Coopersmith R, Leon M
Department of Psychobiology, University of California, Irvine 92717.
J Comp Neurol. 1989 Nov 8;289(2):348-59. doi: 10.1002/cne.902890213.
An understanding of olfactory system glucose metabolism is necessary for the interpretation of radiolabeled 2-deoxyglucose studies of odor processing since the relationship between glucose uptake and neural activity is based on assumptions regarding cellular glucose utilization. As part of an ongoing study examining divergent pathways of glucose metabolism in the olfactory system, the relative activity of glucose-6-phosphate dehydrogenase, the rate-limiting enzyme of the hexose monophosphate shunt, was examined among cells of the rat olfactory bulb and anterior olfactory nucleus, by using enzyme histochemistry on fresh frozen tissue. Optical density measurement of formazan reaction product in stained tissue were quantified by computerized image analysis. To aid in the identification of histochemically stained neurons, alternate sections were Nissl-stained. The highest olfactory bulb dehydrogenase levels were found in the olfactory nerve and glomerular layers. Individual mitral and tufted cells also showed high dehydrogenase activity. In most stained neurons, formazan reaction product filled the cytoplasm and sometimes extended into the proximal part of dendrites and axons. The external plexiform and granule cell layers had low enzyme activity. High activity also was seen in pyramidal cells of pars dorsalis and pars lateralis of the anterior olfactory nucleus, one of the first, and most rostral of the olfactory bulb projection sites. High glucose-6-phosphate dehydrogenase activity in the olfactory system indicates that a significant amount of glucose can be channeled through the hexose monophosphate shunt in these neurons, with a concomitant production of NADPH. This may reflect high activity of cellular detoxification enzymes that rely on NADPH for reducing power. Such detoxification processes may be engaged in response to the potential entry and transsynaptic movement of airborne chemicals into the brain via the olfactory system.
由于葡萄糖摄取与神经活动之间的关系基于有关细胞葡萄糖利用的假设,因此了解嗅觉系统的葡萄糖代谢对于解释放射性标记的2-脱氧葡萄糖气味处理研究至关重要。作为正在进行的一项研究嗅觉系统中葡萄糖代谢不同途径的一部分,通过对新鲜冷冻组织进行酶组织化学,检测了大鼠嗅球和前嗅核细胞中葡萄糖-6-磷酸脱氢酶(己糖磷酸旁路的限速酶)的相对活性。通过计算机图像分析对染色组织中azan反应产物的光密度测量进行定量。为了有助于识别组织化学染色的神经元,对交替切片进行了尼氏染色。在嗅神经和肾小球层中发现嗅球脱氢酶水平最高。单个的二尖瓣细胞和簇状细胞也显示出高脱氢酶活性。在大多数染色的神经元中,azan反应产物充满细胞质,有时延伸到树突和轴突的近端部分。外丛状层和颗粒细胞层的酶活性较低。在前嗅核背侧部和外侧部的锥体细胞中也观察到高活性,前嗅核是嗅球投射部位中最早且最靠前的部位之一。嗅觉系统中高葡萄糖-6-磷酸脱氢酶活性表明,在这些神经元中,大量葡萄糖可以通过己糖磷酸旁路,同时产生NADPH。这可能反映了依赖NADPH提供还原力的细胞解毒酶的高活性。这种解毒过程可能是为了应对空气中的化学物质通过嗅觉系统进入大脑的潜在进入和跨突触移动。