Cargando…
Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats
Prenatal stress impairs cognitive function in rats, while Piromelatine treatment corrects memory decline in male rats with chronic mild stress. In the present study, we aimed to evaluate the effect of chronic treatment with the melatonin analogue Piromelatine on the associative and spatial hippocamp...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864968/ https://www.ncbi.nlm.nih.gov/pubmed/36674787 http://dx.doi.org/10.3390/ijms24021271 |
_version_ | 1784875718853787648 |
---|---|
author | Ivanova, Natasha Atanasova, Milena Nenchovska, Zlatina Tchekalarova, Jana |
author_facet | Ivanova, Natasha Atanasova, Milena Nenchovska, Zlatina Tchekalarova, Jana |
author_sort | Ivanova, Natasha |
collection | PubMed |
description | Prenatal stress impairs cognitive function in rats, while Piromelatine treatment corrects memory decline in male rats with chronic mild stress. In the present study, we aimed to evaluate the effect of chronic treatment with the melatonin analogue Piromelatine on the associative and spatial hippocampus-dependent memory of male and female offspring with a history of prenatal stress (PNS). We report that male and female young adult offspring with PNS treated with a vehicle had reduced memory responses in an object recognition test (ORT). However, the cognitive performance in the radial arm maze test (RAM) was worsened only in the male offspring. The 32-day treatment with Piromelatine (20 mg/kg, i.p.) of male and female offspring with PNS attenuated the impaired responses in the ORT task. Furthermore, the melatonin analogue corrected the disturbed spatial memory in the male offspring. While the ratio of phosphorylated and nonphosphorylated adenosine monophosphate response element binding protein (pCREB/CREB) was reduced in the two sexes with PNS and treated with a vehicle, the melatonin analogue elevated the ratio of these signaling molecules in the hippocampus of the male rats only. Our results suggest that Piromelatine exerts a beneficial effect on PNS-induced spatial memory impairment in a sex-dependent manner that might be mediated via the pCREB/CREB pathway. |
format | Online Article Text |
id | pubmed-9864968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98649682023-01-22 Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats Ivanova, Natasha Atanasova, Milena Nenchovska, Zlatina Tchekalarova, Jana Int J Mol Sci Article Prenatal stress impairs cognitive function in rats, while Piromelatine treatment corrects memory decline in male rats with chronic mild stress. In the present study, we aimed to evaluate the effect of chronic treatment with the melatonin analogue Piromelatine on the associative and spatial hippocampus-dependent memory of male and female offspring with a history of prenatal stress (PNS). We report that male and female young adult offspring with PNS treated with a vehicle had reduced memory responses in an object recognition test (ORT). However, the cognitive performance in the radial arm maze test (RAM) was worsened only in the male offspring. The 32-day treatment with Piromelatine (20 mg/kg, i.p.) of male and female offspring with PNS attenuated the impaired responses in the ORT task. Furthermore, the melatonin analogue corrected the disturbed spatial memory in the male offspring. While the ratio of phosphorylated and nonphosphorylated adenosine monophosphate response element binding protein (pCREB/CREB) was reduced in the two sexes with PNS and treated with a vehicle, the melatonin analogue elevated the ratio of these signaling molecules in the hippocampus of the male rats only. Our results suggest that Piromelatine exerts a beneficial effect on PNS-induced spatial memory impairment in a sex-dependent manner that might be mediated via the pCREB/CREB pathway. MDPI 2023-01-09 /pmc/articles/PMC9864968/ /pubmed/36674787 http://dx.doi.org/10.3390/ijms24021271 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ivanova, Natasha Atanasova, Milena Nenchovska, Zlatina Tchekalarova, Jana Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats |
title | Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats |
title_full | Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats |
title_fullStr | Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats |
title_full_unstemmed | Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats |
title_short | Sex-Dependent Effect of Chronic Piromelatine Treatment on Prenatal Stress-Induced Memory Deficits in Rats |
title_sort | sex-dependent effect of chronic piromelatine treatment on prenatal stress-induced memory deficits in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864968/ https://www.ncbi.nlm.nih.gov/pubmed/36674787 http://dx.doi.org/10.3390/ijms24021271 |
work_keys_str_mv | AT ivanovanatasha sexdependenteffectofchronicpiromelatinetreatmentonprenatalstressinducedmemorydeficitsinrats AT atanasovamilena sexdependenteffectofchronicpiromelatinetreatmentonprenatalstressinducedmemorydeficitsinrats AT nenchovskazlatina sexdependenteffectofchronicpiromelatinetreatmentonprenatalstressinducedmemorydeficitsinrats AT tchekalarovajana sexdependenteffectofchronicpiromelatinetreatmentonprenatalstressinducedmemorydeficitsinrats |