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引用次数: 0
摘要
源自脂肪细胞的激素瘦素在维持能量平衡方面发挥着关键作用。瘦素与其受体的长型结合,该受体主要表达于下丘脑的不同区域,包括下丘脑外侧区(LH)和视上核(SO)。多项研究表明,瘦素可直接激活神经元一氧化氮合酶,导致一氧化氮生成增加。我们使用烟酰胺腺嘌呤二核苷酸磷酸二磷酸酶(NADPH-d)的组织化学方法作为一氧化氮合酶活性的标记物,并评估了瘦素对大鼠 LH 和 SO 中一氧化氮能神经元的影响。我们发现,腹腔注射瘦素后,LH和SO中NADPH-d阳性神经元的数量显著增加。此外,接受瘦素治疗的大鼠与接受生理盐水治疗的大鼠相比,LH和SO神经元中NADPH-d染色的强度(光密度)明显提高。这些研究结果表明,LH和SO中的能硝化神经元可能与瘦素的中枢效应有关。
Effect of leptin on nitrergic neurons in the lateral hypothalamic area and the supraoptic nucleus of rats.
The adipocyte-derived hormone, leptin, plays a key role in the maintenance of energy homeostasis. Leptin binds to the long form of its receptor, which is predominantly expressed in various hypothalamic regions, including the lateral hypothalamic area (LH) and supraoptic nucleus (SO). Several studies have suggested that leptin directly activates neuronal nitric oxide synthase, leading to increased nitric oxide production. We used histochemistry for nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) as a marker for nitric oxide synthase activity and assessed the effect of leptin on nitrergic neurons in the LH and SO of rats. We found that intraperitoneal administration of leptin led to a significant increase in the number of NADPH-d-positive neurons in the LH and SO. In addition, the intensity (optical density) of NADPH-d staining in LH and SO neurons was significantly elevated in rats that received leptin compared with saline-treated rats. These findings suggest that nitrergic neurons in the LH and SO may be implicated in mediating the central effects of leptin.
期刊介绍:
Biotechnic & Histochemistry (formerly Stain technology) is the
official publication of the Biological Stain Commission. The journal has been in continuous publication since 1926.
Biotechnic & Histochemistry is an interdisciplinary journal that embraces all aspects of techniques for visualizing biological processes and entities in cells, tissues and organisms; papers that describe experimental work that employs such investigative methods are appropriate for publication as well.
Papers concerning topics as diverse as applications of histochemistry, immunohistochemistry, in situ hybridization, cytochemical probes, autoradiography, light and electron microscopy, tissue culture, in vivo and in vitro studies, image analysis, cytogenetics, automation or computerization of investigative procedures and other investigative approaches are appropriate for publication regardless of their length. Letters to the Editor and review articles concerning topics of special and current interest also are welcome.