Marianela N. Ceol Retamal
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Marianela N. Ceol Retamal has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Ailen Alba Colapietro
Instituto de Biología Celular y Neurociencias “Prof. E. De Robertis”. Facultad de Medicina. Universidad de Buenos Aires. Buenos Aires, Argentina
1 shared publication - Jazmín Grillo Balboa
Laboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina
1 shared publication - Mariela Chertoff
Laboratorio de Neuroepigenética y Adversidades Tempranas, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina
1 shared publication - Marina Flavia Ponzio
Facultad de Ciencias Médicas, Instituto de Investigaciones en Ciencias de la Salud (INICSA-CONICET), Universidad Nacional de Córdoba, Córdoba, Argentina
1 shared publication - Marta Cristina Antonelli
Instituto de Biología Celular y Neurociencias, “Prof. Dr. E De Robertis”, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina
1 shared publication - María Eugenia Pallarés
Instituto de Biología Celular y Neurociencia “Prof. E. De Robertis”, Facultad de Medicina, Universidad de Buenos Aires, Ciudad de Buenos Aires, Argentina
1 shared publication
Latest Publications
- 18 February 2025
- Published by Springer Nature in Neurotoxicity Research
- Vol. 43 (2) , 1-18
Sex-Specific Outcomes in a Rat Model of Early-Life Stress Due to Adverse Caregiving
Early parental care is critical for the development of cortico-limbic circuits regulating stress responses and emotional well-being. Conversely, infant maltreatment can increase susceptibility to mood disorders—such as anxiety and depression—and impair stress-coping abilities. Here, we employed the Scarcity-Adversity Model (SAM) in rats, limiting nesting resources from postnatal days 8–12, to examine its effects on maternal and adult offspring behavior. SAM-exposed mothers exhibited fragmented care and increased violence towards pups. By postpartum day (PPD) 13, maternal fecal corticosterone metabolites (FCM) were elevated, indicating heightened stress. At weaning, SAM dams also showed increased anxiety-like behavior in the Elevated Plus Maze (EPM), suggesting significant emotional alterations. In adulthood, SAM-exposed offspring underwent anxiogenic tests. Both male and female SAM offspring showed increased latency to enter open arms and reduced risk-assessment in the EPM, though females displayed anxiolytic-like behavior in the Light-Dark Box. Male SAM rats had reduced locomotion in the Open Field, earlier onset and increased immobility in the Forced Swim, and increased latency to groom in the Sucrose Splash. When exposed to acute stress, male SAM rats had lower FCM levels, consistent with their passive stress reactivity. These findings confirm SAM induces long-lasting, sex-specific changes in risk-taking, novelty responsiveness, and stress reactions, underscoring the importance of early nurturing in promoting well-being and reducing psychopathological risk.
- 18 February 2025
- Published by Springer Nature in Neurotoxicity Research
- Vol. 43 (2) , 1-18
Sex-Specific Outcomes in a Rat Model of Early-Life Stress Due to Adverse Caregiving
Early parental care is critical for the development of cortico-limbic circuits regulating stress responses and emotional well-being. Conversely, infant maltreatment can increase susceptibility to mood disorders—such as anxiety and depression—and impair stress-coping abilities. Here, we employed the Scarcity-Adversity Model (SAM) in rats, limiting nesting resources from postnatal days 8–12, to examine its effects on maternal and adult offspring behavior. SAM-exposed mothers exhibited fragmented care and increased violence towards pups. By postpartum day (PPD) 13, maternal fecal corticosterone metabolites (FCM) were elevated, indicating heightened stress. At weaning, SAM dams also showed increased anxiety-like behavior in the Elevated Plus Maze (EPM), suggesting significant emotional alterations. In adulthood, SAM-exposed offspring underwent anxiogenic tests. Both male and female SAM offspring showed increased latency to enter open arms and reduced risk-assessment in the EPM, though females displayed anxiolytic-like behavior in the Light-Dark Box. Male SAM rats had reduced locomotion in the Open Field, earlier onset and increased immobility in the Forced Swim, and increased latency to groom in the Sucrose Splash. When exposed to acute stress, male SAM rats had lower FCM levels, consistent with their passive stress reactivity. These findings confirm SAM induces long-lasting, sex-specific changes in risk-taking, novelty responsiveness, and stress reactions, underscoring the importance of early nurturing in promoting well-being and reducing psychopathological risk.