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Published on: January 5, 2017
Association between intestinal and antioxidant barriers in children with cancer
Teresa Stachowicz-Stencel1, Anna Synakiewicz, Anna Owczarzak
1Department of Paediatrics, Haematology, Oncology and Endocrinology, University of Gdansk, Gdańsk, Poland. tsten@gumed.edu.pl
Objective:
Reactive oxygen species (ROS) play a role in cancerogenesis processing and damage tissues. Furthermore, oncological treatment may impair proper function of the gut barrier. The aim of this study was to measure intestinal permeability in children in clinical remission for solid tumours and to search for a possible relationship between free radicals and the intestinal barrier. No such investigation in children has been reported so far.
Research Methods And Procedures:
The prospective study consisted of 19 paediatric patients with cancer after completion of chemotherapy. 32 healthy children from the outpatients clinics were recruited for measurement of intestinal permeability and antioxidant barrier as a control group. Intestinal permeability was assessed by measurement of urinary lactulose and mannitol after oral challenge. Antioxidant enzymes: superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in erythrocytes were assessed. Ischemia modified albumin (IMA) concentration was measured in serum.
Results:
Cancer patients excreted less mannitol and more lactulose versus controls. The ratio of lactulose to mannitol was significantly higher in oncological children vs control (mean 0.188 and 0.0453, respectively, p=0.0006,). Significantly higher IMA level in the oncological group vs control was noted (mean 123.8 and 87.3 U/ml, respectively, p=0.0037). No correlation between intestinal permeability and oxidative stress barrier was found.
Conclusions:
Our data shows that intestinal barrier is damaged in paediatric cancer patients after chemotherapy. IMA is believed to play a protective role in the defence against tissue damage. No correlation was found between these two barriers.
Insights
Paediatric cancer patients in remission show impaired intestinal barriers after chemotherapy, with higher levels of ischemia modified albumin (IMA). However, no direct link was found between gut permeability and oxidative stress markers.
Area of Science:
- Oncology
- Gastroenterology
- Biochemistry
Background:
- Reactive oxygen species (ROS) are implicated in cancer development and tissue damage.
- Cancer treatments, including chemotherapy, can compromise the integrity of the gut barrier.
- Previous research has not investigated intestinal permeability and its relationship with oxidative stress in pediatric cancer survivors.
Purpose of the Study:
- To assess intestinal permeability in children with solid tumors who are in clinical remission.
- To explore the potential association between free radicals (oxidative stress) and the intestinal barrier function in these patients.
Main Methods:
- A prospective study involving 19 pediatric cancer patients post-chemotherapy and 32 healthy controls.
- Intestinal permeability measured via urinary lactulose and mannitol excretion after oral challenge.
- Antioxidant enzymes (superoxide dismutase, glutathione peroxidase) and serum ischemia modified albumin (IMA) levels were assessed.
Main Results:
- Cancer patients exhibited significantly higher lactulose-to-mannitol ratios, indicating increased intestinal permeability, compared to controls (p=0.0006).
- Elevated serum IMA levels were observed in the pediatric cancer group (p=0.0037).
- No significant correlation was identified between the measured markers of intestinal permeability and oxidative stress.
Conclusions:
- Pediatric cancer patients treated with chemotherapy demonstrate compromised intestinal barrier function.
- Ischemia modified albumin (IMA) may play a role in protecting against tissue damage.
- Despite observed impairments, no direct relationship was found between intestinal permeability and the oxidative stress markers in this cohort.
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