Ohlsson Bodil
Division of Internal Medicine, Department of Clinical Sciences, Skåne University Hospital, Lund University, Malmö, Sweden.
Eur Surg Res. 2016;57(1-2):22-33. doi: 10.1159/000445717. Epub 2016 Apr 19.
Gonadotropin-releasing hormone (GnRH), follicle-stimulating hormone (FSH), and luteinizing hormone (LH) are involved in the reproductive cycle and regulate the secretion of sex steroids from the gonads. In mammals, GnRH1 is secreted as a hormone from the hypothalamus, whereas both GnRH1 and GnRH2 are present as neuropeptides in a variety of tissues. This review describes the role of GnRH in the gastrointestinal tract.
GnRH1, GnRH2, and LH receptors in humans and rats, and GnRH receptors in rats, have been described in the gastrointestinal tract, where they affect motility, gastric and hormone secretion, and cell proliferation. GnRH analogs are clinically used in the treatment of sex hormone-dependent diseases, i.e., endometriosis and malignancies, and as pretreatments for in vitro fertilization. Severe gastrointestinal dysmotility has been shown to develop in some women after such treatment, along with a reduction in the number of enteric neurons and autoantibodies against GnRH. Consequently, a rat model of enteric neurodegeneration has been developed based on the administration of the GnRH analog buserelin. Serum IgM antibodies against GnRH1, the GnRH2 precursor progonadoliberin-2, and the GnRH receptor have also been described in patients with irritable bowel syndrome and dysmotility, as well as in patients with gastrointestinal disorders associated with diabetes mellitus, posterior laryngitis, and primary Sjögren's syndrome, although no treatments using GnRH analogs have been administered.
GnRH and receptors for GnRH and LH are present in the human and rat gastrointestinal tract. Treatment with GnRH analogs may induce severe dysmotility, and a rat model of enteric neurodegeneration has been developed based on stimulation by the GnRH analog buserelin. Autoantibodies against GnRH and its receptor are found in a subgroup of patients with functional bowel disorders and dysmotility, independent of treatment with GnRH analogs.
促性腺激素释放激素(GnRH)、促卵泡生成素(FSH)和促黄体生成素(LH)参与生殖周期,并调节性腺中性类固醇的分泌。在哺乳动物中,GnRH1作为一种激素从下丘脑分泌,而GnRH1和GnRH2在多种组织中均作为神经肽存在。本综述描述了GnRH在胃肠道中的作用。
人类和大鼠胃肠道中已发现GnRH1、GnRH2和LH受体,以及大鼠胃肠道中的GnRH受体,它们会影响胃肠蠕动、胃和激素分泌以及细胞增殖。GnRH类似物在临床上用于治疗性激素依赖性疾病,即子宫内膜异位症和恶性肿瘤,以及作为体外受精的预处理。已证明一些女性在接受此类治疗后会出现严重的胃肠动力障碍,同时肠神经元数量减少以及出现抗GnRH自身抗体。因此,基于GnRH类似物布舍瑞林的给药建立了一种肠神经变性大鼠模型。肠易激综合征和胃肠动力障碍患者,以及患有与糖尿病、喉炎和原发性干燥综合征相关的胃肠道疾病的患者,血清中也存在抗GnRH1、GnRH2前体促性腺激素释放素-2和GnRH受体的IgM抗体,尽管这些患者未接受过GnRH类似物治疗。
人类和大鼠胃肠道中存在GnRH及其GnRH和LH受体。GnRH类似物治疗可能会诱发严重的胃肠动力障碍,并且基于GnRH类似物布舍瑞林的刺激建立了一种肠神经变性大鼠模型。在功能性肠病和胃肠动力障碍患者的一个亚组中发现了抗GnRH及其受体的自身抗体,这与GnRH类似物治疗无关。