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枳壳对睾酮诱导的大鼠前列腺增生的抑制作用。

Inhibitory effects of Ponciri Fructus on testosterone-induced benign prostatic hyperplasia in rats.

作者信息

Jeon Woo-Young, Kim Ohn Soon, Seo Chang-Seob, Jin Seong Eun, Kim Jung-Ae, Shin Hyeun-Kyoo, Kim Yong-Ung, Lee Mee-Young

机构信息

K-herb Research Center, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon, 34054, Republic of Korea.

KM Convergence Research Division, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon, 34054, Republic of Korea.

出版信息

BMC Complement Altern Med. 2017 Aug 3;17(1):384. doi: 10.1186/s12906-017-1877-y.

Abstract

BACKGROUND

Benign prostatic hyperplasia (BPH) is non-cancerous condition of enlargement of the prostate, a common occurrence in older men. The immature fruits of Poncirus trifoliata (L.) Rafinesque (Rutaceae), Ponciri Fructus are widely used in traditional oriental medicine for the therapy of various diseases. However, little is known about the mechanism underlying the pathogenesis of BPH. In the present study, we investigated the protective effects of a Ponciri Fructus extract (PFE) on the development of BPH in a in a rat model of BPH induced by testosterone propionate (TP).

METHODS

Male Sprague Dawley rats were used as a model of BPH after its induction by daily subcutaneous injections of TP/corn oil, for a period of four weeks. PFE was administrated daily 1 h before TP/corn oil injection by oral gavage at a dose level of 200 mg/kg during the 4 weeks of TP/corn oil injections. All rats were sacrificed at the end of the experiment, we measured the relative prostate weight, the levels of testosterone and dihydrotestosterone (DHT), histological changes, activities of antioxidant enzymes (catalase, glutathione peroxidase, glutathione reductase, and superoxide dismutase), and expression of proliferating cell nuclear antigen (PCNA). In addition, we also measured the inhibition (%) of 5α-reductase in the prostatic tissue.

RESULTS

Our findings indicate that PFE significantly inhibited the development of BPH; decreased the relative prostate weight, the level of testosterone and DHT in serum and prostatic tissue, prostatic hyperplasia, expression of PCNA, and increased the antioxidant enzymes. Moreover, PFE showed a weak inhibitory activity on 5α-reductase.

CONCLUSIONS

These results suggest that PFE may be used as a therapeutic agent for BPH via antiproliferative and antioxidant effects.

摘要

背景

良性前列腺增生(BPH)是前列腺非癌性肿大,在老年男性中很常见。枳壳(芸香科)未成熟果实枳实,在传统东方医学中广泛用于治疗各种疾病。然而,关于BPH发病机制的潜在机制知之甚少。在本研究中,我们研究了枳实提取物(PFE)对丙酸睾酮(TP)诱导的BPH大鼠模型中BPH发展的保护作用。

方法

雄性Sprague Dawley大鼠通过每日皮下注射TP/玉米油诱导4周后作为BPH模型。在TP/玉米油注射的4周期间,每天在TP/玉米油注射前1小时通过口服灌胃给予PFE,剂量为200mg/kg。实验结束时处死所有大鼠,我们测量了相对前列腺重量、睾酮和二氢睾酮(DHT)水平、组织学变化、抗氧化酶(过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶和超氧化物歧化酶)活性以及增殖细胞核抗原(PCNA)的表达。此外,我们还测量了前列腺组织中5α-还原酶的抑制率(%)。

结果

我们的研究结果表明,PFE显著抑制了BPH的发展;降低了相对前列腺重量、血清和前列腺组织中睾酮和DHT水平、前列腺增生、PCNA表达,并增加了抗氧化酶。此外,PFE对5α-还原酶表现出较弱的抑制活性。

结论

这些结果表明,PFE可能通过抗增殖和抗氧化作用用作BPH的治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a055/5543435/98a899c430a6/12906_2017_1877_Fig1_HTML.jpg

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