Prenatal morphine exposure induces molecular and structural alterations in the developing hippocampus of neonatal rats
محل انتشار: مجله علوم پایه پزشکی ایران، دوره: 29، شماره: 2
سال انتشار: 1405
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 138
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شناسه ملی سند علمی:
JR_IJBMS-29-2_005
تاریخ نمایه سازی: 7 بهمن 1404
چکیده مقاله:
Objective(s): Prenatal exposure to opioids such as morphine poses significant risks to fetal neurodevelopment, particularly in brain regions critical for cognition, such as the hippocampus. Despite the prescription and use of opioids during pregnancy, the molecular and histological consequences of such exposure remain insufficiently explored. To evaluate the effects of short-term prenatal morphine exposure on the expression of key neurodevelopmental genes and the structural integrity of the hippocampus in neonatal rats.Materials and Methods: Pregnant Sprague Dawley rats were administered intraperitoneal injections of morphine sulfate (۱۰ mg/kg) on gestational days ۱۵ and ۱۶. On postnatal day ۱۲, offspring (n = ۶ per group) were euthanized, and their hippocampal tissues were collected. Quantitative real-time PCR was performed to assess the expression levels of neurodevelopmental genes, including MDH۲, Neurog۱, and BDNF. Histological evaluations were conducted using hematoxylin and eosin and cresyl violet staining to assess cellular architecture and neuronal viability. Immunohistochemical staining for GFAP, S۱۰۰, and synaptophysin was used to evaluate astrocytic integrity and synaptic density.Results: The morphine-exposed group showed significant up-reglation of MDH۲, Neurog۱, and BDNF (P<۰.۰۵). Histological analyses revealed neuronal degeneration and inflammatory infiltration in the hippocampus. Immunohistochemistry demonstrated a marked reduction of GFAP, S۱۰۰, and synaptophysin signals, indicating substantial glial loss and synaptic disruption.Conclusion: Prenatal morphine exposure leads to marked molecular and histopathological changes in the developing hippocampus, suggesting long-term risks for neurocognitive dysfunction. These findings emphasize the importance of limiting opioid use during pregnancy and identifying molecular targets for future therapeutic interventions.
کلیدواژه ها:
نویسندگان
Pooya Nadri
Student Research Committee, Ramsar Campus, Mazandaran University of Medical Sciences, Ramsar, Iran
Zahra Daneshfar
Ramsar Campus, Mazandaran University of Medical Sciences, Ramsar, Iran
Zahra Azarmehr
Department of Hematology, Tehran University of Medical Science, Tehran, Iran
Samaneh Farrokhfar
Department of Anatomical Sciences, Faculty of Medicine, Ramsar Campus, Mazandaran University of Medical Sciences, Ramsar, Iran
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