scholarly journals Acetaminophen changes paracellular transport activity through regulation of the tight junction protein in an intestinal barrier model

2012 ◽  
Vol 13 (S1) ◽  
Author(s):  
Mohammad R Lornejad-Schäfer ◽  
Christine Schäfer ◽  
Klaus R Schröder
2020 ◽  
Author(s):  
Guangmang Liu ◽  
Xiaomei Xu ◽  
Caimei Wu ◽  
Gang Jia ◽  
Hua Zhao ◽  
...  

Abstract Background: Weaning stress can lead to the disruption of tight junctions and increased intestinal permeabilty, which contributes to the initiation and development of many disease, such as Crohn’s disease and ulcerative colitis. Pigs are more ideal models for human studies than other animals. However, no information is found about the relationship of intestinal integrity and spermine supplementation in pigs. The objective of this study is to investigate whether spermine protects intestinal barrier integrity via Rac1/PLC-γ1 signalling pathway in piglets. Methods: In vivo, the piglets were categorised into the control group and the spermine group, which was fed with spermine at 0.4 mmol kg−1 body weight for 7 hours and 3, 6 and 9 days. In vitro, we examined whether spermine protects the intestinal barrier after TNF-α challenge through Ras-related C3 botulinum toxin substrate 1 (Rac1)/Phospho-lipase C-γ1 (PLC-γ1) signalling pathway. Results: In vivo study revealed that the spermine treatment upregulated tight junction protein mRNA levels and Rac1/PLC-γ1 signalling pathway gene expression in the jejunum of piglets. The serum D-lactate content was significantly reduced after spermine treatment (P < 0.05). In vitro study revealed that 0.1 μM spermine significantly increased the levels of tight junction protein expression, Rac1/PLC-γ1 signalling pathway and transepithelial electrical resistance, and decreased paracellular permeability (P < 0.05). Further experiments showed that spermine treatment increased the levels of tight junction protein expression, Rac1/PLC-γ1 signalling pathway and transepithelial electrical resistance, and decreased paracellular permeability compared with the NSC-23766 and U73122 treatment with spermine after TNF-α challenge (P < 0.05). Conclusion: spermine protects intestinal integrity through the Rac1/PLC-γ1 signalling pathway.


2010 ◽  
Vol 285 (44) ◽  
pp. 33584-33588 ◽  
Author(s):  
Kerstin Duning ◽  
Deike Rosenbusch ◽  
Marc A. Schlüter ◽  
Yuemin Tian ◽  
Karl Kunzelmann ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Yi-Fang Tu ◽  
Si-Tse Jiang ◽  
Chi-Wu Chiang ◽  
Li-Ching Chen ◽  
Chao-Ching Huang

AbstractHypoxic-ischemic (HI) encephalopathy is the major cause of mortality and disability in newborns. The neurovascular unit is a major target of acute and chronic brain injury, and therapies that protect simultaneously both neurons and vascular endothelial cells from neonatal HI injury are in demand. Insulin receptors and its key downstream molecule-insulin receptor substrate −1 (IRS-1) are potential neuroprotective targets and expressed both in neuron and endothelial cells. To investigate whether IRS-1 can act similarly in neurons and vascular endothelial cells in protecting neurovascular units and brain form HI injury, we found that neuron-specific IRS-1 transgenic rats showed reduced neurovascular injury and infarct volumes, whereas endothelial-specific IRS-1 transgenic rats showed increased blood-brain barrier (BBB) disruption and exaggerated neurovascular injury after neonatal HI brain injury. Endothelial-specific IRS-1 overexpression increased vascular permeability and disassembled the tight junction protein (zonula occludens-1) complex. Inhibition of mammalian target of rapamycin (mTOR) by rapamycin preserved tight junction proteins and attenuated BBB leakage and neuronal apoptosis after HI in the endothelial-specific IRS-1 transgenic pups. Together, our findings suggested that neuronal and endothelial IRS-1 had opposite effects on the neurovascular integrity and damage after neonatal HI brain injury and that endothelial IRS-1 worsens neurovascular integrity after HI via mTOR-mediated tight junction protein disassembly.


Sign in / Sign up

Export Citation Format

Share Document