کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4337584 | 1614806 | 2014 | 16 صفحه PDF | دانلود رایگان |
• Head direction cells in the limbic system encode the animal’s perceived directional heading.
• Lesions of the vestibular system abolish the head direction signal.
• Responses of vestibular neurons are markedly attenuated during volitional head turns.
• A conundrum arises as to how a vestibular signal is fed forward to update the HD signal.
• This review discusses four possible mechanisms that could resolve this problem.
Head direction (HD) cells have been identified in a number of limbic system structures. These cells encode the animal’s perceived directional heading in the horizontal plane and are dependent on an intact vestibular system. Previous studies have reported that the responses of vestibular neurons within the vestibular nuclei are markedly attenuated when an animal makes a volitional head turn compared to passive rotation. This finding presents a conundrum in that if vestibular responses are suppressed during an active head turn how is a vestibular signal propagated forward to drive and update the HD signal? This review identifies and discusses four possible mechanisms that could resolve this problem. These mechanisms are: (1) the ascending vestibular signal is generated by more than just vestibular-only neurons, (2) not all vestibular-only neurons contributing to the HD pathway have firing rates that are attenuated by active head turns, (3) the ascending pathway may be spared from the affects of the attenuation in that the HD system receives information from other vestibular brainstem sites that do not include vestibular-only cells, and (4) the ascending signal is affected by the inhibited vestibular signal during an active head turn, but the HD circuit compensates and uses the altered signal to accurately update the current HD. Future studies will be needed to decipher which of these possibilities is correct.
Journal: Neuroscience - Volume 270, 13 June 2014, Pages 123–138