首页> 外文期刊>Neuroreport >PAF antagonist treatment reduces pro-inflammatory cytokine mRNA after spinal cord injury.
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PAF antagonist treatment reduces pro-inflammatory cytokine mRNA after spinal cord injury.

机译:PAF拮抗剂治疗可降低脊髓损伤后促炎细胞因子的mRNA。

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摘要

Platelet-activating factor (PAF) is a pro-inflammatory molecule which contributes to secondary damage after spinal cord injury (SCI).To test if PAF contributes to cytokine induction following SCI, female Long-Evans rats were pretreated with the PAF antagonist WEB 2170 prior to receiving a contusion injury at spinal cord level T10 using the NYU impactor. RNase protection assay (RPA) analysis revealed that IL-1alpha mRNA peaked at I h post-injury while IL-1beta and IL-6 mRNA levels were higher and peaked at 6 h.TNF-alpha mRNA was almost undetectable. All mRNA levels approached baseline by 24 h. Treatment with WEB 2170 (1 mg/kg, i.p.) 15 min prior to injury significantly decreased mRNA levels for all three cytokines at 6 h post-injury, but not at I h post-injury. These results demonstrate a role for PAF in proinflammatory cytokine induction after SCI.
机译:血小板活化因子(PAF)是一种促炎分子,在脊髓损伤(SCI)后导致继发性损伤。为测试PAF是否在SCI后诱导细胞因子的诱导,对雌性Long-Evans大鼠进行了PAF拮抗剂WEB 2170的预处理然后使用NYU撞击器在T10级脊髓受到挫伤。 RNase保护分析(RPA)分析显示,IL-1αmRNA在损伤后1 h达到峰值,而IL-1beta和IL-6 mRNA的水平更高并在6 h达到峰值.TNF-αmRNA几乎无法检测到。到24小时,所有mRNA水平均接近基线。损伤前15分钟用WEB 2170(1 mg / kg,i.p.)处理,在伤后6 h显着降低所有三种细胞因子的mRNA水平,而在伤后1 h则没有。这些结果证明了PAF在SCI后在促炎细胞因子诱导中的作用。

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