Neonatal isolation provokes hippocampal apoptosis and recognition memory impairment in rats
Bibliographic Data
| ID | 15799251 |
|---|---|
| Authors | Hussein A Ghanimi (0000-0001-5199-9182, Ferdowsi University of Mashhad, corresponding author), Hawraa M Kadhim (University of Kerbala, corresponding author), Hawraa Hamid Hussein (0000-0002-8465-6706, University of Kerbala, corresponding author), Arash Abdolmaleki (0000-0002-7454-8728, University of Mohaghegh Ardabili, corresponding author), Ali Moghimi (0000-0001-9578-2612, Ferdowsi University of Mashhad, corresponding author) |
| Year | 2022 |
| Pages | 2811-2823 |
| Publication date | 2022-04-08 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | International Journal of Health Sciences (JOURNAL) |
| Journal identifiers | ISSN: 2550-696X • E-ISSN: 2550-6978 |
| Publisher | Universidad Tecnica de Manabi (PUBLISHER • EC) |
| DOI | 10.53730/ijhs.v6ns2.5701 |
| OpenAlex | W4223996989 |
| Language | EN |
Neonatal isolation (NI) has detrimental consequences on the hippocampal neurons of rat neonates. It has been reported to enhance neuronal cell death and impair memory behaviors. We conducted this study to assess the effects of NI on hippocampal apoptosis and recognition memory impairment in the hippocampus of rat neonates. One group of male Wistar rat neonates exposed to NI; rat neonates reared with 1-hour neonatal isolation (NI) for eight consecutive days (P2-P9). On the other hand, the control group reared normally. Novel object recognition test (NOR) test used to evaluate the effects of NI on recognition memory impairment. On day 22 (P22), a TUNEL assay was done. NOR demonstrated that rat neonates who experienced NI had long-term memory deficits (P<0.01). TUNEL assay results showed that NI increased the number of TUNEL positive neurons in CA1, CA3, and DG subfields of the hippocampus (P<0.05, P<0.001, and P<0.001). The present results indicated that NI exerted apoptotic effect and induced recognition memory impairment in the rat neonate’s hippocampus
Apoptosis · Biology · Cognition · Hippocampal formation · Hippocampus · Memory Impairment · Programmed cell death · Recognition memory · TUNEL assay · Anesthesia and Neurotoxicity Research · Medicine · Neonatal and fetal brain pathology · Neuroscience · Neuroscience and Neuropharmacology Research · Psychology · Endocrinology · Internal Medicine
| Highly cited | No |
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