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Uromedic^(■) Pumpkin Seed Derived Δ7-Sterols, Extract and Oil Inhibit 5α-Reductases and Bind to Androgen Receptor in Vitro
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作者 Stefan Heim Stephanie Seibt +1 位作者 Heike Stier Margret I More 《Pharmacology & Pharmacy》 2018年第6期193-207,共15页
Dihydrotestosterone (DHT) is implicated in the development of benign prostate hyperplasia (BPH). We investigated if Uromedic? pumpkin (variety of Cucurbita pepo L. convar. citrullinina GREB. var. styriaca GREB) seed s... Dihydrotestosterone (DHT) is implicated in the development of benign prostate hyperplasia (BPH). We investigated if Uromedic? pumpkin (variety of Cucurbita pepo L. convar. citrullinina GREB. var. styriaca GREB) seed soft extract (active ingredients of GRANUFINK? Prosta forte 500 mg), seed oil and isolated Δ7-sterols could inhibit the conversion of [1,2,6,7-3H(N)]-testosterone to DHT by 5α-reductases. Also, we tested competition with [3H]-DHT for binding to the androgen receptor (AR). Pumpkin seed oil and pumpkin seed soft extract were identified as moderately active inhibitors of 5α-R1 and 5α-R2, with almost similar inhibitory capacities (IC50 5 mg/ml for 5α-R1 and about IC50 = 6 mg/ml for 5α-R2). The isolated Δ7-sterols were more active inhibitors (IC50 = 0.3 mg/ml for 5α-R1, IC50 = 1.0 mg/ml for 5α-R2). All three test compounds bound to the AR dose-dependently, with strong binding by Δ7-sterols (IC50 = 0.2 mg/ml) and weaker binding by pumpkin seed oil (IC50 = 0.4 mg/ml) and pumpkin seed soft extract (IC50 = 1.1 mg/ml). We propose that inhibition of 5α-reductases and competitive binding to the AR are mechanisms of action, by which the Uromedic? pumpkin seed derived test compounds, most specifically Δ7-sterols, counteract DHT and thereby exert clinically positive effects on the prostate, as well as bladder-strengthening effects. 展开更多
关键词 5-Alpha-reductases 5α-r1 and 5α-r2 Androgen Receptor DIHYDROTESTOSTERONE Uromedic? Pumpkin Seed Oil and Soft Extract (Delta-7) Δ7-Sterols
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DEHP对大鼠睾丸氧化应激和血清睾酮水平影响 被引量:7
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作者 杨敏 魏丽 刘长江 《中国公共卫生》 CAS CSCD 北大核心 2017年第11期1599-1602,共4页
目的探讨邻苯二甲酸二乙基己酯(DEHP)对青春期雄性大鼠睾丸及性激素的影响及潜在机制。方法 18日龄SD大鼠24只,按体重随机分为4组(对照组、低、中、高剂量DEHP组),每组6只。DEHP染毒剂量分别为250、500和750 mg/kg,经口连续染毒30 d;颈... 目的探讨邻苯二甲酸二乙基己酯(DEHP)对青春期雄性大鼠睾丸及性激素的影响及潜在机制。方法 18日龄SD大鼠24只,按体重随机分为4组(对照组、低、中、高剂量DEHP组),每组6只。DEHP染毒剂量分别为250、500和750 mg/kg,经口连续染毒30 d;颈部脱臼处死,收集血清,分离睾丸组织;测定血清睾酮、黄体生成素(LH)和卵泡刺激素(FSH)等性激素水平及睾丸组织中谷胱甘肽过氧化物酶(GSH-Px)、超氧化物歧化酶(SOD)、丙二醛和5α-还原酶(5α-R)活性。结果 DEHP处理组,大鼠睾丸和附睾脏器系数降低,睾丸曲精小管管腔缩小,结构坍塌,部分细胞膜破裂,细胞排列紊乱;与对照组比较,高剂量DEHP组大鼠血清睾酮和LH水平[分别为(115.04±14.21)pg/m L、(23.42±3.12)m IU/m L]降低,中、高剂量DEHP组大鼠血清FSH水平[分别为(5.49±0.42)、(4.63±0.51)IU/L]下降,差异有统计学意义(P<0.05);与对照组比较,高剂量DEHP组大鼠睾丸组织中GSH-Px和SOD活力[分别为(728.3±95.3)、(835.8±151.2)U/mg pro]降低,而中、高剂量DEHP组大鼠睾丸组织中丙二醛含量[分别为(79.6±13.9)、(90.6±4.0)nmol/mg pro]和5α-R2活性[分别为(415.9±112.7)、(415.9±147.8)IU/mg pro]升高,差异有统计学意义(P<0.05)。结论 DEHP暴露后,大鼠睾丸发生氧化应激,并通过诱导5α-R2活性降低血清睾酮水平。 展开更多
关键词 邻苯二甲酸二乙基己酯(DEHP) 睾丸 氧化应激 -还原酶2(5α-r2) 睾酮
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