Gonadorelin Acetate
Other names:Gonadorelin, gonadotropin-releasing hormone (GnRH), Kryptocur, LHRH Ferring, Lutamin, Lutrelef, Lutrepulse, Relisorm L, and Relisorm
Gonadorelin Acetate is a synthetic form of the hormone gonadotropin-releasing hormone (GnRH). GnRH is naturally produced in the hypothalamus of the brain and plays a crucial role in regulating the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the pituitary gland. LH and FSH are essential for proper sexual development, fertility, and hormone regulation in both males and females.
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Properties
Description
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Properties
Sequence: | Pyr-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly |
Molecular Formula: | C57H79N17O15 |
Molecular Weight: | 1242.3 g/mol |
PubChem CID: | 11980076 |
CAS Number: | 34973-08-5 (Gonadorelin CAS: 9034-40-6) |
Synonyms: | Gonadorelin, gonadotropin-releasing hormone (GnRH), Cystorelin, Fertiline, Lutrelef, Lutrepulse |
Description
Authoritative source:PubChem
What Is Gonadorelin Acetate Peptide
Gonadorelin Acetate is a synthetic compound that mimics the function of the natural hormone gonadotropin-releasing hormone (GnRH) produced in the hypothalamus of the brain. GnRH plays a crucial role in regulating the release of other hormones such as luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the pituitary gland. These hormones, LH and FSH, are essential for various processes in the body, including proper sexual development, fertility, and hormone regulation.
Gonadorelin Acetate is used to assess the functioning of the hypothalamus and pituitary glands. Administering Gonadorelin Acetate helps determine if these glands are responding appropriately to the signal for hormone release. In women who have irregular ovulation and menstrual periods due to insufficient GnRH release from the hypothalamus, Gonadorelin Acetate can be used to stimulate the ovaries and induce ovulation.[1][2]
The synthetic Gonadorelin Acetate compound serves the same purpose as the natural GnRH hormone, and its administration can aid in restoring proper hormonal balance and function in cases where these processes are disrupted.
Although much progress has been made, the full extent of Gonadorelin Acetate’s mechanisms of action and therapeutic potential is still an active area of research, holding great promise for improving human health and addressing the growing global burden of metabolic diseases. To buy high quality Gonadorelin Acetate peptide to do research. Please ensure to buy it through a regular peptide manufacturer.
How Does Gonadorelin Acetate Peptide Be Used In Various Medical Contexts?
Gonadorelin Acetate mimics the action of naturally occurring gonadotropin-releasing hormone (GnRH) in the body. Its primary mechanism of action is to stimulate the synthesis and release of luteinizing hormone (LH) from the anterior pituitary gland. Additionally, it increases the production and release of follicle-stimulating hormone (FSH), although to a lesser extent. In certain cases, such as prepubertal females and some gonadal function disorders, the FSH response might be greater than the LH response. By simulating the physiological release of GnRH from the hypothalamus, Gonadorelin Acetate leads to increased levels of LH and FSH in the pituitary gland. These elevated levels of gonadotropins then stimulate the gonads (ovaries in females and testes in males) to produce reproductive steroids.[3][4]
Fertility Medicine: Gonadorelin Acetate is used in fertility treatments to stimulate the release of LH and FSH, which in turn can trigger ovulation in women and improve sperm production in men.
Amenorrhea and Hypogonadism: It can be used to treat conditions like amenorrhea (absence of menstrual periods) and hypogonadism (impaired function of the gonads) by restoring the hormonal balance.
Hormone Testing: Gonadorelin Acetate is used diagnostically to assess the functioning of the hypothalamus and pituitary glands. Administering Gonadorelin Acetate can help determine if these glands are responding appropriately to the hormone’s signal.
Cancer Treatment Research: Recent research has explored the potential of Gonadorelin Acetate in cancer treatment. It has shown promise in slowing the growth of breast and prostate cancer cells.
Alzheimer’s Disease Treatment: Studies have suggested potential benefits of Gonadorelin Acetate in the treatment of Alzheimer’s disease. However, this area of research is still developing.
Unlike some other GnRH analogues, Gonadorelin Acetate is not used to suppress sex hormone production. Its primary function is to stimulate the release of LH and FSH, which, in turn, affects the production of reproductive steroids.
What are the benefits of GnRH peptide?
Treating Testicular Atrophy
Gonadorelin Acetate, when used alongside testosterone therapy, can help prevent testicular atrophy (shrinkage of the testicles). By stimulating the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), Gonadorelin Acetate supports the natural production of testosterone, maintaining testicular function and size.[5][6]
Improving Fertility
Gonadorelin Acetate is instrumental in enhancing fertility, particularly in men with low testosterone levels. It stimulates LH production, which, in turn, boosts testosterone production. Adequate testosterone levels are crucial for sperm development and overall fertility.
Increasing Sexual Desire
Increased testosterone production through Gonadorelin Acetate therapy can lead to a higher libido and increased sexual desire in both men and women.
Potential Cancer Prevention
While research on GnRH analogs (like Gonadorelin Acetate) and cancer treatment exists, their preventive effects on cancer are not well-established. Further research is needed to understand this potential aspect.
Promoting Muscle Mass
Gonadorelin Acetate, by stimulating testosterone production, may contribute to increased muscle mass, particularly when combined with appropriate exercise and strength training.
Enhancing Bone Health
Testosterone plays a significant role in maintaining bone density and health. Gonadorelin Acetate’s promotion of testosterone production might help reduce the risk of bone-related issues like osteoporosis.[7][8]
Improving Mood
Optimal hormonal balance, including testosterone levels, is linked to improved mood and emotional well-being. Gonadorelin Acetate therapy might positively impact mood, especially in individuals with hormonal imbalances.
Treating Amenorrhea
In women with hypothalamic amenorrhea (lack of menstrual periods due to hormonal imbalances), Gonadorelin Acetate helps restore regular menstrual cycles by stimulating LH and FSH release. This can be beneficial for women experiencing fertility issues.
Additionally, some points could benefit from further research to establish more concrete connections. As medical understanding evolves, ongoing research will provide greater insights into the potential uses and benefits of Gonadorelin Acetate.
Gonadorelin Acetate Dosage
For Lutrepulse Pump (treating amenorrhea or infertility in women caused by pituitary or hypothalamus problems):
- Adults:5 micrograms (mcg) injected by the pump into a vein or under the skin slowly over 1 minute, every ninety minutes for twenty-one days. The doctor may adjust the dose as needed, within the range of 1 mcg to 20 mcg.
- Children up to 18 years of age:The dose must be determined by the doctor.
For Single-Dose Injection (testing the hypothalamus and pituitary glands):
- Adults: 0.1 milligram (mg) injected once as a single dose under the skin or into a vein.
- Children 12 years of age and older:2 micrograms (mcg) per kilogram (kg) of body weight (0.9 mcg per pound), not to exceed a single dose of 100 mcg, injected once under the skin or into a vein.
- Children up to 12 years of age: The dose must be determined by the doctor.
These dosages are provided as general information and may vary based on individual medical conditions and needs. Always follow the specific dosing instructions given by your healthcare provider and use the medication as directed. If you have any questions or concerns about your medication or dosage, don’t hesitate to discuss them with your doctor.[9][10]
Gonadorelin Acetate side effects and safety
Allergic Reaction: Rarely, an allergic reaction may occur. Symptoms can include difficulty breathing, throat swelling, lip/tongue/face swelling, or hives. Seek emergency medical attention if this occurs.
Less Serious Side Effects:
- Headache
- Flushing (redness and warmth of the skin)
- Nausea or abdominal discomfort
- Dizziness or lightheadedness
- Pain, swelling, or itching at the injection site
- Skin rash
Serious Side Effects:
- Signs of an allergic reaction (rash, hives, itching, swelling of the face/lips/tongue/throat, difficulty breathing)
- Irritation at the injection site
- Agitation
- Depression or mood changes
- Headache
- Upset stomach
- Very heavy menstrual bleeding (menorrhagia)
- Stomach pain
It’s important to note that while these side effects are possible, not everyone will experience them, and their occurrence can vary from person to person. If you’re considering or undergoing Gonadorelin Acetate therapy, it’s crucial to discuss potential side effects and any concerns you might have with your healthcare provider. They can provide personalized guidance and monitor your response to the treatment.[12]
How to recostitute GnRH?
Gonadorelin Acetate is a man-made protein that is like a hormone in the body called gonadotropin-releasing hormone (GnRH). Researchers and scientists can purchase Gonadorelin Acetate peptides from specialized peptide manufacturer or research companies that offer a variety of peptide products.
Materials Needed:
- 100 microgram vial of GonadorelinAcetate
- 1 ml of accompanying solvent
- Syringe
- Needle (if not already attached to the syringe)
- Alcohol swabs
- Sterile vial if necessary
- Refrigerator set at 2-8°C
Procedure:
- Wash Hands:Before starting, make sure to wash your hands thoroughly to maintain a sterile environment.
- Prepare Workspace:Ensure your workspace is clean and organized. You may want to disinfect the surface with an alcohol swab.
- Inspect Vial:Check the vial of Gonadorelin Acetate for any signs of damage or contamination. Do not use it if the seal is broken or if there are visible particles.
- Reconstitute: Follow these steps to reconstitute the medication:
a.Attach Needle: If the syringe doesn’t have a needle attached, carefully attach a new sterile needle to the syringe.
b.Draw Solvent: Use the syringe to draw up exactly 1 ml of the accompanying solvent. Be precise to ensure accurate reconstitution.
c.Inject Solvent: Carefully inject the 1 ml of solvent into the vial containing the GonadorelinAcetatepowder. Direct the solvent towards the side of the vial to prevent excessive foaming. Avoid forcefully injecting the solvent, as this could cause agitation.
d.Mix Gently: Once the solvent is added, gently swirl the vial to help dissolve the powder. Do not shake vigorously, as this can damage the medication.
- Inspect Mixture:After swirling, inspect the mixture to ensure that the Gonadorelin Acetate powder has dissolved completely. The solution should be clear and without visible particles. If there are any particles or clumps, do not use the solution.
- Withdraw Solution: If necessary, use the syringe to withdraw the reconstituted solution from the vial. If the medication needs to be transferred to a sterile vial, follow proper sterile procedures.
- Storage: Keep the reconstituted solution in the refrigerator at a temperature of 2-8°C. Use the solution within 24 hours of reconstitution to ensure its effectiveness.[13]
Gonadorelin Acetate and HCG
Gonadorelin Acetate is a medication that replicates the natural gonadotropin-releasing hormone (GnRH) released by the hypothalamus gland. By stimulating the pituitary gland, it triggers the release of other hormones with various positive effects on the body. It is utilized to assess the functioning of the hypothalamus and pituitary glands and is also beneficial in addressing fertility issues.[11]
On the other hand, HCG, a hormone produced during pregnancy, mimics the action of LH. In men, it stimulates testosterone production, often in combination with testosterone therapy to prevent testicular atrophy. In women, it is used as a fertility treatment to induce ovulation.
While both Gonadorelin Acetate and HCG impact the reproductive system, their mechanisms and medical applications differ. Gonadorelin Acetate stimulates LH and FSH release, whereas HCG mimics LH to influence testosterone production in men and promote ovulation in women. Qualified healthcare professionals should prescribe and monitor the usage of these medications according to individual medical needs.
Gonadorelin Acetate For Sale | Gonadorelin Acetate supplier
Gonadorelin Acetate is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pituitary. Gonadorelin Acetate has demonstrated benefits in the treatment of infertility and hypogonadism. Recent research indicates its potential in slowing the growth of breast and prostate cancer. Additionally, studies have shown promising results in the treatment of Alzheimer’s disease. Researchers interested in experimenting with Gonadorelin Acetate will want to ensure that they source this material from a reliable supplier. lf you’re looking to buying Gonadorelin Acetate online, it is essential to exercise caution and ensure that you obtain the peptide from a reputable and trustworthy manufacuturer. Polypeptide.Ltd is a highly reliable manufacturer that offers pharmaceutical grade peptides.[14]
Manufacturers/Factory
Gonadorelin Acetate is a medicine that is the same as gonadotropin-releasing hormone (GnRH) that is naturally released from the hypothalamus gland. GnRH causes the pituitary gland to release other hormones (luteinizing hormone [LH] and follicle-stimulating hormone [FSH]). LH and FSH control development in children and fertility in adults. Gonadorelin Acetate targets treatment of infertility and hypogonadism. If you are looking for the professional and top peptide Gonadorelin Acetate manufacturer or factory, here is the right place where you are.
Gonadorelin Acetate is an artificial polypeptide hormone with the capacity that it stimulates the release of the luteinizing hormonal hormone from the hypothalamus. Gonadorelin Acetate is used to test how well the hypothalamus and the pituitary glands are working. It is also used to cause ovulation (release of an egg from the ovary) in women who do not have regular ovulation andmenstrual periods because the hypothalamus gland does not release enough GnRH.
As the best Gonadorelin Acetate peptide manufacturer, Polypeptide.ltd is not only supply the peptide Gonadorelin Acetate in powder form but provide the customized standard easy use vial form.
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Coa & MS
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FAQ
What is the precautions using GnRH?
If you are using Gonadorelin Acetate to help you become pregnant, closely follow your doctor’s advice on the best times to have sexual intercourse. Your doctor can help you decide when having sexual intercourse will not result in a pregnancy with twins or triplets. Tell your doctor when you suspect your are pregnant.
What does Gonadorelin Acetate do for men?
In the male reproductive system, GnRH stimulates the production of: Luteinizing hormone, which affects how much testosterone and androgens (male sex hormones) your body makes. Follicle-stimulating hormone, which affects sperm production.
What is a Gonadorelin Acetate injection used for?
Gonadorelin Acetate is a test to determine how well the hypothalamus as well as the pituitary glands function. It can also induce an ovulation (release of eggs out of the ovary) for women who don’t have regular menstrual cycles and ovulation due to the hypothalamus gland’s inability to not produce enough GnRH. That is utilized in fertility medicine as well as to treat hypogonadism, amenorrhea, and amen. It is also utilized in the field of veterinary medicine.
Who should not take Gonadorelin Acetate?
Do not use gonadorelin Acetate if you:
- are allergic to gonadorelinAcetate or any ingredients of the medication
have a medical condition that could be worsened by pregnancy (e.g., certain tumours of the pituitary gland)
- have a medical condition that could be worsened by reproductive hormones (e.g., estrogen or progesterone), such as hormone-dependent tumours
- have ovarian cysts
Can Gonadorelin Acetate be used with testosterone?
Gonadorelin Acetate can be used in conjunction with testosterone therapy in certain cases. Testosterone therapy can sometimes lead to testicular atrophy (shrinkage of the testicles). To counteract this effect and prevent testicular atrophy, Gonadorelin Acetate may be used alongside testosterone therapy. Gonadorelin Acetate stimulates the pituitary gland to release LH and FSH, which in turn supports the natural production of testosterone in the testes.
What is the most important information I should know about GnRH?
Inform your doctor if you take any drugs, including herbal remedies, or if you have any other medical issues prior to using Gonadorelin Acetate. You might not be able to take Gonadorelin Acetate, or you might need to change your dosage or undergo further monitoring.
Reviews
Gonadorelin Peptide dosage calculator
Referenced Citations
[1]Bain J, Moskowitz JP, Clapp JJ. “LH and FSH response to gonadotropin releasing hormone (GnRH) in normospermic, oligospermic and azoospermic men”. Arch. Androl. 1978 May 10;1(2): 147–52. doi:10.3109/01485017808988331. PMID 367302
[2]Shao WM, Bai WJ, Chen YM, Liu L, Wang YJ. “[Micropump infusion of gonadorelin in the treatment of hypogonadotropic hypogonadism in patients with pituitary stalk interruption syndrome: cases analysis and literature review]”. Beijing da Xue Xue Bao (in Chinese). 2014 Jan 12;46(4): 642–5. PMID 25131486
[3]Sweetman, Sean C., ed.. Sex hormones and their modulators. Martindale: The Complete Drug Reference (36th ed.). London: Pharmaceutical Press. 2009 Aug 21;pp. 2106–2108. ISBN 978-0-85369-840-1
[4]Louis Sanford Goodman; Alfred Goodman Gilman. Goodman & Gilman’s the Pharmacological Basis of Therapeutics. McGraw-Hill, Health Professions Division. 1996 Jan 8;p. 1379. ISBN 978-0-07-026266-9
[5]Gautam N Allahbadia; Monika Malhotra Chawla; Rita Basuray Das; Esther Velilla Garcia, Goral Gandhi, Rubina Merchant. The Art & Science of Assisted Reproductive Techniques (ART). JP Medical Ltd. 2017 Jul 17;pp. 731–. ISBN 978-93-86322-82-1
[6]Lu ZL, Gallagher R, Sellar R, Coetsee M, Millar RP: Mutations remote from the human gonadotropin-releasing hormone (GnRH) receptor-binding sites specifically increase binding affinity for GnRH II but not GnRH I: evidence for ligand-selective, receptor-active conformations. J Biol Chem. 2005 Aug 19;280(33):29796-803
[7]Moles G, Carrillo M, Mananos E, Mylonas CC, Zanuy S: Temporal profile of brain and pituitary GnRHs, GnRH-R and gonadotropin mRNA expression and content during early development in European sea bass (Dicentrarchus labrax L.). Gen Comp Endocrinol. 2007 Jan 1;150(1):75-86
[8]Mamputha S, Lu ZL, Roeske RW, Millar RP, Katz AA, Flanagan CA: Conserved amino acid residues that are important for ligand binding in the type I gonadotropin-releasing hormone (GnRH) receptor are required for high potency of GnRH II at the type II GnRH receptor. Mol Endocrinol. 2007 Jan;21(1):281-92
[9] Lee PA, Houk CP: Gonadotropin-releasing hormone analog therapy for central precocious puberty and other childhood disorders affecting growth and puberty. Treat Endocrinol. 2006;5(5):287-96
[10]Bliss SP, Navratil AM, Breed M, Skinner DC, Clay CM, Roberson MS: Signaling complexes associated with the type I gonadotropin-releasing hormone (GnRH) receptor: colocalization of extracellularly regulated kinase 2 and GnRH receptor within membrane rafts. Mol Endocrinol. 2007 Feb;21(2):538-49
[11]Chen X, Ji ZL, Chen YZ: TTD: Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5
[12] Sá Filho MF, Ayres H, Ferreira RM, Marques MO, Reis EL, Silva RC, Rodrigues CA, Madureira EH, Bó GA, Baruselli PS. Theriogenology. 2010 Mar 15;73(5):651-8. doi: 10.1016/j.theriogenology.2009.11.004. Epub 2010 Jan 18.PMID: 20080296
[13] Bergfeld EG, D’Occhio MJ, Kinder JE. Biol Reprod. 1996 Apr;54(4):769-75. doi: 10.1095/biolreprod54.4.769. PMID: 8924495
[14] Hall JB, Staigmiller RB, Short RE, Bellows RA, MacNeil MD, Bellows SE.J Anim Sci. 1997 Jun;75(6):1606-11. doi: 10.2527/1997.7561606x. PMID: 9250524
What Is Gonadorelin?
Gonadorelin, also known as GnRH, is a decapeptide gonadotropin-releasing hormone agonist. It functions by stimulating the synthesis and release of luteinizing hormone and follicle-stimulating hormone. In human medicine, it is utilized to address infertility, menstrual cycle irregularities, and hypogonadism. Additionally, it serves as a diagnostic tool for evaluating pituitary function. Ongoing research has uncovered potential applications of gonadorelin in the treatment of breast and prostate cancer, as well as Alzheimer’s disease. [4][5][6][7]
Gonadorelin Structure

Authoritative source:PubChem
Sequence: Pyr-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly
Molecular Formula: C55H75N17013
Molecular Weight: 1182.311 g/mol
PubChem CID: 638793
CAS Number: 9034-40-6
Synonyms: Growth Hormone Releasing Factor, Somatocrinin, Somatoliberin
Gonadorelin Effects
Gonadorelin Research and Breast Cancer Prevention
Research indicates that women with greater lifetime exposure to estrogen may have an increased likelihood of developing breast cancer. Factors such as early onset of menstruation, later onset of menopause, use of estrogen-containing birth control, and menopausal hormone replacement therapy are associated with a higher risk of breast cancer. However, it is worth noting that the risk diminishes once birth control pills are discontinued, and eventually returns to the baseline level. It is important to recognize that while the use of birth control increases the risk of breast cancer, it simultaneously decreases the risk of ovarian cancer, making it a double-edged sword in terms of cancer risks.[3][4][5]
The growth of certain breast cancer cells relies on estrogen, and for years, reducing estrogen production or blocking estrogen receptors has been a recognized approach in treating specific types of breast cancer. Recent studies on gonadorelin have demonstrated its ability to suppress ovarian estrogen production, presenting a potential method for breast cancer prevention. This concept revolves around the notion that certain women, influenced by genetic and environmental factors, face a higher risk of developing breast cancer during their postmenopausal years. Utilizing gonadorelin in this context has proven to be safe and cost-effective, making it an appealing strategy for reducing the burden of cancer. Research suggests that a 10-year use of gonadorelin could potentially reduce the risk of breast cancer by up to 50%, and extending its use to 15 years may lead to a risk reduction of 70%.
The benefits of gonadorelin extend beyond breast cancer prevention. Research indicates that adjuvant therapy with anti-estrogens can significantly reduce disease progression, up to 50%, in cases where the cancer is sensitive to estrogen. However, currently available treatments face limitations in their effectiveness due to the development of resistance by cancer cells over time. This resistance often occurs due to increased expression of estrogen receptors, making it challenging to block every estrogen receptor without causing severe side effects. Gonadorelin offers a potential solution by reducing estrogen expression from the onset. This approach would not only directly inhibit the growth of estrogen-sensitive cancer cells but also enhance the efficacy of receptor-blocking medications, thereby extending their therapeutic effectiveness.
Gonadorelin a Breakthrough in Prostate Cancer
Contrary to popular media portrayal, prostate cancer is highly responsive to hormonal changes. While this might appear concerning, it actually presents an opportunity for intervention. By disrupting the supply of testosterone and its derivatives to prostate cancer cells, it is possible to significantly slow down and even stop the growth of the cancer. The main challenge lies in completely blocking all hormonal activity.[4][5][7] Initially, surgical removal of the testicles was performed in men with aggressive prostate cancer. However, this procedure was swiftly replaced by the administration of gonadorelin, which was found to be equally effective and potentially reversible in its action.
The use of GnRH in men with prostate cancer dates back to 1979, when it was initially referred to as “medical castration.” However, this mode of treatment led to an interesting discovery—that certain androgens are produced locally in the prostate through a process known as intracrinology. This means that GnRH blockade alone is only partially effective in treating prostate cancer. With the aid of gonadorelin, scientists were able to develop two new drugs that have been approved by the FDA for the treatment of castration-resistant prostate cancer (CRPC). These drugs play a crucial role in combating the progression and metastasis of prostate cancer, and they may even have potential as preventive measures in older men.

The impact of gonadorelin and GnRH analogues on testosterone levels
Authoritative source:PubChem
Gonadorelin May Reduce Dementia Risk
Research suggests that sex hormones, specifically luteinizing hormone (LH), have effects on the brain that go beyond their role in sexual dimorphism or reproductive function. Interestingly, the rise in LH levels during menopause has been linked to a higher risk of Alzheimer’s disease and reduced memory performance in both humans and animals. In-depth studies conducted on rats have shown that LH directly influences the hippocampus, the brain’s key memory center. Rats administered with LH demonstrate impaired memory performance and dysfunction in the hippocampus, which can be reversed by the administration of an LH-blocking drug.
Subsequent investigations into LH have provided additional insights, demonstrating a correlation between elevated hormone levels and increased neuropathology.[1][5][7] Specifically, it has been observed that LH plays a role in the formation of plaques associated with Alzheimer’s disease. Therefore, it is logical to assume that lowering LH levels could potentially slow the progression of Alzheimer’s. This hypothesis has been partially supported by studies using mouse models, where the removal of LH receptors in the brain has shown improvements in amyloid pathology and the preservation of cell health, including astrocytes that provide support and protection to neurons.
Recent findings have revealed that testosterone plays a beneficial role in brain health and the preservation of cognitive function. Consequently, solely inhibiting the entire hypothalamic-pituitary-gonadal axis may not be an effective approach for treating Alzheimer’s disease. As a result, scientists have embarked on testing gonadorelin derivatives to determine if selective interference in LH production is feasible and can yield potential benefits.
Ongoing research has shed light on the effectiveness of leuprolide, a GnRH receptor agonist commonly used to treat uterine fibroids, in reducing the risk of Alzheimer’s compared to other gonadorelin analogues. While the specific reasons behind this discrepancy are still being investigated, it is crucial to note that men undergoing highly effective combined androgen blockade (CAB) treatment for prostate cancer need not face a trade-off between cancer control and Alzheimer’s disease. In this context, leuprolide can be employed to mitigate the risks associated with CAB treatment and Alzheimer’s disease.[1][2][3][7] Particularly, the ability of leuprolide to down-regulate serum gonadotropin levels, including LH, is generally sufficient to counteract the effects of reduced testosterone.
New studies are underway to investigate the impact of gonadorelin and its analogues on APOE and MS4A6A expression in Alzheimer’s disease. Both of these genetic loci are associated with late-onset Alzheimer’s disease. However, research indicates that they need to function in conjunction to manifest significant problems, and disrupting either gene locus alone is sufficient to disrupt the pathological pathway. Gonadorelin affects this process of tandem interaction, although the specific mechanisms and underlying reasons remain unclear. Presently, researchers are diligently working to comprehend how the interplay of genes in Alzheimer’s disease can be disrupted for both treatment and prevention purposes. Gonadorelin plays a pivotal role in this line of research, and its exploration holds great importance.
Gonadorelin Research
Gonadorelin is not a recent discovery in the field of human and mammalian disease treatment. However, researchers continually uncover new insights into the mechanisms of action of GnRH and GnRH analogues in both normal physiology and disease development. The breakthrough revelation that gonadorelin can be used in the treatment of prostate cancer has led to the development of an incredibly effective cure, with a success rate of up to 99% for early-stage prostate cancer patients. Excitingly, similar breakthroughs appear to be on the horizon regarding the involvement of gonadorelin and its downstream hormones in the pathways associated with Alzheimer’s disease risk.
It is worth noting that gonadorelin demonstrates minimal side effects and exhibits excellent subcutaneous bioavailability in mice, although the dosage per kilogram in mice cannot be directly scaled to humans. It is important to emphasize that the sale of gonadorelin at Peptide Sciences is strictly limited to educational and scientific research purposes and is not intended for human consumption. Individuals should only purchase gonadorelin if they are licensed researchers.
Referenced Citations
[1] G. Secreto et al., “A novel approach to breast cancer prevention: reducing excessive ovarian androgen production in elderly women,” Breast Cancer Res. Treat., vol. 158, no. 3, pp. 553–561, 2016.
[2] D. V. Spicer and M. C. Pike, “Sex steroids and breast cancer prevention,” J. Natl. Cancer Inst. Monogr., no. 16, pp. 139–147, 1994.
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Author of this article:
Dr. Jean Zeng graduated from king’s college london Faculty of Life Sciences & Medicine.
scientific journal paper author:
Department of Chemistry ‘Ugo Schiff’, University of Florence, 50019 Sesto Fiorentino, FI, Italy
Department of Animal and Fish Production, Faculty of Agriculture (El-Shatby), Alexandria University, Alexandria 21545, Egypt
Professor of Clinical Pharmacology, Burroughs Wellcome Fund Professorship in Veterinary Pharmacology, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina
Laboratório de Biologia e Cultivo de Peixes de Água Doce (LAPAD), Departamento de Aquicultura, Centro de Ciências Agrárias, Universidade Federal de Santa Catarina, Rodovia SC 406, 3532, Florianópolis, Santa Catarina, CEP 88066-000, Brazil
Université de Toulouse, Institut National Polytechnique de Toulouse, École Nationale Vétérinaire de Toulouse, Toulouse, France
Institute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Am Sportpark Müngersdorf, 50933 Cologne, Germany
Author of this article:
Dr. Jean Zeng graduated from king's college london Faculty of Life Sciences & Medicine.
Scientific Journal paper Author:
Stephen C. Bain
Diabetes Research Group, Swansea University Medical School, Swansea, SA2 8PP, UK
Department of Diabetes and Endocrinology, Singleton Hospital, Swansea Bay University Health Board, Swansea, SA2 8QA, UK
In no way does this doctor/scientist endorse or advocate the purchase, sale, or use of this product for any reason. Polypeptide.ltd has no affiliation or relationship, implied or otherwise, with this physician. The purpose of citing this doctor is to acknowledge, acknowledge and commend the exhaustive research and development work done by the scientists working on this peptide.
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