Arzneimittelforschung 2008; 58(1): 18-23
DOI: 10.1055/s-0031-1296461
Antiallergic Drugs · Antiasthmatics · Antitussives · Bronchodilators · Bronchosecretogogues · Mucolytics
Editio Cantor Verlag Aulendorf (Germany)

Suppressive Activity of Pemirolast Potassium, an Antiallergic Drug, on Glomerulonephritis

Studies in glomerulonephritis model rats and in patients with chronic glomerulonephritis concurrently affected by allergic rhinitis
Tomohito Gohda
1   Division of Nephrology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan
,
Chisei Ra
2   Division of Molecular Cell Immunology and Allergology, Nihon University Graduate School of Medical Sciences, Tokyo, Japan
,
Chieko Hamada
1   Division of Nephrology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan
,
Toshinao Tsuge
1   Division of Nephrology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan
,
Hiroshi Kawachi
3   Department of Cell Biology, Institute of Nephrology Niigata University Graduate School of Medical and Dental Sciences, Niigata City, Niigata, Japan
,
Yasuhiko Tomino
1   Division of Nephrology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan
› Author Affiliations
Further Information

Publication History

Publication Date:
15 December 2011 (online)

Abstract

Background:

It is still difficult to manage chronic glomerulonephritis with corticosteroids because of safety concerns, especially for patients with mild symptoms and infants. Therefore, an alternative approach is greatly required. Pemirolast potassium (CAS 100299-08-9) is an antiallergic drug with high safety.

Methods:

Two glomerulonephritis rat models were prepared to examine the pharmacological actions of pemirolast potassium: one reversible model prepared with the anti-Thy-1 antibody, and another irreversible model by unilateral nephrectomy and with the anti-Thy-1 antibody. Pemirolast potassium was administered to 10 Japanese chronic glomerulonephritis patients concurrently affected by allergic rhinitis in order to examine its efficacy for mild proteinuria.

Results:

Pemirolast potassium 1 and 10 mg/kg markedly inhibited proteinuria in the reversible model. In the irreversible model, pemirolast potassium 3 mg/kg showed a significant decrease in the incidence of glomerulosclerosis. In chronic glomerulonephritis patients, pemirolast potassium, 10 mg twice daily, for 6 months, significantly reduced the severity of proteinuria.

Conclusion:

Our research suggested the efficacy of pemirolast potassium in glomerulonephritis. A well-controlled study is considered necessary to validate pemirolast potassium as a therapeutic drug for glomerulonephritis.

 
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