Guo Tieyun, Li Jiade, Li Jing, Kong Dan, Bi Chunli, He Zheng, Tang Dai, Jin Xiaoming, Jin Lianhong
Department of Histology and Embryology, Basic Medical Science College, Harbin Medical University, Harbin, Heilongjiang 150081, P.R. China.
Department of Pathology, Basic Medical Science College, Harbin Medical University, Harbin, Heilongjiang 150081, P.R. China.
Oncol Lett. 2017 Mar;13(3):1601-1608. doi: 10.3892/ol.2017.5652. Epub 2017 Jan 25.
Advanced malignant ascites is accompanied by gastrointestinal dysmotility, and patients often feel abdominal pain, abdominal distention, nausea and constipation. Gastrointestinal dysmotility is not only painful for the patients, but it reduces the absorption of nutrients and affects the physical recovery of patients with malignant ascites. It is reported that changes in interstitial cells of Cajal (ICCs) are responsible for the gastrointestinal dysmotility induced by malignant ascites, but the mechanism is not completely understood. The present study observed a significantly decreased expression of ion channels, including hyperpolarization-activated cyclic nucleotide-gated potassium channel 2 (HCN2) and cyclic adenosine monophosphate, in the condition of malignant ascites. Using electrophysiology, it was identified that malignant ascites led to lower amplitude and slower frequency signals in cells of the small intestine. In addition, when ICCs were cultured with malignant ascites , the expression of HCN2 of ICCs was significantly reduced, and the data of flow cytometry revealed that the Ca concentration of ICCs was also decreased. The results of electron microscopy analysis demonstrated the nuclei of ICCs were pyknotic, and the processes of ICCs were reduced in malignant ascites. The present study suggests the small intestinal dysmotility caused by malignant ascites may be associated with changes in HCN2 of ICCs, which offers a potential therapeutic target for gastrointestinal dysmotility in advanced malignant ascites.
晚期恶性腹水伴有胃肠动力障碍,患者常感到腹痛、腹胀、恶心和便秘。胃肠动力障碍不仅给患者带来痛苦,还会降低营养物质的吸收,影响恶性腹水患者的身体恢复。据报道, Cajal间质细胞(ICCs)的变化是恶性腹水所致胃肠动力障碍的原因,但机制尚未完全明确。本研究观察到在恶性腹水情况下,包括超极化激活的环核苷酸门控钾通道2(HCN2)和环磷酸腺苷在内的离子通道表达显著降低。通过电生理学方法,确定恶性腹水导致小肠细胞的信号幅度降低、频率减慢。此外,当用恶性腹水培养ICCs时,ICCs的HCN2表达显著降低,流式细胞术数据显示ICCs的钙浓度也降低。电子显微镜分析结果表明,在恶性腹水中ICCs的细胞核固缩,ICCs的突起减少。本研究提示,恶性腹水引起的小肠动力障碍可能与ICCs的HCN2变化有关,这为晚期恶性腹水胃肠动力障碍提供了一个潜在的治疗靶点。