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超活性人瘦素拮抗剂通过阻断瘦素受体,逆转瘦素诱导的猪卵巢卵泡中孕酮和睾酮过度分泌。

Superactive human leptin antagonist reverses leptin-induced excessive progesterone and testosterone secretion in porcine ovarian follicles by blocking leptin receptors.

作者信息

Gregoraszczuk E L, Rak A

机构信息

Department of Physiology and Toxicology of Reproduction, Chair of Animal Physiology, Institute of Zoology, Jagiellonian University, Cracow, Poland.

出版信息

J Physiol Pharmacol. 2015 Feb;66(1):39-46.

Abstract

Accumulating evidence indicates that leptin plays an important role in controlling reproductive function. At physiological levels, leptin stimulates steroidogenesis and follicle maturation, whereas supraphysiological concentrations of leptin have been suggested to be an independent risk factor for cyst formation. Since the discovery of the link between leptin and obesity, which is frequently associated with polycystic ovarian syndrome (PCOS), a number of leptin mutants exhibiting antagonistic properties have been developed, opening new avenues for leptin-related research. Here, using a superactive human leptin antagonist (SHLA), we sought to determine whether blocking leptin receptors can reverse the actions of leptin in ovarian follicles. Antral porcine ovarian follicles, collected from prepubertal and mature animals, were exposed to 100, 250 and 500 ng/ml SHLA for 24 hours, after which leptin receptor (ObR), leptin, CYP11A1 and 17β-hydroxysteroid dehydrogenase (17β-HSD) levels in follicles were evaluated by Western blotting. Levels of secreted leptin, progesterone (P4), and testosterone (T) in the follicle incubation medium were measured using enzyme-linked immunosorbent assays. The effects of SHLA on leptin-stimulated P4 and T secretion were also tested by exposing follicles to 40 ng/ml leptin in the presence and absence of SHLA. These experiments revealed that SHLA acted through inhibition of ObR expression and leptin expression and secretion decreased P4 and T secretion by ovarian follicles from both prepubertal and mature animals. Our data further suggest that the mechanism underlying this action of SHLA involves inhibition of CYP11A1 and 17β-HSD protein expression. Importantly, SHLA reversed leptin-induced increases in P4 and T secretion. Collectively, these data indicate that, in addition to their potential application in novel therapeutic strategies in oncology, which has received considerable recent research attention, leptin receptors antagonists might also be beneficial in controlling reproduction.

摘要

越来越多的证据表明,瘦素在控制生殖功能中发挥着重要作用。在生理水平上,瘦素刺激类固醇生成和卵泡成熟,而超生理浓度的瘦素被认为是囊肿形成的独立危险因素。自从发现瘦素与肥胖之间的联系(肥胖常与多囊卵巢综合征(PCOS)相关)以来,已经开发出了许多具有拮抗特性的瘦素突变体,为瘦素相关研究开辟了新途径。在此,我们使用一种超活性人瘦素拮抗剂(SHLA),试图确定阻断瘦素受体是否能逆转瘦素在卵巢卵泡中的作用。从青春期前和成熟动物收集的猪窦状卵泡暴露于100、250和500 ng/ml的SHLA中24小时,之后通过蛋白质印迹法评估卵泡中瘦素受体(ObR)、瘦素、CYP11A1和17β-羟基类固醇脱氢酶(17β-HSD)的水平。使用酶联免疫吸附测定法测量卵泡孵育培养基中分泌的瘦素、孕酮(P4)和睾酮(T)的水平。还通过在有和没有SHLA的情况下将卵泡暴露于40 ng/ml瘦素,测试了SHLA对瘦素刺激的P4和T分泌的影响。这些实验表明,SHLA通过抑制ObR表达起作用,瘦素表达和分泌的减少降低了青春期前和成熟动物卵巢卵泡的P4和T分泌。我们的数据进一步表明,SHLA这种作用的潜在机制涉及对CYP11A1和17β-HSD蛋白表达的抑制。重要的是,SHLA逆转了瘦素诱导的P4和T分泌增加。总的来说,这些数据表明,除了它们在肿瘤学新治疗策略中的潜在应用(这最近受到了相当多的研究关注)之外,瘦素受体拮抗剂在控制生殖方面可能也有益处。

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