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Sairei-to ameliorates rat peritoneal fibrosis partly through suppression of oxidative stress

Authors :
Takahiko Ono
Kazuhide Uemura
Kozue Kato
Masayuki Kitamoto
Chunmo Wu
Hisayo Kitamura
Tatsuya Morimoto
Akihisa Sugimoto
Fumiaki Nogaki
Toshiya Takeda
Source :
Nephron. Experimental nephrology. 117(3)
Publication Year :
2009

Abstract

Background: Sairei-to is a herbal prescription originating from traditional Chinese medicine. We conducted an experimental study on rat peritoneal fibrosis to clarify the suppressive mechanisms of sairei-to. Methods: Wistar rats were intraperitoneally injected with chlorhexidine gluconate (CG) every day. Peritoneal specimens were collected after 28 days of CG injection and oral administration of sairei-to. Macrophage infiltration, extracellular matrix accumulation, and angiogenesis were evaluated by immunostaining for ED-1, fibronectin, and CD-31, respectively. To observe oxidative stress in the tissue, 4-hydroxy-2-noneal (HNE) accumulation and plasma levels of superoxide dismutase (SOD) activity were detected. As a candidate of antioxidative components in sairei-to, plasma levels of baicalin were determined by high-performance liquid chromatography. Results: Compared with the disease control group, serum total protein levels were significantly recovered in the sairei-to treatment group. Thickness of the submesothelial compact zone, trichrome-stained area, ED-1-positive cells, fibronectin-staining area, and HNE accumulation were suppressed in the treatment group. Concurrently, decreased plasma levels of SOD activity were recovered by sairei-to treatment. Increased CD-31-positive vessel number and area were also suppressed in the sairei-to group. Baicalin was detected in the plasma samples of the sairei-to group at 0.29 ± 0.11 µg/ml (mean±SEM). Conclusion: These results suggest that sairei-to ameliorates peritoneal fibrosis, partly through suppressing oxidative stress and macrophage infiltration.

Details

ISSN :
16602129
Volume :
117
Issue :
3
Database :
OpenAIRE
Journal :
Nephron. Experimental nephrology
Accession number :
edsair.doi.dedup.....f0e6e1db8433b838717dc76c0ace6d9f