Comparative treatment with hyperbaric oxygen therapy in a model of systemic loxoscelism in rats

Mireille Toledo-Blas, Antonio Franco-Vadillo, Selma A. Somilleda-Ventura, Brenda Dominguez-Ruiz, Gustavo Guevara-Balcazar, Alexandre Kormanovski-Kovzova, Pedro Lopez-Sanchez, Rosa A. Jarillo-Luna, Eleazar Lara-Padilla, Maria Carmen Castillo-Hernandez

Research output: Contribution to journalArticlepeer-review

Abstract

Objective(s): Spiders of the Loxosceles genus, known as violin spiders, produce venom with dermonecrotic and systemic effects, as it is a species widely distributed in the world, its study represents a high medical relevance. Systemic loxoscelism, which occurs in 1 in 5 cases and is the most frequent in children, can be fatal, so the study of effective therapy is of great relevance. In the present study, we compared different therapeutic options to mitigate the systemic effects of Loxosceles boneti venom in a model in which prepubertal rats were used. Materials and Methods: A model of systemic intoxication by L. boneti venom was provoked in male Wistar rats. Study groups were formed: healthy control, with venom and untreated control, treatment with N-acetylcysteine, and/or hyperbaric oxygenation therapy. Subsequently, pathological analysis of the kidney and lung was performed. The oxidant-antioxidant response was evaluated, and molecular analysis of the COX-1 and COX-2 enzymes was performed. Results: Regenerative changes were observed at the cellular level in both treatments, being more noticeable in the hyperbaric oxygen therapy (HBO) group. The anti-oxidant response was outstanding in the same group. Conclusion: Both treatments offer considerable benefits, however; further studies are needed to provide adequate therapeutics.

Original languageEnglish
Pages (from-to)1452-1459
Number of pages8
JournalIranian Journal of Basic Medical Sciences
Volume25
Issue number12
DOIs
StatePublished - Dec 2022

Keywords

  • Anti-oxidant therapy
  • Cyclooxygenases
  • Hyperbaric oxygen therapy
  • Spider venoms
  • Systemic inflammatory - response

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