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Potential immunomodulatory response associated with L-mimosine in male Wistar rats. | LitMetric

Potential immunomodulatory response associated with L-mimosine in male Wistar rats.

Toxicon

Research Centre for Veterinary Toxicology (CEPTOX) - Department of Pathology, School of Veterinary Medicine and Animal Sciences, University of São Paulo, Pirassununga, 05508-270, SP, Brazil. Electronic address:

Published: April 2023

AI Article Synopsis

  • Leucaena leucocephala is a plant used for food that contains a toxic compound called L-mimosine, which has potential cancer treatment properties due to its ability to chelate metal ions.
  • This study aimed to understand how L-mimosine affects immune responses in Wistar rats by administering varying doses (25, 40, and 60 mg/kg) over 28 days.
  • Results showed no signs of toxicity, but a decrease in T-dependent immune responses at the highest dose and enhanced phagocytosis by macrophages at medium to high doses, indicating that while L-mimosine inhibited certain immune functions, it did not compromise macrophage activity.

Article Abstract

Leucaena leucocephala is a plant that is used as animal and human food worldwide. This plant contains the toxic compound namely L-mimosine. The main mechanism of action of this compound involves its ability to chelate metal ions, which may interfere with the proliferative activity of cells and being studied for the treatment of cancer. However, little is known about the effect of L-mimosine on immune responses. Thus, the aim of this study was to evaluate the effects of L-mimosine on immune responses in Wistar rats. Different doses of L-mimosine (25, 40 and 60 mg/kg body weight/day) were administered orally by gavage to adult rats for 28 days. No clinical signs of toxicity were observed in animals, but a decrease in the T-dependent response to sheep red blood cells (SRBC) in animals treated with 60 mg/kg L-mimosine and an increase in the intensity of S. aureus phagocytosis by macrophages in animals treated with 40 or 60 mg/kg L-mimosine were observed. Therefore, these findings suggest that L-mimosine did not compromise macrophage activity and inhibited T-dependent clonal expansion during the immune response.

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Source
http://dx.doi.org/10.1016/j.toxicon.2023.107084DOI Listing

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