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Heart and systemic effects of statin pretreatment in a rat model of abdominal sepsis. Assessment by Tc99m-sestamibi biodistribition
Macedo, Robson; Javadi, Som Mehrbod; Higuchi, Takahiro; Carvalho, Marília Daniela Ferreira de; Medeiros, Vanessa de Fátima Lima Paiva; Azevedo, Ítalo Medeiros; Lima, Francisco Pignataro; Medeiros, Aldo Cunha.
Affiliation
  • Macedo, Robson; Federal University of Rio Grande do Norte. Postgraduate Program in Health Sciences. Natal. Brazil
  • Javadi, Som Mehrbod; Johns Hopkins University. Department of Radiology. Division of Nuclear Medicine. Baltimore. United States of America
  • Higuchi, Takahiro; Wuerzburg University. Department of Nuclear Medicine. Wuerzburg. Germany
  • Carvalho, Marília Daniela Ferreira de; Federal University of Rio Grande do Norte. Postgraduate Program in Health Sciences. Natal. Brazil
  • Medeiros, Vanessa de Fátima Lima Paiva; Federal University of Rio Grande do Norte. Postgraduate Program in Health Sciences. Natal. Brazil
  • Azevedo, Ítalo Medeiros; Federal University of Rio Grande do Norte. Department of Surgery. Natal. Brazil
  • Lima, Francisco Pignataro; Federal University of Rio Grande do Norte. Department of Patology. Natal. Brazil
  • Medeiros, Aldo Cunha; Federal University of Rio Grande do Norte. Department of Surgery. Natal. Brazil
Acta cir. bras. ; 30(6): 388-393, June 2015. tab
Article in En | VETINDEX | ID: vti-23104
Responsible library: BR68.1
Localization: BR68.1
ABSTRACT

PURPOSE:

To evaluate the heart and the Tc-99m-sestamibi biodistribution after statin pretreatment in a rat model of abdominal sepsis.

METHODS:

Twenty-four Wistar rats were randomly distributed into four groups (n=6 per group) 1) sepsis with simvastatin treatment, 2) sepsis with vehicle, 3) sham control with simvastatin and 4) sham control with vehicle. 24 hours after cecal ligation and puncture rats received 1.0MBq of Tc-99m-sestamibi i.v. 30min after, animals were euthanized for ex-vivo tissue counting and myocardium histological analysis.

RESULTS:

Myocardial histologic alterations were not detected 24 hours post-sepsis. There was significantly increased cardiac Tc-99m-sestamibi activity in the sepsis group with simvastatin treatment (1.9±0.3%ID/g, p 0.001) in comparison to the sepsis group+vehicle (1.0±0.2%ID/g), control sham group+ simvastatin (1.2±0.3%ID/g) and control sham group (1.3±0.2%ID/g). Significant Tc-99m-sestamibi activity in liver, kidney and lungs was also detected in the sepsis group treated with simvastatinin comparison to the other groups.

CONCLUSIONS:

Statin treatment altered the biodistribution of Tc-99m-sestamibi with increased cardiac and solid organ activity in rats with abdominal sepsis, while no impact on controls. Increased myocardial tracer activity may be a result of a possible protection effect due to increased tissue perfusion mediated by statins.(AU)
Subject(s)
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Full text: 1 Database: VETINDEX Main subject: Sepsis / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Simvastatin / Myocardium Limits: Animals Language: En Journal: Acta cir. bras. Year: 2015 Document type: Article / Project document

Full text: 1 Database: VETINDEX Main subject: Sepsis / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Simvastatin / Myocardium Limits: Animals Language: En Journal: Acta cir. bras. Year: 2015 Document type: Article / Project document