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Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice

Activators of tissue proteolysis including Stachybotrys microspora triprenyl phenol (SMTP)-7 are a new class of agents that are expected to be effective for amelioration of chronic tissue destructive diseases. The present study was performed to examine whether SMTP-7 is effective for the amelioratio...

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Autores principales: Kemmochi, Sayaka, Hayashi, Hitomi, Taniai, Eriko, Hasumi, Keiji, Sugita-Konishi, Yoshiko, Kumagai, Susumu, Mitsumori, Kunitoshi, Shibutani, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Toxicologic Pathology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392907/
https://www.ncbi.nlm.nih.gov/pubmed/22907981
http://dx.doi.org/10.1293/tox.25.149
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author Kemmochi, Sayaka
Hayashi, Hitomi
Taniai, Eriko
Hasumi, Keiji
Sugita-Konishi, Yoshiko
Kumagai, Susumu
Mitsumori, Kunitoshi
Shibutani, Makoto
author_facet Kemmochi, Sayaka
Hayashi, Hitomi
Taniai, Eriko
Hasumi, Keiji
Sugita-Konishi, Yoshiko
Kumagai, Susumu
Mitsumori, Kunitoshi
Shibutani, Makoto
author_sort Kemmochi, Sayaka
collection PubMed
description Activators of tissue proteolysis including Stachybotrys microspora triprenyl phenol (SMTP)-7 are a new class of agents that are expected to be effective for amelioration of chronic tissue destructive diseases. The present study was performed to examine whether SMTP-7 is effective for the amelioration or protection of early-stage IgA nephropathy (IgAN) induced by nivalenol (NIV) in female BALB/c mice. In Experiment 1, mice were administered NIV at 24 ppm in diet for 8 weeks, and during the NIV treatment, they were intraperitoneally injected with SMTP-7 (10 mg/kg) three times a week. In Experiment 2, mice were injected similarly with SMTP-7 during the last 4 weeks of a 16-week NIV treatment. Immunofluorescence analysis revealed an inhibitory effect of SMTP-7 on the glomerular deposition of IgA in Experiment 1; however, it was ineffective in Experiment 2. On the other hand, SMTP-7 did not affect the serum concentration of IgA in both experiments. These results suggest that SMTP-7 has a potential to decrease the progression of IgAN induced by NIV through inhibition of local accumulation of IgA in the glomerular mesangium, while it was ineffective for suppression of IgA production. On the other hand, SMTP-7 was found to be ineffective for already deposited IgA, suggesting that SMTP-7 may not be effective for ameliorating advanced IgAN.
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spelling pubmed-33929072012-08-20 Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice Kemmochi, Sayaka Hayashi, Hitomi Taniai, Eriko Hasumi, Keiji Sugita-Konishi, Yoshiko Kumagai, Susumu Mitsumori, Kunitoshi Shibutani, Makoto J Toxicol Pathol Original Article Activators of tissue proteolysis including Stachybotrys microspora triprenyl phenol (SMTP)-7 are a new class of agents that are expected to be effective for amelioration of chronic tissue destructive diseases. The present study was performed to examine whether SMTP-7 is effective for the amelioration or protection of early-stage IgA nephropathy (IgAN) induced by nivalenol (NIV) in female BALB/c mice. In Experiment 1, mice were administered NIV at 24 ppm in diet for 8 weeks, and during the NIV treatment, they were intraperitoneally injected with SMTP-7 (10 mg/kg) three times a week. In Experiment 2, mice were injected similarly with SMTP-7 during the last 4 weeks of a 16-week NIV treatment. Immunofluorescence analysis revealed an inhibitory effect of SMTP-7 on the glomerular deposition of IgA in Experiment 1; however, it was ineffective in Experiment 2. On the other hand, SMTP-7 did not affect the serum concentration of IgA in both experiments. These results suggest that SMTP-7 has a potential to decrease the progression of IgAN induced by NIV through inhibition of local accumulation of IgA in the glomerular mesangium, while it was ineffective for suppression of IgA production. On the other hand, SMTP-7 was found to be ineffective for already deposited IgA, suggesting that SMTP-7 may not be effective for ameliorating advanced IgAN. Japanese Society of Toxicologic Pathology 2012-07 2012-06 /pmc/articles/PMC3392907/ /pubmed/22907981 http://dx.doi.org/10.1293/tox.25.149 Text en ©2012 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original Article
Kemmochi, Sayaka
Hayashi, Hitomi
Taniai, Eriko
Hasumi, Keiji
Sugita-Konishi, Yoshiko
Kumagai, Susumu
Mitsumori, Kunitoshi
Shibutani, Makoto
Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice
title Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice
title_full Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice
title_fullStr Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice
title_full_unstemmed Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice
title_short Protective Effect of Stachybotrys microspora Triprenyl Phenol-7on the Deposition of IgA to the Glomerular Mesangium in Nivalenol-induced IgA Nephropathy Using BALB/c Mice
title_sort protective effect of stachybotrys microspora triprenyl phenol-7on the deposition of iga to the glomerular mesangium in nivalenol-induced iga nephropathy using balb/c mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392907/
https://www.ncbi.nlm.nih.gov/pubmed/22907981
http://dx.doi.org/10.1293/tox.25.149
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