ORIGINAL RESEARCH article

Front. Pharmacol.

Sec. Experimental Pharmacology and Drug Discovery

Volume 16 - 2025 | doi: 10.3389/fphar.2025.1543166

Therapeutic Potential of Zinc 64 Zn Aspartate for Obesity Management: Impact on Oxidative Stress, Lipid Metabolism, Pancreas and Liver in High-Calorie Diet Model

Provisionally accepted
Max  TemnikMax Temnik1Sergey  GurinSergey Gurin1Alexandr  BalakinAlexandr Balakin1Roman  ByshovetsRoman Byshovets2Olesia  KalmukovaOlesia Kalmukova3*Tetiana  VovkTetiana Vovk3Tetiana  HalenovaTetiana Halenova3Nataliia  RakshaNataliia Raksha3Tetyana  FalalyeyevaTetyana Falalyeyeva3Olexiy  SavchukOlexiy Savchuk3
  • 1Physical Chemistry, Vector Vitale, North Miami Beach, United States
  • 2Department of Internal Diseases, Bogomolets National Medical University, Kyiv, Ukraine
  • 3Institute of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine

The final, formatted version of the article will be published soon.

Zinc is a critical micronutrient that plays multifaceted roles in oxidative stress management, lipid metabolism, pancreatic function, and liver health, which are all closely interconnected with obesity. Maintaining adequate zinc levels is essential for overall metabolic health and proper functioning of these vital systems. The investigational new drug complex of zinc-64 aspartate (KLS-1 or 64Zn-aspartate) was evaluated in this study as a pharmaceutical agent targeting oxidative stress and lipid metabolism using rodent model of obesity. KLS-1 is the isotopically modified zinc aspartate in which stable (non-radioactive) 64Zn atoms were enriched to exceed 99% atomic fraction of total zinc, as compared to natural isotopic ratio of 64Zn of 48.6%. In this paper, we discuss our findings and the effects rendered by KLS-1 on lipid metabolism, pancreas and liver function.This study was conducted on outbred rats, which were divided into 4 experimental groups: 1) the control group consuming standard food (3.81 kcal/g), 2) the obese group consuming a high-calorie diet (5.35 kcal/g), 3) the obese group consuming a high-calorie diet (5.35 kcal/g) treated with intragastric administration of 64Zn- aspartate at a dose of 4.5 mg per animal during 6 weeks (the obese rats), 4) the group consuming standard food diet (3.81 kcal/g) with 64Zn- aspartate form administration. The obese rats treated with 64Zn-64 stable isotope demonstrated decreased area of the hepatocytes, insulin and glucose levels in serum; increased catalase and superoxide dismutase activity, and area of pancreatic islets in comparison with the obese group. The study shows that 64Zn-aspartate is effective as a therapeutic agent for obesity management, significantly reducing body mass, improving histopathological changes in the pancreas and liver and normalizing oxidative stress in high-calorie diet animal models. These findings suggest that 64Zn- aspartate may be a promising monotherapy or adjunct treatment for obesity, offering benefits in weight reduction, organ protection, and antioxidant balance.

Keywords: Prooxidant-antioxidant balance, Glucose, Insulin, Fibrosis, NAFLD, 64 Zn-Asp, Oxidative Stress, ROS

Received: 10 Dec 2024; Accepted: 17 Apr 2025.

Copyright: © 2025 Temnik, Gurin, Balakin, Byshovets, Kalmukova, Vovk, Halenova, Raksha, Falalyeyeva and Savchuk. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Olesia Kalmukova, Institute of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine

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