We thank the University of Texas Southwestern Medical Center Animal Resource Center for their help in surgical training and protocol review. We thank the Wert Lab support team for their invaluable assistance. This work has been supported by funds from the National Institute of Health (NIH P30EY030413). Biorender.com was used for the creation of cartoon schematics.

All animal experiments were approved by the Institutional Animal Care and Use Committee at UTSW (APN#2019-102840).
1. Murine orchiectomy
<ol>
	<li>Prepare an aseptic working field and ensure that necessary surgical instruments have been sterilized and are readily available. Follow aseptic practices for rodent survival surgery.</li>
	<li>Record the weight of the male mouse and administer the preferred method of anesthesia according to the institutional guidelines. In this pro...

<ol>
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O., Theodorsson, A., Ingberg, E., Isaksson, I. M., Theodorsson, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ovariectomy+and+17&#946;-estradiol+replacement+in+rats+and+mice:+a+visual+demonstration.">Ovariectomy and 17&#946;-estradiol replacement in rats and mice: a visual demonstration.</a> Journal of Visualized Experiments. (64), e4013 (2012).</li><li>Valkenburg, K. C., Amend, S. R., Pienta, K. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Murine+prostate+micro-dissection+and+surgical+castration.">Murine prostate micro-dissection and surgical castration.</a> Journal of Visualized Experiments. (111), e53984 (2016).</li><li>Pritchett-Corning, K. R., Luo, Y., Mulder, G. B., White, W. 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D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Evaluation+of+early+bilateral+ovariectomy+in+mice+as+a+model+of+left+heart+disease.">Evaluation of early bilateral ovariectomy in mice as a model of left heart disease.</a> American Journal of Physiology Heart-Circulartory Physiology. 322 (6), H1080-H1085 (2022).</li><li>Lu, H., Ma, K., Jin, L., Zhu, H., Cao, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=17&#946;-estradiol+rescues+damages+following+traumatic+brain+injury+from+molecule+to+behavior+in+mice.">17&#946;-estradiol rescues damages following traumatic brain injury from molecule to behavior in mice.</a> Journal of Cell Physiology. 233 (2), 1712-1722 (2018).</li><li>Meydan, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effects+of+testosterone+on+orchiectomy-induced+oxidative+damage+in+the+rat+hippocampus.">Effects of testosterone on orchiectomy-induced oxidative damage in the rat hippocampus.</a> Journal of Chemical Neuroanatomy. 40 (4), 281-285 (2010).</li><li>Ohlson, N., Bergh, A., Persson, M. L., Wikstr&#246;m, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Castration+rapidly+decreases+local+insulin-like+growth+factor-1+levels+and+inhibits+its+effects+in+the+ventral+prostate+in+mice.">Castration rapidly decreases local insulin-like growth factor-1 levels and inhibits its effects in the ventral prostate in mice.</a> Prostate. 66 (16), 1687-1697 (2006).</li><li>Tehranipour, M., Moghimi, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neuroprotective+effects+of+testosterone+on+regenerating+spinal+cord+motoneurons+in+rats.">Neuroprotective effects of testosterone on regenerating spinal cord motoneurons in rats.</a> Journal of Motor Behavior. 42 (3), 151-155 (2010).</li><li>Yamada, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+impact+of+ovariectomy+on+olfactory+neuron+regeneration+in+mice.">The impact of ovariectomy on olfactory neuron regeneration in mice.</a> Chemical Senses. 45 (3), 203-209 (2020).</li><li>Koebele, S. V., Bimonte-Nelson, H. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Modeling+menopause:+The+utility+of+rodents+in+translational+behavioral+endocrinology+research.">Modeling menopause: The utility of rodents in translational behavioral endocrinology research.</a> Maturitas. 87, 5-17 (2016).</li></ol>

No conflicts of interest.

Surgical removal of testes and ovaries allows for studying murine physiology under controlled hormone deprivation. This technique is important for many fields of science, including neurodegeneration, mineral metabolism, cardiovascular, and reproductive health15,16,17,18,19,20,21. Here, we de...

The testes and ovaries are the primary organs responsible for&#160;sex hormone production. The cascade of hormonal communication leading to the production of testosterone and estrogen is a well-characterized process that begins in the hypothalamus with the release of gonadotropin-releasing hormone (GnRH)1. The release of GnRH causes the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the pituitary gland. As these hormones enter the bloodstream, they then affect other tissues in the body. The primary target of LH is the testes (in males) and the ovaries (in females)2. In response to LH, the testes produce and release testosterone3. Similarly, the ovaries produce estrogen4. While the intended effects of these hormones are to prepare the cells and body for fertilization and ensure a functioning reproductive system, many other bodily systems can be affected.
Sex hormones have been linked to several physiological functions. For instance, estrogen helps maintain bone homeostasis by preventing the resorption of bone by osteoclasts. For this reason, ovariectomized mouse models can be used to study the physiology of bone diseases such as osteoporosis5,6,7. Testosterone and estrogen are also research targets for many cardiovascular and neurodegenerative diseases. Recently, elevated testosterone production coupled with high-fat diet has been linked to vascular oxidative stress8. In the brain, changes in LH after ovariectomy have caused alterations in spatial memory9. Reduction of estrogens following ovariectomy has also become a model system for studying cell death in the hippocampus, as this can induce apoptosis, resulting in memory deficits10. Testosterone has also shown a role in the growth of kidneys both in mouse models and humans following kidney transplantation11.
The creation of a hormone-deprived murine model allows for the study of sex hormones and their hormone cascades on various diseases or tissues. This can be accomplished by surgical removal of the testes (orchiectomy) or ovaries (ovariectomy). This procedure can be performed in mice of any strain when they are as young as weaning age (twenty-one days) or any adult age. Ovariectomy is performed in female mice, while orchiectomy is performed in male mice. By removing these organs, the levels of estrogen and testosterone, and many of their derivatives, such as progesterone, can be greatly reduced12,13. The process of performing orchiectomies or ovariectomies in mice can be rapid and minimally invasive with the proper technique. Rapid excision of these organs in a safe and efficient manner can allow for quick surgical processing while keeping mouse numbers minimal by having a 100% survival rate when performed correctly. Here, we detail a protocol for the rapid excision of the testes and ovaries and demonstrate the proper post-surgical monitoring to enable researchers to perform this surgery quickly and safely. We also include visual examples of the sex organs and surrounding tissues to provide the surgeon with anatomical landmarks when performing this procedure.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
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			<td>Galilean Loupes</td>
			<td>Fine Science Tools</td>
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			<td>Optional, can provide better clarity during procedure</td>
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			<td>Gauze Sponges, 4&#34;x4&#34;</td>
			<td>Fisher Scientific</td>
			<td>13-761-52</td>
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			<td>Graefe Forceps</td>
			<td>Fine Science Tools</td>
			<td>11150-10</td>
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			<td>High Temp Cautery Kit</td>
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			<td>Using the fine tip attachment</td>
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			<td>PGA Absorbable Suture:4-0 / NFS-2 Reverse Cutting 19MM / 30 IN</td>
			<td>Covetrus</td>
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			<td>4-0 or 5-0 Absorbable sutures are best</td>
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			<td>Fine Science Tools</td>
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			<td>Surgical Scissors</td>
			<td>Fine Science Tools</td>
			<td>140-60-09</td>
			<td></td>
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			<td>Vannas Spring Scissors - 2.5mm Cutting Edge</td>
			<td>Fine Science Tools</td>
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			<td>Amazon</td>
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			<td>Wahl Professional Animal Compact Trimmer and Grooming Kit, Blue&#160;</td>
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</table>

murine orchiectomy and ovariectomy to reduce sex hormone production

Sex hormone signaling plays a critical role in multiple organ systems as well as in the progression of various diseases, including neurodegenerative disease. The manipulation of sex hormone levels in the murine model system allows for the study of their impact on organs/tissues and within disease progression. Orchiectomy - the surgical removal of the testes - and ovariectomy - the surgical removal of the ovaries - provide a method to deplete the endogenous sex hormones so that the precise hormone levels can be provided through drug or other delivery methods. Here, we provide rapid and minimally invasive methods for both orchiectomy and ovariectomy in the murine model system for the reduction of sex hormones. This protocol details the surgical preparation and excision of the testes through the scrotal sac, and excision of the ovaries via two incisions in the right and left lateral dorsum.

The procedure presented here is performed in one- to three-month-old mice in the C57BL/6J background. Male mice weighed 16-28 g, and female mice weighed 14-24 g at the time of the procedure. This procedure has been optimized to be applicable for mice of many ages, from weaning through adulthood.
Surgical orchiectomy involves a single skin incision in the ventral scrotal sac, as depicted in Figure 1A. Both testes are removed one at a time and are severed through th...

Watch this Scientific Journal Video about Murine Orchiectomy and Ovariectomy to Reduce Sex Hormone Production at JoVE.com

Murine Orchiectomy and Ovariectomy to Reduce Sex Hormone Production

This manuscript describes a consistent way to quickly perform survival rodent orchiectomies and ovariectomies.

Sex hormone signaling plays a critical role in multiple organ systems as well as in the progression of various diseases, including neurodegenerative ...

The overall goal of this procedure is to demonstrate the surgical removal of murine testes and ovaries in a fast, safe, and effective manner. Murine orchiectomy is performed by a ventral midline incision into the scrotal sac, where the testes are isolated and removed, followed by closure of the skin incision. Murine ovariectomy is performed by a dorsolateral incision into the abdomen where the ovary is isolated and removed, followed by closure of the skin incision, with the option to repeat this procedure on the other side to perform a bilateral ovariectomy.To begin the murine orchiectomy, first start by recording the weight of a male mouse and prepare to administer the appropriate pain medication and anesthetics per your institutional guidelines. Once the mouse is under anesthesia, cover the eyes with a lubricating eye gel to protect them from drying out during the procedure. Before proceeding, ensure that the mouse is at an appropriate plane of anesthesia by performing a toe-pinch response test.Next, shave the inguinal and scrotal areas of the mouse. Using a cotton-tipped applicator, apply a thin layer of depilatory hair removal cream to the surgical site and surrounding areas. After 30 seconds, remove the depilatory cream with the clean gauze sponge.Transfer the mouse to a surgical area and make sure a source of heat is available. Use soft adhesive tape to adhere the mouse's feet to the surgical mat. If the testes have ascended into the abdomen, use gentle pressure on the abdomen to help them descend.Scrub the skin with Betadine solution, starting in the center over the surgical site and working readily outwards towards the border of the shaved area. Follow the Betadine scrub with an alcohol scrub performed in a similar manner. Repeat this process three times to ensure proper skin disinfection.Cover the mouse with the surgical drape. Grasp the skin and make a midline incision about 1 to 1 1/2 centimeters in length. Grasping the cut border of the skin, use a blunt-tipped instrument to separate the skin from the underlying tissue.Take time to do this on the lateral, superior, and inferior borders of the incision. Next, isolate one testicle by sliding the skin incision to be directly atop it. Use a pair of forceps to grasp the thin, transparent cremaster muscle that surrounds the testicle.Identification of the correct tissue can be confirmed by its transparency and its ability to move independently from the underlying tissues enclosed within it. Next, incise the cremaster muscle by making an incision into the apex of the tissue. Place a locking clamp on the posterior border of the cut cremaster muscle to hold tension on the tissue.Use a pair of forceps to grasp the testicle and exteriorize it from its cremaster sheath. Once the testicle is out, roll the tissue laterally and localize the cremaster insertion point that connects the cremaster muscle to the testicle and epididymis on the posterior side of the testicle. Clamp and tear this tissue to sever this connection.Exteriorize the inguinal fat pad by slowly pulling it out. While doing this, watch for signs of bleeding and be sure to not harm any of the blood vessels in the process. Next, use a pair of locking hemostats to clamp the spermatic cord and blood vessels.While holding slight tension on the testicle, cauterize the spermatic cord and blood vessels distal to the hemostat clamp. Slowly release the hemostat and ensure the tissue stump has good hemostasis and does not continue to bleed. Applying a slight outward pressure on the cremaster muscle will allow this tissue stump to retract into the body cavity.Bring the two sides of the cremaster muscle together. Using 4-0 or 5-0 absorbable sutures, place a suture to join the two ends of the cremaster muscle. Once the suture is finished, trim the ends of the suture material to be 1/2 a centimeter in length.Repeat this process for the other testicle by sliding the skin incision to be atop the other side, and follow the same steps used to remove the first testicle. Once both testicles have been removed and both sides of the cremaster have been sutured, evert the skin upwards and prepare to apply a wound clip to the area. Be sure the suture ends will not be caught in the wound clip.The mouse is now ready to continue with postoperative monitoring. To prepare for murine ovariectomy, weigh a female mouse and administer pain medication and anesthesia per your institutional guidelines. Administer lubricating eye gel and check to make sure the mouse has no toe-pinch response.Shave the dorsolateral regions of the mouse's back to prepare the surgical site. Using a cotton-tipped applicator, apply a layer of depilatory hair removal cream to the shaved area. After 30 seconds, remove the cream with a clean gauze sponge.Transfer the mouse to a surgical mat and ensure that a source of heat is available. Scrub the skin with Betadine solution, starting in the center and working readily outwards towards the border of the shaved area. Follow this by scrubbing the skin with 70%alcohol solution applied in a similar manner.Repeat this process for a total of three times to ensure proper skin disinfection. Plan the surgical incision as detailed in the written protocol. Place a surgical drape over the mouse's surgical site.Grasp the skin with forceps and incise the skin with a one-centimeter incision. Use a blunt-tipped instrument or a plain pair of hemostats to separate the skin from the underlying tissue. Take time to do this on the lateral, superior, and inferior borders of the incision.Grasp the abdominal wall and incise with a 1/2-centimeter incision. Use a pair of forceps to locate the ovary within the incision and pull to exteriorize it. Once the tissues have been identified, use a pair of hemostats to clamp and crush the distal uterine horn.Use a second pair of hemostats or a pair of forceps to clamp just distal to the first clamp. Holding the bottom hemostat still, pull the top clamp up and away from the body to perform a crush and tear of the distal uterine horn. Slowly release the hemostat and watch to make sure there is not excessive bleeding coming from the surgical site.Bring the two sides of the abdominal wall together and suture the incision closed, using a single suture with 4-0 absorbable suture material. Once the suture is secured, trim the ends of the suture material to be 1/2 a centimeter in length. Bring the two sides of the skin back together and prepare to place a wound clip.While everting the skin, place a wound clip over the incision site. The mouse is now ready to continue with postoperative monitoring. Document the procedure date and time and analgesic administration per your institutional guidelines.Once a mouse has undergone surgical orchiectomy or ovariectomy, transfer them to a clean, heated cage. Once a mouse has regained sternal recumbency, place them in a clean cage and provide moist chow and water. During their recovery, frequently check on the mouse's surgical site and look for any signs of infection or bleeding.To prevent damage to the wound clip, remove any rodent igloo habitats from the cage of an ovariectomy mouse for one week following surgery. After 14 days, remove the wound clips from the mouse's skin. The demonstrated protocol details how to perform an orchiectomy and ovariectomy in a mouse to generate a sex-hormone-depleted model.This involves removing the testicles through a midline incision in the scrotum, followed by exteriorizing the testicles and severing the spermatic cord in blood vessels, resulting in the removal of the testicle, epididymis, and inguinal fat pads. Surgical ovariectomy can be performed by a dorsolateral incision into the dorsum and exteriorizing the ovary, oviduct, and distal uterine horn. This is followed by severing the distal uterine horn, leading to removal of the ovary and oviduct.Careful surgical technique and proper postoperative care will result in well-healed surgical sites. These surgical procedures can be further validated by analyzing hormone levels in mouse serum samples one week after orchiectomy. Ovariectomy can be confirmed by the observation of uterine atrophy following the removal of the ovaries.This protocol enables the rapid and effective surgical removal of ovaries and testes from mice to generate a sex-hormone-depleted model. This can have many uses to study how depletion of these hormones affects various organs and physiological processes.

murine-orchiectomy-and-ovariectomy-to-reduce-sex-hormone-production

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Medicine

6.5K ビュー.  UT Southwestern Medical Center. この手順の全体的な目標は、マウスの精巣と卵巣の外科的除去を迅速、安全、かつ効果的な方法で実証することです。マウス精巣摘除術は、陰嚢への腹側正中線切開によって行われ、そこで精巣が分離されて除去され、続いて皮膚切開が閉鎖されます。マウス卵巣摘出術は、卵巣を分離して除去する腹部の背外側切開を行い、続いて皮膚切開部を閉鎖し、反対側でこの?...