Therapeutic Neuroendocrine Agonist and Antagonist Analogs of Hypothalamic Neuropeptides as Modulators of the Hypothalamic-Pituitary-Gonadal Axis.

C. Newton, Ross C. Anderson, R. Millar
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引用次数: 18

Abstract

Reproductive hormones play a role at all stages of life and affect most tissues of the body. Gonadotropin-releasing hormone (GnRH) synthesized in the hypothalamus stimulates the secretion of gonadotropins which in turn stimulate gonadal sex hormone production and gamete formation. This hypothalamic-pituitary-gonadal (HPG) axis has, therefore, been the target for the development of numerous drugs which regulate it at various points. These include sex steroid agonists and antagonists, inhibitors of sex steroid biosynthesis, and GnRH agonists and antagonists, which have found extensive applications in treating numerous conditions such as precocious puberty, delayed puberty, prostate cancer, benign prostatic hyperplasia, endometriosis, uterine fibroids and also in in vitro fertilization protocols. The novel neuroendocrine peptides, kisspeptin (KP) and neurokinin B (NKB), were recently discovered as upstream regulators of GnRH, and inactivating mutations of KP and NKB ligands or receptors result in a failure to progress through puberty. Agonists and antagonists of KP and NKB are being developed as more subtle modulators of the HPG axis. These new drugs offer additional and alternative therapeutic options in pediatric and adult hormone-dependent diseases.
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下丘脑神经肽作为下丘脑-垂体-性腺轴调节剂的治疗性神经内分泌激动剂和拮抗剂类似物。
生殖激素在生命的各个阶段都发挥作用,影响身体的大多数组织。下丘脑合成的促性腺激素释放激素(GnRH)刺激促性腺激素的分泌,促性腺激素反过来刺激性腺激素的产生和配子的形成。因此,这种下丘脑-垂体-性腺(HPG)轴已经成为许多药物开发的目标,这些药物可以在不同的点上调节它。这些药物包括性类固醇激动剂和拮抗剂、性类固醇生物合成抑制剂和GnRH激动剂和拮抗剂,它们已被广泛应用于治疗许多疾病,如性早熟、青春期延迟、前列腺癌、良性前列腺增生、子宫内膜异位症、子宫肌瘤以及体外受精方案。新的神经内分泌肽,kisspeptin (KP)和neurokinin B (NKB),最近被发现是GnRH的上游调节因子,KP和NKB配体或受体的失活突变导致青春期发育失败。KP和NKB的激动剂和拮抗剂作为HPG轴的更微妙的调节剂正在开发中。这些新药为儿童和成人激素依赖性疾病提供了额外和替代的治疗选择。
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