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TP0463518(TS-143)可改善肽聚糖-多糖诱导的大鼠炎症性贫血。

TP0463518 (TS-143) Ameliorates Peptidoglycan-Polysaccharide Induced Anemia of Inflammation in Rats.

机构信息

Discovery Research Laboratories, Taisho Pharmaceutical Co., Ltd.

出版信息

Biol Pharm Bull. 2021;44(11):1653-1661. doi: 10.1248/bpb.b21-00038.

Abstract

TP0463518 (TS-143) is a competitive prolyl hydroxylase 1/2/3 pan-inhibitor, and has been shown to specifically stabilize hypoxia-inducible factor-2 alpha in the liver to increase erythropoietin production. While TP0463518 has been shown to improve renal anemia, its effect on anemia of inflammation is still unknown. In this study, we created a rat model of anemia of inflammation by administering peptidoglycan-polysaccharide (PG-PS) to Lewis rats; the PG-PS-treated rats developed anemia within 2 weeks after the PG-PS challenge. The hematopoietic effects of oral TP0463518 administration at 10 mg/kg once daily for 6 weeks were examined in this rat model. The hematocrit values in the TP0463518-treated group increased significantly from 32.8 ± 0.8 to 44.5 ± 2.1% after the treatment, which was comparable to that in the healthy control group. The change of the mean corpuscular volume following TP0463518 treatment was similar to that in the healthy control group up to week 4, and significantly higher than that in the vehicle-treated group. TP0463518 increased divalent metal transporter 1 and duodenal cytochrome b expressions in the intestine. Conversely, TP0465318 did not exert any effects on the expressions of genes involved in iron metabolism in the liver, even though TP0463518 dramatically increased erythropoietin expression. Furthermore, TP0463518 had no effect on the expressions of inflammation markers in the liver. These results suggest that TP0463518 increased iron absorption and improved anemia of inflammation without exacerbating liver inflammation. TP0463518 appears to have an acceptable safety profile and could become a useful new therapeutic option for anemia of inflammation.

摘要

TP0463518(TS-143)是一种竞争性脯氨酰羟化酶 1/2/3 泛抑制剂,已被证明可特异性稳定肝脏中的缺氧诱导因子-2α,从而增加促红细胞生成素的产生。虽然 TP0463518 已被证明可改善肾脏性贫血,但它对炎症性贫血的影响尚不清楚。在这项研究中,我们通过给 Lewis 大鼠施用肽聚糖-多糖(PG-PS)来创建炎症性贫血大鼠模型;PG-PS 处理的大鼠在 PG-PS 挑战后 2 周内出现贫血。我们在该大鼠模型中检查了口服 TP0463518 给药 10mg/kg,每日 1 次,连续 6 周的造血作用。TP0463518 治疗组的红细胞压积值从治疗前的 32.8±0.8%显著增加至治疗后的 44.5±2.1%,与健康对照组相当。TP0463518 治疗后的平均红细胞体积变化与健康对照组相似,直至第 4 周,明显高于载体处理组。TP0463518 增加了肠道中二价金属转运蛋白 1 和十二指肠细胞色素 b 的表达。相反,TP0463518 对肝脏中参与铁代谢的基因表达没有任何影响,尽管 TP0463518 显著增加了促红细胞生成素的表达。此外,TP0463518 对肝脏中炎症标志物的表达没有影响。这些结果表明,TP0463518 通过增加铁吸收和改善炎症性贫血而不加重肝脏炎症。TP0463518 似乎具有可接受的安全性,可能成为炎症性贫血的一种有用的新治疗选择。

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