Trinchese Giovanna, Cimmino Fabiano, Cavaliere Gina, Catapano Angela, Fogliano Chiara, Lama Adriano, Pirozzi Claudio, Cristiano Claudia, Russo Roberto, Petrella Lidia, Meli Rosaria, Mattace Raso Giuseppina, Crispino Marianna, Avallone Bice, Mollica Maria Pina
Department of Biology, University of Naples Federico II, 80126 Naples, Italy.
Department of Pharmaceutical Sciences, University of Perugia, 06123 Perugia, Italy.
Antioxidants (Basel). 2022 Oct 7;11(10):1990. doi: 10.3390/antiox11101990.
The role of the liver in autism spectrum disorders (ASD), developmental disabilities characterized by impairments in social interactions and repetitive behavioral patterns, has been poorly investigated. In ASD, it has been shown a dysregulation of gut-brain crosstalk, a communication system able to influence metabolic homeostasis, as well as brain development, mood and cognitive functions. The liver, with its key role in inflammatory and metabolic states, represents the crucial metabolic organ in this crosstalk. Indeed, through the portal vein, the liver receives not only nutrients but also numerous factors derived from the gut and visceral adipose tissue, which modulate metabolism and hepatic mitochondrial functions. Here, we investigated, in an animal model of ASD (BTBR mice), the involvement of hepatic mitochondria in the regulation of inflammatory state and liver damage. We observed increased inflammation and oxidative stress linked to hepatic mitochondrial dysfunction, steatotic hepatocytes, and marked mitochondrial fission in BTBR mice. Our preliminary study provides a better understanding of the pathophysiology of ASD and could open the way to identifying hepatic mitochondria as targets for innovative therapeutic strategies for the disease.
肝脏在自闭症谱系障碍(ASD)中的作用尚未得到充分研究,ASD是一种以社交互动障碍和重复行为模式为特征的发育障碍。在ASD中,已发现肠-脑串扰失调,这是一种能够影响代谢稳态以及大脑发育、情绪和认知功能的通信系统。肝脏在炎症和代谢状态中起关键作用,是这种串扰中的关键代谢器官。实际上,肝脏通过门静脉不仅接收营养物质,还接收来自肠道和内脏脂肪组织的多种因子,这些因子调节代谢和肝线粒体功能。在此,我们在ASD动物模型(BTBR小鼠)中研究了肝线粒体在炎症状态调节和肝损伤中的作用。我们观察到,BTBR小鼠中与肝线粒体功能障碍、脂肪变性肝细胞和明显的线粒体分裂相关的炎症和氧化应激增加。我们的初步研究有助于更好地理解ASD的病理生理学,并可能为将肝线粒体确定为该疾病创新治疗策略的靶点开辟道路。