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Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice

This study was designed to examine the potential use of the ethyl acetate (EA) extract of Tripterygium wilfordii Hook F (TwHF), a Chinese herbal medicine, in the treatment of systemic lupus erythematosus. A total of 48 28-week-old female NZB/W F1 mice were randomly divided into three groups and oral...

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Autores principales: Tao, Xuelian, Fan, Fred, Hoffmann, Victoria, Longo, Nancy S, Lipsky, Peter E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526566/
https://www.ncbi.nlm.nih.gov/pubmed/16507125
http://dx.doi.org/10.1186/ar1879
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author Tao, Xuelian
Fan, Fred
Hoffmann, Victoria
Longo, Nancy S
Lipsky, Peter E
author_facet Tao, Xuelian
Fan, Fred
Hoffmann, Victoria
Longo, Nancy S
Lipsky, Peter E
author_sort Tao, Xuelian
collection PubMed
description This study was designed to examine the potential use of the ethyl acetate (EA) extract of Tripterygium wilfordii Hook F (TwHF), a Chinese herbal medicine, in the treatment of systemic lupus erythematosus. A total of 48 28-week-old female NZB/W F1 mice were randomly divided into three groups and orally administered vehicle or the EA extract of TwHF at 18.25 mg/kg (EA(low)) or 36.5 mg/kg (EA(high)) for 14 weeks. Proteinuria and serum anti-double-stranded (ds)DNA antibody titers were assayed before and after treatment. At the end of treatment, all animals were sacrificed and pathological changes in the kidneys were examined by observers blinded to the treatment regimens. Immunohistological studies were carried out on kidneys and spleens. At 28 weeks of age, proteinuria (>30 mg/dl) and anti-dsDNA antibodies were found in all mice in the three groups. Fourteen, sixteen and fifteen mice in the vehicle, EA(low )and EA(high )groups, respectively, completed at least four weeks of treatment. At the end of treatment, the mean proteinuria of the EA(low )and EA(high )groups was significantly less than that of the vehicle group and no different from proteinuria at the onset of treatment. Histological evidence of glomerulonephritis, glomerular deposition of IgG and complement 3 and cellular infiltration in the interstitium and perivascular regions were significantly less severe in the EA extract treated mice than in vehicle treated mice. Treatment with the EA extract significantly inhibited the progression of kidney disease in NZB/W F1 mice, though had no significant effect on the levels of anti-dsDNA antibody.
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spelling pubmed-15265662006-08-04 Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice Tao, Xuelian Fan, Fred Hoffmann, Victoria Longo, Nancy S Lipsky, Peter E Arthritis Res Ther Research Article This study was designed to examine the potential use of the ethyl acetate (EA) extract of Tripterygium wilfordii Hook F (TwHF), a Chinese herbal medicine, in the treatment of systemic lupus erythematosus. A total of 48 28-week-old female NZB/W F1 mice were randomly divided into three groups and orally administered vehicle or the EA extract of TwHF at 18.25 mg/kg (EA(low)) or 36.5 mg/kg (EA(high)) for 14 weeks. Proteinuria and serum anti-double-stranded (ds)DNA antibody titers were assayed before and after treatment. At the end of treatment, all animals were sacrificed and pathological changes in the kidneys were examined by observers blinded to the treatment regimens. Immunohistological studies were carried out on kidneys and spleens. At 28 weeks of age, proteinuria (>30 mg/dl) and anti-dsDNA antibodies were found in all mice in the three groups. Fourteen, sixteen and fifteen mice in the vehicle, EA(low )and EA(high )groups, respectively, completed at least four weeks of treatment. At the end of treatment, the mean proteinuria of the EA(low )and EA(high )groups was significantly less than that of the vehicle group and no different from proteinuria at the onset of treatment. Histological evidence of glomerulonephritis, glomerular deposition of IgG and complement 3 and cellular infiltration in the interstitium and perivascular regions were significantly less severe in the EA extract treated mice than in vehicle treated mice. Treatment with the EA extract significantly inhibited the progression of kidney disease in NZB/W F1 mice, though had no significant effect on the levels of anti-dsDNA antibody. BioMed Central 2006 2006-01-03 /pmc/articles/PMC1526566/ /pubmed/16507125 http://dx.doi.org/10.1186/ar1879 Text en Copyright © 2006 Tao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tao, Xuelian
Fan, Fred
Hoffmann, Victoria
Longo, Nancy S
Lipsky, Peter E
Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice
title Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice
title_full Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice
title_fullStr Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice
title_full_unstemmed Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice
title_short Therapeutic impact of the ethyl acetate extract of Tripterygium wilfordii Hook F on nephritis in NZB/W F1 mice
title_sort therapeutic impact of the ethyl acetate extract of tripterygium wilfordii hook f on nephritis in nzb/w f1 mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526566/
https://www.ncbi.nlm.nih.gov/pubmed/16507125
http://dx.doi.org/10.1186/ar1879
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