Objective： To evaluate the expression of glucose transporter-4 （GLUT4） mRNA in skeletal muscle and subcutaneous adipose tissues and investigate the mechanism of posttraumatic insulin resistance. Methods： Sixteen a...Objective： To evaluate the expression of glucose transporter-4 （GLUT4） mRNA in skeletal muscle and subcutaneous adipose tissues and investigate the mechanism of posttraumatic insulin resistance. Methods： Sixteen adult male Wistar rats were randomly divided into 2 group （ n = 8 in each group）, i.e., severe traumatic brain injury （TBI） group due to falls from a height and normal control group. Blood glucose and serum insulin were measured at 0.5 h before trauma and 3 h, 24 h, 72 h, 7 d after trauma, respectively. And insulin sensitivity was calculated by insulin activity index （IAI） formula. Skeletal muscle and subcutaneous adipose tissue samples were collected at the same time when blood was sampled. The changes of expression of GLUT4 mRNA were observed using reverse transcription-polymerase chain reaction （RT-PCR）. Results： Accompanied by the decrease of insulin sensitivity, the expression of GLUT4 mRNA was significantly decreased in adipose tissues at 24 h and 72 h after trauma （ P 〈 0. 01 ）, however, such phenomena did not appear in skeletal muscle samples. Conclusions： To some extent, the development of posttraumatic insulin resistance is related to the abnormality of transcription activity of GLUT4 gene. Adipose tissues show some difference in the transcriptional level of GLUT4 gene after trauma as compared with skeletal muscle tissues.展开更多
文摘Objective： To evaluate the expression of glucose transporter-4 （GLUT4） mRNA in skeletal muscle and subcutaneous adipose tissues and investigate the mechanism of posttraumatic insulin resistance. Methods： Sixteen adult male Wistar rats were randomly divided into 2 group （ n = 8 in each group）, i.e., severe traumatic brain injury （TBI） group due to falls from a height and normal control group. Blood glucose and serum insulin were measured at 0.5 h before trauma and 3 h, 24 h, 72 h, 7 d after trauma, respectively. And insulin sensitivity was calculated by insulin activity index （IAI） formula. Skeletal muscle and subcutaneous adipose tissue samples were collected at the same time when blood was sampled. The changes of expression of GLUT4 mRNA were observed using reverse transcription-polymerase chain reaction （RT-PCR）. Results： Accompanied by the decrease of insulin sensitivity, the expression of GLUT4 mRNA was significantly decreased in adipose tissues at 24 h and 72 h after trauma （ P 〈 0. 01 ）, however, such phenomena did not appear in skeletal muscle samples. Conclusions： To some extent, the development of posttraumatic insulin resistance is related to the abnormality of transcription activity of GLUT4 gene. Adipose tissues show some difference in the transcriptional level of GLUT4 gene after trauma as compared with skeletal muscle tissues.
