Laboratory of Neurophysiology, Multidisciplinary Institute of Cell Biology [IMBICE, Argentine Research Council (CONICET) and Scientific Research Commission, Province of Buenos Aires (CIC-PBA), National University of La Plata], La Plata, Buenos Aires 1900, Argentina.
Department of Biophysics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, CEP: 04023-062, Brazil.
Endocrinology. 2023 Sep 23;164(11). doi: 10.1210/endocr/bqad154.
The hormone ghrelin displays several well-characterized functions, including some with pharmaceutical interest. The receptor for ghrelin, the growth hormone secretagogue receptor (GHSR), is expressed in the hypothalamic paraventricular nucleus (PVH), a critical hub for the integration of metabolic, neuroendocrine, autonomic, and behavioral functions. Here, we performed a neuroanatomical and functional characterization of the neuronal types mediating ghrelin actions in the PVH of male mice. We found that fluorescent ghrelin mainly labels PVH neurons immunoreactive for nitric oxide synthase 1 (NOS1), which catalyze the production of nitric oxide [NO]). Centrally injected ghrelin increases c-Fos in NOS1 PVH neurons and NOS1 phosphorylation in the PVH. We also found that a high dose of systemically injected ghrelin increases the ghrelin level in the cerebrospinal fluid and in the periventricular PVH, and induces c-Fos in NOS1 PVH neurons. Such a high dose of systemically injected ghrelin activates a subset of NOS1 PVH neurons, which do not express oxytocin, via an arcuate nucleus-independent mechanism. Finally, we found that pharmacological inhibition of NO production fully abrogates ghrelin-induced increase of calcium concentration in corticotropin-releasing hormone neurons of the PVH whereas it partially impairs ghrelin-induced increase of plasma glucocorticoid levels. Thus, plasma ghrelin can directly target a subset of NO-producing neurons of the PVH that is involved in ghrelin-induced activation of the hypothalamic-pituitary-adrenal neuroendocrine axis.
生长激素释放肽受体(GHSR)是 ghrelin 的受体,它在下丘脑室旁核(PVH)中表达,PVH 是代谢、神经内分泌、自主和行为功能整合的关键枢纽。在这里,我们对雄性小鼠 PVH 中介导 ghrelin 作用的神经元类型进行了神经解剖学和功能表征。我们发现荧光 ghrelin 主要标记对一氧化氮合酶 1(NOS1)免疫反应性的 PVH 神经元,NOS1 催化一氧化氮 [NO] 的产生。中枢注射 ghrelin 增加 NOS1 PVH 神经元中的 c-Fos 和 PVH 中的 NOS1 磷酸化。我们还发现,系统注射高剂量的 ghrelin 会增加脑脊液和脑室周围 PVH 中的 ghrelin 水平,并诱导 NOS1 PVH 神经元中的 c-Fos。这种系统注射的高剂量 ghrelin 通过弓状核独立的机制激活一组不表达催产素的 NOS1 PVH 神经元。最后,我们发现,NO 产生的药理学抑制完全消除了 ghrelin 诱导的促肾上腺皮质激素释放激素神经元钙浓度的增加,而部分损害了 ghrelin 诱导的血浆糖皮质激素水平的增加。因此,血浆 ghrelin 可以直接靶向参与 ghrelin 诱导的下丘脑-垂体-肾上腺神经内分泌轴激活的 PVH 中的一组产生 NO 的神经元。