六君子水煎剂通过抑制 PERK/eIF2α/ATF4/CHOP 通路和 GDF15/GFRAL 的表达,减轻顺铂诱导的大鼠厌食症

Yongzhao Dai, Wanting Hu, Jinyuan Han, Yaozhong Zhao, Xipei Wu, Xiuxiu Liao, Ke Nie
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摘要

背景与目的六君子汤(LJZD),又称六君子水,是一种传统方剂,在临床治疗化疗引起的厌食症(CIA)方面被证明是有效的。之前的研究表明,GDF15/GFRAL 轴在 CIA 的发病机制中具有重要作用,并提出了内质网应激与 GDF15 表达之间的潜在联系。方法通过腹腔注射顺铂建立大鼠CIA模型,给大鼠口服LJZD 72 h。每天记录大鼠的进食量和体重。结果 LJZD能显著增加大鼠的食物摄入量,并降低顺铂注射后24小时和72小时血清中GDF15的水平。这种效应可能与抑制 Gdf15 转录、改善肝脏和回肠的病理损伤或内质网应激有关。此外,LJZD还抑制了顺铂诱导的肝脏和回肠PERK/eIF2α/ATF4/CHOP通路的激活,从而缓解了中枢GDF15/GFRAL的表达。 结论 LJZD能有效改善大鼠模型中顺铂诱导的厌食症,这可能与它抑制了顺铂激活的PERK/eIF2α/ATF4/CHOP通路和GDF15/GFRAL的表达有关。
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Liujunzi decoction attenuates cisplatin-induced anorexia in rats via inhibiting PERK/eIF2α/ATF4/CHOP pathway and GDF15/GFRAL expression

Background and aim

Liujunzi Decoction (LJZD), also called Rikkunshito, is a traditional formula that has proven effective in clinical treatment against chemotherapy-induced anorexia (CIA). Previous study indicated the importance of GDF15/GFRAL axis in the pathogenesis of CIA, and suggested the potential connection between endoplasmic reticulum stress and GDF15 expression. However, further exploration is required to determine whether the mechanism of LJZD against CIA is related to the PERK/eIF2α/ATF4/CHOP signaling and GDF15/GFRAL expression.

Methods

The CIA model of rats was established via intraperitoneal injection of cisplatin, and the rats were given LJZD orally for 72 ​h. Food intake and body weight were recorded daily. The expression of GDF15/GFRAL and ER stress factors, as well as the histological injuries were investigated.

Results

LJZD led to a significant increase in food intake in rats and a decrease in serum GDF15 levels at 24 ​h and 72 ​h after cisplatin injection. This effect may be associated with the inhibition of Gdf15 transcription and the amelioration of pathological injuries or endoplasmic reticulum stress in the liver and ileum. Moreover, LJZD suppressed the cisplatin-induced activation of the hepatic and ileal PERK/eIF2α/ATF4/CHOP pathway, resulting in the alleviation of central GDF15/GFRAL expression.

Conclusion

LJZD effectively improves cisplatin-induced anorexia in a rat model, which might be attributed to its inhibition of the PERK/eIF2α/ATF4/CHOP pathway and GDF15/GFRAL expression activated by cisplatin.

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