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红参油(KGC11)对丙酸睾酮诱导的良性前列腺增生的影响。

Effects of red ginseng oil(KGC11) on testosterone-propionate-induced benign prostatic hyperplasia.

作者信息

Lee Jeong Yoon, Kim Sohyuk, Kim Seokho, Kim Jong Han, Bae Bong Seok, Koo Gi-Bang, So Seung-Ho, Lee Jeongmin, Lee Yoo-Hyun

机构信息

Department of Food Science and Nutrition, The University of Suwon, Hwasung, Republic of Korea.

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

出版信息

J Ginseng Res. 2022 May;46(3):473-480. doi: 10.1016/j.jgr.2021.11.005. Epub 2021 Nov 13.

Abstract

BACKGROUND

Benign prostatic hyperplasia (BPH) is a disease characterized by abnormal proliferation of the prostate, which occurs frequently in middle-aged men. In this study, we report the effect of red ginseng oil (KGC11) on BPH.

METHODS

The BPH-induced Sprague-Dawley rats were divided into seven groups: control, BPH, KGC11 25, 50, 100, 200, and finasteride groups. KGC11 and finasteride were administered for 8 weeks. The BPH biomarkers, DHT, 5AR1, and 5AR2, androgen receptor, prostate-specific antigen (PSA), Bax, Bcl-2, and TGF-β were determined in the serum and prostate tissue. The cell viability after KGC11 treatment was determined using BPH-1 cells, and, androgen receptor, Bax, Bcl-2, and TGF-β were confirmed by western blotting.

RESULTS

In the in vivo study, administration of KGC11 reduced prostate weight by 18%, suppressed DHT (up to 22%) and 5AR2 (up to 12%) levels from administration of 100 mg/kg KGC11 (P < 0.05). PSA was significantly downregulated dose-dependently from at the concentration of 50 mg/kg KGC11 (P < 0.05). BPH-1 cell viability significantly reduced through the treatment with KGC11. and , AR, Bcl-2 TGF-β levels reduced significantly but Bax was increased (P < 0.05).

CONCLUSION

These results suggest that KGC11 may inhibit the development of BPH by significantly reducing the levels of BPH biomarkers via 5ARI, anti-androgenic effect, and anti-proliferation effect, serving as a potential functional food for treating BPH.

摘要

背景

良性前列腺增生(BPH)是一种以前列腺异常增生为特征的疾病,常见于中年男性。在本研究中,我们报告了红参油(KGC11)对BPH的影响。

方法

将诱导BPH的斯普拉格-道利大鼠分为七组:对照组、BPH组、KGC11 25mg/kg组、50mg/kg组、100mg/kg组、200mg/kg组和非那雄胺组。KGC11和非那雄胺给药8周。测定血清和前列腺组织中的BPH生物标志物、双氢睾酮(DHT)、5α还原酶1(5AR1)、5α还原酶2(5AR2)、雄激素受体、前列腺特异性抗原(PSA)、Bax、Bcl-2和转化生长因子-β(TGF-β)。使用BPH-1细胞测定KGC11处理后的细胞活力,并通过蛋白质免疫印迹法确认雄激素受体、Bax、Bcl-2和TGF-β。

结果

在体内研究中,给予KGC11可使前列腺重量降低18%,从给予100mg/kg KGC11起,DHT(高达22%)和5AR2(高达12%)水平受到抑制(P<0.05)。从KGC11浓度为50mg/kg起,PSA显著呈剂量依赖性下调(P<0.05)。通过KGC11处理,BPH-1细胞活力显著降低。并且,雄激素受体、Bcl-2、TGF-β水平显著降低,但Bax升高(P<0.05)。

结论

这些结果表明,KGC11可能通过5α还原酶抑制剂、抗雄激素作用和抗增殖作用显著降低BPH生物标志物水平,从而抑制BPH的发展,可作为治疗BPH的潜在功能性食品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdf5/9120790/f17a94eb91db/ga1.jpg

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