Abstract | BACKGROUND: METHODS: RESULTS: At 6 hours after the initial brain death, serum levels of cTnT, TNF-alpha, IL-1beta, and IL-6 in Groups B and N began to increase. Levels in Group B increased more dramatically than in Group N. At 24 hours, cardiocyte damage was documented, but the damage in Group N was less severe than that in Group B. The expression of NF-kappaB in Groups B and N increased, and expression in Group B increased more sharply than in Group N. CONCLUSIONS:
N-acetylcysteine can alleviate both structural and functional injury of the heart during brain death, which might be related to the inhibition of NF-kappaB expression and decreasing release of inflammatory mediators.
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Authors | Wenlong Zhai, Ruo Feng, Liang Huo, Jie Li, Shuijun Zhang |
Journal | The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
(J Heart Lung Transplant)
Vol. 28
Issue 9
Pg. 944-9
(Sep 2009)
ISSN: 1557-3117 [Electronic] United States |
PMID | 19716048
(Publication Type: Journal Article)
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Chemical References |
- DNA Primers
- Interleukin-1beta
- Interleukin-6
- Troponin T
- Tumor Necrosis Factor-alpha
- RNA
- Acetylcysteine
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Topics |
- Acetylcysteine
(pharmacology)
- Animals
- Brain Death
(pathology, physiopathology)
- DNA Primers
- Disease Models, Animal
- Fasting
- Heart
(drug effects, physiology)
- Interleukin-1beta
(pharmacology)
- Interleukin-6
(pharmacology)
- Intermittent Positive-Pressure Ventilation
- Intubation, Intratracheal
(methods)
- RNA
(genetics, isolation & purification)
- Reverse Transcriptase Polymerase Chain Reaction
(methods)
- Swine
- Swine, Miniature
- Troponin T
(blood, drug effects)
- Tumor Necrosis Factor-alpha
(pharmacology)
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