Daily profile of glut1 and glut4 expression in tissues inside and outside the blood-brain barrier in control and streptozotocin-treated rats
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24329691
DOI
10.33549/physiolres.932596
PII: 932596
Knihovny.cz E-zdroje
- MeSH
- cirkadiánní hodiny * MeSH
- cirkadiánní rytmus * MeSH
- experimentální diabetes mellitus chemicky indukované metabolismus MeSH
- glukosa metabolismus MeSH
- hematoencefalická bariéra metabolismus MeSH
- krysa rodu Rattus MeSH
- potkani Wistar MeSH
- přenašeč glukosy typ 1 metabolismus MeSH
- přenašeč glukosy typ 4 metabolismus MeSH
- streptozocin MeSH
- tkáňová distribuce účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- glukosa MeSH
- přenašeč glukosy typ 1 MeSH
- přenašeč glukosy typ 4 MeSH
- Slc2a1 protein, rat MeSH Prohlížeč
- Slc2a4 protein, rat MeSH Prohlížeč
- streptozocin MeSH
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.
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