Abstract

Irinotecan, an anticancer drug, induces diarrhea and intestinal inflammation, resulting in an increase in the cost of care and in treatment delays. In this study, we investigated whether alpha-lipoic acid (α-LA) could improve irinotecan-mediated intestinal inflammation, diarrhea and dysmotility. Intestinal mucositis was induced by irinotecan injection (75 mg/kg, i.p., for 4 days) in Swiss mice. α-LA (50, 100 or 200 mg/kg, gavage) was administered daily 1 h before the injection of irinotecan. Duodenum tissues were obtained for inflammation and proliferation analysis. The outcomes: diarrhea, intestinal dysmotility, weight body loss and survival were evaluated. Compared with the control condition, irinotecan diminished (p < 0.05) intestinal villus height, caused a loss of crypt integrity and intense inflammatory cell infiltration, increased myeloperoxidase (MPO), IL-6 and IL-1β levels and decreased reduced glutathione (GSH) levels in duodenum segments and increased gastric retention and decreased liquid retention in the medial intestinal segment, resulting in increased intestinal transit, severe diarrhea and reduced survival (approximately 72%). Furthermore, α-LA (200 mg/kg) pretreatment ameliorated (p < 0.05) these irinotecan-induced effects. Our findings show that α-LA reduced irinotecan-induced inflammation, intestinal dysmotility and diarrhea, resulting in improved survival. α-LA may be a useful therapeutic agent for the treatment of gut dysmotility in patients with intestinal mucositis associated with irinotecan treatment.

Highlights

  • Irinotecan, a DNA topoisomerase I inhibitor, is an anticancer therapeutic widely used for the treatment of breast and colorectal cancer [1]

  • Given that irinotecan induces severe intestinal inflammation and diarrhea in humans and mice, we aimed to investigate whether α-LA can improve the outcome and intestinal damage induced by irinotecan in mice

  • Given that α-LA is an antioxidant, we investigated whether α-LA affects the levels of GSH during intestinal mucositis induced by irinotecan

Read more

Summary

Introduction

Irinotecan, a DNA topoisomerase I inhibitor, is an anticancer therapeutic widely used for the treatment of breast and colorectal cancer [1]. Treatment of the diarrhea induced by irinotecan has been based on dietary modification and administration of antidiarrheal drugs, such as loperamide, the somatostatin analog octreotide and deodorized tincture of opium. These current therapies often worsen existing chronic gastrointestinal symptoms or induce other side effects, including respiratory depression, arrhythmias, seizures, and neurotoxicity [2,3,4]. Whether alpha-lipoic acid (α-LA; 1,2-ditiolane-3-pentanoic acid), known as thioctic acid, can improve the outcomes of intestinal mucositis induced by irinotecan, such as diarrhea, intestinal inflammation and mortality, has not yet been investigated

Objectives
Methods
Findings
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call