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Effect of Valeriana fauriei Extract on the Neurodevelopmental Proteins Expression and Behavioral Patterns in Maternal Immune Activation Animal Modelopen access쥐오줌풀 추출물이 MIA동물모델에서의 신경발달 단백질의 발현과 행동증상에 미치는 영향

Authors
원한솔김영옥이화영임지윤이상현조익현이상원박춘근김형기권준택김학재
Issue Date
Oct-2016
Publisher
한국약용작물학회
Keywords
Valeriana fauriei Briq.; Maternal Immune Activation; Polyriboinosinic-Polyribocytidilic Acid; Schizophrenia
Citation
한국약용작물학회지, v.24, no.5, pp 341 - 350
Pages
10
Journal Title
한국약용작물학회지
Volume
24
Number
5
Start Page
341
End Page
350
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/7867
DOI
10.7783/KJMCS.2016.24.5.341
ISSN
1225-9306
Abstract
Background: Prenatal exposure to infectious and/or inflammatory insults can increase the risk of developing neuropsychiatric disorder such as bipolar disorder, autism, and schizophrenia later in life. We investigated whether Valeriana fauriei (VF) treatment alleviates prepulse inhibition (PPI) deficits and social interaction impairment induced by maternal immune activation (MIA). Methods and Results: Pregnant mice were exposed to polyriboinosinic-polyribocytidilic acid (5㎎/㎏, viral infection mimic) on gestational day 9. The adolescent offspring received daily oral treatment with VF (100㎎/㎏) and injections of clozapine (5㎎/㎏) for 30 days starting on the postnatal day 35. The effects of VF extract treatment on behavioral activity impairment and protein expression were investigated using the PPI analysis, forced swim test (FST), open field test (OFT), social interaction test (SIT), and immunohistochemistry. The MIA-induced offspring showed deficits in the PPI, FST, OFT, and SIT compared to their non MIAinduced counterparts. Treatment with the VF extract significantly recovered the sensorimotor gating deficits and partially recovered the aggressive behavior observed in the SIT. The VF extract also reversed the downregulation of protein expression induced by MIA in the medial prefrontal cortex. Conclusions: Our results provide initial evidence of the fact that the VF extract could reverse MIA-induced behavioral impairment and prevent neurodevelopmental disorders such as schizophrenia.
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