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Title:Hepatic alterations in a BTBR T + Itpr3tf/J mouse model of autism and improvement using melatonin via mitigation oxidative stress, inflammation and ferroptosis
Authors:ID Rezzani, Rita (Author)
ID Gianò, Marzia (Author)
ID Pinto, Daniela (Author)
ID Rinaldi, Fabio (Author)
ID Noorden, Cornelis J. F. van (Author)
ID Favero, Gaia (Author)
Files:URL URL - Source URL, visit https://www.mdpi.com/1422-0067/25/2/1086
 
.pdf PDF - Presentation file, download (12,47 MB)
MD5: 335DEDB060BD841A9D8D6311D16F8742
 
URL URL - Source URL, visit https://doi.org/10.3390/ijms25021086
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Abstract:Autism spectrum disorder (ASD) is a complicated neurodevelopmental disorder, and its etiology is not well understood. It is known that genetic and nongenetic factors determine alterations in several organs, such as the liver, in individuals with this disorder. The aims of the present study were to analyze morphological and biological alterations in the liver of an autistic mouse model, BTBR T + Itpr3tf/J (BTBR) mice, and to identify therapeutic strategies for alleviating hepatic impairments using melatonin administration. We studied hepatic cytoarchitecture, oxidative stress, inflammation and ferroptosis in BTBR mice and used C57BL6/J mice as healthy control subjects. The mice were divided into four groups and then treated and not treated with melatonin, respectively. BTBR mice showed (a) a retarded development of livers and (b) iron accumulation and elevated oxidative stress and inflammation. We demonstrated that the expression of ferroptosis markers, the transcription factor nuclear factor erythroid-related factor 2 (NFR2), was upregulated, and the Kelch-like ECH-associated protein 1 (KEAP1) was downregulated in BTBR mice. Then, we evaluated the effects of melatonin on the hepatic alterations of BTBR mice; melatonin has a positive effect on liver cytoarchitecture and metabolic functions.
Keywords:autism spectrum disorder, liver, oxidative stress, inflammation, ferroptosis
Publication status:Published
Publication version:Version of Record
Publication date:16.01.2024
Year of publishing:2024
Number of pages:str. 1-20
Numbering:Vol. 25, no. 2, [article no.] 1086
PID:20.500.12556/DiRROS-20180 New window
UDC:577.2
ISSN on article:1422-0067
DOI:10.3390/ijms25021086 New window
COBISS.SI-ID:190985987 New window
Note:Nasl. z nasl. zaslona; Soavtorji: Marzia Gianò, Daniela Pinto, Fabio Rinaldi, Cornelis J. F. van Noorden and Gaia Favero; Opis vira z dne 31. 3. 2024;
Publication date in DiRROS:07.08.2024
Views:13
Downloads:7
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Record is a part of a journal

Title:International journal of molecular sciences
Shortened title:Int. j. mol. sci.
Publisher:MDPI
ISSN:1422-0067
COBISS.SI-ID:2779162 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0245-2019
Name:Ekotoksiologija, toksikološka genomika in karcinogeneza

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-2526-2020
Name:Razkrivanje niše matičnih glioma celic v iskanju novih terapevtskih ciljev pri bolnikih z glioblastomom

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License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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