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Depolarizing neuromuscular blocking action induced by electropharmacological coupling in the combined effect of paeoniflorin and glycyrrhizin.
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- KIMURA Masayasu
- Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University
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- KIMURA Ikuko
- Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University
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- NOJIMA Hiroshi
- Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University
Bibliographic Information
- Other Title
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- Depolarizing neuromuscular blocking action induced by electropharmacological coupling in the combined effect of paeomflorin and glycyrrhizin
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Description
Twitch tensions of indirectly stimulated diaphragm muscles of mice were blocked by a combination of paeoniflorin (PF) and glycyrrhizin (GLR). The mechanism of this effect was studied electropharmacologically. When twitch responses were completely prevented, miniature end-plate, end-plate, and muscle action potentials were still observed when PF and GLR were combined, suggesting that the mechanism is postsynaptic. Potential amplitudes induced by acetylcholine (ACh), which was injected iontophoretically, were inhibited by about 70% by PF (25 μg/ml) plus GLR (75 μg/ml), although neither agent alone caused an inhibition. The combined ratio (PF:GLR=1:3) by concentrations (g/ml) potentiated both the inhibition of ACh potential amplitudes and the depolarization of resting membrane potentials. These results indicate that the effect of combined PF and GLR is to depolarize the muscle membrane and to block ACh-receptor-linked processes. In chemically skinned (saponin-treated) muscles, the tension induced by 0.39 μM of free calcium was inhibited by PF (300 μg/ml), but it tended to be increased by GLR (300 μg/ml). Caffeine-induced contractures in the skinned muscles was not influenced by PF, and they tended to be decreased with GLR treatment. Thus, in muscles with sustained depolarization, these combined compounds seem to block intracellular Ca2+ movement.
Journal
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- The Japanese Journal of Pharmacology
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The Japanese Journal of Pharmacology 37 (4), 395-399, 1985
The Japanese Pharmacological Society
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Keywords
Details 詳細情報について
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- CRID
- 1390282679263689984
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- NII Article ID
- 130000834905
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- COI
- 1:CAS:528:DyaL2MXhvFOrtbY%3D
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- ISSN
- 13473506
- 00215198
- http://id.crossref.org/issn/00215198
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- PubMed
- 4010089
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- Text Lang
- en
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- Article Type
- journal article
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- Data Source
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed