Therapeutic Review Leuprolide Acetate

نویسنده

  • Mark A. Mitchell
چکیده

Leuprolide acetate is a potent Gonadotropin Releasing Hormone (GnRH) agonist. The general premise behind leuprolide is that it inhibits the synthesis of lutenizing hormone and follicle stimulating hormone via a negative feedback. By reducing the production of these hormones, the drug effectively reduces estrogen and androgen production. This compound has been formulated as a depot formulation (1-, 3and 4-month) to provide long-term treatment for reproductive diseases in humans, including mammary and prostatic cancer, endometriosis, and precocious puberty.1 In these formulations, the hydrophilic leuprorelin is held in biodegradable highly lipophilic synthetic polymer microspheres.2 The depot is released over a defined length of time depending on the polymer. In humans, peak plasma concentrations can occur rapidly (1-3 hours) following a subcutaneous injection, and the microspheres help maintain plasma concentrations (1-month depot) between 0.4 to 1.4 g/L for almost a month.2 The long-term use of this drug in humans has been found to desensitize the pituitary. Leuprolide acetate is not recommended during pregnancy, as it can cause fetal abnormalities. Although formulated for humans, leuprolide acetate has been used fairly extensively in exotic and avian species. In exotic animal practice, this compound is primarily used to manage adrenal gland disease in ferrets and excessive egg laying in psittacines. However, this compound has also been used to induce molting in chickens, stimulate rat spermatogenesis, and serve as a reversible contraceptive in wapiti (Cervus elaphus nelsoni).3-5 The author also has some anecdotal success using leuprolide acetate (0.15 mg/kg q 4 weeks) as a method of reducing aggression in intact male green iguanas (Iguana iguana). Because the husbandry methods used to manage captive exotic species have improved over the past decade, many of these animals are living longer and successfully reproducing. These captive successes have led to the development of new and challenging health crises for the veterinarian to manage. The purpose of this article is to provide a

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Leuprolide acetate: a drug of diverse clinical applications.

Leuprolide acetate is a synthetic nonapeptide that is a potent gonadotropin-releasing hormone receptor (GnRHR) agonist used for diverse clinical applications, including the treatment of prostate cancer, endometriosis, uterine fibroids, central precocious puberty and in vitro fertilization techniques. As its basic mechanism of action, leuprolide acetate suppresses gonadotrope secretion of lutein...

متن کامل

Luteinizing hormone modulates cognition and amyloid-beta deposition in Alzheimer APP transgenic mice.

Until recently, the study of hormonal influences in Alzheimer disease was limited to the role of sex steroids. Despite numerous epidemiological studies supporting a protective role for estrogen in Alzheimer disease, recent studies show that estrogen administration in elderly women increases the risk of disease. Reconciling these contradictory reports, we previously hypothesized that other hormo...

متن کامل

Leuprolide acetate induces structural and functional recovery of injured spinal cord in rats.

Gonadotropin-releasing hormone (GnRH) and its synthetic analog leuprolide acetate, a GnRH agonist, have neurotrophic properties. This study was designed to determine whether administration of leuprolide acetate can improve locomotor behavior, gait, micturition reflex, spinal cord morphology and the amount of microglia in the lesion epicenter after spinal cord injury in rats. Rats with spinal co...

متن کامل

Ulipristal acetate versus leuprolide acetate for uterine fibroids.

BACKGROUND The efficacy and side-effect profile of ulipristal acetate as compared with those of leuprolide acetate for the treatment of symptomatic uterine fibroids before surgery are unclear. METHODS In this double-blind noninferiority trial, we randomly assigned 307 patients with symptomatic fibroids and excessive uterine bleeding to receive 3 months of daily therapy with oral ulipristal ac...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2005