Effects of a New Non-Steroidal 5α-Reductase Inhibitor, FK143, on the Prostate Gland in Beagle Dogs

The Japanese Journal of Pharmacology

Susumu Tsujimoto¹  Toshitaka Manda¹  Kyoichi Shimomura¹  Ikuo Kawamura¹  Tamotsu Mizota¹  Yoshinori Naoe¹  Masamichi Inami¹ 

[1] Pharmacological Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.

关键词: FK143;    5α-Reductase;    Benign prostatic hyperplasia;   

DOI  :  10.1254/jjp.74.187

学科分类：药理学

来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society

【 摘 要 】

References(28)Cited-By(3)FK143 (4-[3-[3-[bis(4-isobutylphenyl)methylamino]benzoyl]-1H-indol-1-yl]-butyric acid)is a new non-steroidal inhibitor of steroid 5α-reductase (5α-reductase). The effects of FK143 on prostate size and histopathology of mature male beagle dogs were investigated and compared with those of finasteride (a steroidal 5α-reductase inhibitor), and allylestrenol and chlormadinone acetate (CMA)(androgen receptor antagonists). FK143 was orally administered to the dogs daily for 12 weeks. At doses of 10 and 32 mg/kg, FK143 significantly reduced prostate volume to about 60% of the initial value, and dogs treated with FK143 showed a dose-dependent glandular epithelial atrophy in the prostate. FK143 showed no abnormal changes in organ weights and histopathology of the adrenal, testis, pituitary and liver. The degree of prostate reduction in the dogs treated with FK143 (10 and 32 mg/kg)was almost the same as that by finasteride (1.0 mg/kg)and smaller than that by allylestrenol (10 mg/kg)or CMA (10 mg/kg). However, allylestrenol increased liver weights, and CMA increased liver and reduced adrenal weights. These results demonstrate that FK143 can decrease the volume of the dog prostate without any influence on other organs, and they suggest that FK143 is a good candidate for the treatment for benign prostatic hyperplasia.

【 授权许可】

Unknown