Inhibition of gustatory plasticity due to acute nicotine exposure in the nematode Caenorhabditis elegans

被引:10
作者
Matsuura, Tetsuya [1 ,2 ]
Miura, Hitoshi [1 ]
Nishino, Asuka [1 ,2 ]
机构
[1] Iwate Univ, Fac Engn, Lab Behav Physiol, Morioka, Iwate 0208551, Japan
[2] Iwate Univ, United Grad Sch Agr Sci, Div Thermobiosyst Relat, Morioka, Iwate 0208551, Japan
基金
日本学术振兴会;
关键词
Caenorhabditis elegans; Chemotaxis; Gustatory plasticity; Nicotine; Serotonin; C-ELEGANS; CHEMOTACTIC RESPONSE; SODIUM-ACETATE; SEROTONIN; ATTRACTANTS; ADAPTATION; BEHAVIOR; NEURONS; PATHWAY; FAMILY;
D O I
10.1016/j.neures.2013.09.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study investigated the effect of nicotine exposure on gustatory plasticity in the nematode Caenorhabditis elegans. The chemotactic response of wild-type N2 nematodes pre-exposed to 100 mM NaCl with 3.0 mM nicotine was almost the same as that of mock-conditioned nematodes unexposed to NaCl; however, the response of N2 nematodes pre-exposed to NaCl without nicotine was significantly lower than that of mock-conditioned nematodes. These results indicate that gustatory plasticity is inhibited by acute nicotine exposure. Inhibition of gustatory plasticity was observed when cat-2 mutants with a defect in dopamine biosynthesis were pre-exposed to NaCl with 3.0 mM nicotine. Acute nicotine exposure did not cause inhibition of gustatory plasticity in bas-1 mutants, which had defects in both serotonin and dopamine secretion, and tph-1 mutants, which had a defect in serotonin secretion only. However, inhibition of gustatory plasticity was observed when bas-1 and tph-1 mutants were maintained on a growth plate that included serotonin. These results suggest that serotonin signaling plays an essential role in the modulation of the acute effects of nicotine. (C) 2013 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:155 / 161
页数:7
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