College of Pharmacy, Gachon University, Hambakmoero 191, Yeonsu-gu, Incheon, 21936, Republic of Korea.
Gachon Institute of Pharmaceutical Sciences, Hambakmoero 191, Yeonsu-gu, Incheon, 21936, Republic of Korea.
Sci Rep. 2019 Jul 26;9(1):10888. doi: 10.1038/s41598-019-47267-5.
Pruritus is an unexpected symptom observed in cholestasis and its mechanism is still unclear. Here, we show that bovine adrenal medulla (BAM) 8-22, an endogenous itch-inducing peptide, could be involved in cholestatic pruritus. It was found that bile duct ligation (BDL) mice, an obstructive cholestasis model, showed increased spontaneous scratching behaviour. Importantly, the mRNA level of proenkephalin, a precursor polypeptide of BAM8-22, was significantly increased in the skin of BDL mice. Furthermore, the mRNA level of Mrgprx1, which encodes a receptor for BAM8-22, was significantly increased in the dorsal root ganglia (DRG) of BDL mice. This was further confirmed by elevation of intracellular calcium levels upon BAM8-22 treatment in primarily-cultured DRG neurons. In addition, BDL mice showed augmented scratching behaviour by BAM8-22, indicating enhanced activity of MRGPRX1. Moreover, the skin homogenate of BDL mice induced elevation of intracellular calcium levels through MRGPRX1. Finally, among the various bile acids, chenodeoxycholic acid significantly increased proenkephalin transcription in a human keratinocyte cell line (HaCaT). In conclusion, cholestatic pruritus could be attributed in part to enhanced action of both BAM8-22 in the skin and its receptor MRGPRX1 in sensory neurons.
瘙痒是胆汁淤积症中观察到的一种意外症状,其机制尚不清楚。在这里,我们表明牛肾上腺髓质(BAM)8-22,一种内源性瘙痒诱导肽,可能参与胆汁淤积性瘙痒。研究发现,胆管结扎(BDL)小鼠,一种阻塞性胆汁淤积模型,自发性搔抓行为增加。重要的是,BDL 小鼠皮肤中 proenkephalin 的 mRNA 水平显著增加,proenkephalin 是 BAM8-22 的前体多肽。此外,编码 BAM8-22 受体的 Mrgprx1 的 mRNA 水平在 BDL 小鼠的背根神经节(DRG)中显著增加。这进一步通过 BAM8-22 处理原代培养的 DRG 神经元时细胞内钙水平的升高得到证实。此外,BDL 小鼠对 BAM8-22 表现出增强的搔抓行为,表明 MRGPRX1 的活性增强。此外,BDL 小鼠的皮肤匀浆通过 MRGPRX1 诱导细胞内钙水平升高。最后,在各种胆汁酸中,鹅脱氧胆酸显著增加了人角质形成细胞系(HaCaT)中 proenkephalin 的转录。总之,胆汁淤积性瘙痒部分归因于皮肤中 BAM8-22 及其在感觉神经元中的受体 MRGPRX1 的增强作用。