Acute and Chronic Ethanol Effects during Adolescence on Neuroimmune Responses: Consequences and Potential Pharmacologic Interventions

被引:5
|
作者
Nwachukwu, Kala N. [1 ,2 ]
Mohammed, Hassan E. [1 ]
Mebane, DaQuan R. [1 ]
Barber, Andrew W. [1 ]
Swartzwelder, H. Scott [3 ]
Marshall, S. Alex [1 ]
机构
[1] North Carolina Cent Univ, Dept Biol & Biomed Sci, Durham, NC 27707 USA
[2] North Carolina Cent Univ, Integrated Biosci Program, Durham, NC 27707 USA
[3] Duke Univ Med Ctr, Dept Psychiat & Behav Sci, Durham, NC 27708 USA
关键词
adolescent alcohol use; microglia; astrocytes; cytokines; toll-like receptors; neuroimmune system; ALCOHOL-INDUCED NEUROINFLAMMATION; TOLL-LIKE RECEPTORS; RICE BRAN OIL; GENDER-DIFFERENCES; SEX-DIFFERENCES; BINGE; DRINKING; CONSUMPTION; ACTIVATION; EXPRESSION;
D O I
10.3390/cells12101423
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heavy ethanol consumption during adolescence has been linked to neuroimmune response dysregulation and cognitive deficits in the developing adolescent brain. During adolescence, the brain is particularly susceptible to the pharmacological effects of ethanol that are induced by acute and chronic bouts of exposure. Numerous preclinical rodent model studies have used different ethanol administration techniques, such as intragastric gavage, self-administration, vapor, intraperitoneal, and free access, and while most models indicated proinflammatory neuroimmune responses in the adolescent brain, there are various factors that appear to influence this observation. This review synthesizes the most recent findings of the effects of adolescent alcohol use on toll-like receptors, cytokines, and chemokines, as well as the activation of astrocytes and microglia with an emphasis on differences associated with the duration of ethanol exposure (acute vs. chronic), the amount of exposure (e.g., dose or blood ethanol concentrations), sex differences, and the timing of the neuroimmune observation (immediate vs. persistent). Finally, this review discusses new therapeutics and interventions that may ameliorate the dysregulation of neuroimmune maladaptations after ethanol exposure.
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页数:18
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