Astrocytes play a predominant role in energy metabolism and in the catabolism of gamma-aminobutyric acid (GABA) and glutamate, neurotransmitters critically involved in epileptic processes. We show specific astrocytic alterations in the genetic absence epilepsy rats from Strasbourg (GAERS). Spontaneo
Glucocorticoids up-regulate the expression of glial fibrillary acidic protein in the rat suprachiasmatic nucleus
✍ Scribed by Daniel Maurel; Dominique Sage; Mourad Mekaouche; Olivier Bosler
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 262 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
✦ Synopsis
Immunoreactivity against glial fibrillary acidic protein (GFAP) was used as a dynamic index in adrenalectomized rats subjected or not to corticosterone replacement to investigate whether glucocorticoids may interact with astrocytes in the suprachiasmatic nucleus (SCN), the master component of the central circadian clock. GFAP staining in the SCN was significantly higher in rats having received implants that restored physiological plasma levels of corticosterone within diurnal or nocturnal limits than in non-normalized rats. The effects of corticosterone were similar in the parvocellular portion of the paraventricular nucleus but were opposite in the hippocampus, another major site of negative feed-back regulation of the hypothalamic-pituitary-adrenal axis, where a decreased GFAP staining was observed in discrete regions of the dentate gyrus. This indicates that glucocorticoids may positively or negatively regulate GFAP, depending on the target brain structure. In the SCN, that contains only few if any glucocorticoid receptors, indirect mechanisms that may involve serotoninergic neurons are probably responsible for the effects of corticosterone level. It is proposed that the corticosteroneinduced increase in GFAP staining in that nucleus accounts for dynamic changes in neurone-astrocyte interactions that might occur in relation with natural fluctuations of glucocorticoids over the 24 h period.
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