Wesson Daniel W, Carey Ryan M, Verhagen Justus V, Wachowiak Matt
Department of Biology, Boston University, Boston, Massachusetts, United States of America.
PLoS Biol. 2008 Apr 8;6(4):e82. doi: 10.1371/journal.pbio.0060082.
To gain insight into which parameters of neural activity are important in shaping the perception of odors, we combined a behavioral measure of odor perception with optical imaging of odor representations at the level of receptor neuron input to the rat olfactory bulb. Instead of the typical test of an animal's ability to discriminate two familiar odorants by exhibiting an operant response, we used a spontaneously expressed response to a novel odorant-exploratory sniffing-as a measure of odor perception. This assay allowed us to measure the speed with which rats perform spontaneous odor discriminations. With this paradigm, rats discriminated and began responding to a novel odorant in as little as 140 ms. This time is comparable to that measured in earlier studies using operant behavioral readouts after extensive training. In a subset of these trials, we simultaneously imaged receptor neuron input to the dorsal olfactory bulb with near-millisecond temporal resolution as the animal sampled and then responded to the novel odorant. The imaging data revealed that the bulk of the discrimination time can be attributed to the peripheral events underlying odorant detection: receptor input arrives at the olfactory bulb 100-150 ms after inhalation begins, leaving only 50-100 ms for central processing and response initiation. In most trials, odor discrimination had occurred even before the initial barrage of receptor neuron firing had ceased and before spatial maps of activity across glomeruli had fully developed. These results suggest a coding strategy in which the earliest-activated glomeruli play a major role in the initial perception of odor quality, and place constraints on coding and processing schemes based on simple changes in spike rate.
为了深入了解神经活动的哪些参数在塑造气味感知中起重要作用,我们将气味感知的行为测量与在大鼠嗅球的受体神经元输入水平上对气味表征进行的光学成像相结合。我们没有采用通过表现出操作性反应来测试动物区分两种熟悉气味剂能力的典型方法,而是使用对新气味剂的自发表达反应——探索性嗅闻——作为气味感知的一种测量方法。这种测定方法使我们能够测量大鼠进行自发气味辨别所需的速度。采用这种范式,大鼠在短短140毫秒内就能辨别并开始对新气味剂做出反应。这个时间与早期使用经过广泛训练后的操作性行为读数进行的研究中测得的时间相当。在这些试验的一个子集中,当动物对新气味剂进行采样然后做出反应时,我们以近毫秒的时间分辨率同时对背侧嗅球的受体神经元输入进行成像。成像数据显示,大部分辨别时间可归因于气味剂检测背后的外周事件:吸入开始后100 - 150毫秒,受体输入到达嗅球,留给中枢处理和反应启动的时间只有50 - 100毫秒。在大多数试验中,甚至在受体神经元最初的一阵放电停止之前以及在整个肾小球的活动空间图谱完全形成之前,气味辨别就已经发生了。这些结果表明了一种编码策略,其中最早被激活的肾小球在气味质量的初始感知中起主要作用,并对基于放电率简单变化的编码和处理方案施加了限制。