Kurade Mangesh, Bobba-Alves Natalia, Kelly Catherine, Behnke Alexander, Conklin Quinn, Juster Robert-Paul, Hirano Michio, Trumpff Caroline, Picard Martin
Division of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Clinical and Biological Psychology, Institute of Psychology and Education, Ulm University, Ulm, Germany.
medRxiv. 2025 Feb 3:2025.01.30.25321437. doi: 10.1101/2025.01.30.25321437.
FGF21 is a metabolic hormone induced by fasting, metabolic stress, and mitochondrial oxidative phosphorylation (OxPhos) defects that cause mitochondrial diseases (MitoD). Here we report that acute psychosocial stress alone (without physical exertion) decreases serum FGF21 by an average of 20% (<0.0001) in healthy controls but increases FGF21 by 32% (<0.0001) in people with MitoD-pointing to a functional interaction between the stress response and OxPhos capacity in regulating FGF21. We further define co-activation patterns between FGF21 and stress-related neuroendocrine hormones and report novel associations between FGF21 and psychosocial factors related to stress and wellbeing, highlighting a potential role for FGF21 in meeting the energetic needs of acute and chronic psychosocial stress.
成纤维细胞生长因子21(FGF21)是一种由禁食、代谢应激以及导致线粒体疾病(MitoD)的线粒体氧化磷酸化(OxPhos)缺陷所诱导产生的代谢激素。在此我们报告,在健康对照者中,仅急性心理社会应激(无体力消耗)就能使血清FGF21平均降低20%(<0.0001),但在患有线粒体疾病的人群中却能使FGF21升高32%(<0.0001)——这表明应激反应与调节FGF21的氧化磷酸化能力之间存在功能相互作用。我们进一步确定了FGF21与应激相关神经内分泌激素之间的共激活模式,并报告了FGF21与应激及幸福感相关的心理社会因素之间的新关联,突出了FGF21在满足急性和慢性心理社会应激能量需求方面的潜在作用。