古巴皇家棕榈果实脂质提取物D-004对完整和去势啮齿动物睾丸激素诱导的前列腺增生的预防作用。

M L Arruzazabala, D Carbajal, R Más, V Molina, E Rodríguez, V González
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摘要

良性前列腺增生(BPH)是一种非癌性、不受控制的前列腺细胞和基质增生,可引起排尿困难。果脂提取物从锯棕榈,一种棕榈从槟榔科,用于BPH管理。古巴皇家棕榈Roystonea regia也是槟榔科的一员,因此研究Roystonea regia果实脂质提取物对前列腺增生的保护作用是合适的。本研究的目的是研究从皇家Roystonea regia果实中提取的脂质提取物D-004是否能阻止睾丸激素诱导的阉割和完整啮齿动物的PH。进行了两个系列的实验。第一个实验是在阉割和完整的大鼠中进行的,分为五组,每组10只大鼠。阴性对照组注射大豆油并口服载药,4个睾酮注射组分别给予载药(阳性对照)、D-004 100、200、400 mg/kg。另一项实验是在阉割和完整的小鼠中进行的。将这些小鼠分为4组,每组10只:阴性对照组和3个睾酮注射组,其中1个为阳性对照组,2个分别注射D-004 200和400 mg/kg。在研究结束时,啮齿动物被处死,前列腺被切除并称重。D-004在100,200和400mg /kg剂量下显著且剂量依赖地阻止了完整和去势大鼠和小鼠的前列腺肿大。在小鼠中获得的抑制百分比更大:完整小鼠和阉割小鼠分别为77%和84%。D-004治疗对体重没有影响。由此可见,口服D-004均能显著抑制睾丸激素诱导的前列腺增大,这表明内源性睾酮并不是观察前列腺增大的必要条件。本研究结果为D-004对前列腺增生实验模型的进一步研究提供了支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preventive effects of D-004, a lipid extract from Cuban royal palm (Roystonea regia) fruits, on testosterone-induced prostate hyperplasia in intact and castrated rodents.

Benign prostatic hyperplasia (BPH) is the noncancerous, uncontrolled growth of prostate gland cells and stroma that can cause difficulty urinating. Fruit lipid extracts from saw palmetto, a palm from the Arecaceae family, are used for BPH management. The Cuban royal palm, Roystonea regia, is also a member of the Arecaceae family and therefore it was appropriate to investigate the protective effects of Roystonea regia fruit lipid extracts on prostatic hyperplasia. The aim of this study was to investigate whether D-004, a lipid extract from Roystonea regia fruits, prevented testosterone-induced PH in castrated and intact rodents. Two series of experiments were performed. The first one was conducted in castrated and intact rats, distributed into five groups of 10 rats per group. The negative control group was injected with soy oil and treated orally with vehicle, while the four testosterone-injected groups were treated with vehicle (positive control), D-004 100, 200 and 400 mg/kg, respectively. The other experiment was conducted in castrated and intact mice. These were distributed into four groups of 10 mice per group: a negative control group and three testosterone-injected groups, of which one was a positive control, while two received D-004 200 and 400 mg/kg, respectively. At study completion, the rodents were sacrificed and prostates removed and weighed. D-004 at doses of 100, 200 and 400 mg/kg significantly and dose-dependently prevented prostate enlargement in intact and castrated rats and mice. The percentage inhibitions obtained in mice were greater: 77% and 84% for intact and castrated mice, respectively. D-004 therapy did not affect body weight. It is concluded that D-004 administered orally significantly prevented testosterone-induced prostate enlargement in both intact and castrated rodents, indicating that an endogenous supply of testosterone is not necessary to observe such an effect The results of the present investigation support further studies of D-004 on experimental models of prostatic hyperplasia.

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