In-Vivo Electrophysiology Unit, Behavioral Neuroscience Branch, National Institute on Drug Abuse-Intramural Research Program, NIH, DHHS, 333 Cassell Dr., Baltimore, MD 21224, USA.
J Neurophysiol. 2012 Sep;108(6):1669-84. doi: 10.1152/jn.00521.2012. Epub 2012 Jun 20.
Glucose, a primary energetic substrate for neural activity, is continuously influenced by two opposing forces that tend to either decrease its extracellular levels due to enhanced utilization in neural cells or increase its levels due to entry from peripheral circulation via enhanced cerebral blood flow. How this balance is maintained under physiological conditions and changed during neural activation remains unclear. To clarify this issue, enzyme-based glucose sensors coupled with high-speed amperometry were used in freely moving rats to evaluate fluctuations in extracellular glucose levels induced by brief audio stimulus, tail pinch (TP), social interaction with another rat (SI), and intravenous cocaine (1 mg/kg). Measurements were performed in nucleus accumbens (NAcc) and substantia nigra pars reticulata (SNr), which drastically differ in neuronal activity. In NAcc, where most cells are powerfully excited after salient stimulation, glucose levels rapidly (latency 2-6 s) increased (30-70 μM or 6-14% over baseline) by all stimuli; the increase differed in magnitude and duration for each stimulus. In SNr, where most cells are transiently inhibited by salient stimuli, TP, SI, and cocaine induced a biphasic glucose response, with the initial decrease (-20-40 μM or 5-10% below baseline) followed by a reboundlike increase. The critical role of neuronal activity in mediating the initial glucose response was confirmed by monitoring glucose currents after local microinjections of glutamate (GLU) or procaine (PRO). While intra-NAcc injection of GLU transiently increased glucose levels in this structure, intra-SNr PRO injection resulted in rapid, transient decreases in SNr glucose. Therefore, extracellular glucose levels in the brain change very rapidly after physiological and pharmacological stimulation, the response is structure specific, and the pattern of neuronal activity appears to be a critical factor determining direction and magnitude of physiological fluctuations in glucose levels.
葡萄糖是神经活动的主要能量底物,不断受到两种相反力量的影响,这两种力量要么通过增强神经细胞的利用来降低细胞外水平,要么通过增强大脑血流从外周循环中进入来增加水平。在生理条件下如何维持这种平衡,以及在神经激活期间如何改变,仍然不清楚。为了澄清这个问题,使用基于酶的葡萄糖传感器与高速安培法,在自由活动的大鼠中评估短暂音频刺激、尾巴夹(TP)、与另一只大鼠的社交互动(SI)和静脉内可卡因(1mg/kg)引起的细胞外葡萄糖水平波动。测量在伏隔核(NAcc)和黑质网状部(SNr)中进行,这两个区域的神经元活动差异很大。在 NAcc 中,大多数细胞在显著刺激后会被强烈兴奋,葡萄糖水平会迅速(潜伏期 2-6s)升高(相对于基线升高 30-70μM 或 6-14%);每个刺激的增加幅度和持续时间都不同。在 SNr 中,大多数细胞会被显著刺激短暂抑制,TP、SI 和可卡因会引起双相葡萄糖反应,初始下降(相对于基线下降 20-40μM 或 5-10%),随后出现反弹样增加。通过监测局部微注射谷氨酸(GLU)或普鲁卡因(PRO)后的葡萄糖电流,证实神经元活动在介导初始葡萄糖反应中的关键作用。虽然 NAcc 内注射 GLU 会短暂增加该结构中的葡萄糖水平,但 SNr 内注射 PRO 会导致 SNr 葡萄糖迅速、短暂下降。因此,在生理和药理学刺激后,大脑中的细胞外葡萄糖水平会迅速变化,反应具有结构特异性,神经元活动模式似乎是决定葡萄糖水平生理波动方向和幅度的关键因素。