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논문 기본 정보

자료유형
학술저널
저자정보
Park, Byung Kyu (College of Pharmacy, Kangwon National University) So, Kyung Su (College of Pharmacy, Kangwon National University) Ko, Hye Jung (College of Pharmacy, Kangwon National University) Kim, Hyun Joong (College of Pharmacy, Kangwon National University) Kwon, Ki Sun (College of Pharmacy, Kangwon National University) Kwon, Yong Soo (College of Pharmacy, Kangwon National University) Son, Kun Ho (Department of Food and Nutrition, Andong National University) Kwon, Soon Youl (Gyeongbuk Institute for Bio Industry) Kim, Hyun Pyo (College of Pharmacy, Kangwon National University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제26권 제6호
발행연도
2018.1
수록면
553 - 559 (7page)

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Investigations into the development of new therapeutic agents for lung inflammatory disorders have led to the discovery of plant-based alternatives. The rhizomes of Anemarrhena asphodeloides have a long history of use against lung inflammatory disorders in traditional herbal medicine. However, the therapeutic potential of this plant material in animal models of lung inflammation has yet to be evaluated. In the present study, we prepared the alcoholic extract and derived the saponin-enriched fraction from the rhizomes of A. asphodeloides and isolated timosaponin A-III, a major constituent. Lung inflammation was induced by intranasal administration of lipopolysaccharide (LPS) to mice, representing an animal model of acute lung injury (ALI). The alcoholic extract (50-200 mg/kg) inhibited the development of ALI. Especially, the oral administration of the saponin-enriched fraction (10-50 mg/kg) potently inhibited the lung inflammatory index. It reduced the total number of inflammatory cells in the bronchoalveolar lavage fluid (BALF). Histological changes in alveolar wall thickness and the number of infiltrated cells of the lung tissue also indicated that the saponin-enriched fraction strongly inhibited lung inflammation. Most importantly, the oral administration of timosaponin A-III at 25-50 mg/kg significantly inhibited the inflammatory markers observed in LPS-induced ALI mice. All these findings, for the first time, provide evidence supporting the effectiveness of A. asphodeloides and its major constituent, timosaponin A-III, in alleviating lung inflammation.

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