PMID- 37114289 OWN - NLM STAT- MEDLINE DCOM- 20230606 LR - 20230606 IS - 1873-474X (Electronic) IS - 0736-5748 (Linking) VI - 83 IP - 4 DP - 2023 Jun TI - Postnatal melatonin administration to stressed dams for ameliorating risk-taking behaviour in rat pups through maternal care improvement. PG - 374-382 LID - 10.1002/jdn.10265 [doi] AB - BACKGROUND AND AIM: Anxiety often occurs both concurrently and sequentially in childhood and adolescence in association with prenatal stress, which may reduce the quality of maternal care and then cause mood disorders among children in later life. Against this background, melatonin, as a powerful antioxidant, was used in the present study to ameliorate risk-taking behaviour induced by pure maternal care in rat pups. MATERIALS AND METHODS: The Wistar rat dams recruited in this study were exposed to restraint stress from gestational day (GD) 11 until delivery. They further received melatonin (10 mg/kg) during the postnatal days (PNDs) 0-7 by intraperitoneal (IP) injections at 4:00 PM. The pregnant rats were then divided into four groups, namely, control, stress, stress + melatonin and melatonin, and their maternal behaviour and corticosterone levels were measured. In the offspring, the outcomes of some behavioural tasks, including the elevated plus-maze (EPM) and open-field (OF) tests were ultimately assessed. RESULTS: The study results revealed that the quantity and quality of maternal care significantly declined and the plasma corticosterone levels compounded in the stressed dams. Melatonin treatment, however, improved their nursing behaviour and reduced their plasma corticosterone levels. The offspring performance in two tasks also showed an upward trend in risk-taking behaviour in the stress group, and melatonin administration ameliorated the effects of stress and lessened their anxiety-like behaviour. CONCLUSION: It was concluded that prenatal restraint stress could impair stress responses and quality of maternal care, whereas postnatal melatonin administration potentially contributed to the normalization of stress reaction and anxiolysis. CI - (c) 2023 International Society for Developmental Neuroscience. FAU - Bagheri, Farzaneh AU - Bagheri F AUID- ORCID: 0000-0002-9300-6705 AD - School of Biology, Damghan University, Damghan, Iran. FAU - Goudarzi, Iran AU - Goudarzi I AUID- ORCID: 0000-0002-6665-3202 AD - School of Biology, Damghan University, Damghan, Iran. LA - eng PT - Journal Article DEP - 20230427 PL - United States TA - Int J Dev Neurosci JT - International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience JID - 8401784 RN - W980KJ009P (Corticosterone) RN - JL5DK93RCL (Melatonin) SB - IM MH - Humans MH - Female MH - Pregnancy MH - Rats MH - Animals MH - Rats, Wistar MH - Corticosterone MH - *Melatonin/pharmacology/therapeutic use MH - Anxiety/drug therapy MH - Risk-Taking MH - Stress, Psychological/drug therapy MH - *Prenatal Exposure Delayed Effects OTO - NOTNLM OT - early-life stress OT - maternal behaviour OT - melatonin OT - rat OT - risk-taking behaviour EDAT- 2023/04/28 06:41 MHDA- 2023/06/06 06:42 CRDT- 2023/04/28 02:42 PHST- 2023/04/06 00:00 [revised] PHST- 2023/01/22 00:00 [received] PHST- 2023/04/13 00:00 [accepted] PHST- 2023/06/06 06:42 [medline] PHST- 2023/04/28 06:41 [pubmed] PHST- 2023/04/28 02:42 [entrez] AID - 10.1002/jdn.10265 [doi] PST - ppublish SO - Int J Dev Neurosci. 2023 Jun;83(4):374-382. doi: 10.1002/jdn.10265. Epub 2023 Apr 27.