1. A new mechanism of POCD caused by sevoflurane in mice: cognitive impairment induced by cross-dysfunction of iron and glucose metabolism
- Author
-
Peng Yu, Zhenhua Shi, Xincheng Li, Yan Li, Jinhong Xie, Changhao Zhou, Yan-Zhong Chang, Guofen Gao, Anand Thirupathi, Xing Ge, and Yong Zuo
- Subjects
Aging ,medicine.medical_specialty ,glucose metabolism ,Iron ,viruses ,sevoflurane ,Apoptosis ,Carbohydrate metabolism ,medicine.disease_cause ,Hippocampus ,Mice ,Postoperative Cognitive Complications ,Glucose Metabolism Disorder ,Internal medicine ,medicine ,Animals ,iron metabolism ,Cognitive Dysfunction ,POCD ,cognitive impairment ,Chemistry ,Glucose transporter ,Neurotoxicity ,Brain ,Endothelial Cells ,Spectrometry, X-Ray Emission ,virus diseases ,Cell Biology ,Metabolism ,respiratory system ,medicine.disease ,Oxidative Stress ,Glucose ,Endocrinology ,Anesthetics, Inhalation ,Postoperative cognitive dysfunction ,Homeostasis ,Oxidative stress ,Research Paper - Abstract
Sevoflurane (Sev) is a commonly used anesthetic in hospitals that can cause neurotoxicity. Postoperative cognitive dysfunction (POCD) is a common clinical problem induced by some anesthetics. However, the exact mechanism of neurotoxicity induced by Sev is unclear. Here we studied a new mechanism of POCD induced by Sev. We treated 15-month-old mice with 2% Sev for 6 hours, and we had found that Sev causes POCD. Using isobaric tags for relative and absolute quantitation (iTRAQ), we found that the transporter and the metabolism of carbohydrates and inorganic ions were involved in the cognitive impairment induced by Sev. Using synchrotron radiation micro-X-ray fluorescence (μ-XRF), we showed that Sev caused the iron overload in the brain of 15-month-old mice. Subsequently, excessive iron led to oxidative stress and impaired mitochondrial function that further led to glucose metabolism disorder and reduced ATP production by regulating the expression of key enzyme genes or proteins including G6Pase, Pck1, and Cs. Meanwhile, Sev also inhibited the oxygen consumption rate and glucose absorption by downregulating the expression of glucose transporter 1 in cerebral vascular endothelial cells. The cross-dysfunction of iron and glucose metabolism caused the apoptosis in the cortex and hippocampus through Bcl2/Bax pathway. In conclusion, the data here showed a new mechanism that Sev caused apoptosis by cross-dysregulation of iron and glucose metabolism and induced energy stress in mice. Maintaining iron and glucose metabolism homeostasis may play an important role in cognitive impairment induced by Sev.
- Published
- 2021