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Selective lesions of the cholinergic neurons within the posterior pedunculopontine do not alter operant learning or nicotine sensitization

机译:后足小脑桥骨桥胆碱能神经元的选择性病变不会改变操作学习或尼古丁敏化

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摘要

Cholinergic neurons within the pedunculopontine tegmental nucleus have been implicated in a range of functions, including behavioral state control, attention, and modulation of midbrain and basal ganglia systems. Previous experiments with excitotoxic lesions have found persistent learning impairment and altered response to nicotine following lesion of the posterior component of the PPTg (pPPTg). These effects have been attributed to disrupted input to midbrain dopamine systems, particularly the ventral tegmental area. The pPPTg contains a dense collection of cholinergic neurons and also large numbers of glutamatergic and GABAergic neurons. Because these interdigitated populations of neurons are all susceptible to excitotoxins, the effects of such lesions cannot be attributed to one neuronal population. We wished to assess whether the learning impairments and altered responses to nicotine in excitotoxic PPTg-lesioned rats were due to loss of cholinergic neurons within the pPPTg. Selective depletion of cholinergic pPPTg neurons is achievable with the fusion toxin Dtx-UII, which targets UII receptors expressed only by cholinergic neurons in this region. Rats bearing bilateral lesions of cholinergic pPPTg neurons (>90 % ChAT+ neuronal loss) displayed no deficits in the learning or performance of fixed and variable ratio schedules of reinforcement for pellet reward. Separate rats with the same lesions had a normal locomotor response to nicotine and furthermore sensitized to repeated administration of nicotine at the same rate as sham controls. Previously seen changes in these behaviors following excitotoxic pPPTg lesions cannot be attributed solely to loss of cholinergic neurons. These findings indicate that non-cholinergic neurons within the pPPTg are responsible for the learning deficits and altered responses to nicotine seen after excitotoxic lesions. The functions of cholinergic neurons may be related to behavioral state control and attention rather than learning.
机译:足小脑桥骨被盖核内的胆碱能神经元与一系列功能有关,包括行为状态控制,注意力以及中脑和基底神经节系统的调节。先前对兴奋性毒性病变的实验发现,在PPTg(pPPTg)的后部成分受损后,持续的学习障碍和对尼古丁的反应改变。这些影响归因于中脑多巴胺系统输入的中断,尤其是腹侧被盖区。 pPPTg包含密集的胆碱能神经元集合以及大量的谷氨酸能和GABA能神经元。因为这些相互交叉的神经元群体都容易受到兴奋毒素的影响,所以这种损害的影响不能归因于一个神经元群体。我们希望评估兴奋性PPTg损伤大鼠的学习障碍和对尼古丁的反应是否改变是由于pPPTg内胆碱能神经元的丧失引起的。胆碱能pPPTg神经元的选择性消耗可以通过融合毒素Dtx-UII实现,该毒素靶向仅由胆碱能神经元在该区域表达的UII受体。携带胆碱能pPPTg神经元双侧病变(> 90%ChAT +神经元丢失)的大鼠在学习或固定或可变比例的颗粒强化计划表学习或表现方面均无缺陷。具有相同病变的独立大鼠对尼古丁具有正常的运动反应,而且对以与假对照相同的速率重复施用尼古丁敏感。兴奋毒性pPPTg损伤后这些行为的先前变化不能仅归因于胆碱能神经元的丧失。这些发现表明,pPPTg内的非胆碱能神经元是造成兴奋性损害后出现的学习缺陷和对尼古丁反应改变的原因。胆碱能神经元的功能可能与行为状态控制和注意力有关,而不是学习。

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