Daily Profile of glut1 and glut4 Expression in Tissues Inside and Outside the Blood-Brain Barrier in Control and Streptozotocin-Treated Rats

被引:10
作者
Soltesova, D. [1 ]
Vesela, A. [1 ]
Mravec, B. [2 ,3 ]
Herichova, I. [1 ]
机构
[1] Comenius Univ, Dept Anim Physiol & Ethol, Bratislava 84215, Slovakia
[2] Comenius Univ, Fac Med, Inst Pathophysiol, Bratislava 84215, Slovakia
[3] Slovak Acad Sci, Inst Expt Endocrinol, Bratislava, Slovakia
关键词
Frontal cortex; Heart; Cerebellum; Glucose transporter; Circadian; GLUCOSE-TRANSPORTER EXPRESSION; SUPRACHIASMATIC NUCLEUS; GENE-EXPRESSION; CIRCADIAN-RHYTHMS; MESSENGER-RNA; CEREBRAL-CORTEX; INSULIN; METABOLISM; PHYSIOLOGY; PROTEIN;
D O I
10.33549/physiolres.932596
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Glucose is molecule usually studied in relation to metabolism. Except for this traditional view, it is known that under certain conditions glucose can serve as a signal molecule for the circadian system. The circadian system is entrained by relevant synchronizing cues that can be tissue-dependent. Central oscillator is synchronized mainly by light-dark cycle, while peripheral oscillators can be entrained by food intake. Glucose transport in the organism is controlled by insulin dependent and independent mechanism. Therefore, we employed streptozotocin-induced diabetes to elucidate the influence of metabolic changes on glucose transporter (glut1, glut4) 24-h expression profile in peripheral oscillators in tissues, inside (frontal cortex, cerebellum) and outside (heart) the blood-brain barrier. Diabetes was induced by streptozotocin injection. Seventeen days later, sampling was performed during a 24-h cycle. Gene expression was measured using real-time PCR. We observed down-regulation of glut1 and glut4 expression in the heart of diabetic rats. The expression of glut1 and glut4 in brain areas was not down-regulated, however, we observed trend to phase advance in glut1 expression in the cerebellum. These results may indicate higher glucose levels in diabetic brain, which might influence regulation of clock gene expression in different manner in brain compared to periphery.
引用
收藏
页码:S115 / S124
页数:10
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