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首页> 外文期刊>Journal of Neurophysiology >Differential neural representation of oral ethanol by central taste-sensitive neurons in ethanol-preferring and genetically heterogeneous rats.
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Differential neural representation of oral ethanol by central taste-sensitive neurons in ethanol-preferring and genetically heterogeneous rats.

机译:偏爱乙醇和遗传异质大鼠的中枢味觉敏感神经元对口服乙醇的差异神经表示。

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In randomly bred rats, orally applied ethanol stimulates neural substrates for appetitive sweet taste. To study associations between ethanol's oral sensory characteristics and genetically mediated ethanol preference, we made electrophysiological recordings of oral responses (spike density) by taste-sensitive nucleus tractus solitarii neurons in anesthetized selectively bred ethanol-preferring (P) rats and their genetically heterogeneous Wistar (W) control strain. Stimuli (25 total) included ethanol [3%, 5%, 10%, 15%, 25%, and 40% (vol/vol)], a sucrose series (0.01, 0.03, 0.1, 0.3, 0.5, and 1 M), and other sweet, salt, acidic, and bitter stimuli; 50 P and 39 W neurons were sampled. k-means clustering applied to the sucrose response series identified cells showing high (S(1)) or relatively low (S(0)) sensitivity to sucrose. A three-way factorial analysis revealed that activity to ethanol was influenced by a neuron's sensitivity to sucrose, ethanol concentration, and rat line (P = 0.01). Ethanol produced concentration-dependent responses in S(1) neurons that were larger than those in S(0) cells. Although responses to ethanol by S(1) cells did not differ between lines, neuronal firing rates to ethanol in S(0) cells increased across concentration only in P rats. Correlation and multivariate analyses revealed that ethanol evoked responses in W neurons that were strongly and selectively associated with activity to sweet stimuli, whereas responses to ethanol by P neurons were not easily associated with activity to representative sweet, sodium salt, acidic, or bitter stimuli. These findings show differential central neural representation of oral ethanol between genetically heterogeneous rats and P rats genetically selected to prefer alcohol.
机译:在随机饲养的大鼠中,口服乙醇刺激神经底物具有令人愉悦的甜味。为了研究乙醇的口感特性与遗传介导的乙醇偏爱之间的关联,我们通过麻醉敏感的选择性乙醇偏爱(P)大鼠和其遗传异质Wistar(P)大鼠中的味觉敏感核孤索神经元对口服反应(穗密度)进行电生理记录。 W)控制应变。刺激物(总共25个)包括乙醇[3%,5%,10%,15%,25%和40%(体积/体积)],蔗糖系列(0.01、0.03、0.1、0.3、0.5和1 M ),以及其他甜,盐,酸性和苦味刺激;采样了50 P和39 W神经元。应用于蔗糖反应系列的k均值聚类确定了对蔗糖表现出高(S(1))或相对低(S(0))敏感性的细胞。三因素分析显示,对乙醇的活性受神经元对蔗糖的敏感性,乙醇浓度和大​​鼠品系的影响(P = 0.01)。乙醇在S(1)神经元中产生的浓度依赖性响应大于在S(0)细胞中的响应。尽管品系之间对S(1)细胞对乙醇的反应没有差异,但仅在P大鼠中,S(0)细胞对乙醇的神经元激发速率会增加。相关性和多变量分析表明,乙醇诱发了W神经元中与甜味刺激活性强烈且选择性相关的反应,而P神经元对乙醇的反应并不容易与代表性甜味,钠盐,酸性或苦味刺激活性相关。这些发现表明,在遗传异质大鼠和经遗传选择偏爱酒精的P大鼠之间,口服乙醇的中枢神经表征存在差异。

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