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Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients

Processed aconite root (PA), the tuberous root of Aconitum carmichaelii prepared by autoclaving, is a crude drug used in Japanese traditional Kampo medicine and traditional Chinese medicine for the symptoms of kidney deficiency, that is related to the muscle atrophy in modern medicine. The objective...

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Autores principales: Kondo, Taishi, Ishida, Tomoaki, Ye, Ke, Muraguchi, Marin, Tanimura, Yohei, Yoshida, Masato, Ishiuchi, Kan’ichiro, Abe, Tomoki, Nikawa, Takeshi, Hagihara, Keisuke, Hayashi, Hidetoshi, Makino, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008256/
https://www.ncbi.nlm.nih.gov/pubmed/35178660
http://dx.doi.org/10.1007/s11418-022-01606-5
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author Kondo, Taishi
Ishida, Tomoaki
Ye, Ke
Muraguchi, Marin
Tanimura, Yohei
Yoshida, Masato
Ishiuchi, Kan’ichiro
Abe, Tomoki
Nikawa, Takeshi
Hagihara, Keisuke
Hayashi, Hidetoshi
Makino, Toshiaki
author_facet Kondo, Taishi
Ishida, Tomoaki
Ye, Ke
Muraguchi, Marin
Tanimura, Yohei
Yoshida, Masato
Ishiuchi, Kan’ichiro
Abe, Tomoki
Nikawa, Takeshi
Hagihara, Keisuke
Hayashi, Hidetoshi
Makino, Toshiaki
author_sort Kondo, Taishi
collection PubMed
description Processed aconite root (PA), the tuberous root of Aconitum carmichaelii prepared by autoclaving, is a crude drug used in Japanese traditional Kampo medicine and traditional Chinese medicine for the symptoms of kidney deficiency, that is related to the muscle atrophy in modern medicine. The objective of the present study is to evaluate the effectiveness of PA on muscle atrophy and to find its active ingredients using dexamethasone-induced muscle ring finger protein-1 (MuRF1) mRNA expression in murine myoblast C2C12 cells. Dexamethasone-induced MuRF1 expression was significantly suppressed by methanol-soluble part of boiling water extract of PA in a concentration-dependent manner with its IC(50) value of 1.5 mg/ml. By the activity-guided fractionations of PA extract using the partition between organic solvents and its aqueous solution, the activity of PA did not transfer into the fraction containing aconitine-type diterpenoid alkaloids but into BuOH layer. Then, we found higenamine and salsolinol as the active ingredients in PA. Higenamine and salsolinol significantly suppressed dexamethasone-induced MuRF1 expression, and their IC(50) values were 0.49 and 50 µM, respectively. The contents of higenamine and salsolinol in the decoctions of commercially available fourteen PA products are 0.12 and 14 µg/ml as the average values, and varied with the coefficient of variation (CV) values of 97 and 63%, respectively. Higenamine also significantly suppressed dexamethasone-induced mRNA expressions of muscle atrophy F-box protein (MAFbx)/atrogin1, casitas B-lineage lymphoma-b (Cbl-b), troponin, branched-chain amino acid aminotransferase 2 (BCAT2), and Bcl-2 binding and pro-apoptotic protein3 (Bnip3). Although the quality control of PA is regulated by the contents of diterpene alkaloids, salsolinol and higenamine can be used as the marker compounds to certificate the pharmacological activities of PA. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-100082562023-03-13 Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients Kondo, Taishi Ishida, Tomoaki Ye, Ke Muraguchi, Marin Tanimura, Yohei Yoshida, Masato Ishiuchi, Kan’ichiro Abe, Tomoki Nikawa, Takeshi Hagihara, Keisuke Hayashi, Hidetoshi Makino, Toshiaki J Nat Med Original Paper Processed aconite root (PA), the tuberous root of Aconitum carmichaelii prepared by autoclaving, is a crude drug used in Japanese traditional Kampo medicine and traditional Chinese medicine for the symptoms of kidney deficiency, that is related to the muscle atrophy in modern medicine. The objective of the present study is to evaluate the effectiveness of PA on muscle atrophy and to find its active ingredients using dexamethasone-induced muscle ring finger protein-1 (MuRF1) mRNA expression in murine myoblast C2C12 cells. Dexamethasone-induced MuRF1 expression was significantly suppressed by methanol-soluble part of boiling water extract of PA in a concentration-dependent manner with its IC(50) value of 1.5 mg/ml. By the activity-guided fractionations of PA extract using the partition between organic solvents and its aqueous solution, the activity of PA did not transfer into the fraction containing aconitine-type diterpenoid alkaloids but into BuOH layer. Then, we found higenamine and salsolinol as the active ingredients in PA. Higenamine and salsolinol significantly suppressed dexamethasone-induced MuRF1 expression, and their IC(50) values were 0.49 and 50 µM, respectively. The contents of higenamine and salsolinol in the decoctions of commercially available fourteen PA products are 0.12 and 14 µg/ml as the average values, and varied with the coefficient of variation (CV) values of 97 and 63%, respectively. Higenamine also significantly suppressed dexamethasone-induced mRNA expressions of muscle atrophy F-box protein (MAFbx)/atrogin1, casitas B-lineage lymphoma-b (Cbl-b), troponin, branched-chain amino acid aminotransferase 2 (BCAT2), and Bcl-2 binding and pro-apoptotic protein3 (Bnip3). Although the quality control of PA is regulated by the contents of diterpene alkaloids, salsolinol and higenamine can be used as the marker compounds to certificate the pharmacological activities of PA. GRAPHICAL ABSTRACT: [Image: see text] Springer Nature Singapore 2022-02-18 2022 /pmc/articles/PMC10008256/ /pubmed/35178660 http://dx.doi.org/10.1007/s11418-022-01606-5 Text en © The Author(s) 2022, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Kondo, Taishi
Ishida, Tomoaki
Ye, Ke
Muraguchi, Marin
Tanimura, Yohei
Yoshida, Masato
Ishiuchi, Kan’ichiro
Abe, Tomoki
Nikawa, Takeshi
Hagihara, Keisuke
Hayashi, Hidetoshi
Makino, Toshiaki
Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
title Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
title_full Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
title_fullStr Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
title_full_unstemmed Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
title_short Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
title_sort suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008256/
https://www.ncbi.nlm.nih.gov/pubmed/35178660
http://dx.doi.org/10.1007/s11418-022-01606-5
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