https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:55018 Wed 03 Apr 2024 13:22:37 AEDT ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:25914 Thu 17 Mar 2022 14:37:50 AEDT ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:27349 Sat 24 Mar 2018 07:39:38 AEDT ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:50760 24 months) mice had impaired performance in a balance beam task compared to young (3-4 months) adult mice. While there was no qualitative loss of cholinergic axon varicosities in the crista ampullaris of old mice, qPCR analysis revealed reduced expression of nicotinic receptor subunit genes Chrna1, Chrna9, and Chrna10 in the cristae of old relative to young mice. Functionally, single-cell patch clamp recordings taken from type II vestibular hair cells exposed to acetylcholine show reduced conductance through alpha9/10 subunit-containing nicotinic receptors in older mice, despite preserved passive membrane properties and voltage-activated conductances. These findings suggest that cholinergic signaling in the peripheral vestibular sensory organs is vulnerable to aging processes, manifesting in dynamic molecular and functional age-related changes. Given the importance of these organs to our everyday activities, and the dramatic increase in fall incidence in the elderly, further investigation into the mechanisms of altered peripheral vestibular function in older humans is warranted.]]> Mon 07 Aug 2023 14:22:26 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:47281 Fri 13 Jan 2023 10:24:38 AEDT ]]>