Maternal diabetes decreases the expression of GABA Aα1 , GABA B1, and mGlu2 receptors in the visual cortex of male rat neonates

This study examines the impact of maternal diabetes on the expression of GABA , GABA , and mGlu2 receptors in the primary visual cortex layers of male rat newborns. In diabetic group (Dia), diabetes was induced in adult female rats using an intraperitoneal dose of Streptozotocin (STZ) 65 (mg/kg). Di...

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Veröffentlicht in:Neuroscience letters 2023-07, Vol.809, p.137309
Hauptverfasser: Bagheri, Javad, Fallahnezhad, Somaye, Alipour, Nasim, Babaloo, Hamideh, Tahmasebi, Fatemeh, Kheradmand, Hamed, Sazegar, Ghasem, Haghir, Hossein
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Sprache:eng
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Zusammenfassung:This study examines the impact of maternal diabetes on the expression of GABA , GABA , and mGlu2 receptors in the primary visual cortex layers of male rat newborns. In diabetic group (Dia), diabetes was induced in adult female rats using an intraperitoneal dose of Streptozotocin (STZ) 65 (mg/kg). Diabetes was managed by daily subcutaneous injection of NPH insulin in insulin-treated diabetic group (Ins). Control group (Con) received normal saline intraperitoneally rather than STZ. Male offspring born to each group of female rats were euthanized via CO2 inhalation at P0, P7, and P14 days after delivery and the expression of GABA , GABA , and mGlu2 receptors in their primary visual cortex was determined using immunohistochemistry (IHC). The expression of GABAB1, GABAAα1, and mGlu2 receptors increased gradually with age in the male offspring born to Con group while the highest expression was detected in layer IV of the primary visual cortex. In Dia group newborns, the expression of these receptors was significantly reduced in all layers of the primary visual cortex at every three days. Insulin treatment in diabetic mothers restored the expression of these receptors to normal levels in their newborns. The study indicates that diabetes reduces the expression of GABAB1, GABAAα1, and mGlu2 receptors in the primary visual cortex of male offspring born to diabetic rats at P0, P7, and P14. However, insulin treatment can counteract these effects.
ISSN:1872-7972
DOI:10.1016/j.neulet.2023.137309