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魔芋低聚糖通过激活5-HT4R/cAMP/PKA/p-CREB通路缓解小鼠便秘。

Konjac Oligosaccharide Alleviates Constipation in Mice via 5-HT4R/cAMP/PKA/p-CREB Pathway Activation.

作者信息

Sun Guang-Jun, Li Ming, Zhang Xiao-Yu, Liu Jin-Shuang, Lin Ai-Zhen, Cai Qiong

机构信息

Department of Proctology, Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan, 430061, China.

Hubei Shizhen Laboratory, Wuhan, 430061, China.

出版信息

Curr Med Sci. 2025 Aug 29. doi: 10.1007/s11596-025-00102-7.

Abstract

BACKGROUND

Konjac oligosaccharide (KOS), which is produced through the degradation of konjac glucomannan via enzymatic, chemical, or physical treatments, has been found to have laxative effects. The current study aimed to elucidate the mechanisms underlying the laxative effect of KOS.

METHODS

KOS was administered by gavage to wild-type and 5-hydroxytryptamine 4 receptor (5-HT4R)-knockout C57BL/6 mice subjected to loperamide-induced constipation for four weeks. Following treatment, feces, blood, small intestine, colonic tissue, and intestinal contents were collected. Constipation-related parameters, gastrointestinal hormones, and Ca concentrations were evaluated. Histopathological changes were examined via hematoxylin and eosin staining. Immunofluorescence staining, Western blotting, and immunohistochemical staining were performed to detect the 5-HT4R/cyclic adenosine monophosphate (cAMP)/protein kinase A (PKA) pathway. Isolated smooth muscle cells (SMCs) were treated with KOS and GR113808 (a 5-HT4R antagonist), morphologically observed under an inverted microscope, and identified by α-SMA immunofluorescence staining. Cell viability was assessed via CCK-8 assays. 5-HT4R/cAMP/PKA/p-CREB pathway activity in SMCs was detected via Western blotting.

RESULTS

KOS alleviated loperamide-induced constipation in mice. KOS activated the 5-HT4R/cAMP/PKA/p-CREB pathway in loperamide-induced constipated mice. The protective effect of KOS was significantly diminished in 5-HT4R mice. KOS promoted the proliferation of SMCs by activating the 5-HT4R/cAMP/PKA/p-CREB signaling pathway.

CONCLUSION

KOS improves loperamide-induced constipation by activating the 5-HT4R/cAMP/PKA/p-CREB signaling pathway.

摘要

背景

魔芋寡糖(KOS)是通过酶解、化学或物理处理降解魔芋葡甘露聚糖而产生的,已发现其具有通便作用。本研究旨在阐明KOS通便作用的潜在机制。

方法

通过灌胃给予野生型和5-羟色胺4受体(5-HT4R)基因敲除的C57BL/6小鼠KOS,这些小鼠因洛哌丁胺诱导便秘持续四周。治疗后,收集粪便、血液、小肠、结肠组织和肠内容物。评估便秘相关参数、胃肠激素和钙浓度。通过苏木精和伊红染色检查组织病理学变化。进行免疫荧光染色、蛋白质印迹法和免疫组织化学染色以检测5-HT4R/环磷酸腺苷(cAMP)/蛋白激酶A(PKA)信号通路。用KOS和GR113808(一种5-HT4R拮抗剂)处理分离的平滑肌细胞(SMC),在倒置显微镜下进行形态学观察,并通过α-SMA免疫荧光染色进行鉴定。通过CCK-8试验评估细胞活力。通过蛋白质印迹法检测SMC中5-HT4R/cAMP/PKA/p-CREB信号通路的活性。

结果

KOS缓解了洛哌丁胺诱导的小鼠便秘。KOS激活了洛哌丁胺诱导的便秘小鼠中的5-HT4R/cAMP/PKA/p-CREB信号通路。在5-HT4R基因敲除小鼠中,KOS的保护作用显著减弱。KOS通过激活5-HT4R/cAMP/PKA/p-CREB信号通路促进SMC的增殖。

结论

KOS通过激活5-HT4R/cAMP/PKA/p-CREB信号通路改善洛哌丁胺诱导的便秘。

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