Introduction
Alcoholism is a major health issue that afflicts people all over the world. In addition, researchers have raised concerns about health and the social consequences of excessive drinking (Das, Balakrishnan, & Vasudevan, 2006). The consumption of alcohol and the subsequent production of its oxidative metabolites have many direct and indirect effects both on the developing and the developed nervous system, and have acute and chronic complications (Alderazi & Brett, 2007). Alcohol impairs cognitive function and is associated with a variety of behavioral changes resulting in deficits in perceptual and emotional function. Alcohol consumption has immediate effects on multiple cognitiveâmotor processing domains and leads to damage of multiple attentional abilities (Mongrain & Standing, 1989). Given the high prevalence of alcohol abuse, and the current limited and inefficient treatment options, the need for a better understanding of the effects of alcohol is clear (Nielsen & Nielsen, 2015).
Alcohol and Neurological Dysfunction
Historically, it is well documented that acute alcohol intoxication could result in changes in regional brain function, as assessed by changes in glucose metabolism or cerebral blood flow (Volkow et al., 1988, 1990), cognitive performance (Lau, Pihl, & Peterson, 1995; Lindman, Sjoholm, & Lang, 2000; Reynolds, Richards, & de Wit, 2006), motor function (Lemon, 1993), and behavior (Kong, Zheng, Lian, & Zhang, 2012; Zheng, Kong, Chen, Zhang, & Zheng, 2015; Mongrain & Standing, 1989).
Laboratory studies, which typically examine blood alcohol concentrations (BACs) in the range of 0.03â0.08%, indicate that, at these doses, the influence of alcohol on memory depends on the cognitive functions required by the particular experimental task (e.g., Bisby, Leitz, Morgan, & Curran, 2010; Söderlund, Parker, Schwartz, & Tulving, 2005).
Acute alcohol intake has pronounced effects on brain function in a general way. Until recently, the effect of alcohol on neural mechanisms had not been fully elucidated. These effects include neurotoxicity of the ethanol molecule itself, and the consequences of nutritional deficiencies or liver dysfunction, each of which can lead to the possibility of alcohol-induced neuro-inflammation. A number of measures have been used to investigate these issues. For example, George used the P300 event-related potentials (ERPs) component to assess the relationship of alcoholism with frontal lobe damage, indicating that the frontal lesion subject group of the study had significant P300 amplitude reduction. There was a similar trend for the alcohol-dependent group, but not for the subcortical group when compared to the control subjects (George, Potts, Kothman, Martin, & Mukundan, 2004).
The misuse of alcohol can affect the adult central and peripheral nervous systems, and direct effects are the result of the toxic and intoxicating effects of alcohol. It is well accepted that alcohol intoxication results in changes in physical and mental impairments including thought, judgment, coordination, concentration, and reasoning. Moreover, alcohol can lead to confusion, ataxia, and loss of social inhibition, and in some circumstances, aggression, putting a person at risk of traumatic injury.
Neuroimaging in Acute Ethanol Consumption
A number of measures have been used to examine the effects of acute ethanol consumption on the brain. Previously, magnetic resonance (MR) imaging has been applied to the study of human chronic alcoholism. Early observations utilizing structural MR imaging studies reported that white matter (WM) subjacent to the cortex and the pons suffers structural volume in those with uncomplicated alcoholism. Specific brain regions affected by chronic alcohol exposure as determined on structural MR imaging include the cortical gray matter (GM) and WM, the thalamus (Bellis et al., 2005), and particularly the prefrontal areas in older alcoholic individuals (Cardenas, Studholme, & Gazdzinski, 2007).
Traditionally, neuroimaging has provided noninvasive anatomic views of the brain, but the applications of neuroimaging have now expanded to include the measurement of neurochemical concentrations and specific proteins, such as subtypes of neurotransmitter receptors or transporters, rates of metabolic pathways and blood flow, and the detection of functional or pharmacological changes in the brain and evaluations of connections among brain regions (Niciu & Mason, 2014). In vivo modern neuroimaging modalities, including diffusion tensor imaging (DTI), magnetic resonance spectroscopy (MRS), and functional magnetic resonance imaging (fMRI), provide important information regarding coexistent structural and functional brain damage, are powerful approaches to the study of brain function, and may provide novel opportunities for investigating the impact of alcohol on the nervous system. The effects of chronic alcohol exposure on the brain and its neurochemistry can be assessed through MRS (Kroenke et al., 2013). In addition, as the microstructural scale can also be assessed through DTI, neuroimaging has dramatically improved researchers' ability to understand the neuropathology of alcoholism (Nagel & Kroen, 2008). Neuroimaging data delineating alcohol effects on brain function are, however, scant. Therefore, the use of these techniques will no doubt provide important information in the near future regarding the mechanisms related to alcohol-induced brain function impairments. This chapter reviews what we have done, to date, regarding the specific imaging features of acute alcohol-induced brain dysfunction, including microstructural changes on the brain and metabolic product concentrations using these noninvasive functional brain imaging techniques.
DTI- and DKI-Detected Acute Ethanol-Induced Changes on Microstructures in the Brain
DTI has identified reduced diffusion anisotropy within the frontal WM of chronic alcoholics (Harris et al., 2008) in the genu of the corpus callosum, the centrum semiovale (Rosenbloom, Sullivan, & Pfefferbaum, 2003), and the frontal and superior sites, such as frontal forceps, internal and external capsules, and the fornix (Pfefferbaum, Rosenbl...