Here, we investigated the protein network regulating cholesterol metabolism in the liver and brain of adolescent and adult male and female rats prenatally exposed to valproate (VPA), a well validated experimental model of autism spectrum disorders (ASD). We were aimed at studying whether prenatal VPA exposure affected the proteins involved in cholesterol homeostasis in a sex-dependent manner. To this aim the protein network of cholesterol metabolism, in term of synthesis and plasma membrane trafficking, was analyzed by Western blot in liver and different brain areas (Amygdala, Cerebellum, Cortex, Hippocampus, Nucleus accumbens, and Dorsal striatum) of adolescent and adult male and female rats prenatally exposed to VPA. Our results show that physiological sex-dependent differences are present both in liver and in brain of rats. Interestingly, VPA affects specifically the brain in an age- and region-specific manner; indeed, Cerebellum, Cortex, Hippocampus and Nucleus accumbens are affected in a sex-dependent way, while this does not occur in Amygdala and Dorsal striatum. Overall, we demonstrate that each brain area responds differently to the same external stimulus and males and females respond in a different way, suggesting that this could be related to the diverse incidences, between the sexes, of some neurodevelopmental pathologies such as autism, which displays a 3:1 male to female ratio.

Cartocci, V., Tonini, C., Tiziana Di Pippo, ., Florenzia, V., Schiavi, S., Marino, M., et al. (2019). Prenatal exposure to valproate induces sex-, age- and tissue-dependent alterations of cholesterol metabolism: potential implications on autism. JOURNAL OF CELLULAR PHYSIOLOGY, 234(4), 4362-4374 [10.1002/jcp.27218].

Prenatal exposure to valproate induces sex-, age- and tissue-dependent alterations of cholesterol metabolism: potential implications on autism.

Veronica Cartocci
Membro del Collaboration Group
;
TONINI, CLAUDIA
Membro del Collaboration Group
;
Sara Schiavi
Membro del Collaboration Group
;
Maria Marino
Membro del Collaboration Group
;
Viviana Trezza
Membro del Collaboration Group
;
Valentina Pallottini
Supervision
2019-01-01

Abstract

Here, we investigated the protein network regulating cholesterol metabolism in the liver and brain of adolescent and adult male and female rats prenatally exposed to valproate (VPA), a well validated experimental model of autism spectrum disorders (ASD). We were aimed at studying whether prenatal VPA exposure affected the proteins involved in cholesterol homeostasis in a sex-dependent manner. To this aim the protein network of cholesterol metabolism, in term of synthesis and plasma membrane trafficking, was analyzed by Western blot in liver and different brain areas (Amygdala, Cerebellum, Cortex, Hippocampus, Nucleus accumbens, and Dorsal striatum) of adolescent and adult male and female rats prenatally exposed to VPA. Our results show that physiological sex-dependent differences are present both in liver and in brain of rats. Interestingly, VPA affects specifically the brain in an age- and region-specific manner; indeed, Cerebellum, Cortex, Hippocampus and Nucleus accumbens are affected in a sex-dependent way, while this does not occur in Amygdala and Dorsal striatum. Overall, we demonstrate that each brain area responds differently to the same external stimulus and males and females respond in a different way, suggesting that this could be related to the diverse incidences, between the sexes, of some neurodevelopmental pathologies such as autism, which displays a 3:1 male to female ratio.
2019
Cartocci, V., Tonini, C., Tiziana Di Pippo, ., Florenzia, V., Schiavi, S., Marino, M., et al. (2019). Prenatal exposure to valproate induces sex-, age- and tissue-dependent alterations of cholesterol metabolism: potential implications on autism. JOURNAL OF CELLULAR PHYSIOLOGY, 234(4), 4362-4374 [10.1002/jcp.27218].
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11590/338031
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 13
  • ???jsp.display-item.citation.isi??? 13
social impact