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Laxative Effect of Spicatoside A by Cholinergic Regulation of Enteric Nerve in Loperamide-Induced Constipation: ICR Mice Model

机译:肠神经胆碱能调节洛哌丁胺诱导的便秘中蛇毒苷A的通便作用:ICR小鼠模型

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摘要

Researches on spicatoside A (SpiA)-containing natural products suggest the possibility of SpiA as a potential laxative to alleviate chronic constipation. However, no studies have been conducted with single compound administration of SpiA. To verify the laxative effects and mechanism of action of SpiA on chronic constipation, we investigated alterations in the excretion parameters, histological structure, and cholinergic regulation of the enteric nerve in the colons of Institute of Cancer Research (ICR) mice with loperamide (Lop)-induced constipation after exposure to 20 mg/kg of SpiA. Decrease in the number, weight and water contents of stools in the Lop+Vehicle treated group significantly recovered after SpiA treatment, and alterations in the histological structure and transmission electron microscopy (TEM) images were improved in the Lop+SpiA treated group. Similar recovery effects were observed in the ability for mucin secretion and expression of the membrane water channel gene (aquaporin 8, AQP8). Furthermore, significant improvements were observed in the acetylcholinesterase (AChE) activity and acetylcholine receptors’ (AChRs) downstream signaling pathway after treatment of SpiA. The levels of gastrointestinal (GI) hormones including cholecystokinin (CCK) and gastrin were also remarkably enhanced in the Lop+SpiA treated group as compared to the Lop+Vehicle treated group. The expression of receptor tyrosine kinase (C-kit) and protein gene product 9.5 (PGP9.5) in Cajal and neural cells, as well as the phosphorylation of myosin light chain (MLC) in smooth muscle cells, were recovered after SpiA exposure. Taken together, the results of the present study provide the first strong evidence that SpiA improves chronic constipation through muscarinic cholinergic regulation of the enteric nerve in a Lop-induced constipation ICR mice model.
机译:对含有蛇藤苷A(SpiA)的天然产物的研究表明,SpiA作为缓解慢性便秘的潜在缓泻剂的可能性。但是,尚未对单一化合物的SpiA进行研究。为了验证SpiA对慢性便秘的通便作用和作用机理,我们研究了洛哌丁胺(Lop)对癌症研究所(ICR)小鼠结肠中肠神经的排泄参数,组织学结构和胆碱能调节的改变。暴露于20 mg / kg SpiA后引起的便秘。 Lop + Vehicle处理组的粪便数量,重量和水含量的减少在SpiA处理后显着恢复,并且Lop + SpiA处理组的组织学结构和透射电子显微镜(TEM)图像改变得到改善。在粘蛋白分泌和膜水通道基因(水通道蛋白8,AQP8)的表达能力方面观察到类似的恢复效果。此外,在治疗SpiA后,乙酰胆碱酯酶(AChE)活性和下游乙酰胆碱受体(AChRs)下游信号通路也得到了显着改善。与Lop +载体治疗组相比,Lop + SpiA治疗组的包括胆囊收缩素(CCK)和胃泌素在内的胃肠道(GI)激素水平也显着提高。暴露于SpiA后,恢复了Cajal和神经细胞中受体酪氨酸激酶(C-kit)和蛋白质基因产物9.5(PGP9.5)的表达以及平滑肌细胞中肌球蛋白轻链(MLC)的磷酸化。综上所述,本研究的结果提供了第一个有力的证据,表明在Lop诱发的便秘ICR小鼠模型中,SpA通过毒蕈碱对肠神经的胆碱能调节来改善慢性便秘。

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