Qu T, Uz T, Manev H
The Psvchiatric Institute, University of Illinois at Chicago, IL 60612, USA.
Neurobiol Aging. 2000 Sep-Oct;21(5):647-52. doi: 10.1016/s0197-4580(00)00167-6.
5-Lipoxygenase (5-LOX) is the key enzyme in the synthesis of leukotrienes, inflammatory mediators of arachidonic acid. 5-LOX is also expressed in neurons (in particular in the hippocampus and the cerebellum), and it seems to be capable of promoting neurodegeneration. Recently, we observed greater 5-LOX mRNA content in the hippocampus of older (24 months) than younger (2 months) rats. In this study, we measured in the hippocampus and the cerebellum of younger and older male F344 rats the contents of: 5-LOX mRNA, FLAP (5-LOX activating protein) mRNA, and 5-LOX protein. By using a quantitative reverse transcription/polymerase chain reaction (PCR) (RT-PCR) with internal standards we found that 5-LOX but not FLAP mRNA content is greater (both in hippocampus and cerebellum) of older than younger rats. By using quantitative Western immunoblotting, we found a greater content of 5-LOX protein in the hippocampus and the cerebellum of older rats; we also established that the membrane/cytosol 5-LOX content ratio is larger in the brains of older than younger rats (statistically significant in the cerebellum). The latter can be considered an indication of 5-LOX translocation/activation during aging. Together these results suggest that aging increases both neuronal 5-LOX expression and protein translocation, and indicate that the 5-LOX system might play a significant role in the pathobiology of aging-associated neurodegenerative diseases.
5-脂氧合酶(5-LOX)是白三烯合成中的关键酶,白三烯是花生四烯酸的炎症介质。5-LOX也在神经元中表达(特别是在海马体和小脑中),并且似乎能够促进神经退行性变。最近,我们观察到老年(24个月)大鼠海马体中的5-LOX mRNA含量比幼年(2个月)大鼠的更高。在本研究中,我们测量了幼年和老年雄性F344大鼠海马体和小脑中的以下物质含量:5-LOX mRNA、FLAP(5-LOX激活蛋白)mRNA和5-LOX蛋白。通过使用带有内标的定量逆转录/聚合酶链反应(PCR)(RT-PCR),我们发现老年大鼠(海马体和小脑中)的5-LOX mRNA含量比幼年大鼠更高,而FLAP mRNA含量则不然。通过定量Western免疫印迹法,我们发现老年大鼠海马体和小脑中5-LOX蛋白的含量更高;我们还确定老年大鼠大脑中膜/胞质5-LOX含量比大于幼年大鼠(在小脑中具有统计学意义)。后者可被视为衰老过程中5-LOX易位/激活的一个指标。这些结果共同表明,衰老会增加神经元5-LOX的表达和蛋白易位,并表明5-LOX系统可能在与衰老相关的神经退行性疾病的病理生物学中起重要作用。