Korean Red Ginseng Ameliorates the Level of Serum Uric Acid via Downregulating URAT1 and Upregulating OAT1 and OAT3.

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY Biological & pharmaceutical bulletin Pub Date : 2024-01-01 DOI:10.1248/bpb.b24-00293
Soon-Young Lee, Seung-Sik Cho, Kang Min Han, Min-Jae Lee, Taeho Ahn, Byungcheol Han, Chun-Sik Bae, Dae-Hun Park
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Abstract

Hyperuricemia is caused by an imbalance of uric acid and is associated with many diseases. Although gout which is one of hyperuricemia-related diseases is curable with anti-hyperuricemic drugs some medications have side effects, such as hypersensitivity in patients with circulatory system disorders, flare reoccurrences, and increased cardiac risk. This study consisted of test tube (xanthine oxidase's inhibition) and animal study. Animal study using with ICR mice was composed of control, potassium oxonate-induced hyperuricemia, allopurinol, and 3 Korean red ginseng water extract (KRGWE) treatment groups (62.5; 125, and 500 mg/kg). We orally administered KRGWE once a day for 7 d to induce hyperuricemia and injected PO 2 h before the final KRGWE administration. We measured serum uric acid, glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT), blood urea nitrogen, and creatinine and analyzed the genes such as organic anion transport (OAT)-1, OAT-3, and urate transport (URAT)-1. KRGWE dose-dependently controlled xanthine oxidase activity in the serum and completely inhibited serum uric acid. KRGWE affected both uric acid excretion-related and uric acid reabsorption-related gene expression. KRGWE stimulated uric acid excretion-related gene expressions, such as OAT-1 and OAT-3, but inhibited uric acid reabsorption-related gene expression, such as URAT-1. KRGWE improved liver and kidney functioning. KRGWE improved liver/kidney functioning and is promising anti-hyperuricemic agent which can control serum uric acid via downregulating URAT1 and upregulating OAT1 and OAT3.

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高丽红参通过下调 URAT1 和上调 OAT1 和 OAT3 改善血清尿酸水平
高尿酸血症是由尿酸失衡引起的,与许多疾病相关。痛风是高尿酸血症相关疾病中的一种,虽然抗高尿酸血症药物可以治愈痛风,但有些药物会产生副作用,如循环系统疾病患者的过敏反应、复发和增加心脏风险。这项研究包括试管研究(抑制黄嘌呤氧化酶)和动物研究。使用 ICR 小鼠进行的动物研究包括对照组、氧化钾诱导的高尿酸血症组、别嘌呤醇组和 3 个高丽红参水提取物(KRGWE)治疗组(62.5、125 和 500 毫克/千克)。我们每天口服一次高丽红参水提取物,连续7天诱导高尿酸血症,并在最后一次服用高丽红参水提取物前2小时注射PO。我们测定了血清尿酸、谷氨酸草酰乙酸转氨酶(GOT)、谷氨酸丙酮酸转氨酶(GPT)、血尿素氮和肌酐,并分析了有机阴离子转运(OAT)-1、OAT-3和尿酸盐转运(URAT)-1等基因。KRGWE剂量依赖性地控制了血清中黄嘌呤氧化酶的活性,并完全抑制了血清尿酸。KRGWE 影响尿酸排泄相关基因和尿酸重吸收相关基因的表达。KRGWE 可刺激尿酸排泄相关基因(如 OAT-1 和 OAT-3)的表达,但抑制尿酸重吸收相关基因(如 URAT-1)的表达。KRGWE 可改善肝脏和肾脏功能。KRGWE 可改善肝脏/肾脏功能,通过下调 URAT1、上调 OAT1 和 OAT3 控制血清尿酸,是一种很有前景的抗高尿酸血症药物。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
247
审稿时长
2 months
期刊介绍: Biological and Pharmaceutical Bulletin (Biol. Pharm. Bull.) began publication in 1978 as the Journal of Pharmacobio-Dynamics. It covers various biological topics in the pharmaceutical and health sciences. A fourth Society journal, the Journal of Health Science, was merged with Biol. Pharm. Bull. in 2012. The main aim of the Society’s journals is to advance the pharmaceutical sciences with research reports, information exchange, and high-quality discussion. The average review time for articles submitted to the journals is around one month for first decision. The complete texts of all of the Society’s journals can be freely accessed through J-STAGE. The Society’s editorial committee hopes that the content of its journals will be useful to your research, and also invites you to submit your own work to the journals.
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