Retinoids, derivatives of vitamin A, inhibit mesangial cell proliferation, glomerular inflammation, and extracellular matrix deposition in acute anti-Thy1.1 glomerulonephritis (Thy-GN) of the rat. We examined a model, chronic mesangioproliferative Thy-GN (MoAb 1-22-3), which is more akin to human disease. Treatment started on day 23 when Thy-GN had already been established. Nonnephritic control and Thy-GN rats were treated orally for 67days with vehicle or with two doses of either the retinoic acid receptor -specific agonist AGN195183 (RAR agonist) or the retinoid X receptor specific agonist AGN194204 (RXR agonist). Doses of either the RAR or the RXR agonist significantly reduced albuminuria and normalized blood pressure during the course of treatment. The glomerulosclerosis index, glomerular cell and interstitial cell counts, and area of the interstitial space were significantly lower in nephritic rats treated with the RAR agonist or RXR agonist than with vehicle. The RAR and RXR agonist significantly reduced the infiltration of the glomerulus by macrophages. The increase in glomerular TGF1 and prepro-ET1 gene expression in vehicle-treated nephritic rats was significantly attenuated by RAR or RXR agonists. Glomerular expression of RXR and RAR receptor mRNA was significantly greater in vehicle-treated nephritic rats than in nonnephritic controls. Treatment with RAR or RXR agonists tended to normalize retinoid-receptor gene expression. Our data indicate that both RAR agonists and RXR agonists reduce renal damage in rats with established chronic glomerulonephritis. Receptor-specific retinoids may provide a novel therapeutic approach for the treatment of chronic glomerulonephritis.