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Nesfatin-1: An Overview and Future Clinical Application

机译:Nesfatin-1:概述和未来的临床应用。

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References(23) Cited-By(34) Nesfatinucleobindin 2 (NUCB2) is expressed in the appetite-control hypothalamic nuclei and brainstem nuclei. Nesfatin/NUCB2 expression in the paraventricular nucleus of the hypothalamus was modulated by starvation and refeeding. Intracerebroventricular administration of nesfatin-1 dose-dependently inhibited food intake for 6 hours in male Wistar and leptin resistant, Zucker fatty rats. Intraperitoneal administration of nesfatin-1 and its mid-segment (M30) dosedependentlyinhibited food intake for 3 hours in male ICR mice. Intraperitoneal administration of M30 also decreased foodintake in leptin-resistant, genetically obese (ob/ob), diabetic (db/db) mice and mice fed a 45% high fat diet for 28 days. Intraperitoneal administration of M30 increased proopiomelanocortin and cocaine- and amphetamine- related peptide mRNA expression in the nucleus of the solitary tract of mice. In addition, intranasal administration of nesfatin-1 significantly inhibited food intake for 6 hours in male Wistar rats. We summarize recent observations about nesfatin-1, and attempt to present future direction of nesfatin-1 research for developing a new anti-obesity treatment.
机译:参考文献(23)被引用的By(34)Nesfatin / nucleobindin 2(NUCB2)在食欲控制的下丘脑核和脑干核中表达。下丘脑室旁核中Nesfatin / NUCB2的表达受到饥饿和重新喂养的调节。在雄性Wistar和瘦素抵抗性Zucker脂肪大鼠中,nesfatin-1的脑室内给药可剂量依赖性地抑制6小时的食物摄入。 nesfatin-1及其中段(M30)的腹膜内给药剂量依赖性地抑制了雄性ICR小鼠的3小时食物摄取。腹膜内施用M30还可降低耐瘦素的,遗传性肥胖(ob / ob),糖尿病(db / db)小鼠和喂食45%高脂饮食28天的小鼠的食物摄入。腹膜内施用M30可增加小鼠孤立道核中proopiomelanocortin以及可卡因和苯丙胺相关肽mRNA的表达。此外,在雄性Wistar大鼠中鼻内注射nesfatin-1可显着抑制6小时的食物摄入。我们总结了有关nesfatin-1的最新观察,并试图提出nesfatin-1研究的未来方向,以开发一种新型的抗肥胖症治疗方法。

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