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Neurobehavioral Assessments in a Mouse Model of Neonatal Hypoxic-ischemic Brain Injury
Published on: November 24, 2017
Basic fibroblast growth factor enhances cell proliferation in the dentate gyrus of neonatal rats following
Huan Zhu1, Lixing Qiao1, Yao Sun2
1Department of Pediatrics, Zhongda Hospital, Southeast University, Nanjing, Jiangsu Province 210009, China.
Insights
Hypoxic-ischemic insult in newborns can cause brain damage. Basic fibroblast growth factor (bFGF) was found to promote cell proliferation in the hippocampus, offering a potential therapeutic avenue for hypoxic-ischemic brain damage (HIBD).
Area of Science:
- Neuroscience
- Developmental Biology
- Pediatrics
Background:
- Perinatal hypoxic-ischemic insult (HIBD) is a leading cause of infant mortality and neurological deficits.
- Limited neurotherapeutic options exist for infant HIBD.
- This study explores neurogenesis and basic fibroblast growth factor (bFGF) in neonatal rat HIBD models.
Purpose of the Study:
- To investigate the relationship between neurogenesis and bFGF in the hippocampal dentate gyrus (DG) following neonatal HIBD.
- To determine the role of bFGF in promoting cell proliferation in the DG after HIBD.
Main Methods:
- Bromodeoxyuridine (BrdU) labeling was used to assess cell proliferation.
- bFGF's effect on cell proliferation in the DG was examined in neonatal rats post-HIBD.
Main Results:
- HIBD induced cell proliferation in the hippocampal DG of neonatal rats.
- bFGF gene expression increased in the hippocampus 7-14 days after HIBD.
- Exogenous bFGF administration enhanced cell proliferation in the DG following HIBD.
Conclusions:
- Neonatal HIBD stimulates cell proliferation in the dentate gyrus.
- bFGF plays a crucial role in promoting this proliferation, suggesting therapeutic potential.
Background:
Perinatal hypoxic-ischemic insult is considered a major contributor to child mortality and morbidity and leads to neurological deficits in newborn infants. There has been a lack of promising neurotherapeutic interventions for hypoxic-ischemic brain damage (HIBD) for clinical application in infants. The present study aimed to investigate the correlation between neurogenesis and basic fibroblast growth factor (bFGF) in the hippocampal dentate gyrus (DG) region in neonatal rats following HIBD.
Material And Methods:
Cell proliferation was examined by detecting BrdU signals, and the role of bFGF in cell proliferation in the DG region following neonatal HIBD was investigated.
Results:
Cell proliferation was induced by HIBD in the hippocampal DG of neonatal rats. Furthermore, bFGF gene expression was upregulated in the hippocampus in neonatal rats, particularly between 7 and 14 days after HIBD. Moreover, intraperitoneal injection of exogenous bFGF enhanced cell proliferation in the hippocampal DG following neonatal HIBD.
Conclusions:
Taken together, these data indicate that cell proliferation in the DG could be induced by neonatal HIBD, and bFGF promotes proliferation following neonatal HIBD.
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