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Identification and Characterization of Baicalin as a Phosphodiesterase 4 Inhibitor
Author(s) -
Park Kyuhee,
Lee Jong Suk,
Choi Jung Suk,
Nam YeonJu,
Han JongHeon,
Byun HooDhon,
Song MyungJin,
Oh JoaSup,
Kim Sung Gyu,
Choi Yongmun
Publication year - 2016
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.5515
Subject(s) - baicalin , rolipram , pharmacology , phosphodiesterase , cyclic adenosine monophosphate , medicine , tumor necrosis factor alpha , chemistry , biochemistry , enzyme , immunology , high performance liquid chromatography , receptor , chromatography
Asthma is a chronic inflammatory disease of lung airways, and pharmacological inhibitors of cyclic adenosine monophosphate‐specific phosphodiesterase 4 (PDE4) have been considered as therapeutics for the treatment of asthma. However, development of PDE4 inhibitors in clinical trials has been hampered because of the severe side effects of non‐selective PDE4 inhibitors. Here, screening of a plant extract library in conjunction with dereplication technology led to identification of baicalin as a new type of PDE4‐selective inhibitor. We demonstrated that while rolipram inhibited the enzyme activity of a range of PDE4 subtypes in in vitro enzyme assays, baicalin selectively inhibited the enzyme activity of PDE4A and 4B. In addition, baicalin suppressed lipopolysaccharide‐induced TNF‐α expression in macrophage where PDE4B plays a key role in lipopolysaccharide‐induced signaling. Furthermore, baicalin treatment in an animal model of allergic asthma reduced inflammatory cell infiltration and TNF‐α levels in bronchoalveolar lavage fluids, indicating that the antiinflammatory effects of baicalin in vivo are attributable, in part, to its ability to inhibit PDE4. Copyright © 2015 John Wiley & Sons, Ltd.