Pålbrink Ann-Ki, Kopietz Franziska, Morén Björn, In 't Zandt René, Kalinec Federico, Stenkula Karin, Göransson Olga, Holm Cecilia, Magnusson Måns, Degerman Eva
Experimental Medical Science, Section for Diabetes, Metabolism and Endocrinology, Lund University Diabetes Centre, Lund University, Lund, Sweden.
Lund University Bioimaging Center, Lund University, Lund, Sweden.
BMJ Open Diabetes Res Care. 2020 Mar;8(1). doi: 10.1136/bmjdrc-2019-000820.
The mechanisms underlying the association between diabetes and inner ear dysfunction are not known yet. The aim of the present study is to evaluate the impact of obesity/insulin resistance on inner ear fluid homeostasis in vivo, and to investigate whether the organ of Corti could be a target tissue for insulin signaling using auditory House Ear Institute-Organ of Corti 1 (HEI-OC1) cells as an in vitro model.
High fat diet (HFD) fed C57BL/6J mice were used as a model to study the impact of insulin resistance on the inner ear. In one study, 12 C57BL/6J mice were fed either control diet or HFD and the size of the inner ear endolymphatic fluid compartment (EFC) was measured after 30 days using MRI and gadolinium contrast as a read-out. In another study, the size of the inner ear EFC was evaluated in eight C57BL/6J mice both before and after HFD feeding, with the same techniques. HEI-OC1 auditory cells were used as a model to investigate insulin signaling in organ of Corti cells.
HFD feeding induced an expansion of the EFC in C57BL/6J mice, a hallmark of inner ear dysfunction. Insulin also induced phosphorylation of protein kinase B (PKB/Akt) at Ser473, in a PI3-kinase-dependent manner. The phosphorylation of PKB was inhibited by isoproterenol and IBMX, a general phosphodiesterase (PDE) inhibitor. PDE1B, PDE4D and the insulin-sensitive PDE3B were found expressed and catalytically active in HEI-OC1 cells. Insulin decreased and AICAR, an activator of AMP-activated protein kinase, increased the phosphorylation at the inhibitory Ser79 of acetyl-CoA carboxylase, the rate-limiting enzyme in de novo lipogenesis. Furthermore, the activity of hormone-sensitive lipase, the rate-limiting enzyme in lipolysis, was detected in HEI-OC1 cells.
The organ of Corti could be a target tissue for insulin action, and inner ear insulin resistance might contribute to the association between diabetes and inner ear dysfunction.
糖尿病与内耳功能障碍之间关联的潜在机制尚不清楚。本研究的目的是在体内评估肥胖/胰岛素抵抗对内耳液体稳态的影响,并使用听觉豪斯耳研究所 - 柯蒂氏器1(HEI-OC1)细胞作为体外模型,研究柯蒂氏器是否可能是胰岛素信号传导的靶组织。
使用高脂饮食(HFD)喂养的C57BL/6J小鼠作为模型来研究胰岛素抵抗对内耳的影响。在一项研究中,12只C57BL/6J小鼠分别喂食对照饮食或HFD,30天后使用MRI和钆造影剂作为读出指标测量内耳内淋巴液腔(EFC)的大小。在另一项研究中,使用相同技术在8只C57BL/6J小鼠喂食HFD前后评估内耳EFC的大小。HEI-OC1听觉细胞用作研究柯蒂氏器细胞中胰岛素信号传导的模型。
HFD喂养导致C57BL/6J小鼠的EFC扩张,这是内耳功能障碍的一个标志。胰岛素还以PI3激酶依赖性方式诱导蛋白激酶B(PKB/Akt)在Ser473处的磷酸化。PKB的磷酸化被异丙肾上腺素和一种通用磷酸二酯酶(PDE)抑制剂IBMX抑制。发现PDE1B、PDE4D和胰岛素敏感的PDE3B在HEI-OC1细胞中表达并具有催化活性。胰岛素降低,而AMP激活的蛋白激酶激活剂AICAR增加了从头脂肪生成的限速酶乙酰辅酶A羧化酶抑制性Ser79处的磷酸化。此外,在HEI-OC1细胞中检测到脂解限速酶激素敏感脂肪酶的活性。
柯蒂氏器可能是胰岛素作用的靶组织,内耳胰岛素抵抗可能导致糖尿病与内耳功能障碍之间的关联。