Jen P H, Sun X D
Division of Biological Sciences, University of Missouri, Columbia 65211.
Chin J Physiol. 1990;33(3):231-46.
Postnatal development of auditory sensitivity in the big brown bat, Eptesicus fuscus, was studied by determining the auditory spatial sensitivity of inferior collicular (IC) neurons of juvenile bats which were raised under normal (control) or monaurally plugged conditions. The auditory spatial sensitivity of each IC neuron was determined by measuring its variation in number of impulses and minimum threshold to a best frequency sound delivered from different azimuthal angles under free field stimulation conditions. Monaural plugging was performed on different juvenile bats at 7, 14, and 35 days of age. Auditory spatial sensitivity was then determined for IC neurons of monaurally plugged bats at 58-69 days after birth. Monaural plugging did not alter the discharge pattern, distribution of best frequency and latency of IC neurons, but it raised the minimum threshold of IC neurons of plugged juvenile bats by an average of 21-24 dB. Monaural plugging also appeared to modify postnatal development of auditory spatial sensitivity. The auditory spatial sensitivity of IC neurons was sharper when the earplug was intact than when the earplug was removed. Thus, the distribution of response center and the spatial sensitivity of IC neurons of the monaurally plugged bats was more comparable to IC neurons of the control bats before the earplug was removed. These findings suggest that the neural circuits underlying auditory spatial sensitivity of IC neurons of the monaurally plugged juvenile bats have undergone modifications to compensate for the unnatural binaural disparity during postnatal development. The auditory spatial sensitivity was also determined for two control juvenile bats at 49 and 60 days of age and for an adult bat (more than 1 year). Our data show that auditory spatial sensitivity of IC neurons sharpens with postnatal age. Furthermore, the sharpening process appears to be still in progress even at 60 days after birth.
通过测定在正常(对照)或单耳堵塞条件下饲养的幼年大棕蝠(Eptesicus fuscus)下丘(IC)神经元的听觉空间敏感性,研究了其出生后听觉敏感性的发育情况。在自由场刺激条件下,通过测量每个IC神经元对从不同方位角发出的最佳频率声音的脉冲数量变化和最小阈值,来确定其听觉空间敏感性。在7、14和35日龄时对不同的幼年蝙蝠进行单耳堵塞。然后在出生后58 - 69天测定单耳堵塞蝙蝠IC神经元的听觉空间敏感性。单耳堵塞并未改变IC神经元的放电模式、最佳频率分布和潜伏期,但使堵塞幼年蝙蝠IC神经元的最小阈值平均提高了21 - 24 dB。单耳堵塞似乎也改变了听觉空间敏感性的出生后发育。耳塞完整时IC神经元的听觉空间敏感性比移除耳塞时更敏锐。因此,单耳堵塞蝙蝠IC神经元的反应中心分布和空间敏感性在移除耳塞之前与对照蝙蝠的IC神经元更具可比性。这些发现表明,单耳堵塞幼年蝙蝠IC神经元听觉空间敏感性的神经回路在出生后发育过程中发生了改变,以补偿不自然的双耳差异。还测定了两只49日龄和60日龄对照幼年蝙蝠以及一只成年蝙蝠(超过1岁)的听觉空间敏感性。我们的数据表明,IC神经元的听觉空间敏感性随出生后年龄而增强。此外,即使在出生后60天,这种增强过程似乎仍在进行。