The Attenuation of Lung Ischemia Reperfusion Injury by Oxymatrine
Autor: | Yue Quan Jiang, Shi-feng Chen, Jian-ru Yang, Bing Zhu |
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Rok vydání: | 2014 |
Předmět: |
medicine.medical_specialty
Biophysics Ischemia Apoptosis Lung injury Biochemistry Gastroenterology Alveolar cells chemistry.chemical_compound Alkaloids Internal medicine Lung ischemia medicine Animals Interleukin 8 Lung Tumor Necrosis Factor-alpha business.industry Interleukin-8 Cell Biology General Medicine medicine.disease Interleukin-10 medicine.anatomical_structure Oxymatrine chemistry Reperfusion Injury Anesthesia Rabbits business Reperfusion injury Quinolizines |
Zdroj: | Cell Biochemistry and Biophysics. 70:333-336 |
ISSN: | 1559-0283 1085-9195 |
DOI: | 10.1007/s12013-014-9917-4 |
Popis: | To investigate the protective effects of oxymatrine (OMT) on lung ischemia reperfusion injury (LIRI) in rabbits, models of LIRI in rabbit were used. Thirty-two rabbits were randomly divided into four groups: control group (n = 8), ischemia reperfusion group (I/R group, n = 8), OMTl group (n = 8), OMT2 group (n = 8). Lung tissue samples were collected at 40, 80, 120 min time-points after lung ischemia reperfusion. TNF-α, 1I-8, IL-10, apoptosis index (AI), and index of quantitative assessment of histologic lung injury (IQA) were measured in each group. TNF-α and IL-8 in I/R group were significantly higher than those of the control group and OMT2 group (P < 0.01), but in OMT2 group they were significantly lower than those of OMTl group (P < 0.05). IL-10 in OMT2 group and OMTl group was significantly higher than that of I/R group (P < 0.01). But in OMTl group it was significantly lower than that of OMT2 group (P < 0.05). AI in I/R group was significantly higher than that of OMT2 group and the control group at 80 min after lung ischemia reperfusion (P < 0.01). IQA in OMTl group and OMT2 group was significantly lower than that of the I/R group (P < 0.01). Oxymatrine can protect against LIRI in rabbits by upregulating levels of IL-10 and downregulating levels of TNF-α and IL-8, inhibiting the alveolar cells apoptosis and inflammatory response, and attenuating the acute LIRI. |
Databáze: | OpenAIRE |
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