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Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats

INTRODUCTION. Cyclophosphamide (CP) is used to treat malignant neoplasias and control autoimmune diseases. Still, one of its metabolites, acrolein, is toxic to the urothelium and can lead to hemorrhagic cystitis and severe discomfort. OBJECTIVE. To evaluate the ability of red propolis to prevent and...

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Autores principales: Ramos Melo, Nayanna de Oliveira, Peres Júnior, Helio De Sousa, Diniz, Clara Araujo, Silva, Matheus De Sousa, Gomes de Lemos, Telma Leda, Jamacaru, Francisco Vagnaldo Fechine, Dornelas, Conceição Aparecida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Nacional de Salud 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365036/
https://www.ncbi.nlm.nih.gov/pubmed/35867919
http://dx.doi.org/10.7705/biomedica.6087
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author Ramos Melo, Nayanna de Oliveira
Peres Júnior, Helio De Sousa
Diniz, Clara Araujo
Silva, Matheus De Sousa
Gomes de Lemos, Telma Leda
Jamacaru, Francisco Vagnaldo Fechine
Dornelas, Conceição Aparecida
author_facet Ramos Melo, Nayanna de Oliveira
Peres Júnior, Helio De Sousa
Diniz, Clara Araujo
Silva, Matheus De Sousa
Gomes de Lemos, Telma Leda
Jamacaru, Francisco Vagnaldo Fechine
Dornelas, Conceição Aparecida
author_sort Ramos Melo, Nayanna de Oliveira
collection PubMed
description INTRODUCTION. Cyclophosphamide (CP) is used to treat malignant neoplasias and control autoimmune diseases. Still, one of its metabolites, acrolein, is toxic to the urothelium and can lead to hemorrhagic cystitis and severe discomfort. OBJECTIVE. To evaluate the ability of red propolis to prevent and treat CP-induced hemorrhagic cystitis in rats. MATERIALS AND METHODS. Red propolis was extracted in 1% gum arabic and administered subcutaneously (sc). In the first experiment, groups IA, IIA, and IIIA and groups IB, IIB, and IIIB received water, gum arabic (GA), or propolis, respectively, for 30 days. Then water (controls) or CP (treatment) was administered i.p. In the second experiment, groups IVA, VA, and VIA received water i.p. while groups IVB, VB, and VIB received CP i.p. This was followed by 5 injections at 2-hour intervals with either water, GA, or propolis. Bladder tissue was examined according to Gray’s criteria. RESULTS. The total inflammatory histology score was significantly smaller in group VIB (11.33 ± 2.07). Mild inflammation predominated in group VIB while most of the animals in group IVB had severe inflammation (p=0.0375). Ulcers were predominantly multiple in Groups IVA and VB but rare or absent in Group VIB (p=0.0118). Urothelial cells were mostly absent in groups IVB and VB and present/normal in group VIB (p=0.0052). Fibrin was abundant in groups IVB and VA but mostly absent in group VIB (p=0.0273). CONCLUSIONS. Red propolis can reduce inflammation in CP-induced hemorrhagic cystitis in rats.
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spelling pubmed-93650362022-08-11 Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats Ramos Melo, Nayanna de Oliveira Peres Júnior, Helio De Sousa Diniz, Clara Araujo Silva, Matheus De Sousa Gomes de Lemos, Telma Leda Jamacaru, Francisco Vagnaldo Fechine Dornelas, Conceição Aparecida Biomedica Artículos Originales INTRODUCTION. Cyclophosphamide (CP) is used to treat malignant neoplasias and control autoimmune diseases. Still, one of its metabolites, acrolein, is toxic to the urothelium and can lead to hemorrhagic cystitis and severe discomfort. OBJECTIVE. To evaluate the ability of red propolis to prevent and treat CP-induced hemorrhagic cystitis in rats. MATERIALS AND METHODS. Red propolis was extracted in 1% gum arabic and administered subcutaneously (sc). In the first experiment, groups IA, IIA, and IIIA and groups IB, IIB, and IIIB received water, gum arabic (GA), or propolis, respectively, for 30 days. Then water (controls) or CP (treatment) was administered i.p. In the second experiment, groups IVA, VA, and VIA received water i.p. while groups IVB, VB, and VIB received CP i.p. This was followed by 5 injections at 2-hour intervals with either water, GA, or propolis. Bladder tissue was examined according to Gray’s criteria. RESULTS. The total inflammatory histology score was significantly smaller in group VIB (11.33 ± 2.07). Mild inflammation predominated in group VIB while most of the animals in group IVB had severe inflammation (p=0.0375). Ulcers were predominantly multiple in Groups IVA and VB but rare or absent in Group VIB (p=0.0118). Urothelial cells were mostly absent in groups IVB and VB and present/normal in group VIB (p=0.0052). Fibrin was abundant in groups IVB and VA but mostly absent in group VIB (p=0.0273). CONCLUSIONS. Red propolis can reduce inflammation in CP-induced hemorrhagic cystitis in rats. Instituto Nacional de Salud 2022-06-01 /pmc/articles/PMC9365036/ /pubmed/35867919 http://dx.doi.org/10.7705/biomedica.6087 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Artículos Originales
Ramos Melo, Nayanna de Oliveira
Peres Júnior, Helio De Sousa
Diniz, Clara Araujo
Silva, Matheus De Sousa
Gomes de Lemos, Telma Leda
Jamacaru, Francisco Vagnaldo Fechine
Dornelas, Conceição Aparecida
Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
title Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
title_full Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
title_fullStr Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
title_full_unstemmed Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
title_short Red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
title_sort red propolis reduces inflammation in cyclophosphamide-induced hemorrhagic cystitis in rats
topic Artículos Originales
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365036/
https://www.ncbi.nlm.nih.gov/pubmed/35867919
http://dx.doi.org/10.7705/biomedica.6087
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