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Anti-Inflammatory and Antioxidant Effects of Kelong-Capsule on Testosterone-Induced Benign Prostatic Hyperplasia in Rats

机译:科龙胶囊对大鼠睾丸良性前列腺增生的抗炎抗氧化作用

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摘要

Benign prostatic hyperplasia (BPH) is a common disease in the current ageing male population. This research aims to study the effects of Kelong-Capsules (KLC) on testosterone-induced BPH. Thirty rats were randomly divided into normal group, model group, and three treatment groups. Three treatment groups were given KLC (3.6 g/kg), KLC (7.2 g/kg), and finasteride (0.9 mg/kg), respectively, for 28 days after establishing the animal model. The BPH rat models were evaluated by Traditional Chinese Medicine (TCM) symptoms and prostate index (PI). Results indicated that three treatment groups all alleviated the pathological changes of prostate and kidney at different levels. Compared with the model group, the PI of the groups treated with KLC (7.2 g/kg) and finasteride decreased significantly. The expressions of NF-E2 related factor 2 (Nrf-2) and quinine oxidoreductase (NQO1) in the group treated with KLC (3.6 g/kg) increased markedly (p < 0.01). The cyclooxygenase-2 (COX-2) protein expression of the group treated with KLC (7.2 g/kg) was increased (p < 0.01). In conclusion, KLC could obviously inhibit the growth of prostate, and KLC (3.6 g/kg) could promote the expressions of Nrf2 and NQO1.
机译:良性前列腺增生(BPH)是当前老龄男性人群中的常见疾病。这项研究旨在研究克龙胶囊(KLC)对睾丸激素诱导的BPH的影响。将30只大鼠随机分为正常组,模型组和三个治疗组。在建立动物模型后的28天中,三个治疗组分别给予KLC(3.6μg/ kg),KLC(7.2μg/ kg)和非那雄胺(0.9μmg/ kg)。通过中药(TCM)症状和前列腺指数(PI)评估了BPH大鼠模型。结果表明,三个治疗组均以不同水平减轻了前列腺和肾脏的病理变化。与模型组相比,KLC(7.2μg/ kg)和非那雄胺治疗组的PI显着降低。 KLC(3.6μg/ kg)治疗组中NF-E2相关因子2(Nrf-2)和奎宁氧化还原酶(NQO1)的表达显着增加(p <0.01)。用KLC处理的组(7.2μg/ kg)的环氧合酶2(COX-2)蛋白表达增加(p <0.01)。总之,KLC可以明显抑制前列腺的生长,而KLC(3.6μg/ kg)可以促进Nrf2和NQO1的表达。

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