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Orthogonal Array Design for Antidepressant Compatibility of Polysaccharides from Banxia-Houpu Decoction, a Traditional Chinese Herb Prescription in the Mouse Models of Depression
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  • Orthogonal Array Design for Antidepressant Compatibility of Polysaccharides from Banxia-Houpu Decoction, a Traditional Chinese Herb Prescription in the Mouse Models of Depression
  • Orthogonal Array Design for Antidepressant Compatibility of Polysaccharides from Banxia-Houpu Decoction, a Traditional Chinese Herb Prescription in the Mouse Models of Depression
저자명
Yi. Li-Tao,Zhang. Li,Ding. An-Wei,Xu. Qun,Zhu. Qin,Kong. Ling-Dong
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2009년|32권 10호|pp.1417-1423 (7 pages)
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대한약학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The present study investigated antidepressant-like interaction of five herb polysaccharide fractions from Banxia-Houpu decoction, composed of rhizome pinelliae (PRP), magnolia bark (PMB), poria (PPO), ginger rhizome (PGR) and folium perillae (PFP) by a $L_{16}(2^5)$ orthogonal array design with a two-factor interaction in the tail suspension and forced swimming and tests (TST, FST) in mice. Serotonin (5-HT) and dopamine (DA) levels in whole mouse brain were simultaneously examined after the FST exposure. Polysaccharides PMB, PPO, PFP, and interactions of PRP ${ imes}$ PGR, PMB ${ imes}$ PFP, PPO ${ imes}$ PFP reduced immobility in the mouse FST. Furthermore, PMB and PPO were two principal components of polysaccharides elevating brain 5-HT levels. PFP was an adjuvant component elevating brain DA levels. These results demonstrated that ineffective PRP exhibited antidepressant-like effects when combined with another ineffective PGR, and PFP played a role in assisting effects of PMB and PPO. Therefore, PMB ${ imes}$ PFP and PPO ${ imes}$ PFP interactions on antidepressant-like effects were the cores in compatibility of polysaccharides from Banxia-Houpu decoction by attenuating abnormalities in the serotonergic and dopaminergic system functions in animal models of depression.