Erythromycin pretreatment induces tolerance against focal cerebral ischemia through up-regulation of nNOS but not down-regulation of HIF-1α in rats

被引:6
|
作者
Lu, Wei-cheng [1 ]
Li, Guang-yu [1 ]
Xie, Hui [2 ]
Qiu, Bo [1 ]
Yang, Ri-miao [1 ]
Guo, Zong-ze [1 ]
机构
[1] China Med Univ, Dept Neurosurg, Affiliated Hosp 1, Shenyang 110001, Liaoning, Peoples R China
[2] Shenyang Med Coll, Dept Histol & Embryol, Coll Basic Med, Shenyang 110034, Peoples R China
基金
中国国家自然科学基金;
关键词
Erythromycin; Preconditioning; Cerebral ischemia; Neuronal nitric oxide synthase; Hypoxia-inducible factor-1 alpha; PRECONDITIONING-INDUCED CARDIOPROTECTION; INDUCIBLE FACTOR-I; NITRIC-OXIDE; PROTEIN EXPRESSION; ARTERY OCCLUSION; INJURY; BRAIN; MICE; NO; NEUROPROTECTION;
D O I
10.1007/s10072-013-1584-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The purpose of this study was to determine whether the antibiotic erythromycin induces tolerance against focal cerebral ischemia, and the possible underlying mechanism including the involvement of neuronal nitric oxide synthase (nNOS) and hypoxia-inducible factor-1 alpha (HIF-1 alpha). In rat focal cerebral ischemia models, we found that erythromycin preconditioning could significantly decrease the cerebral infarct volume and brain edema. Meanwhile, the neurological deficits from day 4 through 7 after surgery were also remarkably decreased after erythromycin preconditioning. Moreover, erythromycin preconditioning induced significantly increased nNOS levels and decreased HIF-1 alpha levels in both mRNA and protein expression. This study for the first time indicated that erythromycin preconditioning could induce focal brain ischemic tolerance and attenuate brain injury of subsequent transient focal cerebral ischemia. The potential mechanism may be due to up-regulation of nNOS, but the HIF-1 alpha system was not involved.
引用
收藏
页码:687 / 693
页数:7
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