The Effect Of Continuously Dutasteride Monotherapy on The Expression Of Protein Kinase C-Alpha Enzyme In BPH Model Of Wistar Strain Rattus Novergicus Rat.

Q2 Medicine Medicinski arhiv Pub Date : 2023-01-01 DOI:10.5455/medarh.2023.77.202-206
Besut Daryanto, I Gusti Lanang Andi Suharibawa, Athaya Febriantyo Purnomo, Pradana Nurhadi, Viera Wardhani
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Abstract

Background: Benign prostate hyperplasia (BPH) is frequently found in the elderly and significantly impacts the quality of life. One of the risk factors that induce BPH is the androgen hormone. One of the effective medications in reducing the severity of Lower Urinary Tract Symptoms caused by BPH is the α-adrenergic receptor 5α-reductase inhibitor.

Objective: The study aims to see the effect of long-term dutasteride on the expression of the PKC-α enzyme in prostatic stromal tissue in the BPH Model of Wistar strain Rattus norvegicus rats.

Method: This study was an experimental, post-test-only, control group design that used randomization in sample selection. The objective is to measure the expression of PKC-α enzyme from prostate tissue of an adult male Wistar Strain of Rattus Novergicus rat that was given testosterone to induce BPH and given dutasteride in 1,3 and 6 days continuously. Data is shown in mean±SD, and all of the data were analyzed using the software SPSS 21st version with the One Way ANOVA Statistical method after fulfilling the normality test and variant homogeneity test. Data analysis with confidence rate 95% and a=0,05.

Results: There was a decrease of PKC-α enzyme and prostate weight in dutasteride monotherapy in 1,3,6 days compared to the positive control, and the lowest value was on the sixth day (SD ± 2876.8). There was a constant decrease of PKC-α enzyme from the first day until the sixth day.

Conclusion: In conclusion, long-term dutasteride monotherapy could significantly decrease the level of PKC-α enzyme. There was no upregulation of the PKC-α enzyme in the long term of dutasteride monotherapy.

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持续使用度他雄胺单药对Wistar种大鼠良性前列腺增生模型中蛋白激酶C-α酶表达的影响
背景:良性前列腺增生症(BPH)常见于老年人,严重影响他们的生活质量。诱发良性前列腺增生症的风险因素之一是雄性激素。α-肾上腺素能受体 5α 还原酶抑制剂是减轻良性前列腺增生症引起的下尿路症状的有效药物之一:本研究旨在观察长期服用度他雄胺对前列腺增生模型Wistar株Rattus norvegicus大鼠前列腺基质组织中PKC-α酶表达的影响:本研究采用随机抽样的实验、后测、对照组设计。研究目的是测量成年雄性 Wistar 株大鼠前列腺组织中 PKC-α 酶的表达情况,该大鼠服用睾酮诱导前列腺增生,并连续服用 1、3 和 6 天度他雄胺。数据以均数±SD 表示,所有数据均在满足正态性检验和变异同质性检验后使用 SPSS 21st 版软件进行单因素方差分析。数据分析置信度为 95%,a=0.05:与阳性对照组相比,度他雄胺单药治疗 1、3、6 天后 PKC-α 酶和前列腺重量均有所下降,最低值出现在第 6 天(SD ± 2876.8)。从第一天到第六天,PKC-α酶持续下降:结论:总之,长期服用度他雄胺单药可显著降低PKC-α酶的水平。结论:长期使用度他雄胺单药治疗可明显降低PKC-α酶的水平,长期使用度他雄胺单药治疗也不会导致PKC-α酶上调。
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Medicinski arhiv
Medicinski arhiv Medicine-Medicine (all)
CiteScore
2.10
自引率
0.00%
发文量
54
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