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DOI 10.3390/molecules21121739

Медицинская библиотека · Molecules (Basel, Switzerland) · 2016

Effects of Quercetin in a Rat Model of Hemorrhagic Traumatic Shock and Reperfusion.

Chamorro Virginia, Pandolfi Rachele, Moreno Laura, Barreira Bianca, Martínez-Ramas Andrea, Morales-Cano Daniel, Ruiz-Cabello Jesús, Lorente José Angel, Duarte Juan, Cogolludo Ángel, Alvarez-Sala José Luis, Perez-Vizcaino Francisco

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Аннотация

BACKGROUND

We hypothesized that treatment with quercetin could result in improved hemodynamics, lung inflammatory parameters and mortality in a rat model of hemorrhagic shock.

METHODS

Rats were anesthetized (80 mg/kg ketamine plus 8 mg/kg xylazine i.p.). The protocol included laparotomy for 15 min (trauma), hemorrhagic shock (blood withdrawal to reduce the mean arterial pressure to 35 mmHg) for 75 min and resuscitation by re-infusion of all the shed blood plus lactate Ringer for 90 min. Intravenous quercetin (50 mg/kg) or vehicle were administered during resuscitation.

RESULTS

There was a trend for increased survival 84.6% (11/13) in the treated group vs. the shock group 68.4% (13/19, p > 0.05 Kaplan-Meier). Quercetin fully prevented the development of lung edema. The activity of aSMase was increased in the shock group compared to the sham group and the quercetin prevented this effect. However, other inflammatory markers such as myeloperoxidase activity, interleukin-6 in plasma or bronchoalveolar fluid were similar in the sham and shock groups. We found no bacterial DNA in plasma in these animals.

CONCLUSIONS

Quercetin partially prevented the changes in blood pressure and lung injury in shock associated to hemorrhage and reperfusion.

Для цитирования: Chamorro Virginia, Pandolfi Rachele, Moreno Laura, Barreira Bianca, Martínez-Ramas Andrea, Morales-Cano Daniel, Ruiz-Cabello Jesús, Lorente José Angel, Duarte Juan, Cogolludo Ángel, Alvarez-Sala José Luis, Perez-Vizcaino Francisco. Effects of Quercetin in a Rat Model of Hemorrhagic Traumatic Shock and Reperfusion.. Molecules (Basel, Switzerland). 2016. DOI: 10.3390/molecules21121739.

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