Effects of asparaginases and L-carnitine on Western-diet-induced hepatosteatosis in mice

F1000Res. 2022 Feb 1:11:128. doi: 10.12688/f1000research.75870.1. eCollection 2022.

Abstract

Background: Asparaginases are common chemotherapeutic agents used for the treatment of acute lymphoblastic leukemia as a single or combinational therapy. Accompanying hepatotoxicity makes its use in elderly patients with pre-conditions, as obesity or other hepatopathies, difficult. Various hepatoprotective compounds like, L-carnitine, are discussed to ameliorate the induced hepatotoxicity. Methods: Here we aimed to establish a mouse model to study the effect of asparaginases (L-asparaginase and Oncaspar) and L-carnitine on Western-diet-induced hepatosteatosis in mice. Dose-escalation studies were performed to analyze asparaginases induced hepatotoxicity in C57BL/6 mice with normal or fatty livers. Subsequently, the effect of L-carnitine to improve the induced toxicity was tested. Results: Our results showed mild-to-moderate hepatotoxic effects while the Western-diet induced a higher degree of vacuolization and hepatocyte damage in liver tissue. Testing of L-carnitine in the established models did not show any protective effect on the toxicity or impairment of the efficacy of asparaginases. Conclusion: The here established models were able to demonstrate the asparaginase-induced hepatotoxic effects which were enhanced by the Western-diet. However, to test potential ameliorating drugs, the models might need some improvements.

Keywords: L-carnitine; asparaginases; hepatosteatosis; hepatotoxicity..

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Asparaginase* / pharmacology
  • Carnitine / pharmacology
  • Carnitine / therapeutic use
  • Chemical and Drug Induced Liver Injury* / drug therapy
  • Diet
  • Mice
  • Mice, Inbred C57BL

Substances

  • Asparaginase
  • Carnitine

Associated data

  • figshare/10.6084/m9.figshare.17032946

Grants and funding

This work was supported with a stipend to Mona Ali Mahmoud Assar by the Egyptian cultural affairs and missions’ sector and ministry of higher education and by the European Union and NRW government (NRW-EU.Ziel2, (EFRE), 005-0908-0112).