Alcohol sensitivity and tolerance encoding in sleep regulatory circadian neurons in Drosophila

被引:2
|
作者
Lange, Anthony P. P. [1 ,3 ]
Wolf, Fred W. W. [1 ,2 ]
机构
[1] Univ Calif Merced, Quantitat & Syst Biol Grad Program, Merced, CA 95343 USA
[2] Univ Calif Merced, Dept Mol & Cell Biol, Merced, CA 95343 USA
[3] Univ Iowa, Dept Neurosci & Pharmacol, Iowa City, IA USA
关键词
alcohol tolerance; circadian rhythms; circuitry; Drosophila; sleep; ETHANOL TOLERANCE; RAPID TOLERANCE; MUSHROOM BODY; CLOCK; GENE; MODULATION; PREFERENCE; PEPTIDE; COMPLEX; SUBSET;
D O I
10.1111/adb.13304
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alcohol tolerance is a simple form of behavioural and neural plasticity that occurs with the first drink. Neural plasticity in tolerance is likely a substrate for longer term adaptations that can lead to alcohol use disorder. Drosophila develop tolerance with characteristics similar to vertebrates, and it is a useful model for determining the molecular and circuit encoding mechanisms in detail. Rapid tolerance, measured after the first alcohol exposure is completely metabolized, is localized to specific brain regions that are not interconnected in an obvious way. We used a forward neuroanatomical screen to identify three new neural sites for rapid tolerance encoding. One of these was composed of two groups of neurons, the DN1a and DN1p glutamatergic neurons, that are part of the Drosophila circadian clock. We localized rapid tolerance to the two DN1a neurons that regulate arousal by light at night, temperature-dependent sleep timing, and night-time sleep. Two clock neurons that regulate evening activity, LNd6 and the 5th LNv, are postsynaptic to the DN1as, and they promote rapid tolerance via the metabotropic glutamate receptor. Thus, rapid tolerance to alcohol overlaps with sleep regulatory neural circuitry, suggesting a mechanistic link.
引用
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页数:12
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