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外周给予脂化的NPAF和NPFF类似物不影响中枢食物摄入调节,但会诱发焦虑样行为。

Peripheral administration of lipidized NPAF and NPFF analogs does not influence central food intake regulation but induces anxiety-like behavior.

作者信息

Strnadová Veronika, Morgan Alena, Škrlová Magdalena, Haasová Eliška, Bardová Kristina, Myšková Aneta, Sýkora David, Kuneš Jaroslav, Železná Blanka, Maletínská Lenka

机构信息

Institute of Organic Chemistry and Biochemistry, CAS, Prague, Czech Republic.

Institute of Organic Chemistry and Biochemistry, CAS, Prague, Czech Republic; First Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Neuropeptides. 2024 Apr;104:102417. doi: 10.1016/j.npep.2024.102417. Epub 2024 Feb 23.

Abstract

RF-amide peptides influence multiple physiological processes, including the regulation of appetite, stress responses, behavior, and reproductive and endocrine functions. In this study, we examined the roles of neuropeptide FF receptors (NPFFR1 and NPFFR2) by generating several lipidized analogs of neuropeptide AF (NPAF) and 1DMe, a stable analog of neuropeptide FF (NPFF). These analogs were administered peripherally for the first time to investigate their effects on food intake and other potential physiological outcomes. Lipidized NPAF and 1DMe analogs exhibited enhanced stability and increased pharmacokinetics. These analogs demonstrated preserved high affinity for NPFFR2 in the nanomolar range, while the binding affinity for NPFFR1 was tens of nanomoles. They activated the ERK and Akt signaling pathways in cells overexpressing the NPFFR1 and NPFFR2 receptors. Acute food intake in fasted mice decreased after the peripheral administration of oct-NPAF or oct-1DMe. However, this effect was not as pronounced as that observed after the injection of palm-PrRP31, a potent anorexigenic compound used as a comparator that binds to GPR10 and the NPFFR2 receptor with high affinity. Neither oct-1DMe nor oct-NPAF decreased food intake or body weight in mice with diet-induced obesity during long-term treatment. In mice treated with oct-1DMe, we observed decreased activity in the central zone during the open field test and decreased activity in the open arms of the elevated plus maze. Furthermore, we observed a decrease in plasma noradrenaline levels and an increase in plasma corticosterone levels, as well as an increase in Crh expression in the hypothalamus. Moreover, neuronal activity in the hypothalamus was increased after treatment with oct-1DMe. In this study, we report that oct-1DMe did not have any long-term effects on the central regulation of food intake; however, it caused anxiety-like behavior.

摘要

RF-酰胺肽影响多种生理过程,包括食欲调节、应激反应、行为以及生殖和内分泌功能。在本研究中,我们通过生成神经肽AF(NPAF)的几种脂化类似物以及神经肽FF(NPFF)的稳定类似物1DMe,研究了神经肽FF受体(NPFFR1和NPFFR2)的作用。这些类似物首次通过外周给药来研究它们对食物摄入和其他潜在生理结果的影响。脂化的NPAF和1DMe类似物表现出增强的稳定性和增加的药代动力学。这些类似物在纳摩尔范围内对NPFFR2表现出保留的高亲和力,而对NPFFR1的结合亲和力为数十纳摩尔。它们在过表达NPFFR¹和NPFFR2受体的细胞中激活了ERK和Akt信号通路。禁食小鼠外周注射八肽-NPAF或八肽-1DMe后,急性食物摄入量减少。然而,这种作用不如注射棕榈酰-PrRP31后观察到的明显,棕榈酰-PrRP31是一种强效的厌食化合物,用作对照物,它与GPR10和NPFFR2受体具有高亲和力结合。在长期治疗期间,八肽-1DMe和八肽-NPAF均未降低饮食诱导肥胖小鼠的食物摄入量或体重。在用八肽-1DMe治疗的小鼠中,我们在旷场试验中观察到中央区域的活动减少,在高架十字迷宫的开放臂中活动减少。此外,我们观察到血浆去甲肾上腺素水平降低,血浆皮质酮水平升高,以及下丘脑促肾上腺皮质激素释放激素(Crh)表达增加。此外,用八肽-1DMe治疗后下丘脑的神经元活动增加。在本研究中,我们报告八肽-1DMe对食物摄入的中枢调节没有任何长期影响;然而,它引起了焦虑样行为。

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