Gonadorelin acetate is a synthetic decapeptide analog of gonadotropin-releasing hormone (GnRH) and acts as a specific agonist for the GnRH receptor[1]. By binding to the GnRH receptors in the anterior pituitary gland, Gonadorelin acetate triggers a signaling cascade that promotes the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), both of which play a key role in regulating the reproductive system[2]. Gonadorelin acetate is usually used in the study of reproductive-related diseases[3][4].
In vitro, treatment of rat spinal ganglion neurons with Gonadorelin acetate (50µM; 30s-10min) significantly inhibits GABA-induced depolarization and reduces GABA-activated currents[5]. Gonadorelin acetate (1μM; 72h) significantly inhibited the proliferation, migration, and multi-lineage differentiation potential of endometrial stem cells[6].
In vivo, Gonadorelin acetate (150ng/mouse; subcutaneous injection; five days a week for three weeks) significantly reduced small intestinal polyp multiplicity and size and inhibited colon tumor formation in female ApcMin/+ mice[7].
References:
[1] Nederpelt I, Georgi V, Schiele F, et al. Characterization of 12 GnRH peptide agonists - a kinetic perspective. Br J Pharmacol. 2016;173(1):128-141.
[2] Resta C, Moustogiannis A, Chatzinikita E, et al. Gonadotropin-Releasing Hormone (GnRH)/GnRH Receptors and Their Role in the Treatment of Endometriosis. Cureus. 2023;15(4):e38136.
[3] Carel JC, Eugster EA, Rogol A, et al. Consensus statement on the use of gonadotropin-releasing hormone analogs in children. Pediatrics. 2009;123(4):e752-e762.
[4] Edi R, Cheng T. Endometriosis: Evaluation and Treatment. Am Fam Physician. 2022;106(4):397-404.
[5] Zhou XP, Wu XP, Guan BC, Li ZW. Modulatory effects of gonadorelin on GABA-induced depolarization and GABA-activated current in rat spinal ganglion neurons. Zhongguo Yao Li Xue Bao. 1996;17(1):31-34.
[6] Park SR, Cho A, Park ST, et al. Double-edged sword of gonadotropin-releasing hormone (GnRH): A novel role of GnRH in the multiple beneficial functions of endometrial stem cells. Cell Death Dis. 2018;9(8):828.
[7] Janakiram NB, Mohammed A, Brewer M, et al. Raloxifene and antiestrogenic gonadorelin inhibits intestinal tumorigenesis by modulating immune cells and decreasing stem-like cells. Cancer Prev Res (Phila). 2014;7(3):300-309.
Gonadorelin acetate是一种促性腺激素释放激素(GnRH)的合成十肽类似物,是GnRH受体的特异性激动剂[1]。Gonadorelin acetate通过与垂体前叶的GnRH受体结合,触发信号级联反应,促使黄体生成素(LH)和促卵泡激素(FSH)的分泌,这些激素在调节生殖系统方面发挥着关键作用[2]。Gonadorelin acetate通常用于生殖相关疾病研究[3][4]。
体外实验中,用50µM的Gonadorelin acetate处理大鼠脊髓神经节细胞30秒至10分钟,可显著抑制由GABA引起的去极化,并减少GABA激活的电流[5]。Gonadorelin acetate(1μM;72小时)处理子宫内膜干细胞显著抑制其增殖、迁移和多系分化潜能[6]。
体内实验中,Gonadorelin acetate (150ng/只;皮下注射;每周五天、连续三周)显著减少了雌性ApcMin/+小鼠小肠息肉的数量和大小,并抑制了结肠肿瘤的形成[7]。
















