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Doxycycline reduces liver and kidney injuries in a rat hemorrhagic shock model.
Sordi, Regina; Bojko, Luana; Oliveira, Filipe R M B; Rosales, Thiele Osvaldt; Souza, Camila Fernandes; Moreno, Lucas Wenceslau; Ferreira Alves, Gustavo; Vellosa, José Carlos Rebuglio; Fernandes, Daniel; Gomes, Jose Rosa.
Afiliación
  • Sordi R; Department of Pharmacology, Graduate Program in Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
  • Bojko L; Department of Structural Biology, Molecular and Genetics, Post Graduation Program in Biomedical Science, Universidade Estadual de Ponta Grossa, Avenida Carlos Cavalcanti, 4748, Ponta Grossa, PR, 84030-900, Brazil.
  • Oliveira FRMB; Department of Structural Biology, Molecular and Genetics, Universidade Estadual de Ponta Grossa, Ponta Grossa, PR, Brazil.
  • Rosales TO; Department of Pharmacology, Graduate Program in Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
  • Souza CF; Department of Pharmacology, Graduate Program in Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
  • Moreno LW; Department of Pharmacology, Graduate Program in Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
  • Ferreira Alves G; Department of Structural Biology, Molecular and Genetics, Universidade Estadual de Ponta Grossa, Ponta Grossa, PR, Brazil.
  • Vellosa JCR; Department of Pharmacology, Graduate Program in Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
  • Fernandes D; Department of Clinical and Toxicological Analysis, Universidade Estadual de Ponta Grossa, Ponta Grossa, PR, Brazil.
  • Gomes JR; Department of Pharmacology, Graduate Program in Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
Intensive Care Med Exp ; 12(1): 2, 2024 Jan 09.
Article en En | MEDLINE | ID: mdl-38194181
ABSTRACT

BACKGROUND:

Hemorrhagic shock (HS), which causes insufficient tissue perfusion, can result in multiple organ failure (MOF) and death. This study aimed to evaluate whether doxycycline (DOX) protects cardiovascular, kidney, and liver tissue from damage in a rat model of HS. Immediately before the resuscitation, DOX (10 mg/kg; i.v.) was administered, and its protective effects were assessed 24 h later. Mean arterial pressure, renal blood flow, heart rate, vasoactive drug response, and blood markers such as urea, creatinine, AST, ALT, CPK, CPR, and NOx levels were determined.

RESULTS:

We showed that DOX has a significant effect on renal blood flow and on urea, creatinine, AST, ALT, CPK, and NOx. Morphologically, DOX reduced the inflammatory process in the liver tissue.

CONCLUSIONS:

We conclude that DOX protects the liver and kidney against injury and dysfunction in a HS model and could be a strategy to reduce organ damage associated with ischemia-and-reperfusion injury.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_kidney_renal_pelvis_ureter_cancer Idioma: En Revista: Intensive Care Med Exp Año: 2024 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_kidney_renal_pelvis_ureter_cancer Idioma: En Revista: Intensive Care Med Exp Año: 2024 Tipo del documento: Article País de afiliación: Brasil
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