Treatment of benign prostatic hyperplasia with Croton membranaceus in an experimental animal model
- PMID: 25256687
- DOI: 10.1016/j.jep.2014.09.007
Treatment of benign prostatic hyperplasia with Croton membranaceus in an experimental animal model
Abstract
Ethnopharmacological relevance: Croton membranaceus leaf extracts are used in the Bahamas to aromatize tobacco. In Nigeria it is used to improve digestion and in Ghana, the root extract is used for the treatment of benign prostatic hyperplasia (BPH). Despite claims of efficacy no data exists to support this. The aim of this study was to determine if Croton membranaceus aqueous root extract (CMARE) could attenuate the development of BPH in an animal model.
Materials and methods: Fifty (50) adult male Sprague-Dawley rats weighing 200-250g were randomly divided into 5 groups. Group 1 served as the control and received normal saline p.o. Groups 2-5 were castrated and injected with 5mg/kg b.wt. testosterone propionate subcutaneously for 28 days. Group 2 (model group) had no further treatment. Group 3 was simultaneously given 0.5mg/kg b.wt. finasteride p.o. throughout. Groups 4 and 5 received 30mg/kg b.wt. [low dose (LD)] and 300mg/kg b.wt. [high dose (HD)] CMARE, respectively, for 28 days. Rats were sacrificed at the end of the study and all prostate organs harvested. Wet weights, volumes and prostatic index (PI) were determined. Tissues were histologically examined. Serum prostate specific antigen (PSA) and dihydrotestosterone (DHT) levels were determined.
Results: Prostate volume of the control group was 0.67±0.23cm(3). The model, finasteride, CMARE LD and HD groups had the following volumes: 0.92±0.12, 0.84±0.16, 0.79±0.16 and 0.80±0.19cm(3), respectively. Only the model group showed significant statistical differences with the control (p=0.007). PI for control, model, finasteride, LD and HD groups was as follows: 0.19±0.04, 0.30±0.04, 0.25±0.04, 0.21±0.05 and 0.22±0.05. No statistical differences between the control PI and the CMARE treated groups were observed. Histologically, the model group had massive growth of columnar stromal and epithelial cells. CMARE and finasteride attenuated this growth with a resultant thin layer of stromal and epithelial cells similar to the control. PSA levels were significantly lower in the treatment groups.
Conclusion: CMARE reduces stromal and epithelial cell growth, and subsequently shrinks enlarged prostate. This is the first scientific proof validating the anecdotal evidence of CMARE efficacy in the management of BPH.
Keywords: Benign prostatic hyperplasia; Croton membranaceus; Finasteride; Prostate; Testosterone.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.
Similar articles
-
Prostate-specific targeting of the aqueous root extract of Croton membranaceus in experimental animals.Andrologia. 2014 Sep;46(7):753-60. doi: 10.1111/and.12144. Epub 2013 Aug 19. Andrologia. 2014. PMID: 23957252
-
Mitochondria-dependent apoptogenic activity of the aqueous root extract of Croton membranaceus against human BPH-1 cells.Genet Mol Res. 2015 Jan 15;14(1):149-62. doi: 10.4238/2015.January.15.18. Genet Mol Res. 2015. PMID: 25729946
-
Acute toxicity studies of Croton membranaceus root extract.J Ethnopharmacol. 2011 Apr 12;134(3):938-43. doi: 10.1016/j.jep.2011.02.004. Epub 2011 Feb 16. J Ethnopharmacol. 2011. PMID: 21335084
-
The effect of finasteride on prostate specific antigen: review of available data.J Urol. 1996 Jan;155(1):3-9. J Urol. 1996. PMID: 7490873 Review.
-
5alpha-reductase inhibitors/finasteride.Prostate Suppl. 1996;6:82-7. Prostate Suppl. 1996. PMID: 8630236 Review.
Cited by
-
Protective effects of combination of Stauntonia hexaphylla and Cornus officinalis on testosterone-induced benign prostatic hyperplasia through inhibition of 5α- reductase type 2 and induced cell apoptosis.PLoS One. 2020 Aug 13;15(8):e0236879. doi: 10.1371/journal.pone.0236879. eCollection 2020. PLoS One. 2020. PMID: 32790676 Free PMC article.
-
Oral exposure of sulpiride promotes the proliferation of Brown-Norway rat prostates.Exp Ther Med. 2020 Apr;19(4):2551-2562. doi: 10.3892/etm.2020.8521. Epub 2020 Feb 11. Exp Ther Med. 2020. PMID: 32256734 Free PMC article.
-
Inhibitory effects of Ponciri Fructus on testosterone-induced benign prostatic hyperplasia in rats.BMC Complement Altern Med. 2017 Aug 3;17(1):384. doi: 10.1186/s12906-017-1877-y. BMC Complement Altern Med. 2017. PMID: 28774334 Free PMC article.
-
Protective effect of the hydroethanolic extract of camelthorn (Alhagi maurorum) on benign prostatic hyperplasia induced by testosterone in rats.BMC Complement Med Ther. 2025 Apr 12;25(1):136. doi: 10.1186/s12906-025-04862-6. BMC Complement Med Ther. 2025. PMID: 40221684 Free PMC article.
-
Inhibitory effects of Nigella sativa seed oil on the testosterone-induced benign prostatic hyperplasia in rats.Biomedicine (Taipei). 2021 Mar 1;11(1):19-25. doi: 10.37796/2211-8039.1083. eCollection 2021. Biomedicine (Taipei). 2021. PMID: 35223391 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous