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Oral administration of ginsenoside Rh1 inhibits the development of atopic dermatitis-like skin lesions induced by oxazolone in hairless mice.

Abstract
In the present study, we examined the inhibitive effect of ginsenoside Rh1 on oxazolone-induced atopic dermatitis-like skin lesions in hairless mice. Oral administration of ginsenoside Rh1 improved clinical symptoms, and it was confirmed by histophathological analysis. In ginsenoside Rh1 (20mg/kg) group, ear swellings and ear weights were significantly lower than the control group. Moreover, elevation of IL-6 and total IgE levels in serum were suppressed by ginsenoside Rh1 (20mg/kg). In addition, ginsenoside Rh1 (20mg/kg) significantly increased mRNA expression of IFNγ and Foxp3, and slightly decreased IL-4 expression in draining lymph nodes. The results suggest that ginsenoside Rh1 can alleviate inflammatory symptoms in atopic dermatitis (AD) by reduction of IgE and IL-6 levels in peripheral blood, increase of Foxp3 expression in draining lymph nodes and suppression of inflammation in skin regions. Indeed, ginsenoside Rh1 exhibited therapeutic possibility in immune disorders.
AuthorsHua Zheng, Yunju Jeong, Jeongmin Song, Geun Eog Ji
JournalInternational immunopharmacology (Int Immunopharmacol) Vol. 11 Issue 4 Pg. 511-8 (Apr 2011) ISSN: 1878-1705 [Electronic] Netherlands
PMID21238621 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2010 Elsevier B.V. All rights reserved.
Chemical References
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Ginsenosides
  • Immunologic Factors
  • Interleukin-6
  • Oxazolone
  • Immunoglobulin E
  • ginsenoside Rh1
  • Interferon-gamma
Topics
  • Administration, Oral
  • Animals
  • Dermatitis, Atopic (immunology, pathology, prevention & control)
  • Disease Models, Animal
  • Forkhead Transcription Factors (biosynthesis, immunology)
  • Ginsenosides (administration & dosage, therapeutic use)
  • Immunoglobulin E (biosynthesis, blood, immunology)
  • Immunologic Factors (administration & dosage, therapeutic use)
  • Interferon-gamma (biosynthesis)
  • Interleukin-6 (biosynthesis, blood, immunology)
  • Lymph Nodes (immunology, metabolism)
  • Mice
  • Mice, Hairless
  • Molecular Structure
  • Oxazolone (immunology)
  • Skin (drug effects, immunology, pathology)

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