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Rapatar, a nanoformulation of rapamycin, decreases chemically-induced benign prostate hyperplasia in rats

E. Lesovaya, K. Kirsanov, E. Antoshina, L. Trukhanova, T. G. Gorkova, E. Shipaeva, R. Salimov, G. Belitsky et al.

OncoTarget, 2015

31 citations

Abstract

Benign prostatic hyperplasia (BPH) is the most common age-related disease in men. Here we tested the efficacy of Rapatar, a micellar nanoformulation of rapamycin, in two rat models of BPH: testosterone-induced and sulpiride-induced hyperplasia in ventral lobes and lateral/dorsal lobes, respectively. We found that Rapatar prevented hypertrophic and hyperplastic abnormalities and degenerative alterations in both BPH models. Rapatar normalized weight of the lateral lobes in sulpiride-induced BPH, the most relevant animal model of human BPH. Unlike Finasteride, a standard therapy of BPH, Rapatar reduced inflammation caused by sulpiride. No obvious side effects of Rapatar were detected. Our data provide a rationale for clinical trials of Rapatar in patients suffering from BPH.

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