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PMID: 7685635 Published · ppublish English Journal Article

An activator of calcium-dependent potassium channels isolated from a medicinal herb.

Biochemistry ·Vol. 32 ·No. 24 ·1993-06-22 ·Pages 6128-33

McManus OB, Harris GH, Giangiacomo KM, Feigenbaum P, Reuben JP, Addy ME, Burka JF, Kaczorowski GJ, Garcia ML

Abstract

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.

MeSH Terms
Animals Calcium/metabolism Cattle Charybdotoxin In Vitro Techniques Ion Channel Gating Magnetic Resonance Spectroscopy Mass Spectrometry Muscle, Smooth/drug effects,metabolism,physiology Oleanolic Acid/analogs & derivatives Plant Extracts/pharmacology Plants, Medicinal/chemistry Potassium Channels/drug effects,metabolism Saponins/pharmacology Scorpion Venoms/metabolism Structure-Activity Relationship Triterpenes/pharmacology
Chemicals
Plant Extracts Potassium Channels Saponins Scorpion Venoms Triterpenes Charybdotoxin dehydrosoyasaponin I soyasaponin I soyasaponin III Oleanolic Acid Calcium
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
McManus O B
Department of Membrane Biochemistry and Biophysics, Merck Research Laboratories, Rahway, New Jersey 07065.
Harris G H
Giangiacomo K M
Feigenbaum P
Reuben J P
Addy M E
Burka J F
Kaczorowski G J
Garcia M L
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1993-06-22
Pages
6128-33
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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