Department of Biomaterials Science (BK21 FOUR Program), College of Natural Resources & Life Science/Life and Industry Convergence Research Institute/Laboratory Animal Resources Center, Pusan National University, Miryang 50463, Korea.
College of Pharmacy, Pusan National University, Busan 46241, Korea.
Int J Mol Sci. 2021 May 29;22(11):5845. doi: 10.3390/ijms22115845.
Indirect evidence has determined the possibility that microplastics (MP) induce constipation, although direct scientific proof for constipation induction in animals remains unclear. To investigate whether oral administration of polystyrene (PS)-MP causes constipation, an alteration in the constipation parameters and mechanisms was analyzed in ICR mice, treated with 0.5 μm PS-MP for 2 weeks. Significant alterations in water consumption, stool weight, stool water contents, and stool morphology were detected in MP treated ICR mice, as compared to Vehicle treated group. Also, the gastrointestinal (GI) motility and intestinal length were decreased, while the histopathological structure and cytological structure of the mid colon were remarkably altered in treated mice. Mice exposed to MP also showed a significant decrease in the GI hormone concentration, muscarinic acetylcholine receptors (mAChRs) expression, and their downstream signaling pathway. Subsequent to MP treatment, concentrations of chloride ion and expressions of its channel (CFTR and CIC-2) were decreased, whereas expressions of aquaporin (AQP)3 and 8 for water transportation were downregulated by activation of the mitogen-activated protein kinase (MAPK)/nuclear factor (NF)-κB signaling pathway. These results are the first to suggest that oral administration of PS-MP induces chronic constipation through the dysregulation of GI motility, mucin secretion, and chloride ion and water transportation in the mid colon.
间接证据已经确定了微塑料(MP)引起便秘的可能性,尽管动物中直接引起便秘的科学证据尚不清楚。为了研究聚苯乙烯(PS)-MP 的口服给药是否会引起便秘,我们用 0.5μm PS-MP 处理 ICR 小鼠 2 周,分析了便秘参数和机制的变化。与 Vehicle 处理组相比,MP 处理的 ICR 小鼠的饮水量、粪便重量、粪便含水量和粪便形态均发生显著变化。此外,胃肠道(GI)蠕动和肠长度减少,而处理组小鼠的中结肠组织学结构和细胞学结构发生明显改变。暴露于 MP 的小鼠也表现出 GI 激素浓度、毒蕈碱型乙酰胆碱受体(mAChRs)表达及其下游信号通路的显著下降。在 MP 处理后,氯离子浓度及其通道(CFTR 和 CIC-2)的表达降低,而水转运的水通道蛋白(AQP)3 和 8 的表达通过丝裂原激活蛋白激酶(MAPK)/核因子(NF)-κB 信号通路的激活被下调。这些结果首次表明,PS-MP 的口服给药通过调节中结肠的 GI 运动、粘蛋白分泌以及氯离子和水的转运,引起慢性便秘。