Department of Physiology, Jichi Medical University, School of Medicine, Japan.
Department of Physiology, Jichi Medical University, School of Medicine, Japan; Department of Physiology, Wakayama Medical University School of Medicine, Japan.
Biochem Biophys Res Commun. 2018 Jun 12;500(4):910-916. doi: 10.1016/j.bbrc.2018.04.192. Epub 2018 Apr 30.
In the hypothalamic arcuate nucleus (ARC), orexigenic agouti-related peptide (AgRP) neurons regulate feeding behavior and energy homeostasis. The 3-phosphoinositide-dependent protein kinase-1 (PDK1) in AgRP neurons serves as a major signaling molecule for leptin and insulin, the hormones regulating feeding behavior, energy homeostasis and circulation. However, it is unclear whether PDK1 in AGRP neurons is also involved in regulation of blood pressure. This study explored it by generating and analyzing AgRP neuron-specific PDK1 knockout (Agrp-Pdk1) mice and effect of high salt diet on blood pressure in KO and WT mice was analyzed. Under high salt diet feeding, systolic blood pressure (SBP) of Agrp-Pdk1 mice was significantly elevated compared to Agrp-Cre mice. When the high salt diet was switched to control low salt diet, SBP of Agrp-Pdk1 mice returned to the basal level observed in Agrp-Cre mice within 1 week. In Agrp-Pdk1 mice, urinary noradrenalin excretion and NUCB2 mRNA expression in hypothalamic paraventricular nucleus (PVN) were markedly upregulated. Moreover, silencing of NUCB2 in the PVN counteracted the rises in urinary noradrenalin excretions and SBP. These results demonstrate a novel role of PDK1 in AgRP neurons to counteract the high salt diet-induced hypertension by preventing hyperactivation of PVN nesfatin-1 neurons.
在下丘脑弓状核(ARC)中,食欲肽 agouti 相关肽(AgRP)神经元调节摄食行为和能量平衡。AgRP 神经元中的 3-磷酸肌醇依赖性蛋白激酶-1(PDK1)是调节摄食行为、能量平衡和循环的激素(如瘦素和胰岛素)的主要信号分子。然而,PDK1 在 AgRP 神经元中是否也参与血压的调节尚不清楚。本研究通过生成和分析 AgRP 神经元特异性 PDK1 敲除(Agrp-Pdk1)小鼠,并分析 KO 和 WT 小鼠高盐饮食对血压的影响,对此进行了研究。在高盐饮食喂养下,Agrp-Pdk1 小鼠的收缩压(SBP)明显高于 Agrp-Cre 小鼠。当高盐饮食转换为对照低盐饮食时,Agrp-Pdk1 小鼠的 SBP 在 1 周内恢复到 Agrp-Cre 小鼠观察到的基础水平。在 Agrp-Pdk1 小鼠中,下丘脑室旁核(PVN)中的尿去甲肾上腺素排泄和 NUCB2 mRNA 表达明显上调。此外,PVN 中 NUCB2 的沉默抵消了尿去甲肾上腺素排泄和 SBP 的升高。这些结果表明,PDK1 在 AgRP 神经元中具有通过防止 PVN nesfatin-1 神经元的过度激活来对抗高盐饮食诱导的高血压的新作用。