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DOI 10.1080/13880209.2017.1412468

Медицинская библиотека · Pharmaceutical biology · 2018

The suppressive effect of the three-herb extract mixture on vascular and liver inflammation in atherogenic diet with high fructose-fed mice.

Song Hae Seong, Koo Hyun Jung, Park Bong Kyun, Kwon Jeong Eun, Jang Seon-A, Baek Hyun Jin, Kim Se Young, Lee Sung Ryul, Kang Se Chan

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Аннотация

CONTEXT: Cynanchum wilfordii (Maximowicz) Hemsley (Apocynaceae), Arctium lappa L. var. rubescens Frivald (Asteraceae) and Dioscorea opposite Thunb (Dioscoreaceae) root extracts have been widely used as an alternative for intervening obesity.

OBJECTIVES

The synergistic effect of three-herb mixture of C. wilfordii, A. lappa and D. opposita was determined on aortic and liver inflammatory responses.

MATERIALS AND

METHODS

CWE, ALE and DOE were prepared from the root of C. wilfordii, A. lappa and D. opposite by 70% ethanol extraction, respectively. CADE was prepared using a powder mixture of 2 CWE:1 ALE:1 DOE. C57BL/6 mice were fed an atherogenic diet combined with 10% fructose (ATHFR) in the presence of 200 mg/kg/day CWE, ALE, DOE or CADE for 8 weeks (each group, n = 6). Biochemical profiles, protein expression of vascular cell adhesion molecule-1 (VCAM-1) on the aorta and liver were determined.

RESULTS

CADE could significantly suppress the protein expression of VCAM-1 in both the aorta and liver (80% reduction) compared to ATHFR-fed mice. Impairment of liver function was significantly ameliorated by CADE supplement, as determined by GOT (60% reduction) and GPT (51% reduction) levels.

CONCLUSIONS

CADE should be considered when developing medications to suppress the vascular and liver inflammatory responses for individuals who are either non-responsive or resistant to lipid-lowering drugs.

Для цитирования: Song Hae Seong, Koo Hyun Jung, Park Bong Kyun, Kwon Jeong Eun, Jang Seon-A, Baek Hyun Jin, Kim Se Young, Lee Sung Ryul, Kang Se Chan. The suppressive effect of the three-herb extract mixture on vascular and liver inflammation in atherogenic diet with high fructose-fed mice.. Pharmaceutical biology. 2018. DOI: 10.1080/13880209.2017.1412468.

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