芍药苷激活 ASIC3/ERK 通路可改善慢速便秘大鼠的肠液代谢和内脏敏感性

Yuan Deng, Qiong Zhao, Hong‐Yun Zhou, Zi‐Qi Zhang, Yu Zhan
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引用次数: 0

摘要

慢传输性便秘(STC)是全球儿童和成人最常见的胃肠道疾病之一。芍药苷(PF)是从芍药的干根中提取的一种单萜烯苷化合物,已被发现能缓解慢传输性便秘,但其作用机制仍不清楚。本研究旨在探讨 PF 对复方地芬诺酯诱导的 STC 大鼠肠液代谢和内脏敏感性的影响和机制。在评估通便效果的基础上,采用腹部退缩反射试验、酶联免疫吸附试验、实时定量聚合酶链反应、Western 印迹和免疫组织化学方法检测内脏敏感性、体液代谢相关蛋白和酸敏感离子通道 3/ 细胞外信号调节激酶(ASIC3/ERK)通路相关分子。PF 治疗不仅减轻了复合二苯氧胺诱导的大鼠便秘症状和结肠病理损伤,还改善了结肠液体代谢紊乱和内脏敏感性异常,具体表现为结肠小管细胞数量和粘蛋白 2 蛋白表达增加,水肿素 3 蛋白表达减少,腹部退缩反射评分提高,内脏痛阈降低,血清 5- 羟色胺上调,血管活性肠肽水平下调。此外,PF 还激活了 STC 大鼠结肠的 ASIC3/ERK 通路,而 ASIC3 抑制则部分抵消了 PF 对肠液和内脏感觉的调节作用。总之,PF 通过激活 ASIC3/ERK 通路,缓解了 STC 大鼠受损的肠液代谢和异常的内脏敏感性,从而缓解了它们的症状。
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Activation of ASIC3/ERK pathway by paeoniflorin improves intestinal fluid metabolism and visceral sensitivity in slow transit constipated rats
Slow transit constipation (STC) is one of the most common gastrointestinal disorders in children and adults worldwide. Paeoniflorin (PF), a monoterpene glycoside compound extracted from the dried root of Paeonia lactiflora, has been found to alleviate STC, but the mechanisms of its effect remain unclear. The present study aimed to investigate the effects and mechanisms of PF on intestinal fluid metabolism and visceral sensitization in rats with compound diphenoxylate‐induced STC. Based on the evaluation of the laxative effect, the abdominal withdrawal reflex test, enzyme‐linked immunosorbent assay, quantitative real‐time polymerase chain reaction, western blot, and immunohistochemistry were used to detect the visceral sensitivity, fluid metabolism‐related proteins, and acid‐sensitive ion channel 3/extracellular signal‐regulated kinase (ASIC3/ERK) pathway‐related molecules. PF treatment not only attenuated compound diphenoxylate‐induced constipation symptoms and colonic pathological damage in rats but also ameliorated colonic fluid metabolic disorders and visceral sensitization abnormalities, as manifested by increased colonic goblet cell counts and mucin2 protein expression, decreased aquaporin3 protein expression, improved abdominal withdrawal reflex scores, reduced visceral pain threshold, upregulated serum 5‐hydroxytryptamine, and downregulated vasoactive intestinal peptide levels. Furthermore, PF activated the colonic ASIC3/ERK pathway in STC rats, and ASIC3 inhibition partially counteracted PF's modulatory effects on intestinal fluid and visceral sensation. In conclusion, PF alleviated impaired intestinal fluid metabolism and abnormal visceral sensitization in STC rats and thus relieved their symptoms through activation of the ASIC3/ERK pathway.
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