Biochemical and Histopathological evaluation of prostatic tissue under effect of Pterostilbene in benign prostatic hyperplasia rat model

Mohammed Ridha Jawad, Ghaith Ali Jasim
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Abstract

Background: Benign prostatic hyperplasia [BPH] is the urologic condition that affects elderly men the most frequently Benign prostatic hyperplasia. Benign prostatic hyperplasia must be distinguished from lower urinary tract symptoms and benign prostatic enlargement. which refers to an enlarged prostate, benign prostatic hyperplasia is a purely histological term the development, maintenance, and secretory activity of the prostate and other sex-accessory tissues are stimulated by the presence of certain hormones and growth factors. the pathophysiology of Benign prostatic hyperplasia is significantly influenced by the activity of the enzyme 5α-reductase. It's important to remember that 5-αreductase is responsible for creating Dihydrotestosterone a stronger androgen. Pterostilbene Mostly found in blueberries and grapes and pterostilbene substance with a number of biological properties including anticancer properties. pterostilbene is a lipid-soluble molecule that exists in both cis and trans forms with the latter being more prevalent. The conventional medication for Benign prostatic hyperplasia utilized in this trial was finasteride which inhibits the 5α-reductase enzyme and lowers the amount of Dihydrotestosterone. Methods: Forty-eight male rats were divided into six groups; the control group consisted of eight rats who received subcutaneous injections of oil vehicle for a period of 42 days. The induction group consisted of eight rats who received subcutaneous injections of testosterone propionate for a period of fourteen days. The finasteride group consisted of eight rats who received finasteride 0.44 mg/kg by oral gavage for a period of twenty-eight days following the induction of Benign prostatic hyperplasia and Pterostilbene 200 group included 8 rats were given pterostilbene 200mg/kg by oral gavage for 28 days after 14 days of Benign prostatic hyperplasia induction. pterostilbene 100 group included 8 rats were given a pterostilbene 100mg/kg per day kg by oral gavage for 28 days after 14 days of induction Benign prostatic hyperplasia dose and the resveratrol group included 8 rats were given a resveratrol 100mg/kg per day kg by oral gavage for 28 days after 14 days of induction Benign prostatic hyperplasia After twenty-eight days. Results: Histological section of prostate Pterostilbene 200 were similar those in control negative revealed numerous variable sizes alveoli that filled with homogenous eosinophilic secretion, had normal epithelial and stromal tissue. Conclusion: Pterostilbene have a potent anti-proliferative effect by decrease the hyperplastic nodules for prostate and return epithelial cell to normal and have a very good scavenging activity for free radical [very good as antioxidant] in compare with Vitamin c and resveratrol. Aim of study: evaluate the effect of Pterostilbene as Anti proliferative on Benign prostatic hyperplasia and assess the antioxidant activity for Pterostilbene by DPPH Assay.
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紫檀芪对前列腺增生模型大鼠前列腺组织的生化及病理影响
背景:良性前列腺增生(BPH)是影响老年男性最常见的泌尿系统疾病。良性前列腺增生必须与下尿路症状和良性前列腺肿大相鉴别。它指的是前列腺肥大,良性前列腺增生是一个纯粹的组织学术语,前列腺和其他性附属组织的发育、维持和分泌活动受到某些激素和生长因子的刺激。5α-还原酶活性显著影响良性前列腺增生的病理生理。重要的是要记住,5-α还原酶负责产生双氢睾酮,一种更强的雄激素。紫檀芪主要存在于蓝莓和葡萄中,紫檀芪具有多种生物特性,包括抗癌特性。紫檀芪是一种脂溶性分子,以顺式和反式两种形式存在,后者更为普遍。本试验采用非那雄胺治疗良性前列腺增生,抑制5α-还原酶,降低双氢睾酮水平。方法:48只雄性大鼠分为6组;对照组8只大鼠皮下注射油载体,为期42天。诱导组8只大鼠皮下注射丙酸睾酮,持续14天。非那雄胺组8只大鼠,在诱导良性前列腺增生后给予非那雄胺0.44 mg/kg灌胃,持续28天;紫檀芪200组8只大鼠,在诱导良性前列腺增生14天后给予紫檀芪200mg/kg灌胃,持续28天。紫檀芪100组8只大鼠,在诱导良性前列腺增生14 d后给予紫檀芪100mg/kg /天kg灌胃,持续28 d;白藜芦醇组8只大鼠,在诱导良性前列腺增生14 d后给予白藜芦醇100mg/kg /天kg灌胃,持续28 d。结果:前列腺紫檀芪200组织切片与对照阴性相似,可见大量大小不等的肺泡,充满均匀的嗜酸性粒细胞分泌,上皮和间质组织正常。结论:与维生素c和白藜芦醇相比,紫檀芪具有减少前列腺增生性结节、使上皮细胞恢复正常的抗增殖作用,对自由基有较好的清除作用。目的:探讨紫檀芪对前列腺增生的抗增殖作用,并采用DPPH法评价紫檀芪的抗氧化活性。
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