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Maternal diabetes decreases the expression of α2-adrenergic and M2 muscarinic receptors in the visual cortex of male rat neonates.

Authors :
Bagheri, Javad
Fallahnezhad, Somaye
Alipour, Nasim
Babaloo, Hamideh
Tahmasebi, Fatemeh
Kheradmand, Hamed
Sazegar, Ghasem
Haghir, Hossein
Source :
Journal of Chemical Neuroanatomy. Oct2023, Vol. 132, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

This study investigates the impact of maternal diabetes on the expression of α2-adrenergic and M2 muscarinic receptors in the primary visual cortex of male offspring born to diabetic rats. In adult female rats, a single dose of intraperitoneal streptozotocin (STZ) was used to induce diabetes (Diabetic group). Diabetes was controlled with insulin in the Insulin-treated group. Female rats in the control group received normal saline instead of STZ. Male newborns were euthanized at P0, P7, and P14, and the expression of α2-adrenergic and M2 muscarinic receptors in the primary visual cortex was determined using immunohistochemistry (IHC). The study showed that α2-adrenergic and M2 muscarinic receptors were significantly suppressed in all layers of the primary visual cortex of male neonates born to diabetic rats at P0, P7, and P14 compared to the control group. The highest expression was for the Con group at P14 and the lowest one was in the Dia group at P0 for both receptors. The insulin treatment in diabetic mothers modulated the expression of these receptors to normal levels in their newborns. The results demonstrate maternal diabetes decreases the expression of α2-adrenergic and M2 muscarinic receptors in the primary visual cortex of male offspring born to diabetic rats. Insulin treatment can offset these effects of diabetes. [Display omitted] • The expression levels of α2-adrenergic and M2 muscarinic receptors showed an increase with age across all groups. • There was a notable decrease in the expression of both receptors across all layers on P0, P7, and P14 in diabetic group. • Diabetic group who received insulin exhibited a restoration of receptor expression to normal levels. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08910618
Volume :
132
Database :
Academic Search Index
Journal :
Journal of Chemical Neuroanatomy
Publication Type :
Academic Journal
Accession number :
171850969
Full Text :
https://doi.org/10.1016/j.jchemneu.2023.102326