Microglial activation increases cocaine self-administration following adolescent nicotine exposure

被引:45
|
作者
Linker, K. E. [1 ]
Elabd, M. G. [1 ]
Tawadrous, P. [1 ]
Cano, M. [1 ]
Green, K. N. [2 ]
Wood, M. A. [2 ]
Leslie, F. M. [1 ,3 ]
机构
[1] Univ Calif Irvine, Dept Anat & Neurobiol, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA USA
[3] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92717 USA
关键词
CIGARETTE-SMOKING; MODULATION; RECEPTORS; MEDIATORS; ABUSE; CELL; RAT;
D O I
10.1038/s41467-019-14173-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
y With the rise of e-cigarette use, teen nicotine exposure is becoming more widespread. Findings from clinical and preclinical studies show that the adolescent brain is particularly sensitive to nicotine. Animal studies have demonstrated that adolescent nicotine exposure increases reinforcement for cocaine and other drugs. However, the mechanisms that underlie these behaviors are poorly understood. Here, we report reactive microglia are critical regulators of nicotine-induced increases in adolescent cocaine self-administration. Nicotine has dichotomous, age-dependent effects on microglial morphology and immune transcript profiles. A multistep signaling mechanism involving D2 receptors and CX3CL1 mediates nicotine-induced increases in cocaine self-administration and microglial activation. Moreover, nicotine depletes presynaptic markers in a manner that is microglia-, D2- and CX3CL1-dependent. Taken together, we demonstrate that adolescent microglia are uniquely susceptible to perturbations by nicotine, necessary for nicotine-induced increases in cocaine-seeking, and that D2 receptors and CX3CL1 play a mechanistic role in these phenomena.
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页数:14
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