This article has Open Peer Review reports available.
Inhibitory effect of Yukmijihwang-tang, a traditional herbal formula against testosterone-induced benign prostatic hyperplasia in rats
© Shin et al.; licensee BioMed Central Ltd. 2012
Received: 2 January 2012
Accepted: 20 April 2012
Published: 20 April 2012
Yukmijihwang-tang, a traditional herbal formula, has been used for treating disorder, diabetic mellitus and neurosis in China (Liu-wei-di-huang-tang in Chinese), Japan (Lokumijio-to in Japanese) and Korea for many years. In this study, we investigated the effects of Yukmijihwang-tang water extract (YJT) on the development of benign prostatic hyperplasia (BPH) using a rat model of testosterone propionate (TP)-induced BPH.
A total of 30 rats were divided into five groups. One group was used as a control and the other groups received subcutaneous injections of TP for 4 weeks to induce BPH. YJT (200 or 400 mg/kg) was administered daily for 4 weeks to two groups by oral gavage concurrently with the TP. The animals were euthanized, the prostate and body weights were recorded, and tissues were subjected to hormone assays and histomorphology. In addition, we investigated proliferating cell nuclear antigen (PCNA) expression in the prostate using immunoblotting.
Animals with BPH showed significantly increased absolute and relative prostate weights, increased dihydrotestosterone levels in the serum or prostate and increased PCNA expression in the prostate; however, YJT-treated animals showed significant reductions compared with the animals with TP-induced BPH. Histomorphology also showed that YJT inhibited TP-induced prostatic hyperplasia.
These findings indicate that YJT effectively inhibited the development of BPH and might be a useful drug clinically.
Benign prostate hyperplasia (BPH) is a urological disorder caused by the noncancerous enlargement of the prostate as men age. As the prostate enlarges, it can constrict the urethra, inducing various symptoms including a weak urinary stream, incomplete bladder emptying, nocturia, dysuria and bladder outlet obstruction [1, 2]. These symptoms associated with BPH are known as lower urinary tract symptoms (LUTS) . Currently, the two main medications used for treatment of BPH are α1-adrenergic receptor antagonists and 5α-reductase inhibitors . The α1-adrenergic receptor antagonists, including doxazosin, terazosin and tamsulosin, are the initial drugs for treating BPH, and they alleviate LUTS by relaxation of smooth muscle in the prostate and the neck of the bladder [5, 6]. On the other hand, the 5α-reductase inhibitors inhibit the development of BPH via a reduction in dihydrotestosterone (DHT) production . In the development of BPH, 5α-reductase catalyzes the conversion of testosterone to DHT, which induces an increase in the DHT level in the prostate. This accelerates hyperplasia of the stromal and epithelial cells of the prostate, resulting in prostatic enlargement . As mentioned above, α1-adrenergic receptor antagonists and 5α-reductase inhibitors are effective in treating men with BPH. However, these drugs are limited because of their side effects, including decreased libido, ejaculatory or erectile dysfunction, and nasal congestion [9, 10].
Yukmijihwang-tang (Liu-wei-di-huang-tang in Chinese; Lokumijio-to in Japanese), an oriental herbal formula, has been used for many years in Korea, China and Japan. It is composed of six herbs: Rehmannia glutinosa Cornus officinalis Dioscorea batatas Paeonia suffruticosa Poria cocos Alisma orientale . In particular, Yukmijihwang-tang is one of the most widely used herbal formulas in Korea and China. A Recent report showed that Yukmijihwang-tang was ranked first in consumption in the Korean herbal medicine market . In China, the annual market turnover of Yukmijihwang-tang in herbal medicine is about US$633 million . Traditionally, Yukmijihwang-tang is applied in treating renal disorders, diabetes mellitus, and neurosis . There have been many studies on the pharmacological effects of Yukmijihwang-tang, such as protection against renal ischemia/reperfusion , memory enhancement , stimulation of spermatogenesis , inhibition of bone loss , anti-asthmatic effects  and antidiabetic effects . Although many researchers have investigated the pharmacological effects of Yukmijihwang-tang, there has been no study on its possible protective effects against BPH.
Therefore, this study investigated the effects of an aqueous extract of Yukmijihwang-tang (YJT) on testosterone-induced BPH in rats by measuring prostate weight changes and the DHT levels in the serum and prostate, by western immunoblotting and histomorphology.
Preparation of Yukmijihwang-tang
Composition of YJT
Company of purchase
Male 12-week-old Wistar rats (n = 30) weighing 250 – 350 g (Central Lab. Animal. Inc., Seoul, Korea) were housed in a room maintained at 18–23°C and at a relative humidity of 40–60% with an alternating 12 /12 h light/dark cycle. They were offered a standard laboratory diet and water ad libitum . All experimental procedures were carried out in accordance with the NIH Guidelines for the Care and Use of Laboratory Animals and were approved by Korea Institute of Oriental Medicine Institutional Animal Care and Use Committee. The animals were cared for in accordance with the dictates of the National Animal Welfare Law of Korea.
BPH was induced by subcutaneous injection of testosterone propionate (TP, 3 mg/kg, Tokyo Chemical Ins. Co., Tokyo, Japan) for 4 weeks. After 1 week of acclimatization, the rats were divided into five groups: (A) a normal control group that received phosphate-buffered saline (PBS, p.o.) with corn oil (s.c.); (B) a BPH group that received PBS (p.o.) with TP (s.c.); (C) a positive control group that received finasteride (10 mg/kg, p.o.) with TP (s.c.); and (D and E) YJT groups that received YJT at 200 or 400 mg/kg (p.o.), respectively, with TP (s.c.). Finasteride, a 5α-reductase inhibitor, was used as a positive anti-BPH drug and was purchased from Sigma-Aldrich (St Louis, MO, USA). Its effective dose for treating BPH was determined based on a previous study . All materials were administered to animals once daily for 4 weeks, and body weight was measured weekly. The application volumes were 5 mL/kg for oral administration (PBS, finasteride and YJT) and 3 mL/kg for subcutaneous injection (corn oil and TP) and were calculated in advance based on the most recently recorded body weights of individual animals. After the last treatment, all animals were fasted overnight and euthanized using pentobarbital at 100 mg/kg body weight injected intraperitoneally (Han Lim Pharmaceutical. Co. Ltd., Yongin, Korea). Blood samples were drawn from the caudal vena cava, and the serum was separated by centrifugation. Serum was stored at at −80°C for hormone assays. The prostates were removed immediately and weighed. Relative prostate weight was calculated as the ratio of prostate weight to body weight. The percentage inhibition of the increase in prostate weight induced by YJT was determined according to previous study . The ventral lobe of the prostate was divided in half. One half was fixed using 10% neutral-buffered formalin and embedded in paraffin for histomorphology and the other was stored at −80°C for other analyses.
Preparation of prostate homogenates
Prostatic tissue was homogenized (1/10 w/v) in tissue lysis/extraction reagent containing protease inhibitors (Sigma-Aldrich) using an IKA T10 Basic (IKA Works, Staufen, Germany). Homogenates were centrifuged at 12,000 g for 25 min at 4°C. Protein concentrations in the supernatant fractions were determined using Bradford reagent (Bio-Rad Laboratories, Inc., Hercules, CA, USA).
Measurement of DHT levels in the serum and prostate
Levels of DHT in serum and the prostate were determined using an enzyme-linked immunosorbent assay (ELISA) kit according to the manufacturer’s instructions (ALPCO Diagnostics, Salem, NH, USA). The absorbance was measured at 450 nm using a microplate ELISA reader (Bio-Rad Laboratories, Inc.). Values are expressed per mg protein for the prostate and per mL for serum.
Equal aliquots (30 μg) of total lung protein were heated at 100°C for 5 min then loaded onto 12% SDS−PAGE gels, followed by transfer to nitrocellulose membranes at 100 V for 2 h. The membranes were blocked for 1 h with Tris-buffered saline containing 0.05% Tween-20 (TBST) plus 5% skim milk and were incubated with anti-proliferating cell nuclear antigen (anti-PCNA, 1:1000 dilution; Santa Cruz Biotechnology, Santa Cruz, CA, USA) and anti-β-actin (1:1000 dilution; Cell Signaling Technology, Danvers, MA, USA) overnight at 4°C. The membranes were washed three times with TBST and then incubated with a 1:10,000 dilution of horseradish peroxidase-conjugated secondary antibody (Jackson ImmunoResearch, West Grove, PA, USA) for 1 h at room temperature. The membranes were again washed three times with TBST and were then developed using an enhanced chemiluminescence kit (Amersham Biosciences, Little Chalfont, UK). For quantitative anlaysis, band densities were determined using Chemi-Doc (Bio-Rad Laboratories, Inc.).
Fixed prostate tissue embedded in paraffin wax were cut into 4 μm thick sections and stained with hematoxylin (Sigma-Aldrich MHS-16) and eosin (Sigma-Aldrich HT110-1-32). The sections were mounted and coverslipped using mounting medium (Invitrogen, Carlsbad, CA, USA) and then examined under a microscope (Nikon, Tokyo, Japan). Measurement of prostate epithelial thickness was performed using an image analyzer (Molecular Devices Inc., CA, USA).
Data are expressed as the means ± standard deviation (S.D.). Statistical significance was determined using analysis of variance. When tests showed a significant difference among groups, data were analyzed further using a multiple comparison procedure and Dunnett’s test. The significance levels were set at P < 0.05 and < 0.01.
Effect of YJT on prostate weights
Effects of YJT on body weights and prostate weights
Body weights (g)
1.44 ± 0.10
0.35 ± 0.02
273.5 ± 8.50
416.7 ± 12.75
3.05 ± 0.55##
0.78 ± 0.15##
273.9 ± 8.94
391.5 ± 23.47
1.95 ± 0.28**
0.51 ± 0.04**
276.0 ± 13.01
380.3 ± 46.58
2.14 ± 0.25**
0.54 ± 0.06**
277.2 ± 13.08
394.2 ± 27.11
2.25 ± 0.27**
0.56 ± 0.10**
278.9 ± 9.34
404.8 ± 26.01
Effects of YJT on DHT levels in serum
Effects of YJT on DHT levels in the prostate
Effects of YJT on PCNA expression in the prostate
Effects of YJT on prostatic epithelial hyperplasia
We evaluated the inhibitory effects of YJT on the development of BPH using TP-induced BPH in rats. Animals with BPH induced by TP treatment showed significant increases in absolute and relative prostate weights, increased DHT levels in the serum and prostate and elevated prostatic epithelial hyperplasia with elevated PCNA expression. In contrast, the YJT-treated animals showed significant reductions in absolute and relative prostate weights and in DHT levels in the serum and prostate, and mild prostatic epithelial hyperplasia with decreased PCNA expression.
Rats with BPH showed significantly increased absolute and relative prostate weight compared with the negative control animals; however, YJT-treated animals showed significant reductions in these measures compared with the BPH animals. According to previous studies, increased prostate weight is an important marker indicating the development of BPH [20, 21]. BPH involves epithelial and stromal hyperplasia of the prostate, resulting in an increase in the prostate weight. When sufficiently large, the prostate constricts the urethral canal to cause partial or sometimes complete obstruction . For these reason, many studies have tested the inhibitory effects of various substances on the development of BPH by measuring prostate weights [22, 23]. In the results from histomorphology of the prostate, the rats with BPH showed epithelial hyperplasia with an increase in epithelial thickness compared with the negative control animals. In contrast, the YJT-treated rats showed mild prostatic epithelial hyperplasia with a reduction in epithelial thickness compared with BPH animals. These results are in agreement with the prostate weight results. In addition, we evaluated PCNA expression in the prostate to test the inhibitory effects of YJT on epithelial cell proliferation in rats with TP-induced BPH. Measuring PCNA is commonly used to evaluate cellular proliferation in benign and malignant proliferating tissues, as the PCNA level is correlated directly with the degree of proliferation [24, 25]. Previous studies on BPH demonstrated that PCNA is a meaningful indicator of prostatic proliferation, and that its expression in the prostate is significantly increased in animals with experimentally induced BPH [26, 27]. In the present study, YJT significantly decreased PCNA expression in the prostate compared with the BPH group, in parallel with a reduction in the prostatic hyperplasia. Thus, YJT treatment effectively inhibited the prostatic hyperplasia induced by TP.
DHT, a steroid hormone produced from testosterone by the enzyme 5α-reductase, is the primary active metabolite of testosterone . The role of DHT in BPH is well known, as it is the androgen responsible for prostate growth [8, 29]. Because DHT has a 10 times higher affinity for the androgen receptor than testosterone, DHT easily binds to androgen receptors, which stimulates the transcription of growth factors that are mitogenic for the epithelial and stromal cells of the prostate . Therefore, DHT is ultimately responsible for prostatic epithelial and stromal cell hyperplasia . As mentioned above, because DHT is formed from testosterone by 5α-reductase, many studies have focused on reducing the DHT level by inhibiting this enzyme. Finasteride, a 5α-reductase inhibitor, is used as an elective drug for treating human BPH . In previous studies, finasteride reduced DHT levels in the serum and prostate, inhibiting prostate enlargement and attenuating the LUTS caused by BPH [32, 33]. However, there is limited clinical use of 5α-reductase inhibitors including dutasteride and finasteride, because of their adverse effects [9, 10]. In the present study, YJT-treated animals showed significant reductions in DHT levels of the serum and prostate compared with the BPH animals, as did the finasteride-treated rats. These results were consistent with the changes in prostate weights, PCNA expression levels and histomorphology. These findings indicate that YJT suppressed the development of BPH in this animal model, in a manner closely associated with reductions in DHT levels. In addition, YJT has been proved to be safe through toxicity studies [11, 12]. In particular, there was no observed adverse effect from YJT at up to 2000 mg/kg in acute and subchronic toxicity studies .
In conclusion, YJT significantly reduced prostate weights, prostatic hyperplasia, PCNA expression, and DHT levels in the serum and prostates of experimental rats. These results indicate that YJT effectively inhibits the development of BPH. Combined with the proven safety of YJT, these findings strongly support the feasibility of using YJT therapeutically in treating BPH.
This research was part of a research project (The Evidence Based Medicine for Herbal Formula) funded by the Basic Herbal Medicine Research Group of the Korea Institute of Oriental Medicine.
- Pais P: Potency of a novel saw palmetto extract, SPET-85, for inhibition of 5alpha-reductase II. Adv Ther. 2010, 27: 555-563. 10.1007/s12325-010-0041-6.View ArticlePubMedGoogle Scholar
- Roehrborn CG: Male lower urinary tract symptoms (LUTS) and benign prostatic hyperplasia (BPH). Med Clin North Am. 2011, 95: 87-100. 10.1016/j.mcna.2010.08.013.View ArticlePubMedGoogle Scholar
- Barkin J: Benign prostatic hyperplasia and lower urinary tract symptoms: evidence and approaches for best case management. Can J Urol. 2011, 18: 14-19.PubMedGoogle Scholar
- McVary KT: A review of combination therapy in patients with benign prostatic hyperplasia. Clin Ther. 2007, 29: 387-398. 10.1016/S0149-2918(07)80077-4.View ArticlePubMedGoogle Scholar
- Black L, Naslund MJ, Gilbert TD, Davis EA, Ollendorf DA: An examination of treatment patterns and costs of care among patients with benign prostatic hyperplasia. Am J Managed Care. 2006, 12: 99-110.Google Scholar
- Roehrborn CG, Rosen RC: Medical therapy options for aging men with benign prostatic hyperplasia: focus on alfusozin 10 mg once daily. Clin Interv Aging. 2008, 3: 511-524.PubMedPubMed CentralGoogle Scholar
- Gravas S, Oelke M: Current status of 5alpha-reductase inhibitors in the management of lower urinary tract symptoms and BPH. World J Urol. 2010, 28: 9-15. 10.1007/s00345-009-0493-y.View ArticlePubMedGoogle Scholar
- Andriole G, Bruchovsky N, Chung LW, Matsumoto AM, Rittmaster R, Roehrborn C, Russell D, Tindall D: Dihydrotestosterone and the prostate: the scientific rationale for 5alpha-reductase inhibitors in the treatment of benign prostatic hyperplasia. J Urol. 2004, 172: 1399-1403. 10.1097/01.ju.0000139539.94828.29.View ArticlePubMedGoogle Scholar
- Bullock TL, Andriole GL: Emerging drug therapies for benign prostatic hyperplasia. Expert Opin Emerg Drugs. 2006, 11: 111-123. 10.1517/1472822.214.171.124.View ArticlePubMedGoogle Scholar
- Traish AM, Hassani J, Guay AT, Zitzmann M, Hansen ML: Adverse side effects of 5α-reductase inhibitors therapy: persistent diminished libido and erectile dysfunction and depression in a subset of patients. J Sex Med. 2011, 8: 872-884. 10.1111/j.1743-6109.2010.02157.x.View ArticlePubMedGoogle Scholar
- Ha H, Lee JK, Lee HY, Seo CS, Lee MY, Huh JI, Shin H: Evaluation of genotoxicity of Yukmijihwang-tang, a herbal formula. Regul Toxicol Pharmacol. 2011, 59: 391-396. 10.1016/j.yrtph.2011.01.002.View ArticlePubMedGoogle Scholar
- Ha H, Lee JK, Lee HY, Koh WS, Seo CS, Lee MY, Huang DS, Shin H: Safety evaluation of Yukmijihwang-tang: assessment of acute and subchronic toxicity in rats. Evid Based Complement Alternat Med. 2011, 2011: 672136-View ArticlePubMedGoogle Scholar
- Song XY, Chen Q, Qi XY: Effects of liuwei dihuang pill on erythrocyte aldose reductase activity in early diabetic nephropathy patients. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2004, 24: 1087-1090.PubMedGoogle Scholar
- Kang DG, Sohn EJ, Moon MK, Mun YJ, Woo WH, Kim MK, Lee HS: Yukmijihwang-tang ameliorates ischemia/reperfusion-induced renal injury in rats. J Ethnopharmacol. 2006, 104: 47-53. 10.1016/j.jep.2005.08.044.View ArticlePubMedGoogle Scholar
- Kang M, Kim JH, Cho C, Lee KY, Shin M, Hong M, Shim I, Bae H: Effects of Yukmijihwang-tang derivatives (YMJd) on ibotenic acid-induced amnesia in the rat. Biol Pharm Bull. 2006, 29: 1431-1435. 10.1248/bpb.29.1431.View ArticlePubMedGoogle Scholar
- Oh MS, Chang MS, Park W, Kim DR, Bae H, Huh Y, Park SK: Yukmijihwang-tang protects against cyclophosphamide-induced reproductive toxicity. Reprod Toxicol. 2007, 24: 365-370. 10.1016/j.reprotox.2007.05.007.View ArticlePubMedGoogle Scholar
- Shim KS, Ma CJ, Kim DS, Ma JY: Yukmijihwang-tang inhibits receptor activator for nuclear Factor-κB ligand-induced osteoclast differentiation. J Med Food. 2011, 14: 1439-1447. 10.1089/jmf.2010.1502.View ArticlePubMedGoogle Scholar
- Shen JJ, Lin CJ, Hiang JL, Hsieh KH, Kuo ML: The effect of liu-wei-di-huang wan on cytokine gene expression from human peripheral blood lymphocytes. Am J Chin Med. 2003, 31: 247-257. 10.1142/S0192415X03000886.View ArticlePubMedGoogle Scholar
- Huynh H: Induction of apoptosis in rat ventral prostate by finasteride is associated with alteration in MAP kinase pathways and Bcl-2 related family of proteins. Int J Oncol. 2002, 20: 1297-1303.PubMedGoogle Scholar
- Veeresh Babu SV, Veeresh B, Patill AA, Warke YB: Lauric acid and myristic acid prevent testosterone induced prostatic hyperplasia in rats. Eur J Pharmacol. 2010, 625: 262-265.View ArticleGoogle Scholar
- Arruzazabala ML, Mas R, Molina V, Noa M, Carbajal D, Mendoza N: Effect of D-004, a lipid extract from the Cuban royal palm fruit, on atypical prostate hyperplasia induced by phynylephrine in rats. Drugs R&D. 2006, 7: 233-241. 10.2165/00126839-200607040-00003.View ArticleGoogle Scholar
- Bisson JF, Hidalgo S, Rozan P, Messaoudi M: Therapeutic effect of ACTICOA powder, a cocoa polyphenolic extract on experimentally induced prostate hyperplasia in Wistar-Unilever rats. J Med Food. 2007, 10: 628-635. 10.1089/jmf.2006.242.View ArticlePubMedGoogle Scholar
- Jang H, Ha US, Kim SJ, Yoon BI, Han DS, Yuk SM, Kim SW: Anthocyanin extracted from black soybean reduces prostate weight and promotes apoptosis in the prostatic hyperplasia-induced rat model. J Agric Food Chem. 2010, 58: 12686-12691. 10.1021/jf102688g.View ArticlePubMedGoogle Scholar
- Essers J, Theil AF, Baldeyron C, van Cappellen WA, Houtsmuller AB, Kanaar R, Vermeulen W: Nuclear dynamics of PCNA in DNA replication and repair. Mol Cell Biol. 2005, 25: 9350-9359. 10.1128/MCB.25.21.9350-9359.2005.View ArticlePubMedPubMed CentralGoogle Scholar
- Li SH, Ryu JH, Park SE, Cho YS, Park JW, Lee WJ, Chun YS: Vitamin C supplementation prevents testosterone-induced hyperplasia of rat prostate by down-regulating HIF-1alpha. J Nutr Biochem. 2010, 21: 801-808. 10.1016/j.jnutbio.2009.06.004.View ArticlePubMedGoogle Scholar
- Zhong W, Peng J, He H, Wu D, Han Z, Bi X, Dai Q: Ki-67 and PCNA expression in prostate cancer and benign prostatic hyperplasia. Clin Invest Med. 2008, 31: 8-15.Google Scholar
- Vikram A, Kushwaha S, Jena GB: Relative influence of testosterone and insulin in the regulation of prostatic cell proliferation and growth. Steroids. 2011, 76: 416-423. 10.1016/j.steroids.2010.12.014.View ArticlePubMedGoogle Scholar
- Miller J, Tarter TH: Combination therapy with dutasteride and tamsulosin for the treatment of symptomatic enlarged prostate. Clin Interv Aging. 2009, 4: 251-258.PubMedPubMed CentralGoogle Scholar
- Rittmaster R, Hahn RG, Ray P, Shannon JB, Wurzel R: Effect of dutasteride on intraprostatic androgen levels in men with benign prostatic hyperplasia or prostate cancer. Urology. 2008, 72: 808-812. 10.1016/j.urology.2008.06.032.View ArticlePubMedGoogle Scholar
- Carson C, Rittmaster R: The role of dihydrotestosterone in benign prostatic hyperplasia. Urology. 2003, 61: 2-7.View ArticlePubMedGoogle Scholar
- Mizokami A, Koh E, Izumi K, Narimoto K, Takeda M, Honma S, Dai J, Keller ET, Namiki M: Prostate cancer stromal cells and LNCaP cells coordinately activate the androgen receptor through synthesis of testosterone and dihydrotestosterone from dehydroepiandrosterone. Endocr Relat Cancer. 2009, 16: 1139-1155. 10.1677/ERC-09-0070.View ArticlePubMedGoogle Scholar
- Tarter TH, Vaughan ED: Inhibitors of 5alpha-reductase in the treatment of benign prostatic hyperplasia. Curr Pharm Des. 2006, 12: 775-783. 10.2174/138161206776056010.View ArticlePubMedGoogle Scholar
- Aggarwal S, Thareja S, Verma A, Bhardwaj TR, Kumar M: An overview on 5alpha-reductase inhibitors. Steroids. 2010, 75: 109-153. 10.1016/j.steroids.2009.10.005.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6882/12/48/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.