EVALUATION OF THE EFFECTS OF OZONE THERAPY AND CISPLATIN IN AN EXPERIMENTAL MODEL IN MICE WITH EHRLICH CARCINOMA

The present objective was to evaluate Swiss albino mice (Mus muscullus) with Ehrlich carcinoma treated with intrarectal ozone therapy and cisplatin. Twenty-four female mice, approximately 60 days of age, varying between 35g and 40g in weight were divided into four groups, Group G1: Positive control:...

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Published in:Medicina veterinária (Recife, Brazil) Vol. 17; no. 3
Main Authors: Laís Albuquerque van der Linden, Rhaysa Allayde Silva Oliveira, Ykaro Kyokay Vieira Serafim, Yasmim Theonise Ferreira Chaves, Alluanan Adelson do Nascimento Silva, Renan Felipe Silva Santos, Fernando Leandro dos Santos, Ivone Antônia de Souza, Evilda Rodrigues de Lima
Format: Journal Article
Language:English
Published: Universidade Federal Rural de Pernambuco 01-11-2023
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Abstract The present objective was to evaluate Swiss albino mice (Mus muscullus) with Ehrlich carcinoma treated with intrarectal ozone therapy and cisplatin. Twenty-four female mice, approximately 60 days of age, varying between 35g and 40g in weight were divided into four groups, Group G1: Positive control: 2.5mg/kg of cisplatin; Group G2: Ozone-oxygen mix via rectal insufflation (MOO IR); Group G3: 2.5mg/kg of cisplatin + (MOO IR), and Group G4: Negative control with 1ml of saline 0.9%. All animals underwent an eight-day adaptation period. Forty-eight hours after inoculation, the treatments were performed for six days. The mice were euthanized at the end of the experiment and the tumor was removed. There were statistically significant differences between groups for tumor weight. Mean tumor weight was greater in group G4, and lesser in group G3. These significant differences were observed between the negative control and other groups. On histopathology, there were no significant differences between groups. It is concluded that combined ozone therapy and cisplatin was shown to be the treatment where mice with Ehrlich carcinoma had the least tumor weight.
AbstractList The present objective was to evaluate Swiss albino mice (Mus muscullus) with Ehrlich carcinoma treated with intrarectal ozone therapy and cisplatin. Twenty-four female mice, approximately 60 days of age, varying between 35g and 40g in weight were divided into four groups, Group G1: Positive control: 2.5mg/kg of cisplatin; Group G2: Ozone-oxygen mix via rectal insufflation (MOO IR); Group G3: 2.5mg/kg of cisplatin + (MOO IR), and Group G4: Negative control with 1ml of saline 0.9%. All animals underwent an eight-day adaptation period. Forty-eight hours after inoculation, the treatments were performed for six days. The mice were euthanized at the end of the experiment and the tumor was removed. There were statistically significant differences between groups for tumor weight. Mean tumor weight was greater in group G4, and lesser in group G3. These significant differences were observed between the negative control and other groups. On histopathology, there were no significant differences between groups. It is concluded that combined ozone therapy and cisplatin was shown to be the treatment where mice with Ehrlich carcinoma had the least tumor weight.
Author Fernando Leandro dos Santos
Laís Albuquerque van der Linden
Rhaysa Allayde Silva Oliveira
Renan Felipe Silva Santos
Ykaro Kyokay Vieira Serafim
Yasmim Theonise Ferreira Chaves
Alluanan Adelson do Nascimento Silva
Evilda Rodrigues de Lima
Ivone Antônia de Souza
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  fullname: Rhaysa Allayde Silva Oliveira
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  fullname: Ivone Antônia de Souza
  organization: Departamento de Farmácia, Universidade Federal de Pernambuco, Recife-PE, Brasil
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  fullname: Evilda Rodrigues de Lima
  organization: Programa de Pós-Graduação em Medicina Veterinária, Universidade Federal Rural de Pernambuco, Recife-PE, Brasil
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Snippet The present objective was to evaluate Swiss albino mice (Mus muscullus) with Ehrlich carcinoma treated with intrarectal ozone therapy and cisplatin....
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Oncology
Ozone
Rectal Insufflation
Title EVALUATION OF THE EFFECTS OF OZONE THERAPY AND CISPLATIN IN AN EXPERIMENTAL MODEL IN MICE WITH EHRLICH CARCINOMA
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