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猴子触觉辨别背后的皮层机制。I. 初级体感皮层在被动质地辨别中的作用。

Cortical mechanisms underlying tactile discrimination in the monkey. I. Role of primary somatosensory cortex in passive texture discrimination.

作者信息

Tremblay F, Ageranioti-Bélanger S A, Chapman C E

机构信息

Département de Physiologie and Ecole de Réadaptation, Faculté de Médecine, Université de Montréal, Quebec.

出版信息

J Neurophysiol. 1996 Nov;76(5):3382-403. doi: 10.1152/jn.1996.76.5.3382.

Abstract
  1. The discharge patterns of 359 single neurons in the hand representation of primary somatosensory cortex (SI) of two monkeys (Macaca mulatta) were recorded during the performance of a passive texture discrimination task with the contralateral hand (104 in area 3b, 149 in area 1, and 106 in area 2). Three nyloprint surfaces were mounted on a drum that was rotated under the digit tips. One surface was entirely smooth, whereas the other two were smooth over the first half and rough over the second half (smooth/ rough) (raised dots, 1 mm high and 1 mm diam, in a rectangular array; spatial period of 3 mm across the rows and columns for most recordings; 9 mm between columns for selected recordings). The monkeys were trained to distinguish between the smooth and smooth/rough surfaces. After the surface presentation, the monkey indicated the texture of the second half of the surface by pushing or pulling, respectively, on a lever with the other arm. For most recordings an average tangential speed of 49 mm/s was tested. For selected recordings motor speed was incremented (63, 75, or 89 mm/s). 2. Two hundred eighty-three neurons had a cutaneous receptive field (RF) on the hand (96 in area 3b, 120 in area 1, and 67 in area 2). Thirty-five neurons had a deep RF (4 in area 3b, 15 in area 1, and 16 in area 2). Seven neurons had mixed cutaneous and deep RFs (4 in area 1, 3 in area 2). Thirty-four neurons had no identifiable RF (4 in area 3b, 10 in area 1, and 20 in area 2). 3. The discharge of 185 of 359 neurons was significantly modulated during the presentation of one or both surfaces compared with the discharge at rest. Cells with a cutaneous RF that included part or all of the distal phalangeal pads of the digits used in the task (usually digits III and IV) were more likely to be modulated during surface presentation (132 of 179, 74%) than those with a cutaneous RF not in contact with the surfaces (24 of 104, 23%). The remaining neurons (mixed, deep, or no RF) were also infrequently modulated (29 of 76, 38%). 4. Of the 185 modulated units, 118 cells were classified as texture related because there was a significant difference in the discharge rate evoked by the smooth/rough and smooth surfaces. Cells with a cutaneous RF that included the digital pads in contact with the surfaces were frequently texture related (100 of 132, 76%). Texture sensitivity was less frequently observed in the remaining modulated neurons (18 of 53, 34%: cutaneous RF not in contact with the surfaces, deep RF, mixed cutaneous and deep RF, no identifiable RF). 5. Texture-related neurons were found in areas 3b, 1, and 2. Two patterns of texture-related responses were observed in the 100 cutaneous units with an RF in contact with the surfaces. Thirty-one units were classified as showing a phasic response at the time the digits encountered the leading edge of the rough half of the surface. Fifty-eight cells were classified as phasic-tonic (or sometimes tonic at the slowest motor speeds) because the response lasted for the duration of the presentation of the rough portion of the surface. The remaining 11 neurons could not be readily classified into one or the other category and, indeed, generally showed clear texture-related responses only at higher motor speeds (> 49 mm/s, 9 of 11). 6. Speed sensitivity was systematically evaluated in 41 of 100 texture-related units with a cutaneous RF in contact with the surfaces. The discharge of 66% of the units (27 of 41) varied significantly with the speed of surface presentation, with discharge increasing at higher speeds. Speed sensitivity was found in all three cytoarchitectonic areas (6 of 6 cells in area 3b, 11 of 22 in area 1, and 10 of 13 in area 2). 7. Contact force was also systematically monitored in these experiments (69 of 100 texture-related cells with a cutaneous RF in contact with the surfaces). Linear regression analyses indicated than 22% (15 of 69) of the texture-related units were sensitive to contact force (13
摘要
  1. 在两只猕猴(恒河猴)的初级体感皮层(SI)手部代表区记录了359个单神经元的放电模式,实验中使用对侧手执行被动纹理辨别任务(3b区104个,1区149个,2区106个)。三个尼龙印花表面安装在一个滚筒上,滚筒在指尖下方旋转。一个表面完全光滑,而另外两个表面前半部分光滑,后半部分粗糙(光滑/粗糙)(凸起的圆点,高1毫米,直径1毫米,呈矩形阵列;大多数记录中行和列的空间周期为3毫米;部分记录列间距为9毫米)。训练猕猴区分光滑表面和光滑/粗糙表面。在表面呈现后,猕猴通过用另一只手臂分别推或拉杠杆来指示表面后半部分的纹理。大多数记录测试的平均切向速度为49毫米/秒。部分记录中运动速度增加(63、75或89毫米/秒)。2. 283个神经元在手部分别有皮肤感受野(RF)(3b区96个,1区120个,2区67个)。35个神经元有深部RF(3b区4个,1区15个,2区16个)。7个神经元有混合的皮肤和深部RF(1区4个,2区3个)。34个神经元没有可识别的RF(3b区4个,1区10个,2区20个)。3. 与静息放电相比,359个神经元中的185个在一个或两个表面呈现期间放电有显著调制。在任务中使用的手指(通常是第三和第四指)的皮肤RF包括部分或全部远端指腹的细胞,在表面呈现期间比那些皮肤RF不与表面接触的细胞更有可能被调制(179个中的132个,74%)比(104个中的24个,23%)。其余神经元(混合、深部或无RF)也很少被调制(76个中的29个,38%)。4. 在185个被调制的单元中,118个细胞被归类为与纹理相关,因为光滑/粗糙表面和平滑表面诱发的放电率有显著差异。皮肤RF包括与表面接触的指腹的细胞经常与纹理相关(132个中的100个,76%)。在其余被调制的神经元中较少观察到纹理敏感性(53个中的18个,34%:皮肤RF不与表面接触、深部RF、混合皮肤和深部RF、无可识别RF)。5. 在3b区、1区和2区发现了与纹理相关的神经元。在100个皮肤RF与表面接触的单元中观察到两种与纹理相关的反应模式。31个单元被归类为在手指遇到表面粗糙部分前缘时表现出相位反应。58个细胞被归类为相位 - 紧张型(或有时在最慢运动速度下为紧张型),因为反应持续到表面粗糙部分呈现的持续时间。其余11个神经元不能轻易归类为这两类中的任何一类,实际上,通常仅在较高运动速度(>49毫米/秒,11个中的9个)时才表现出明显的与纹理相关的反应。6. 在100个皮肤RF与表面接触的与纹理相关的单元中的41个中系统地评估了速度敏感性。66%的单元(41个中的27个)放电随表面呈现速度有显著变化,放电在较高速度时增加。在所有三个细胞构筑区都发现了速度敏感性(3b区6个中的6个,1区22个中的11个,2区13个中的10个)。7. 在这些实验中也系统地监测了接触力(100个皮肤RF与表面接触的与纹理相关的细胞中的69个)。线性回归分析表明,22%(69个中的15个)的与纹理相关的单元对接触力敏感(13

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