Bulbar acetylcholine enhances neural and perceptual odor discrimination.
Bulbar acetylcholine enhances neural and perceptual odor discrimination.
复制标题
延髓乙酰胆碱增强神经和感知气味辨别能力。
DOI:
10.1523/jneurosci.4036-08.2009
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发表时间:
2009-01-07
期刊:
影响因子:
--
通讯作者:
Linster C
中科院分区:
文献类型:
--
作者:
Chaudhury D;Escanilla O;Linster C
Experimental and modeling data suggest that the circuitry of the main olfactory bulb (OB) plays a critical role in olfactory discrimination. Processing of such information arises from the interaction between OB output neurons local interneurons, as well as interactions between the OB network and centrifugal inputs. Cholinergic input to the OB in particular has been hypothesized to regulate mitral cell odorants receptive fields (ORFs) and behavioral discrimination of similar odorants. We recorded from individual mitral cells in the OB in anesthetized rats in order to determine the degree of overlap in ORFs of individual mitral cells following exposure to odorant stimuli. Increasing the efficacy of the cholinergic neurotransmission in the OB by addition of the anticholinesterase drug neostigmine (20mM) sharpened the olfactory receptive field (ORF) responses of mitral cells. Furthermore, co-addition of either the nicotinic antagonist MLA (20mM) or muscarinic antagonist scopolamine (40mM) together with neostigmine (20mM) attenuated the neostigmine-dependent sharpening of ORF. These electrophysiological findings are predictive of accompanying behavioral experiments in which cholinergic modulation was manipulated by direct infusion of neostigmine, MLA and scopolamine into the OB during olfactory behavioral tasks. Increasing the efficacy of cholinergic action in the OB increased perceptual discrimination of odorants in these experiments, whereas blockade of nicotinic or muscarinic receptors decreased perceptual discrimination. These experiments show that behavioral discrimination is modulated in a manner predicted by the changes in mitral cell ORFs by cholinergic drugs. These results together present a first direct comparison between neural and perceptual effects of a bulbar neuromodulator.