Background: Autism Spectrum Disorder (ASD) is defined by ongoing problems in social interaction and communication and repetitive, constrained behavior patterns. The link between oxidative stress (OS) and inflammation with ASD has been shown in previous studies. E. purpurea is well-known for its potential antioxidant and anti-inflammatory pharmacological properties. In this study, we aimed to evaluate the effects of E. purpurea hydroalcoholic extract on autistic-like behaviors following a mouse model of maternal separation (MS) stress, focusing on possible anti-neuroinflammation and antioxidative stress.
Methods: 70% hydro-ethanolic extract was macerated from the aerial parts of E. purpurea. Standardization was done by determining the amount of chicoric acid in the extract using the UHPLC method. Then, behavioral analysis was done on 75 male mice that underwent MS. Mice were treated with normal saline or 75, 150, and 300 mg/kg of the extract. Sociability behaviors and stereotyping behaviors have been evaluated. Also, their total antioxidant capacity (TAC), nitrite levels, and malondialdehyde (MDA) were measured in the hippocampus. In addition, the expression of inflammatory factors, including interleukin-1 (IL-1), NLRP3, and TLR4, has been determined by quantitative real-time PCR (qRT-PCR). Data were analyzed after collection using PRISM statistical software.
Results: Our findings indicated that MS caused autistic-like behaviors in mice (increased sociability index and social preference index) and increased repetitive behaviors (increased number of buried marbles). These autistic-like behaviors are associated with increased MDA, nitrite, over-expression of inflammatory genes, decreased MDA, nitrite, over-expression of inflammatory genes, and decreased TAC in the hippocampus. E. purpurea extract significantly reversed these adverse effects of MS.
Conclusion: The results of this study showed that E. purpurea extract might reduce autistic-like behaviors in MS by attenuating neuroinflammation and oxidative stress states.
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http://dx.doi.org/10.1016/j.jpsychires.2025.02.038 | DOI Listing |
Sci Rep
March 2025
Department of Experimental Medicine, University of Rome Tor Vergata, Via Montpellier, 1, 00133, Rome, Italy.
Endogenous retroviruses (ERVs) are genetic elements derived from a process of germline infection by exogenous retroviruses. Some ERVs have been co-opted for physiological functions, and their activation has been associated with complex diseases, including Autism Spectrum Disorder (ASD). We have already demonstrated an abnormal expression of ERVs in the BTBR T + tf/J (BTBR) mouse model of ASD during intrauterine life till adulthood.
View Article and Find Full Text PDFJ Psychiatr Res
February 2025
Medical Plants Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address:
Background: Autism Spectrum Disorder (ASD) is defined by ongoing problems in social interaction and communication and repetitive, constrained behavior patterns. The link between oxidative stress (OS) and inflammation with ASD has been shown in previous studies. E.
View Article and Find Full Text PDFIntroduction: Group B Streptococcus (GBS) colonization lead to placental infection and inflammation, known as chorioamnionitis (CA). Fetal exposure to CA is linked to elevated risks of neurobehavioral impairments in offspring, including autism spectrum disorder, which is more prominent in males than females. In our preclinical model of GBS-induced CA, males exhibited heightened placental inflammation compared to females, correlating with more severe subsequent neurobehavioral impairments.
View Article and Find Full Text PDFFront Neurosci
February 2025
The Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Zhejiang University School of Medicine, Hangzhou, China.
Background: Increasing evidence have shown that gestational diabetes mellitus (GDM) is associated with the risk of autism in offspring. However, the underlying mechanisms have not yet been fully elucidated.
Methods: A mouse model of gestational diabetes mellitus (GDM) was established to investigate its impact on offspring.
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