以黄芪为基础的Eefooton对慢性肾病患者的治疗潜力:从临床到实验室研究。

IF 3.2 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Kuo-Cheng Lu, Ko-Lin Kuo, San-Chiang Wu, Chih-Hui Lin, Cheng-Ju Lin, Yi-Chou Hou, Jin-Shuen Chen
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引用次数: 0

摘要

目的:慢性肾脏疾病(CKD)是一个全球性的健康问题,最近的临床证据表明中药(TCM)具有减缓CKD进展的潜力。这为CKD患者提供了替代策略,降低了与多药和药物不良反应相关的风险。我们的自我控制、前瞻性研究旨在评估Eefooton (EFT),一种基于tcm的方案,对3-5期CKD患者肾脏健康的影响。此外,我们还进行了细胞培养研究,以探索EFT保护肾功能的潜在机制。材料和方法:2021 - 2022年间,75例3-5期CKD患者(56%男性;平均年龄68.20岁)在高雄退伍军人总医院及吴三江门诊部接受6个月的EFT治疗及常规CKD药物治疗。评估的主要结局是6个月时估计的肾小球滤过率(eGFR)的变化,次要结局包括肾脏大小和血液生物标志物的变化。监测不良事件。在体外研究中,研究了EFT对HK-2细胞活力和克隆原性的影响,并通过Western blot分析了凋亡和纤维化相关蛋白。结果:治疗后第6个月,中位eGFR由34.37±13.58改善至42.47±18.82 mL/min/1.73 m2 (p < 0.001)。值得注意的是,不同基线CKD分期均观察到改善(第3期:p < 0.001,第4期:p = 0.037)。超声扫描显示肾脏平均大小略有增加。在体外,EFT提高了HK-2细胞的活力和克隆原性。吲哚酚硫酸盐暴露提高了裂解酶和总PARP-1活性。EFT和IS共处理可降低裂解PARP-1活性。EFT降低is诱导的纤维化相关蛋白(α-平滑肌肌动蛋白)的表达,而不影响凋亡相关蛋白(Caspase 3)。结论:当与传统CKD药物联合使用时,EFT在3-5期CKD患者中显示出增强肾功能的有效性,没有报道的安全性问题。EFT的PARP-1抑制和抗纤维化特性在CKD的背景下显示出潜在的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic potential of Astragalus-based Eefooton in patients with chronic kidney disease: from clinical to bench study.

Objective: Chronic kidney disease (CKD) is a global health concern, and recent clinical evidence suggests the potential of traditional Chinese medicine (TCM) to slow CKD progression. This offers alternative strategies for CKD patients, mitigating risks related to polypharmacy and adverse drug reactions. Our self-controlled, prospective study aims to assess the impact of Eefooton (EFT), a TCM-based regimen, on kidney health in stage 3-5 CKD patients. Additionally, we conduct a cell culture study to explore the potential mechanisms of EFT in protecting renal function. Materials and methods: Between 2021 and 2022, 75 stage 3-5 CKD patients (56% males; mean age 68.20y) at Kaohsiung Veterans General Hospital and Wu San-Chiang Medical Clinic received six months of EFT treatment alongside conventional CKD medications. The primary outcome assessed was the change in estimated glomerular filtration rate (eGFR) at 6 months, with secondary outcomes including kidney size and blood biomarker changes. Adverse events were monitored. In an in vitro study, EFT effects on HK-2 cell viability and clonogenicity, as well as analysis of apoptosis and fibrosis-related proteins through Western blot, were investigated. Results: Median eGFR significantly improved from 34.37 ± 13.58 to 42.47 ± 18.82 mL/min/1.73 m2 (p < 0.001) at month 6 post-treatment. Notably, improvements were observed across different baseline CKD stages (stage 3: p < 0.001, stage 4: p = 0.037). Ultrasonography scans indicated a slight increase in mean kidney size. In vitro, EFT enhanced HK-2 cell viability and increased clonogenicity. Indoxyl sulfate exposure raised cleaved and total PARP-1 activity. Co-treatment with EFT and IS reduced cleaved PARP-1 activity. EFT decreased IS-induced expression of fibrosis-related proteins (α-smooth muscle actin) without affecting apoptosis-related proteins (Caspase 3). Conclusions: When combined with conventional CKD medications, EFT has shown effectiveness in enhancing kidney function in individuals with stage 3-5 CKD, with no reported safety concerns. The PARP-1 inhibition and anti-fibrosis properties of EFT present potential benefits in the context of CKD.

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来源期刊
International Journal of Medical Sciences
International Journal of Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
7.20
自引率
0.00%
发文量
185
审稿时长
2.7 months
期刊介绍: Original research papers, reviews, and short research communications in any medical related area can be submitted to the Journal on the understanding that the work has not been published previously in whole or part and is not under consideration for publication elsewhere. Manuscripts in basic science and clinical medicine are both considered. There is no restriction on the length of research papers and reviews, although authors are encouraged to be concise. Short research communication is limited to be under 2500 words.
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