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Anatomical pathways for auditory memory II: information from rostral superior temporal gyrus to dorsolateral temporal pole and medial temporal cortex

机译:听觉记忆的解剖途径II:从延髓上颞回到背外侧颞极和颞内侧皮层的信息

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摘要

Auditory recognition memory in non-human primates differs from recognition memory in other sensory systems. Monkeys learn the rule for visual and tactile delayed matching-to-sample within a few sessions, and then show one-trial recognition memory lasting 10–20 min. In contrast, monkeys require hundreds of sessions to master the rule for auditory recognition, and then show retention lasting no longer than 30–40 s. Moreover, unlike the severe effects of rhinal lesions on visual memory, such lesions have no effect on the monkeys' auditory memory performance. The anatomical pathways for auditory memory may differ from those in vision. Long-term visual recognition memory requires anatomical connections from the visual association area TE with areas 35 and 36 of the perirhinal cortex (PRC). We examined whether there is a similar anatomical route for auditory processing, or that poor auditory recognition memory may reflect the lack of such a pathway. Our hypothesis is that an auditory pathway for recognition memory originates in the higher order processing areas of the rostral superior temporal gyrus (rSTG), and then connects via the dorsolateral temporal pole to access the rhinal cortex of the medial temporal lobe. To test this, we placed retrograde (3% FB and 2% DY) and anterograde (10% BDA 10,000 mW) tracer injections in rSTG and the dorsolateral area 38DL of the temporal pole. Results showed that area 38DL receives dense projections from auditory association areas Ts1, TAa, TPO of the rSTG, from the rostral parabelt and, to a lesser extent, from areas Ts2-3 and PGa. In turn, area 38DL projects densely to area 35 of PRC, entorhinal cortex (EC), and to areas TH/TF of the posterior parahippocampal cortex. Significantly, this projection avoids most of area 36r/c of PRC. This anatomical arrangement may contribute to our understanding of the poor auditory memory of rhesus monkeys.
机译:非人类灵长类动物的听觉识别记忆与其他感觉系统的识别记忆不同。猴子会在几个会话中了解视觉和触觉延迟匹配到采样的规则,然后显示持续10至20分钟的一次测试记忆。相比之下,猴子需要数百次训练才能掌握听觉识别的规则,然后保持时间不超过30–40 s。而且,不同于鼻部病变对视觉记忆的严重影响,这种病变对猴子的听觉记忆性能没有影响。听觉记忆的解剖途径可能与视觉不同。长期的视觉识别记忆需要从视觉关联区域TE与周围神经皮层(PRC)的区域35和36的解剖学联系。我们检查了听觉加工是否存在类似的解剖学途径,或者听觉识别记忆差可能反映出缺乏这种途径。我们的假设是,识别记忆的听觉通路起源于前额颞上回(rSTG)的高阶处理区域,然后通过背外侧颞极连接以进入内侧颞叶的鼻皮质。为了对此进行测试,我们在rSTG和颞极背外侧区域38DL中放置了逆行(3%FB和2%DY)和顺行(10%BDA 10,000 mW)示踪剂注入。结果表明,区域38DL从rSTG的听觉关联区域Ts1,TAa,TPO,从延髓旁带,以及在较小程度上从区域Ts2-3和PGa接收到密集的投影。继而,区域38DL密集地突出到PRC的35区域,内嗅皮层(EC)和海马后皮层的TH / TF区域。显着地,该投影避开了中华人民共和国的大部分区域36r / c。这种解剖结构可能有助于我们了解恒河猴的听觉记忆差。

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