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Naloxone Effects Against Cutaneous Leishmaniasis Caused by Leishmania Major Strain Mrho/Ir/75/Er in the Balb/C Mice Publisher Pubmed



Azizi H1, 2 ; Mahdavinik E1 ; Hataminejad M3, 4, 5 ; Khamesipour A6 ; Montazeri S1
Authors
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Authors Affiliations
  1. 1. Department of Parasitology and Mycology, School of Medicine Zabol, University of Medical Sciences, Zabol, Iran
  2. 2. Zabol Medicinal Plants Research Center, Zabol University of Medical Sciences, Zabol, Iran
  3. 3. Department of Medical Parasitology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
  4. 4. Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran
  5. 5. Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran
  6. 6. Center for Research and Training in Skin Diseases and Leprosy, Tehran University of Medical Sciences, Tehran, Iran

Source: Infectious Disorders - Drug Targets Published:2023


Abstract

Introduction: Cutaneous leishmaniasis (CL) is a serious health problem in some parts of the world, such as Iran. Since the use of pentavalent antimonial compounds such as meglumine antimoniate (Glucantime, MA) for the treatment of CL has side effects, naloxone as a new treatment in the footpad of Leishmania major (L. major)-infected BALB/c mice was investigated by evaluating the lesion size and the parasite burden. Method: The animals were infected with L. major (MRHO/IR/75/ER). 40 BALB/c mice were divided into 4 groups (10/group), and were treated as follows 39 days after L. major infection: Group 1 treated with intraperitoneal injections of MA (100 mg/kg, positive control group) daily for six weeks; Group 2 received a 100 μl injection of PBS (negative control group); Group 3 received subcutaneous (SC) injections of naloxone (10 mg/kg) daily for six weeks (Naloxone1), and Group 4 was SC injected with nalox-one (10 mg/kg) weekly for six weeks (Naloxone2). The lesion size was measured using a digital caliper. Result: After the end of treatment, the lesion parasite burden was evaluated. As compared to the negative control group, the groups that received MA and naloxone (groups 1, 3, and 4) showed fewer para-sites. Also, the naloxone-treated mice showed significantly smaller lesion sizes than the negative control group (p˂0.05), but they did not differ significantly from the MA-treated mice. Conclusion: Taken together, the results suggest that naloxone might be a promising and alternative treatment for CL. © 2023 Bentham Science Publishers.
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