Journal
GENE
Volume 828, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.gene.2022.146440
Keywords
Autism spectrum disorder (ASD); Autism; Electroacupuncture; Zusanli (ST36); Nrf2
Categories
Funding
- Major Project of Synergistic Innovation in Zhengzhou (Zhengzhou University) [18XTZX12003]
- Henan Medical Science and Technology Research Project [LHGJ20190410]
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This study found that electroacupuncture at ST36 can improve autistic-like behaviors and nerve function in rats by activating Nrf2 and the antioxidant response.
Objective: Emerging evidence suggests that acupuncture plays a neumprotective role in autism. This study aimed to explore the effect of electroacupuncture at Zusanli (ST36) on autistic-like behaviors and the underlying mechanism. Method: Pregnant rats were administered with valpmic acid (VPA) on gestational day 12.5 to induce an autism spectrum disorder (ASD) model. The pups were given electroacupuncture at ST36 daily from postnatal day (PND) 28-48. On PND28, the adenoviral vector containing small interfering RNA Nrf2 (Ad-siRNA-Nrf2) was injected into the prefrontal cortex of rats. The behavioral analysis was performed on PND 44-48. On PND48, the animals were euthanized and the brains were collected for further detection. Nissl staining was performed to detect neuronal viability. The biochemical markers of oxidative stress were subsequently measured. Result: Electroacupuncture at ST36 ameliorated the locomotor activity, social behavior, spatial learning and memory and repetitive behavior compared with ASD rats. It was notable that the electroacupuncture decreased oxidative stress markers in the tissues of prefrontal cortex, enhanced translocation of nuclear factor erythroid2-related factor2 (Nrf2) from cytoplasm to nucleus, and up-regulated the levels of NADP(H) quinone oxidoreductase (NQO1) and heme oxygenase (HO-1). However, these effects induced by electroacupuncture at ST36 were abolished after injection of Ad-siRNA-Nrf2. Conclusion: These data suggested that electroacupuncture at ST36 protected nerve function in ASD rats through Nrf2 activation and the antioxidant response.
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