HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Therapeutic mechanism of Saikosaponin-d in anti-Thy1 mAb 1-22-3-induced rat model of glomerulonephritis.

AbstractAIMS:
Mesangioproliferative glomerulonephritis is a common kidney disease and at present, there is no effective treatment. Our previous studies have demonstrated that Sairei-to can significantly prevent progression of experimental glomerulonephritis in rats. Although we have reported that the active component of Sairei-to in treatment of glomerulonephritis was Saikosaponin-d (Ssd), mechanism of Ssd in prevention of mesangioproliferative glomerulonephritis progression is still unknown. Therefore, current study examines the effects of Ssd on progression of mesangioproliferative glomerulonephritis induced by anti-Thy1 monoclonal antibody 1-22-3 (mAb 1-22-3) in uninephrectomized rats.
METHODS:
Eighteen female Wistar rats first received uninephrectomy and mAb 1-22-3 injection and were then divided into 3 groups: treated daily with phosphate-buffered saline (PBS), 0.6 or 1.8 mg/kg of Ssd. Urinary protein concentration and systolic blood pressure were evaluated and the kidneys were collected and subjected to histological and immunohistological evaluation. The mRNA and protein of the kidneys were extracted and subjected to reverse transcriptase polymerase chain reaction and Western blot analysis, respectively.
RESULTS:
Ssd reduced the amount of urinary protein and systolic blood pressure. Ssd administration also decreased extracellular matrix expansion, crescentic formation as well as infiltration of macrophages and CD8+ T lymphocytes. Moreover, Ssd significantly reduced expression of transforming growth factor beta 1 (TGF-beta1) and type I collagen in the kidneys.
CONCLUSION:
Ssd inhibits the progression of mesangioproliferative glomerulonephritis through reduction of the expression of TGF-beta1 and the infiltration of macrophages and CD8+ T lymphocytes.
AuthorsPing Li, Yuewen Gong, Ning Zu, Yajun Li, Bin Wang, Fujio Shimizu
JournalNephron. Experimental nephrology (Nephron Exp Nephrol) Vol. 101 Issue 4 Pg. e111-8 ( 2005) ISSN: 1660-2129 [Electronic] Switzerland
PMID16103731 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2005 S. Karger AG, Basel.
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Antibodies, Monoclonal
  • Collagen Type I
  • Isoantibodies
  • RNA, Messenger
  • Saponins
  • Tgfb1 protein, rat
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • anti-Thy antibody
  • Oleanolic Acid
  • saikosaponin D
Topics
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal (pharmacology, therapeutic use)
  • Antibodies, Monoclonal
  • Blood Pressure (drug effects, physiology)
  • Blotting, Western
  • CD8-Positive T-Lymphocytes (pathology)
  • Collagen Type I (analysis, genetics)
  • Disease Progression
  • Female
  • Fluorescent Antibody Technique
  • Gene Expression Regulation (drug effects)
  • Glomerulonephritis, Membranoproliferative (drug therapy, physiopathology)
  • Isoantibodies
  • Kidney Glomerulus (chemistry, drug effects, pathology)
  • Macrophages (pathology)
  • Mesangial Cells (chemistry, drug effects, pathology)
  • Oleanolic Acid (analogs & derivatives, pharmacology, therapeutic use)
  • Proteinuria (drug therapy, physiopathology)
  • RNA, Messenger (analysis)
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • Saponins (pharmacology, therapeutic use)
  • Transforming Growth Factor beta (analysis, genetics)
  • Transforming Growth Factor beta1

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: