He Baoguo, Zhu Zhenming, Tian Zibin, Wang Dandan, Li Yijing, Luan Xiao, Ma Li
Department of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, 266000, China.
Department of Clinical Nutrition, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, 266000, China.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Apr;398(4):4593-4605. doi: 10.1007/s00210-024-03587-6. Epub 2024 Nov 7.
The effect of fucoidan on postoperative ileus (POI) has not been studied. In this study, how fucoidan ameliorates POI in a rat POI model was investigated. The results showed that in the model animals, when the first defecation time was prolonged, the amount of food consumed decreased, the small intestinal propulsion rate dramatically slowed, and the motility index (MI%) of the small intestine decreased. In vitro experiments revealed that the contractile response of small intestinal smooth muscle strips to carbachol (CCh) was reduced. Immunohistochemistry revealed evident macrophage infiltration in the intestinal muscularis. However, after oral pretreatment with fucoidan, the time to first defecation decreased, and food intake, the small intestinal propulsion rate, and MI% of the small intestine increased. Additionally, the contractile response of the intestinal strips to CCh became stronger, and macrophage infiltration decreased. Mechanistically, fucoidan alleviated POI by exerting anti-inflammatory and antioxidant effects as well as likely through the TrkB/ERK1/2/Akt signalling pathways. When POI occurred, the expression levels of inflammatory factors in the intestines significantly increased while the phosphorylation of TrkB, ERK1/2, and Akt significantly decreased; malondialdehyde (MDA) levels in the intestines increased but the levels of superoxide dismutase (SOD) and glutathione (GSH) decreased. In contrast, after pretreatment with fucoidan, the expression levels of inflammatory factors decreased; the phosphorylation levels of TrkB, ERK1/2, and Akt increased; the MDA level decreased; and SOD and GSH levels increased. Thus, fucoidan alleviated POI-induced impairment of rat intestinal motility through anti-inflammatory and antioxidant effects possibly associated with the TrkB/ERK1/2 and Akt signalling pathways.
岩藻依聚糖对术后肠梗阻(POI)的影响尚未得到研究。在本研究中,探究了岩藻依聚糖如何改善大鼠POI模型中的POI。结果显示,在模型动物中,首次排便时间延长、食物摄入量减少、小肠推进率显著减慢、小肠运动指数(MI%)降低。体外实验表明,小肠平滑肌条对卡巴胆碱(CCh)的收缩反应减弱。免疫组织化学显示,肠肌层有明显的巨噬细胞浸润。然而,用岩藻依聚糖进行口服预处理后,首次排便时间缩短,食物摄入量、小肠推进率和小肠MI%增加。此外,肠条对CCh的收缩反应增强,巨噬细胞浸润减少。从机制上讲,岩藻依聚糖通过发挥抗炎和抗氧化作用以及可能通过TrkB/ERK1/2/Akt信号通路来缓解POI。当发生POI时,肠道中炎症因子的表达水平显著增加,而TrkB、ERK1/2和Akt的磷酸化水平显著降低;肠道中丙二醛(MDA)水平升高,但超氧化物歧化酶(SOD)和谷胱甘肽(GSH)水平降低。相比之下,用岩藻依聚糖预处理后,炎症因子的表达水平降低;TrkB、ERK1/2和Akt的磷酸化水平升高;MDA水平降低;SOD和GSH水平升高。因此,岩藻依聚糖通过抗炎和抗氧化作用,可能与TrkB/ERK1/2和Akt信号通路相关,减轻了POI诱导的大鼠肠道运动障碍。