gene constitutively expressed glyceraldehyde phosphate dehydrogenase (GAPDH). Use the web application Primer-BLAST (www.ncbi.nlm.nih.gov/tools/primer-blast) to choose the best primers that would guarantee the specificity of the pairing only to the gene of interest and obtain the oligonucleotides synthesized by a commercial supplier. The sequences of the used primer pairs are reported in Table 5.
   2. Resuspend the lyophilized primers with RNAse-free distilled water at a final concentration of 100 mM. Use a dedicated kit to perform qPCR analysis. Carry out the reactions in a final volume of 20 µL, diluting the annealed cDNA 1:40. Load each sample in duplicate in 96-well PCR plates.
   3. Perform qPCR runs on thermal cycler following this program: 1 cycle at 95 °C for 10 min; 40 cycles at 95°C for 15 s, 58 °C for 30 s, and 72 °C for 1min. At the end, perform a dissociation cycle from 55° C to 95° C (30 s/°C) to verify the specificity of the amplified product. Using the machine's dedicated software, obtain threshold cycle values (Cycle Threshold, Ct) for each sample. Express the results as ΔΔ Ct (delta delta Ct) according to the Pfaffl formula³²:
      ΔCt Target gene = Ct Control - Ct Treated
      ΔCt Reference gene = Ct Control - Ct Treated
      ΔCt = ΔCt Target gene - ΔCt Reference gene

8. Data analysis

1. Perform data management using a spreadsheet. Perform analysis using statistical analysis software. Design graphics using specific software.
2. Represent bw gain, feed consumption, absolute and relative organ weight, hormone serum levels, tissue morphometrical data, and gene expression data as mean ± standard deviation. Perform a non-parametric Kruskal-Wallis analysis, followed by post-hoc pairwise comparisons (Mann-Whitney test).
3. Analyze histological data using a 2-way Fisher Exact Test to identify significant differences from the Control group, including samples that are assigned to a category without any reference to severity gradations (total finding incidence). Use the Cochran-Armitage Trend Test to identify the dose-response trend. Consider differences among groups as significant if the p-value is < 0.05.

Results

As demonstrated by Tassinari et al.¹⁴ and by Tammaro et al.³³, the following results showed the success of GAHT on rats and the appropriateness of the models.

No mortality or abnormal behavior, such as aggressiveness, are recorded, and no clinical signs of toxicity or suffering (e.g., decreased activity, piloerection, and an ungroomed appearance) are observed¹⁴.

Plasma T concentrations in a...

Discussion

The implementation of rodent models mimicking GAHT is crucial to studying the potential specific susceptibility and vulnerability of TG people and the long-term outcomes of the therapies, usually lasting all their lives.

Given the scarce number of similar studies in the literature, the critical point of this experiment is the selection of the doses to set the models; such doses should be sufficiently low to be compatible with long-term administration in animals without causing adverse effects,...

Materials

Name	Company	Catalog Number	Comments
Analytical balance ABJ 320-4NM	Kern	Z741091
Bouin	Biooptica	05-M01008
Centrifuge 5415 R	Eppendorf		For eppendorf
Cyproterone Acetate	Sigma-Aldrich	C3412
D-MEM medium	Gibco
ExcelTaq 2X Fast Q-PCR Master Mix (SYBR, ROX), 200 RXN	Smobio	TQ1210
Formalin solution, neutral buffered, 10%	Sigma-Aldrich	HT501128
GraphPad Prism software version 5.0  for Windows	GraphPad Software
Hematoxylin	Biooptica	05-06002/L
Heosin	Biooptica	05-10007/L
Imaging Software	Nikon		NIS-BR
JMP 10 statistical software	SAS Institute
Microm	Thermo Scientific	HM 325
Microscopy	Nikon Microphot FX
Mouse/Rat Testosterone ELISA	Biovendor	RTC001R	96T
NanoDrop 1000 Spectrophotometer	Thermo Scientific		ND-1000
Paraffina	Biooptica	087910
Portable Balances SCOUT STX2202	OHAUS	30253064
Primers	Life Technologies		Designed by PrimerBlast
Rat Estradiol ELISA	Biovendor	RTC009R	96T
Rat TSH(Thyroid Stimulating Hormone) ELISA Kit	ELK Biotechnology	ELK2283	96T
Rat TSH(Thyroid Stimulating Hormone) ELISA Kit	ELK Biotechnology	ELK2283	96T
SensiFASTcDNA Synthesis Kit	Bioline	BIO-65053	50 reaction
Sesam Oil	ACROS	AC241000010
Sprague Dawley rats male and female	Envigo		8/9 weeks old
Standard diets	Mucedola	4RF18
T4(Thyroxine) ELISA Kit	ELK Biotechnology	ELK8716	96T
Testosterone enanthate	Sigma-Aldrich	T3006
Thermal Cycler LineGene 9600 Plus Bioer	Aurogene
Tissue processor	Shandon Excelsior ES, Thermo Scientific)
Total RNA purification KIT	Norgen	17200	50 column
Victor 3 Multilabel reader	Perkin Elmer
β-Estradiol 17-valerate	Sigma-Aldrich	E1631