McManus O B, Harris G H, Giangiacomo K M, Feigenbaum P, Reuben J P, Addy M E, Burka J F, Kaczorowski G J, Garcia M L
Department of Membrane Biochemistry and Biophysics, Merck Research Laboratories, Rahway, New Jersey 07065.
Biochemistry. 1993 Jun 22;32(24):6128-33. doi: 10.1021/bi00075a002.
Large-conductance calcium-dependent potassium (maxi-K) channels play an important role in regulating the tone of airway smooth muscle and the release of bronchoconstrictive substances from nerves in the lung. Crude extracts of Desmodium adscendens, a medicinal herb used in Ghana as a treatment for asthma, inhibit binding of monoiodotyrosine charybdotoxin (125I-ChTX) to receptor sites in bovine tracheal smooth muscle membranes that have been shown to be associated with maxi-K channels. Using this assay, three active components have been purified and identified by NMR and MS. Comparison with authentic samples revealed the three active components as the known triterpenoid glycosides dehydrosoyasaponin I (DHS-I), soyasaponin I, and soyasaponin III. The most potent of these compounds, DHS-I, is a partial inhibitor of 125I-ChTX binding (Ki = 120 nM, 62% maximum inhibition). Inhibition of 125I-ChTX binding is primarily due to a decrease in the observed maximum number of binding sites, with a smaller decrease in affinity. DHS-I increases the rate of toxin dissociation from its receptor, suggesting that modulation of ChTX binding occurs through an allosteric mechanism. DHS-I reversibly increases the open probability of maxi-K channels from bovine tracheal smooth muscle incorporated into planar lipid bilayers when applied to the intracellular, but not the extracellular, side of the membrane at concentrations as low as 10 nM. In contrast, DHS-I had no effect on several other types of potassium channels or membrane transporters. This natural product is the first example of a high-affinity activator of calcium-dependent potassium channels and is the most potent known potassium channel opener.
大电导钙依赖性钾通道(大电导钾通道)在调节气道平滑肌张力以及肺部神经释放支气管收缩物质方面发挥着重要作用。在加纳被用作治疗哮喘的药用植物攀援山蚂蝗的粗提物,可抑制单碘酪氨酸美洲蝎毒素(125I - ChTX)与牛气管平滑肌膜上已被证明与大电导钾通道相关的受体位点的结合。利用该检测方法,通过核磁共振(NMR)和质谱(MS)已纯化并鉴定出三种活性成分。与标准样品比较后发现,这三种活性成分是已知的三萜糖苷脱氢大豆皂苷I(DHS - I)、大豆皂苷I和大豆皂苷III。这些化合物中活性最强的DHS - I是125I - ChTX结合的部分抑制剂(Ki = 120 nM,最大抑制率为62%)。125I - ChTX结合的抑制主要是由于观察到的结合位点最大数量减少,亲和力降低幅度较小。DHS - I增加了毒素从其受体解离的速率,表明ChTX结合的调节是通过变构机制发生的。当以低至10 nM的浓度应用于膜的胞内侧而非胞外侧时,DHS - I可逆地增加了整合到平面脂质双分子层中的牛气管平滑肌大电导钾通道的开放概率。相比之下,DHS - I对其他几种类型的钾通道或膜转运体没有影响。这种天然产物是钙依赖性钾通道高亲和力激活剂的首个实例,也是已知最有效的钾通道开放剂。