Gene and protein expressions of nitric oxide synthases in ischemia-reperfused peripheral nerve of the rat

被引:31
作者
Qi, WN
Yan, ZQ
Whang, PG
Zhou, Q
Chen, LE
Seaber, AV
Stamler, JS
Urbaniak, JR
机构
[1] Duke Univ, Med Ctr, Dept Surg, Orthopaed Microsurg Res Lab, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Orthopaed Cell Biol Lab, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Med, Pulm Div,Howard Hughes Med Inst, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Med, Cardiovasc Div,Howard Hughes Med Inst, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 281卷 / 03期
关键词
nitric oxide synthase transcription; nitric oxide synthase translation; reperfusion; sciatic nerve;
D O I
10.1152/ajpcell.2001.281.3.C849
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study examined mRNA and protein expressions of neuronal (nNOS), inducible (iNOS), and endothelial nitric oxide synthases (eNOS) in peripheral nerve after ischemia-reperfusion (I/R). Sixty-six rats were divided into the ischemia only and I/R groups. One sciatic nerve of each animal was used as the experimental side and the opposite untreated nerve as the control. mRNA levels in the nerve were quantitatively measured by competitive PCR, and protein was determined by Western blotting and immunohistochemical staining. The results showed that, after ischemia (2 h), both nNOS and eNOS protein expressions decreased. After I/R (2 h of ischemia followed by 3 h of reperfusion), expression of both nNOS and eNOS mRNA and protein decreased further. In contrast, iNOS mRNA significantly increased after ischemia and was further upregulated (14-fold) after I/R, while iNOS protein was not detected. The results reveal the dynamic expression of individual NOS isoforms during the course of I/R injury. An understanding of this modulation on a cellular and molecular level may lead to understanding the mechanisms of I/R injury and to methods of ameliorating peripheral nerve injury.
引用
收藏
页码:C849 / C856
页数:8
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