Ilex kudingcha extract ameliorates alterations in behaviors, neurochemical markers and Purkinje cells in the sodium valproate murine model of autism spectrum disorder

被引:0
|
作者
Pham, Hang Thi Nguyet [1 ,2 ]
Nguyen, Ly Thi [1 ]
Le, Xoan Thi [1 ]
Do, Ha Thi [3 ]
Nguyen, Chien Le [4 ]
Vu, Tung Manh [5 ]
Matsumoto, Kinzo [6 ]
Lei, Zhentian [7 ]
Folk, William R. [7 ]
机构
[1] Natl Inst Med Mat, Dept Pharmacol & Biochem, Hanoi 100000, Vietnam
[2] Vietnam Natl Univ, Univ Med & Pharm, Hanoi 100000, Vietnam
[3] Natl Inst Med Mat, Dept Analyt Chem & Standardizat, Hanoi 100000, Vietnam
[4] Mil Med Acad, Hanoi 100000, Vietnam
[5] Monash Univ, Parkville, Vic 3052, Australia
[6] Daiichi Univ Pharm, Ctr Supporting Pharmaceut Educ, Fukuoka 8158511, Japan
[7] Univ Missouri, Dept Biochem, Columbia, MO 65211 USA
关键词
Ilex kudingcha; Autism spectrum disorder; PTEN protein; Purkinje cells; OXIDATIVE STRESS; IN-VITRO; MICE; DEFICITS; SUPPLEMENTATION; INVOLVEMENT; MICROBIOTA; ACID; RATS; TEA;
D O I
10.1007/s13596-024-00758-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ilex kudingcha C.J. Tseng is a nootropic used throughout Asia that shares a number of metabolites with Ilex paraguariensis used throughout South America. Our previous study using a Drosophila melanogaster rugose model of autism spectrum disorders (ASD) showed that consumption of an Ilex kudingcha extract (IKE) mitigates phenotypic characteristics of ASD and in normal mice, alters gene expression involved in cognition, metabolism, and protein synthesis. This study investigated the effects of IKE on prenatal sodium valproate (VPA) treatment-induced ASD core behavioral deficits and ASD associated behaviors, neurochemical markers and histological changes. IKE administration significantly mitigated these behavioral deficits and damaged Purkinje cells, PTEN expression and oxidative stress and resembled treatment with methylphenidate in its effect upon social behavior. These findings extend our previous study with D. melanogaster and together, indicate that IKE consumption ameliorates ASD-like properties in two animal models of ASD with different etiologies. Potential mechanisms involve reduction of oxidative stress, increased PTEN expression and cerebral Purkinje cell health. These data support further studies of IKE and related species for treatment of ASD. [GRAPHICS] .
引用
收藏
页码:1065 / 1077
页数:13
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