Maier Donna L, Grieb Ginny M, Stelzner Dennis J, McCasland James S
Department of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Exp Neurol. 2003 Dec;184(2):737-45. doi: 10.1016/S0014-4886(03)00335-2.
Using the 2DG/immunostaining method [McCasland, J.S., Graczyk, G.M., 2000. Metabolic mapping-Unit 1.6. In: Gerfen, C.R. (Ed.), Current Protocols in Neuroscience. Wiley, New York, pp 1.6.1-1.6.15], we have previously demonstrated large-scale plasticity in whisker/barrel fields of young adult hamsters subject to follicle ablation on postnatal day 7 (P7) [Somatosens. Motor Res. 13 (1996) 245]. This plasticity occurs after the barrel field has formed, but before neuronal differentiation and synaptogenesis are complete. The present study tested for similar large-scale plasticity following whisker deprivation in young adult hamsters, when neuronal and synaptic development are more mature. Beginning around P40, animals had all whiskers except row C trimmed on alternating days for periods ranging from 1 h to 2 weeks, after which they were administered (3)H 2DG (i.p.) and allowed to explore a fresh empty cage. Autoradiograms from these animals showed a clear expansion in the zone of heavy 2DG labeling with continued whisker trimming. Hamsters with row C spared overnight showed markedly higher labeling in the row C barrels, as expected. After 2 weeks of repeated trimming, the pattern of 2DG labeling in the barrel field ranged from complete activation of all large-whisker columns, as in a previous study of P7 follicle ablation, down to a more localized activation of rows B, C, and D. Intermediate periods of trimming produced more localized label in the region of row C. There was a clear trend toward larger areas of activation with longer periods of trimming. Because inhibitory neurons are strongly activated in all cases, this large-scale neuronal plasticity must take place in the presence of strong inhibition. The data show that simple trimming of all but a few whiskers in normally reared adults leads to abnormally widespread metabolic labeling encompassing virtually the entire barrel field. Taken together, our findings suggest that a large-scale synaptic reorganization occurs in barrel fields deprived of normal sensory input in the adult as well as during postnatal development.
使用2DG/免疫染色方法[McCasland, J.S., Graczyk, G.M., 2000. 代谢图谱 - 单元1.6。载于:Gerfen, C.R.(编),《神经科学实验指南》。Wiley,纽约,第1.6.1 - 1.6.15页],我们之前已经证明,在出生后第7天(P7)接受毛囊消融的成年幼龄仓鼠的触须/桶状皮层区域存在大规模可塑性[《躯体感觉与运动研究》13(1996)245]。这种可塑性发生在桶状皮层形成之后,但在神经元分化和突触形成完成之前。本研究测试了成年幼龄仓鼠在触须剥夺后是否存在类似的大规模可塑性,此时神经元和突触发育更为成熟。从P40左右开始,动物除了C排触须外,其余触须每隔一天修剪一次,修剪时长从1小时到2周不等,之后给它们腹腔注射(3)H 2DG,并让它们探索一个新的空笼子。这些动物的放射自显影片显示,随着触须持续修剪,2DG高标记区域明显扩大。如预期的那样,C排触须保留过夜的仓鼠在C排桶状皮层中的标记明显更高。经过2周的重复修剪后,桶状皮层区域的2DG标记模式范围从所有大触须柱完全激活(如同之前对P7毛囊消融的研究)到B、C和D排更局部的激活。中间修剪期在C排区域产生了更局部的标记。修剪时间越长,激活区域越大的趋势越明显。由于在所有情况下抑制性神经元都被强烈激活,这种大规模神经元可塑性必定是在强抑制存在的情况下发生的。数据表明,在正常饲养的成年动物中,简单修剪少数几根触须以外的所有触须会导致异常广泛的代谢标记,几乎涵盖整个桶状皮层区域。综上所述