Ennequin Gaël, Boisseau Nathalie, Caillaud Kevin, Chavanelle Vivien, Etienne Monique, Li Xinyan, Sirvent Pascal
Université Clermont Auvergne, Université Blaise Pascal, EA 3533, Laboratoire des Adaptations Métaboliques à l'Exercice en Conditions Physiologiques et Pathologiques (AME2P), BP 80026, F-63171, Aubière Cedex, France; CRNH-Auvergne, Clermont-Ferrand, F-63001, France.
Zensun Sci & Tech Ltd., Shanghai, China.
PLoS One. 2015 Jul 31;10(7):e0130568. doi: 10.1371/journal.pone.0130568. eCollection 2015.
In vitro experiments using rodent skeletal muscle cells suggest that neuregulin 1 (NRG1) is involved in glucose metabolism regulation, although no study has evaluated the role of NRG1 in systemic glucose homeostasis. The purpose of this study was to investigate the effect of chronic and acute NRG1 treatment on glucose homeostasis in db/db mice. To this aim, glucose tolerance tests were performed in 8-week-old male db/db mice after treatment with NRG1 (50μg.kg-1) or saline 3 times per week for 8 weeks. In other experiments, glucose tolerance and pyruvate tolerance tests were performed in db/db mice 15 minutes after a single NRG1 (50μg.kg-1) or saline injection. Liver, adipose tissue, hypothalamus and skeletal muscle were also collected 30 minutes after acute NRG1 (50μg.kg-1) or saline treatment, and the phosphorylation status of the ERBB receptors, AKT (on Ser473) and FOXO1 (on Ser256) was assessed by western blotting. Chronic treatment (8 weeks) with NRG1 improved glucose tolerance in db/db mice. Acute treatment also lowered glycemia and insulinemia during glucose or pyruvate tolerance tests. NRG1 acute injection induced activation of ERBB3 receptors and phosphorylation of AKT and FOXO1 only in liver. Altogether, this study shows that acute and chronic NRG1 treatments improve glucose tolerance in db/db mice. This effect could be mediated through inhibition of hepatic gluconeogenesis.
使用啮齿动物骨骼肌细胞进行的体外实验表明,神经调节蛋白1(NRG1)参与葡萄糖代谢调节,尽管尚无研究评估NRG1在全身葡萄糖稳态中的作用。本研究的目的是调查长期和急性给予NRG1对db/db小鼠葡萄糖稳态的影响。为此,对8周龄雄性db/db小鼠每周3次给予NRG1(50μg·kg-1)或生理盐水,持续8周后进行葡萄糖耐量试验。在其他实验中,单次注射NRG1(50μg·kg-1)或生理盐水15分钟后,对db/db小鼠进行葡萄糖耐量和丙酮酸耐量试验。在急性给予NRG1(50μg·kg-1)或生理盐水处理30分钟后,还收集肝脏、脂肪组织、下丘脑和骨骼肌,并通过蛋白质印迹法评估ERBB受体、AKT(Ser473位点)和FOXO1(Ser256位点)的磷酸化状态。长期(8周)给予NRG1可改善db/db小鼠的葡萄糖耐量。急性处理在葡萄糖或丙酮酸耐量试验期间也降低了血糖和胰岛素水平。NRG1急性注射仅在肝脏中诱导ERBB3受体激活以及AKT和FOXO1磷酸化。总之,本研究表明,急性和长期给予NRG1均可改善db/db小鼠的葡萄糖耐量。这种作用可能是通过抑制肝脏糖异生介导的。