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In vivo imaging of the progression of acute lung injury using hyperpolarized [1-13 C] pyruvate.
Pourfathi, Mehrdad; Xin, Yi; Kadlecek, Stephen J; Cereda, Maurizio F; Profka, Harrilla; Hamedani, Hooman; Siddiqui, Sarmad M; Ruppert, Kai; Drachman, Nicholas A; Rajaei, Jennia N; Rizi, Rahim R.
Afiliação
  • Pourfathi M; Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Xin Y; Department of Electrical and Systems Engineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Kadlecek SJ; Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Cereda MF; Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Profka H; Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Hamedani H; Department of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Siddiqui SM; Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Ruppert K; Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Drachman NA; Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Rajaei JN; Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Rizi RR; Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Magn Reson Med ; 78(6): 2106-2115, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28074497
ABSTRACT

PURPOSE:

To investigate pulmonary metabolic alterations during progression of acute lung injury.

METHODS:

Using hyperpolarized [1-13 C] pyruvate imaging, we measured pulmonary lactate and pyruvate in 15 ventilated rats 1, 2, and 4 h after initiation of mechanical ventilation. Lung compliance was used as a marker for injury progression. 5 untreated rats were used as controls; 5 rats (injured-1) received 1 ml/kg and another 5 rats (injured-2) received 2 ml/kg hydrochloric acid (pH 1.25) in the trachea at 70 min.

RESULTS:

The mean lactate-to-pyruvate ratio of the injured-1 cohort was 0.15 ± 0.02 and 0.15 ± 0.03 at baseline and 1 h after the injury, and significantly increased from the baseline value 3 h after the injury to 0.23 ± 0.02 (P = 0.002). The mean lactate-to-pyruvate ratio of the injured-2 cohort decreased from 0.14 ± 0.03 at baseline to 0.08 ± 0.02 1 h after the injury and further decreased to 0.07 ± 0.02 (P = 0.08) 3 h after injury. No significant change was observed in the control group. Compliance in both injured groups decreased significantly after the injury (P < 0.01).

CONCLUSIONS:

Our findings suggest that in severe cases of lung injury, edema and hyperperfusion in the injured lung tissue may complicate interpretation of the pulmonary lactate-to-pyruvate ratio as a marker of inflammation. However, combining the lactate-to-pyruvate ratio with pulmonary compliance provides more insight into the progression of the injury and its severity. Magn Reson Med 782106-2115, 2017. © 2017 International Society for Magnetic Resonance in Medicine.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Isótopos de Carbono / Ácido Láctico / Ácido Pirúvico / Lesão Pulmonar Aguda / Pulmão Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Isótopos de Carbono / Ácido Láctico / Ácido Pirúvico / Lesão Pulmonar Aguda / Pulmão Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article