• Asian Pacific Journal of Cancer Prevention
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• 제16권3호
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• pp.1033-1036
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• 2015

Background: Testosterone, a primary androgen in males, is converted into its most active form, dihydrotestosterone (DHT), by $5{\alpha}$-reductase type 2 (encoded by the SRD5A2 gene) in the prostate. DHT is necessary for prostatic growth and has five times higher binding affinity than testosterone for androgen receptors. We hypothesized that polymorphic variations in the SRD5A2 gene may affect the risk of benign prostatic hyperplasia and prostate cancer. Materials and Methods: We analyzed SRD5A2 gene polymorphisms in 217 BPH patients, 192 PCa cases, and 171 controls. Genotyping was undertaken using direct DNA sequencing. Genotype data were compared between cases and controls using a Chi square statistical tool. Results: We found that the A49T locus was monomorphic with 'AA' genotype in all subjects. At V89L locus, the presence of 'VV' showed a marginally significant correlation with increased BPH risk (p=0.047). At the $(TA)_n$ locus, longer TA repeats were found to be protective against BPH (p=0.003). However, neither of these polymoprhisms correlated with the risk of PCa. Conclusions: We conclude that A49T is monomorphic in the study population, VV marginally correlates with BPH risk, and longer $(TA)_n$ repeats are protective against BPH. None of these polymorphisms affect the risk of PCa.

• Natural Product Sciences
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• 제13권2호
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• pp.160-163
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• 2007

Four glycosides, rosamultin (1), tetracentronside B (2), 4-O-methylellagic acid 3-O-${\alpha}$-$_L$-rhamnopyranoside (3), and vanillic acid 4-O-${\beta}$-$_L$-glucopyranoside (4), isolated from the roots extract of Potentilla discolor, were subjected to in vitro bioassays to evaluate the inhibitory activity on advanced glycation end products (AGEs) formation and rat lens aldose reductase (RLAR). Compound 3 exhibited a significant inhibitory activity against both AGEs formation and RLAR with IC$_{50}$ values of 79.5 and 8.03 ${\mu}$M, respectively. All the compounds (1-4) were isolated for the first time from this plant.

• 미생물학회지
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• 제29권4호
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• pp.258-262
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• 1991

Rhizopus nigricans에 의한 progest$\xi$rone의 Iia-hydroxylation 반응은 포도당에 의하여 촉진되었으며 그 효과가 전자 수용체인 NADPH와 NaJD. 를 투입하였을 때의 효과와 유사한 것으로 부터 표도당은 이 반응에 필요한 보조요소의 생성에 기여하며 hydroxylation 반응을 촉진한다고 생각되었다 포도당의 소모량은 hydroxy lation 반응 속도가 빠을수록 크게 나타났으며 포도당의 농도가 증가함에 따라 반응 속도는 점차 증가하다가 균사체는 0.5 g/l 포자체는 20 g/l에서 거의 일정해지는 경향을 나타내었다. 그러나 polyacrylamide gel에 고정화한 균사체의 경우 배양 기간 동안 gel내에 축적되어 있는 포도당 만으로도 반응이 충분히 촉진되었다. a-Hydroxy progesterone의 Sa-reduction 반응은 p progesterone의 11a-hyroxylation 반응에 버하여 훨씬 더 높은 포도당 농도가 필요하므로 포노당의 농도를 낮게 유지시킴으로써 5a-reducrion 반응을 억제하여 11 a-hydroxyprogesterone의 수득융을 높힐 수 있음 갯으로 판단되었다.

• Journal of Acupuncture Research
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• 제31권1호
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• pp.95-103
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• 2014

Objectives : The aim of this study is to evaluate the effect of Paljeong-san pharmac-opuncture(PJS) on the rat model of benign prostatic hyperplasia(BPH). Methods : Rats were divided into 5 groups, with 6 rats in each group. The 5 groups included sham-operated group(sham group), BPH model group(BPH group), finasteride-treated group (fina group), PJS-treated groups(PJS 10 and PJS 100 group). Testosterone was injected subcutaneously to the castrated rats except sham group for BPH model. During 4-week experimental period, finasteride(5 mg/kg) was administrated orally once daily in fina group, PJS in PJS 10(10 mg/kg) and PJS 100(100 mg/kg) group and normal saline in sham and BPH group were injected subcutaneously once daily at Jungwan($CV_{12}$). We checked prostate weights, serum concentration of dihydrotestosterone(DHT), morphologic changes of the prostate, and the amount of expression of the proliferating cell nuclear antigen(PCNA) and $5{\alpha}$-reductase gene to evaluate the effect of PJS after 4-week experimental period. Results : 1. PJS and finasteride treatment reduced prostate weights comparing with BPH group, but PJS-treated groups showed no significant changes, unlikely fina group. 2. PJS-treated groups showed significant degreases in concentration of DHT. 3. PJS-treated groups showed significant degreases concentration-dependently in the amount of expression of the PCNA and $5{\alpha}$-reductase gene. 4. PJS treatment showed shrinking of thickness in the prostatic epithelial tissue. Conclusions : PJS has the effects that improve the symptoms of BPH through inhibiting proliferation of the prostatic tissues.

• 한국발생생물학회지:발생과생식
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• 제13권2호
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• pp.79-87
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• 2009

출산과 수유 과정에서의 잘 알려진 기능 때문에, 옥시토신(oxytocin, OT)은 '여성 뇌하수체후엽 호르몬(female nerohypophyseal hormone)'으로 알려져 왔다. 그러나 최신 연구들에 따르면 OT가 중추신경계와 말초조직 수준에서 수컷 생식을 조절하는 국부적인 기능을 가짐이 알려졌다. 일부 실험용 설치류에서, OT는 사회적인 자극들에 반응하여 뇌의 특정 지역으로 분비되는데, 이 뇌 OT와 그 수용체(OTR)를 매개로한 작용들은 수컷의 다양한 행동, 특히 교미 관련 행동의 조절에 깊이 관여한다. 최근에 개발된 OT와 OTR knockout 생쥐 모델들의 사회적, 성적 행도으이 분자 조절 기작들에 대한 중요한 실마리들을 제공하다. OT는 또한 설치류의 정소, 부정소, 전립선에서도 합성되며, 이들 조직에서도 OTR이 발현됨이 보고되어왔다. OT는 말초적으로 testosterone(T)을 dihydrotestosterone(DHT)로 전환시키는 5alpha-reductase의 활성조절을 통해 정소의 스테로이드호르몬 합성과 분비에 관여한다. 안드로겐 전환을 유도하는 OT 작용들이 부정소와 전립선에서도 발견되는데, 이는 OT가 이들 안드로겐 의존적인 생식도관의 기능들, 예를 들어 평활근 수축 유도와 같은 기능을 조절함을 시사한다. 이러한 맥락에서, 수컷의 뇌와 생싯기간 중추신경계와 생식기관에서의 OT의 기능들에 대한 향후 연구들은 복잡한 사회적, 성적 행동에 대한 이해 증진과 심리적 혹은 남성과학적 이상에 대한 치료법 개발에 대한 기반을 제공할 수 있을 것이다.

• Applied Biological Chemistry
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• 제27권2호
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• pp.100-106
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• 1984

신생 쥐 간의 subcellular fraction의 특징과 $6{\alpha}$-steroid hydroxylase의 subcellular localization및 특성을 살펴본 결과는 다음과 같다. 1000g 30초 침전 fraction은 총 DNA의 95%를 차지하므로써 crude nuclei fraction으로 나타났으며 또한 5'-nucleotidase의 specific activity가 높은 것은 파괴되지 않은 세포에 기인된 것으로 생각이 되며, 1450g 10분 침전 fraction은 5'-nucleotidase의 activity가 가장 높으므로 crude plasma membrane fraction으로 동정하였으나 mitochondria가 같이 침전되어 있었으며, 9000g 20분 침전 fraction은 succinate-cytochrome C reductase의 activity가 가장 높아 mitochondria fraction으로 하였고, 105,000g 60분 상등액은 LDH가 가장 높아 cytosol로 하였으며, 105,000g 60분 침전은 남은 부분으로 microsome fraction으로 추정하였다. 각 fraction에 기질인 $3{\beta}$-hydroxy-$5{\alpha}$-pregnan-20-one을 incubation시킨 후의 생성된 steroid를 보면 crude nuclei fraction에서는 pregnadiol($5{\alpha}$-pregnane-$3{\alpha}/{\beta}$, $20{\alpha}$-diol)의 형성으로 $20{\alpha}$-reduction과 $3{\alpha}$-$3{\beta}$ iso${\beta}$merization을 볼 수 있었으며 crude plasma membrane fraction에서는 $20{\alpha}$-reduction과 $6{\alpha}$-hydroxylation을 볼 수 있었으며 crude mitochondria와 cytosol에서는 $20{\alpha}$-reduction만을 crude microsome에서는 $16{\alpha}$-hydroxylation을 볼 수 있었으므로 $6{\alpha}$-hydroxylase는 crude plasma membrane에 존재함을 확인하였다. 한편 $6{\alpha}$-steroid hydroxylase에 존재함을 확인하였다. 한편 $6{\alpha}$-steroid hydroxylase의 최대 활성도는 pH 7에서 나타났으며 progesterone은 hydroxylation을 시키지 못한 반면 $3{\alpha}$-hydroxy-$5{\alpha}$-pregnan-20-one은 $6{\alpha}$-hydroxylation이 되었다.

• 한국임상약학회지
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• 제25권3호
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• pp.171-177
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• 2015

Background: Androgenetic alopecia (AGA), one of alopecias, requires continuous treatment in order to prevent or stop it, and patient's compliance is very important. Currently, only two drugs (finasteride, minoxidil) have been approved for AGA by Food and Drug Administration of United States (US FDA). However, another ${\alpha}-2$ reductase inhibitor, dutasteride, is approved by Korea Ministry of Food and Drug Safety (MFDS) through a phase III trial. For treatment, pharmacotherapy of AGA usually combines topical minoxidil 7% with one of oral <${\alpha}-2$ reductase inhibitor. Objectives: We evaluated the comparative efficacy and adverse effect between topical minoxidil 7%/finasteride 1 mg and topical minoxidil 7%/dutasteride 0.5 mg pharmacotherapy for outpatients with AGA. Also we evaluated the relationship between therapeutic effect and regular hospital visit. Method: This study was performed retrospectively based on electronic medical record (EMR) data of total 98 patients (topical minoxidil 7% with dutasteride 0.5 mg ($Avodart^{(R)}$) or finasteride 1 mg ($Alopecia^{(R)}$, $Propecia^{(R)}$) with diagnosis of AGA from department of dermatology at a secondary hospital from January $1^{st}$, to May $31^{st}$, 2014. Results: The efficacy and adverse event of topical minoxidil 7%/dutasteride 0.5 mg (DUTA group) were 100% and 45.7%, and of topical minoxidil 7%/finasteride 1 mg (FINA group) were 92.1% and 33.3%, respectively. The mean onset time of responses and adverse events in the FINA group were 3.86 months and 4.43 months. Those in the DUTA group were 3.97 months and 5.06 months. Conclusion: Both FINA and DUTA group were highly effective, but the DUTA group showed higher efficacy and adverse effects than those in the FINA group. Dutasteride may be another alternative in AGA treatment.

• Biomolecules & Therapeutics
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• 제21권1호
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• pp.49-53
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• 2013

A number of naturally-occurring or synthetic chemicals have been reported to exhibit prostate chemopreventive effects. Synthetic $5{\alpha}$-reductase (5-AR) inhibitors, e.g. finasteride and durasteride, gained special interests as possible prostate chemopreventive agents. Indeed, two large-scale epidemiological studies have demonstrated that finasteride or durasteride significantly reduced the incidence of prostate cancer formation in men. However, these studies have raised an unexpected concern; finasteride and durasteride increased the occurrence of aggressive prostate tumor formation. In the present study, we have observed that treatment of finasteride did not affect the growth of androgen-refractory PC-3 prostate cancer cells. Finasteride also failed to induce apoptosis or affect the expression of proto-oncogenes in PC-3 cells. Interestingly, we found that treatment of finasteride induced the expression of Nrf2 and HO-1 proteins in PC-3 cells. In particular, basal level of Nrf2 protein was higher in androgen-refractory prostate cancer cells, e.g. DU-145 and PC-3 cells, compared with androgen-responsive prostate cancer cells, e.g. LNCaP cells. Also, treatment of finasteride resulted in a selective induction of Nrf2 protein in DU-145 and PC-3 cells, but not in LNCaP cells. In view of the fact that upregulation of Nrf2-mediated phase II cytoprotective enzymes contribute to attenuating tumor promotion in normal cells, but, on the other hand, confers a selective advantage for cancer cells to proliferate and survive against chemical carcinogenesis and other forms of toxicity, we propose that finasteride-mediated induction of Nrf2 protein might be responsible, at least in part, for an increased risk of high-grade prostate tumor formation in men.

• Nutrition Research and Practice
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• 제17권1호
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• pp.32-47
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• 2023

BACKGROUND/OBJECTIVES: Benign prostatic hyperplasia (BPH) characterized by an enlarged prostate gland is common in elderly men. Corni Fructus (CF) and Schisandrae Fructus (SF) are known to have various pharmacological effects, including antioxidant and anti-inflammatory activities. In this study, we evaluated the inhibitory efficacy of CF, SF, and their mixture (MIX) on the development of BPH using an in vivo model of testosterone-induced BPH. MATERIALS/METHODS: Six-week-old male Sprague-Dawley rats were randomly divided into seven groups. To induce BPH, testosterone propionate (TP) was injected to rats except for those in the control group. Finasteride, saw palmetto (SP), CF, SF, and MIX were orally administered along with TP injection. At the end of treatment, histological changes in the prostate and the level of various biomarkers related to BPH were evaluated. RESULTS: Our results showed that BPH induced by TP led to prostate weight and histological changes. Treatment with MIX effectively improved TP-induced BPH by reducing prostate index, lumen area, epithelial thickness, and expression of BPH biomarkers such as 5α-reductase type 2, prostate-specific antigen, androgen receptor, and proliferating cell nuclear antigen compared to treatment with CF or SF alone. Moreover, MIX further reduced levels of elevated serum testosterone, dihydrotestosterone, and prostate-specific antigen in BPH compared to the SP, a positive control. BPH was also improved more by MIX than by CF or SF alone. CONCLUSIONS: Based on the results, MIX is a potential natural therapeutic candidate for BPH by regulating 5α-reductase and AR signaling pathway.

• 동의생리병리학회지
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• 제24권4호
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• pp.653-660
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• 2010

Pulsatillae Radix and Cicadidae Periostracum have long been used for treatment of injuries, inflammations or itchiness in Korea. This study was carried out to examine the acne-remedy effects of the mixture made with equal parts of Pulsatillae Radix extract and Cicadidae Periostracum extract (PRCP) compared with 2%-benzoyl peroxide (Standard) used commercially as anti-acne. The results showed the mixture (PRCP) was more effective than each crude drug extract. The 10%-PRCP showed significant antimicrobial activity against Propionibacterium acnes, the major cause of acne, and also showed significant inhibition from type 1 $5{\alpha}$-reductase ($5{\alpha}R$), another cause of acne, And the cream made with PRCP demonstrated anti-sebum and acne-improvement effects on examinee's facial skin.