Leuprolide acetate
Leuprolide acetate
Leuprolide acetate is a synthetic nonapeptide analog of gonadotropin-releasing hormone (GnRH or LHRH). It acts as an agonist at pituitary GnRH receptors, leading to an initial surge in luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels, followed by a profound hypogonadal effect due to receptor downregulation.
Medical Uses[edit | edit source]
Leuprolide acetate is primarily used in the treatment of hormone-sensitive cancers such as prostate cancer and breast cancer. It is also used in the management of endometriosis, uterine fibroids, and precocious puberty. Additionally, it is utilized in assisted reproductive technology (ART) protocols to control ovarian stimulation.
Prostate Cancer[edit | edit source]
In the treatment of prostate cancer, leuprolide acetate is used to reduce the levels of testosterone, which can stimulate the growth of cancer cells. It is often administered as part of androgen deprivation therapy (ADT).
Breast Cancer[edit | edit source]
For breast cancer, particularly in premenopausal women, leuprolide acetate helps to lower estrogen levels, which can fuel the growth of certain types of breast cancer cells.
Endometriosis[edit | edit source]
Leuprolide acetate is effective in reducing the symptoms of endometriosis by decreasing the production of estrogen, which is involved in the growth of endometrial tissue.
Uterine Fibroids[edit | edit source]
In the case of uterine fibroids, leuprolide acetate helps to shrink the fibroids and reduce symptoms such as heavy menstrual bleeding and pelvic pain.
Precocious Puberty[edit | edit source]
Leuprolide acetate is used to treat precocious puberty by delaying the onset of puberty until a more appropriate age.
Mechanism of Action[edit | edit source]
Leuprolide acetate works by initially stimulating the release of gonadotropins (LH and FSH) from the pituitary gland. However, with continuous administration, it desensitizes the GnRH receptors, leading to a decrease in the production of sex hormones (testosterone and estrogen).
Administration[edit | edit source]
Leuprolide acetate is available in various formulations, including daily subcutaneous injections, monthly intramuscular injections, and long-acting depot formulations that can be administered every three, four, or six months.
Side Effects[edit | edit source]
Common side effects of leuprolide acetate include hot flashes, headaches, mood changes, and injection site reactions. Long-term use can lead to decreased bone density and an increased risk of osteoporosis.
Related Pages[edit | edit source]
- Gonadotropin-releasing hormone
- Luteinizing hormone
- Follicle-stimulating hormone
- Prostate cancer
- Breast cancer
- Endometriosis
- Uterine fibroids
- Precocious puberty
- Androgen deprivation therapy
- Assisted reproductive technology
Categories[edit | edit source]
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Contributors: Prab R. Tumpati, MD