SITE SEARCH

To study alcohol’s effects on the structure and function of the brain in living human beings, researchers can use various imaging techniques. Positron emission tomography (PET) is a functional imaging approach used to study the metabolism and physiology of the brain. PET studies have found that both acute and chronic alcohol ingestion alter blood flow and metabolism in various brain regions, including the frontal lobes and cerebellum. Other analyses focusing on alcohol’s effects on brain chemical (i.e., neurotransmitter) systems have found that both acute and chronic alcohol consumption alter the activities of the inhibitory neurotransmitter gamma–aminobutyric acid (GABA) and the excitatory neurotransmitters glutamate, dopamine, and serotonin. These alterations may contribute to the reinforcing and rewarding effects of alcohol as well as to symptoms of alcohol withdrawal. Imaging studies also have demonstrated that some of alcohol’s adverse effects on brain function can be reversed by abstinence or alcoholism treatment interventions. In addition, imaging studies may help in the development of new medications for alcoholism treatment. Key words: positron emission tomography; chronic AODE (alcohol and other drug effects); neurobiological theory of AODU (alcohol and other drug use); AOD dependence; brain reward pathway; neuroimaging; excitatory neurotransmitters; hyperexcitability; GABA receptors; glutamate; dopamine; mesolimbic system; serotonin; endogenous opioids; glucose metabolism; cerebral blood flow; AODR (alcohol and other drug related) structural brain damage

Alcohol exerts profound and harmful effects on the human nervous system. One way of determining how the brain is affected by alcohol consumption—particularly chronic excessive consumption that has led to alcohol dependence—is to look directly at the brain and its structures. Obviously, these examinations can be performed only during autopsies of deceased alcoholics. Investigations of the progression of alcohol–induced brain damage over time, its reversibility with abstinence, and the effectiveness of pharmacological and other interventions, however, require analyses in living subjects who can be studied repeatedly. Over the past few decades, various imaging techniques have been developed that allow researchers to study the structure and function of the brain both in healthy people and in people with alcoholism or other disorders. By allowing investigators to visualize alcohol’s actions on the brain in living human beings, these techniques are essential tools for documenting alcohol–induced damage as well as the effects of interventions for alcoholism.

This article focuses primarily on the contributions of one imaging technique—positron emission tomography (PET)—to the analysis of alcohol–related brain damage. Following a description of PET technology, the article explores how this approach has helped elucidate alcohol’s effects on the structures and functions of the brain, particularly its effects on various brain chemical (i.e., neurotransmitter) systems. Methodological considerations relevant to applying PET technology to studies of alcohol dependence also are discussed.

PET AND OTHER NEUROIMAGING TECHNIQUES

The various techniques to visually represent the nervous system that have been developed over the past few decades generally fall into two broad categories, structural and functional imaging approaches. Structural neuroimaging techniques, such as computerized tomography¹ (CT), magnetic resonance imaging (MRI), and an MRI subtype known as diffusion tensor imaging (DTI), illustrate the anatomy of the nervous system. (¹ For a definition of this and other technical terms used in this article, see the glossary, below.) In alcohol research, these approaches are ideally suited for demonstrating anatomical changes that alcohol causes in the nervous system. In contrast, functional neuroimaging procedures—such as PET, functional MRI, magnetic resonance spectroscopy (MRS), and single photon emission computerized tomography (SPECT)—show the metabolic and physiologic processes of the nervous system in action. These imaging procedures are preferable for detecting alcohol–induced metabolic and physiologic alterations in the brain. Because each procedure has its strengths and weaknesses in the evaluation of people with alcoholism (Wong and Brašic 2001), clinicians and investigators must carefully consider the questions they want to address before deciding on the most appropriate approach.

Structural and functional neuroimaging techniques may be combined for certain research questions. For example, consecutive structural and functional neuroimaging analyses can be used to determine the exact anatomic location of alcohol’s physiological and metabolic effects on the nervous system, and the results can be superimposed to obtain the most accurate estimates (Wong and Brašic 2001). An example of this procedure is the concomitant acquisition of both MRI (a structural technique) and PET (a functional technique) images on a person with alcoholism. The MRI and PET images then are realigned to obtain a composite image that has the benefits of the detailed structural information of MRI and the functional information from PET (see figure 1) (Wong and Brašic 2001).² (² The MRI–PET procedure described here is time consuming and technically demanding and can therefore be used only in a few specialized research settings, but is not widely available for clinical purposes.)

PET makes it possible to visualize the physiology of living human beings by tracking radioactive compounds (i.e., radiotracers) that are of potential biological importance in the body (Wong and Brašic 2001). A radiotracer is produced in the laboratory by attaching a radioactive atom or molecule to a compound of interest. It then is usually injected into the patient’s bloodstream, from which it can be taken up into the brain. This uptake of the radiotracer and its subsequent distribution within the brain can be measured over time to obtain information about the physiological process being studied. The amount of radiotracer administered is so small that it does not disturb the conditions in the living organism.³ (³ If a large amount of radiotracer was administered, the sudden excess of the compound under investigation could alter the rate or location of the biological processes in which that compound is involved. In general, the dose of a radiotracer for a routine PET scan is roughly 1,000 times [or three orders of magnitude] lower than the dose required to produce a pharmacological effect.) As a result, one can get direct information on the process being studied by tracking the radioactive molecule using a measuring device called a PET scanner (see figure 2). In addition, one can obtain quantitative information about the biological processes as they occur in the living organism by processing the data with sophisticated computer software, which also can generate three–dimensional images of the structures where the radiotracer is found. (For more information on the technical details of PET, see the textbox, below.)

To conduct functional brain imaging using PET, investigators need radiotracers that can cross the blood–brain barrier,⁴ distribute proportionally with the blood flow through the brain (i.e., regional cerebral blood flow [rCBF]), and remain in the brain long enough to permit PET imaging. (⁴ The blood–brain barrier is a physiological property of the blood vessels in the brain that prevents many substances from entering the brain, thereby protecting the brain from potentially harmful molecules.) PET tracers typically are identical or similar in structure (i.e., are analogs) to a naturally occurring molecule that acts specifically in the particular brain area, except that the radiotracers contain a radioactive atom. For example, the commonly used clinical radiotracer [¹⁸F]fluorodeoxyglucose (FDG) is an analog of the ordinary sugar, glucose, which serves as the source of energy in active brain cells. A tracer commonly used for research purposes is a radioactive antagonist of the neurotransmitter dopamine. This tracer can interact with proteins called dopamine receptors that are located on many nerve cells (neurons) and mediate dopamine’s actions on the cells (for more information on neurotransmitters and their actions, see the next section), but the antagonist’s effect is the opposite from that of dopamine. By measuring the levels of the radioactive dopamine antagonist in various brain regions, one can estimate how many dopamine receptors are present in those regions. For example, neurons in certain brain areas (e.g., the basal ganglia) carry particularly high numbers of dopamine receptors and are therefore especially likely to be governed by dopamine’s actions.

The radioactive atoms most commonly used in PET for studying the effect of alcohol on the brain are radioactive fluorine (¹⁸F), carbon (¹¹C), and oxygen (¹⁵O). Of these, ¹¹C, and ¹⁵O have relatively short half–lives of 20 minutes and 2 minutes, respectively. This means that after those times, only half of the original radioactivity remains in the radiotracers. As a result, PET radiotracers that incorporate ¹¹C and ¹⁵O must be produced at the same site where the PET study is conducted to avoid losing most of the radioactivity before the patient is injected with the radiotracer. Radiotracers can be produced only by machines called cyclotrons, which are extremely expensive, bulky, and require radioactive shielding. Therefore, few facilities can afford to conduct PET analyses using ¹¹C and ¹⁵O. In contrast, ¹⁸F has a relatively long half–life of 109 minutes, which together with the possibility of rapid regional transfer of ¹⁸F, permits the performance of FDG PET scans in many facilities without cyclotrons.

USING PET TO DETERMINE ALCOHOL’S EFFECTS ON BRAIN STRUCTURE AND FUNCTION

Alcohol’s Acute Effects on the Brain

Both acute and chronic alcohol consumption can alter brain function—for example, changing blood flow through various brain regions and metabolic activities of those regions. PET and other neuroimaging approaches have detected such alterations, as follows:

• PET analyses following alcohol consumption in social drinkers showed reduced blood flow to the cerebellum, a region at the base of the brain that controls voluntary movements and coordination (Volkow et al. 1988). These findings may explain the muscular incoordination resulting from the consumption of alcohol.

• Acute alcohol ingestion reduces the metabolic activity of the brain. The pattern of this reduced activity suggests that alcohol increases nerve signal transmission through the inhibitory neurotransmitter gamma–aminobutyric acid (GABA) (Wang et al. 2003) (see the table). This effect is more pronounced in men than in women.

* These actions represent the primary effects of the various neurotransmitters; however, depending on the brain region and cell type studied, each transmitter also may have other effects.

Effects of Chronic Alcohol Consumption

Chronic alcohol consumption affects the brain both directly through its effects on brain cells and their functions and indirectly by causing nutritional deficiencies, liver disease, and disturbances of the hormonal and immune systems. Head trauma sustained during inebriation may also damage the brain. One approach commonly used to study the effects of long–term excessive alcohol consumption is to conduct autopsies of deceased alcoholics. Autopsy studies have demonstrated that people with a history of chronic alcohol consumption have smaller brains than age– and gender–matched nonalcoholics. Other autopsy studies have focused on alcoholics with Wernicke’s encephalopathy, a severe brain disease resulting from a deficiency of the vitamin thiamine that often is associated with chronic excessive alcohol consumption. These studies have shown marked reductions in the number of neurons in the outer layer of the upper surface of the front of the brain (i.e., the superior frontal cortex), particularly in patients with liver cirrhosis (Dodd et al. 1996). Additional autopsy studies of alcoholics with Wernicke’s encephalopathy have detected reduced numbers of neurons in the cerebellum (Baker et al. 1999).

Although autopsy studies can provide valuable information, imaging studies in living humans beings often are preferable, particularly when investigating the progression of alcohol–related brain damage or when determining alcohol’s effects on brain function. Structural imaging techniques such as CT and MRI (Wong and Brašic 2001) have confirmed the findings of brain shrinkage and reduced the number of brain cells in living subjects with Wernicke’s encephalopathy and other disorders associated with alcoholism (Viola et al. 2001). Additionally, DTI studies of alcoholics suggest the presence of abnormalities in the white matter of the brain, which consists of the extensions (i.e., axons) of neurons (Pfefferbaum and Sullivan 2002; Sullivan and Pfefferbaum 2003). Brain shrinkage and other abnormalities primarily affect the frontal lobes (Moselhy et al. 2001), although shrinkage also occurs in other brain regions in people with chronic excessive alcohol consumption.

Imaging analyses that have identified structural brain changes are complemented by functional imaging methods such as PET, which reveal changes in blood flow and other metabolic activities associated with specific sensory, motor, or cognitive functions and are impaired in people with alcohol dependence. (It is important to note, however, that neuropsychological changes may not necessarily correlate with the metabolic changes seen on PET scans of alcoholics.)

When conducting PET analyses, researchers often perform two scans on each participant to study metabolic changes throughout the brain that may be associated with particular activities. The first scan typically is performed when the patient is in a resting state to determine the basal metabolism of the stable brain. The second scan is performed during the activated condition—that is, after exposure to a psychological or pharmacological stimulus. For example, psychological activation can be accomplished by engaging the person in an activity such as viewing a videotape or performing a mental task. Alternatively, pharmacological activation may consist of administering a pharmacological agent such as an amphetamine to simulate the maximal release of dopamine in physiological excitation or stress (Wong and Brašic 2001). The findings of such analyses are summarized in the following sections.

EFFECTS OF CHRONIC ALCOHOL CONSUMPTION ON NEUROTRANSMITTERS

Overview of Neuronal Communication

To understand how chronic excessive alcohol use associated with alcohol dependence affects brain function, it is important to understand how neurons communicate with each other through electrical and chemical signals. Nerve signals are transmitted from one region of the brain to another region of the brain or to the rest of the body through serial communication between two or more neurons located next to each other. When a neuron is activated, an electrical signal is generated (usually near the neuron’s body), which travels along the membrane surrounding the cell body and the long extension protruding from it (i.e., the axon). When the signal reaches the end of the axon, it triggers the release of neurotransmitters from the cell. These neurotransmitters travel across the narrow space separating one neuron from another (i.e., the synaptic cleft). On the signal–receiving neuron, the neurotransmitter molecules then interact with receptors, and this interaction either promotes or prevents the generation of new electrical signals in that neuron, depending on the neurotransmitter. Neurotransmitters that promote the generation of a new nerve signal are called excitatory neurotransmitters; those that prevent the generation of a new nerve signal are called inhibitory neurotransmitters. Many neurotransmitters can have both excitatory and inhibitory effects, depending on which brain region is studied and which receptors are present on the signal–receiving neurons. Neurotransmitters that often have excitatory effects include dopamine, glutamate, and serotonin; neurotransmitters that primarily have inhibitory effects are GABA and glycine. (For a list of excitatory and inhibitory neurotransmitters that may play a role in alcohol’s actions, see the table, above).

Alcohol’s effects on the brain are mediated by numerous neurotransmitters and their highly complex interactions. In general, the pleasurable psychological experiences associated with alcohol consumption appear to be mediated by dopamine, noradrenaline, and the endogenous opioids and their receptors (Basavarajappa and Hungund 2002). Other neurotransmitters commonly affected by alcohol are glutamate and GABA.

Alcohol’s Effects on Inhibitory Neurotransmitters

Alcohol is thought to influence two inhibitory neurotransmitters—GABA (Korpi et al. 2002; Nevo and Hamon 1995) and glycine. Alcohol appears to enhance the inhibitory actions of GABA (Nevo and Hamon 1995), which may contribute to both the acute and the chronic effects of alcohol and to the phenomena of alcohol dependence, tolerance, and withdrawal (Nevo and Hamon 1995). Chronic alcohol consumption leads to a decline in the number of GABA receptors in the brain and reduces GABA’s ability to bind to its receptors, thereby allowing the body to compensate for the alcohol–induced enhancement of GABA’s actions. These effects are a part of the changes in brain function that lead to tolerance and dependence on alcohol (Nevo and Hamon 1995). When alcohol is withheld, however, and its stimulating effect on GABA is eliminated, the body suddenly has too few GABA receptors to balance the actions of the excitatory neurotransmitters. As a result, the brain experiences an excess of excitatory nerve signals, a phenomenon known as rebound hyperexcitability. This hyperexcitability may contribute to the physical and psychological manifestations of alcohol withdrawal (Nevo and Hamon 1995).

Alcohol’s effects on the inhibitory neurotransmitter glycine are controversial, however. Studies have found that both acute and chronic alcohol consumption exerted only minimal effects on the role of glycine in the nervous system (Nevo and Hamon 1995).

Alcohol’s Effects on Excitatory Neurotransmitters

Alcohol consumption appears to influence the transmission of signals mediated by many excitatory neurotransmitters, most prominently glutamate, dopamine, and serotonin (Nevo and Hamon 1995).

Glutamate. Glutamate exerts its effects by interacting with several types of receptors, including one called the N–methyl–D–aspartate (NMDA) receptor. Alcohol acts on these NMDA receptors, inhibiting their functions and thereby diminishing glutamate–mediated neurotransmission. NMDA receptors may play a role in memory formation; prenatal, acute, or chronic alcohol exposure may hinder the person’s ability to learn and to retain new information (Nevo and Hamon 1995).

Dopamine. In contrast to its dampening effects on the activity of the glutamate system, acute alcohol ingestion enhances the excitatory effect of dopamine (Nevo and Hamon 1995). Correspondingly, acute withdrawal from alcohol reduces dopamine’s excitatory effect. PET studies have confirmed that dopamine and its actions in the brain are involved in the subjective experience of reward (Koob and Weiss 1992; Oswald et al. 2003). Anatomically, the reward system is located deep in the brain in a region called the ventral striatal area, with nerve fibers projecting to an area known as the nucleus accumbens and subsequently to higher regions of the brain (see figure 3). This also is called the mesolimbic dopamine system. Alcohol and other drugs (AODs), as well as food or sex, can trigger the release of dopamine in this reward system and reinforce the subjective pleasurable experiences therefore associated with alcohol or the other stimuli and are a component of the reward process. PET studies have allowed researchers to directly investigate the role of dopamine and the reward system in alcohol consumption in humans (Oswald et al. 2003).

When alcohol induces the release of dopamine in the nucleus accumbens, nerve signals are sent to the cortex, where they are registered as “experience” and memories of the rewarding effects of alcohol, such as its taste or the feelings of relaxation after drinking. Once registered, these memories can stimulate further alcohol intake, completing the reward system. Because memories of the rewarding effects of alcohol also include the environment in which drinking occurred, even sights or smells related to that environment can subsequently trigger the reward system. Indeed, several studies have suggested that alcoholics are predisposed to relapse and that environmental stimuli related to alcohol can trigger the impulse to drink (Flannery et al. 2001). Animal studies have confirmed that the nucleus accumbens is probably involved in the rewarding aspects of alcohol consumption and also may mediate the stimulatory effects of environmental cues associated with past drinking (Katner and Weiss 1999). Another study using single photon emission computed tomography (SPECT) found that alcoholics ingesting a sip of alcohol during brain imaging showed enhanced neuronal activity in a certain region of the ventral striatal area (i.e., a part of the basal ganglia) that correlated highly with their increase in craving (Modell et al. 1990). Because alcohol consumption increases dopamine release preferentially in the ventral striatal area, these findings support the view that dopamine activation is a common property of AODs and contributes to their reinforcing effects.

Recent studies have suggested a link between stress and altered activity of the mesolimbic dopamine system. Stressful situations result in the increased release of hormones called glucocorticoids, most prominently cortisol. Studies have found that glucocorticoids can increase mesolimbic dopamine release (Piazza and Le Moal 1996; Biron et al. 1992; Fahlke et al. 1994; Piazza et al. 1994). It has been suggested that the stress–induced increase in dopamine release may make the person more sensitive to the rewarding effects of AODs, which may represent one of the pathways leading to abuse of those drugs (Deroche et al. 1995; Piazza et al. 1990; Kalivas and Stewart 1991). Recently, researchers have utilized PET to study the relationship between cortisol release and amphetamine–induced dopamine release (Maini et al. 2003). These preliminary studies, which suggest a high correlation between cortisol release and dopamine release, may open the way for future studies of these relationships in alcoholics and their relatives. Other studies have found that actively drinking alcoholics appear to have an abnormal hormonal response to stress, which also may be present in the offspring of alcoholics who are not yet heavy drinkers (Wand et al. 1998, McCaul et al. 2000).

Serotonin. Serotonin, another excitatory neurotransmitter involved in the brain’s reward system, appears to play an important role in alcohol abuse. As with dopamine, animal studies have demonstrated that acute alcohol administration resulted in enhanced serotonin release (Yoshimoto et al. 2000), and withdrawal from alcohol was associated with reduced serotonin release (De Witte et al. 2003). Moreover, studies have found that alcoholics with years of excessive alcohol consumption appeared to exhibit impaired serotonin and dopamine activity (Berggren et al. 2002).⁵ (⁵ The reduction in serotonin in the brain is hypothesized to lead to the reduction in dopamine [Berggren et al. 2002].) Finally, studies using SPECT found a genetic defect in the gene encoding a serotonin transporter in some people who were particularly sensitive to the toxic effects of chronic excessive alcohol consumption on the brain (Heinz et al. 2000). The serotonin transporter is a protein located in serotonin–producing neurons that removes serotonin from the space between neurons to stop serotonin’s effect on the signal–receiving neuron. Thus, people with abnormal serotonin transporter function may be particularly susceptible to the reduced excitatory effect of serotonin caused by heavy alcohol consumption. The reduced effect of serotonin, in turn, probably leads to reduced effects of dopamine. Thus, alcoholics with abnormal serotonin transporter function are likely to need greater amounts of alcohol to attain the pleasurable feelings associated with alcohol consumption (Heinz et al. 2000).

One goal of research on serotonin and other neurotransmitters in alcoholism is to identify distinct biological subtypes of alcoholism and biological markers for them, which may then help to develop more targeted treatment approaches. For example, if one biological subtype of alcoholism was characterized by defective serotonin transporter function, brain scans for the presence of the serotonin transporter could serve as a tool to obtain a biological marker for this alcoholism subtype. Similarly, repeated scans after the administration of a potential treatment for the serotonin transporter deficiency could help identify the effect of that treatment. Future studies of the effects of chronic alcohol consumption on the serotonin system may clarify the role of serotonin and dopamine in alcoholism subtypes. Neuroimaging techniques may help to identify the specific chemicals, such as dopamine and serotonin, that are deficient in particular biological subtypes of alcoholism, and to monitor the effects of potential therapies targeted for the specific deficiency of the biological subtype (Wong et al. 2002).

Other Neurotransmitters. In addition to glutamate, dopamine, and serotonin, alcohol also acts on various other excitatory neurotransmitters conveying signals within the brain as well as to other organs, as follows (also see the table, above):

• Acute administration of alcohol increases the excitatory effects of the neurotransmitter norepinephrine (Nevo and Hamon 1995).

• Acetylcholine is an excitatory neurotransmitter that among other functions plays a role in memory. Chronic consumption of alcohol reduces the number of neurons containing acetylcholine (Nevo and Hamon 1995). This reduction may be associated with the memory deficits commonly associated with heavy chronic alcohol consumption.

• Bombesin and cholecystokinin are compounds produced in the brain that stimulate the functioning of the intestines. Alcohol does not appear to influence the actions of these compounds, but both bombesin and cholecystokinin reduce the intake of alcohol (Nevo and Hamon 1995).

Alcohol’s Effects on Endogenous Opioids

Endogenous opioids are molecules produced in the body that resemble opium; they apparently act like excitatory neurotransmitters to stimulate neurons. It is hypothesized that endogenous opioids reinforce the effects of alcohol and play a role in the pleasurable effects of both acute and chronic alcohol consumption, but their specific part in alcohol abuse and dependence remains to be clarified (Nevo and Hamon 1995). What is known is that alcohol influences one of the opioid receptors—the mu receptor—in the brain. For example, chronic heavy drinkers have alterations of mu receptors in neurons both in the outer layer of the brain and in structures deep in the center of the brain (Bencherif et al. 2004). In addition, studies have found that a medication called naltrexone that inhibits opiate receptors in the brain is an effective treatment for alcoholism (Romach et al. 2002; Terenius 1996), particularly for people with a family history of alcoholism or with a strong craving for alcohol (Monterosso et al. 2001). Other studies have found that alcoholics carrying a specific variant of the mu receptor have a lower relapse rate after treatment with naltrexone than do those carrying other receptor variants (Oslin et al. 2003). These findings suggest that alcoholics with a particular genetic makeup are particularly likely to benefit from treatment with naltrexone. Because PET technology offers promise as a tool for determining the density and the distribution of mu opiate receptors in the brain, this technique may help identify alcoholics who could benefit from interventions such as naltrexone, which affect these receptors. Thus, PET studies to identify mu opiate receptors in the brain may be a tool for identifying a distinct biological subtype of alcoholism; and PET findings could serve as a biological marker of mu opiate receptor dysfunction in the brain (Wong et al. 2002).

PET STUDIES OF BRAIN GLUCOSE METABOLISM AND BLOOD FLOW

Glucose Metabolism

To function properly, the brain needs a continuous supply of the sugar glucose, whose breakdown provides most of the energy the cells need for their diverse functions. Brain regions that are more active, including the cells of rapidly growing tumors, require more glucose. Similarly, lower–than–normal glucose metabolism suggests reduced brain activity indicative of neurological or cognitive problems. PET studies can help researchers identify brain regions that are active at any given time by administering radioactively labeled glucose (i.e., [¹⁸F]fluorodeoxyglucose [FDG]) and measuring its distribution in the brain. Brain glucose metabolism detectable with PET occurs mainly in the gray matter—the brain regions where the bodies of neurons are located. The amount (or volume) of gray matter in the brain, however, can vary substantially among subjects. For example, chronic alcoholics frequently have smaller gray–matter volumes than nonalcoholics (Sullivan 2000). Therefore, data regarding glucose metabolism must be expressed in terms of the gray–matter volume of a specific region, which can be determined by structural imaging techniques such as MRI.

PET studies have shown that glucose metabolism in alcoholics is decreased in the entire brain (Volkow et al. 1992), with the most marked reductions in the frontal lobes and cerebellum. However, an assessment of the effects that reduced glucose metabolism may have on brain functioning in people with alcohol dependence is complicated by the alcohol–induced damage to other organs (e.g., the liver, stomach, or other vital organs) often found in those people. For example, people with liver cirrhosis resulting from chronic alcohol consumption exhibit decreased glucose utilization by gray matter in the frontal and temporal lobes as well as the basal ganglia (Kato et al. 2000). Thus, neurological and cognitive problems of alcoholics may not only be a consequence of reduced glucose metabolism but may reflect the effects of alcohol–induced liver, kidney, and heart dysfunction on the brain. Furthermore, glucose may play a different role in brain metabolism in alcoholics with clear neurological or cognitive problems than in healthy people. Further research is needed to clarify glucose metabolism in alcoholics with neurological and cognitive problems.

Regional Blood Flow

Glucose is brought to the brain via the bloodstream; accordingly, the rates of regional cerebral blood flow (rCBF) within various areas of the brain are regulated depending on the changing demands of these areas. This variability in blood flow depending on regional brain activity is the basis for using PET to measure rCBF. To detect changes in rCBF, investigators inject a radiotracer (typically radioactively labeled water, [¹⁵O]H₂O) into the bloodstream and measure its deposition in the brain tissue, which is determined by the regional distribution of blood flow. ¹⁵O has a short half–life of 2 minutes and therefore can be injected repeatedly while the subjects perform various motor, sensory, or cognitive tasks under different conditions. Assessing the differences in blood flow between tasks enables investigators to identify the brain regions involved in each specific task. This approach can also be used to track the effects of acute alcohol ingestion on regional blood flow over a period of time (Sullivan 2000).

CORRELATING STRUCTURAL AND PHYSIOLOGICAL CHANGES WITH ALCOHOL–RELATED BEHAVIORS

Once PET and other studies have identified changes in brain structure and functioning of alcoholics, investigators must correlate these changes to alcohol–related behaviors in those patients. For example, studies have linked both shrinkage of the cerebellum and decreased blood flow in this region, as determined by imaging studies, to impaired balance and gait, which may cause falls, particularly in older alcoholics (Volkow et al. 1988). Falls can result in head injuries and further deterioration in brain function. Other functional imaging studies have shown that decreases in blood flow and metabolism in the frontal lobes precede shrinkage of that brain region and major cognitive abnormalities (Johnson–Greene et al. 1997).

Imaging studies also have demonstrated that cognitive functions and motor coordination may improve partially within 3 to 4 weeks of abstinence and that these improvements are accompanied by a partial reversal of brain shrinkage (Johnson–Greene et al. 1997). Frontal lobe blood flow also increases with abstinence, returning to normal levels within 4 years, whereas a relapse to drinking leads to renewed brain shrinkage and blood flow reductions (Johnson–Greene et al. 1997).

Finally, PET studies have helped researchers assess risk factors for alcoholism. In nonalcoholics, certain sedatives (i.e., benzodiazepines) produce a temporary impairment in coordination and cognition and a decrease in brain glucose metabolism similar to the effects of alcohol consumption. In alcoholics, however, some regions in the frontal lobe respond to benzodiazepines less strongly than they do in nonalcoholics (Gilman et al. 1996). These results suggest that alcoholics may have a diminished capacity to dampen excessive neuronal activity and therefore may be less able to inhibit behavior.

METHODOLOGICAL CONSIDERATIONS FOR PET STUDIES IN ALCOHOLICS

Developing Models for Interpreting Findings of PET Analyses

The data obtained in alcoholics with functional imaging techniques such as PET typically must undergo a set of processing steps to yield information that is useful to researchers. For example, researchers must develop mathematical representations (i.e., kinetic models) of physiological processes such as the metabolism of neurotransmitters or their receptors. With these models, investigators can develop a mathematical equation describing the tissue response curve expected in the measurements. The tissue–response curve plots the radioactivity of specific parts of the brain before, during, and after the injection of the radiotracer. Thus, the tissue–response curve correlates with the amount of the chemical identified by the radiotracer in the regions of interest. By performing the scans on groups of people with and without alcoholism, the increases and decreases of chemicals in the brains of alcoholics can be identified. By identifying those variables in the model that give the best agreement between the expected and measured values, one can quantify the physiological process.

To develop appropriate models and provide a basis for interpreting the measured behavior of the tracer, all available qualitative information about the physiology and biochemistry of the tracer is collected. For example, it is important to know how fast and to what extent the tracer is transported from the site of the injection in the bloodstream to the tissue being analyzed (e.g., a specific brain region). The basic steps of this transport are as follows:

• The tracer is transported by the blood to the small blood vessels (i.e., capillaries) in the brain.

• The tracer moves across the capillary wall into the fluid–filled spaces between the brain cells.

• The tracer crosses the membrane surrounding the cells or binds to neurotransmitter receptors in the synaptic clefts between neurons.

• If it enters the cells, the tracer participates in various biochemical reactions.

PET can follow the progress of the tracer by measuring the amounts of radioactivity in different areas of the brain as well as the tracer concentrations in the blood. To interpret the data obtained in this way, investigators can use a variety of mathematical or statistical modeling methods (e.g., the compartment model, graphical model, and tissue input graphical model approaches). In many cases, researchers attempt to simplify their models by making assumptions about the processes involved in the model (e.g., about how easily the tracer can cross the capillary walls). To make sure these assumptions are reasonable or correct, however, the simplified model must first be validated. To this end, the investigators must make sure that the model yields reasonable values for the variables tested and that it can distinguish the disease state (e.g., conditions in an alcoholic) from the healthy state (e.g., conditions in a nonalcoholic).

Correcting for Partial Volume Errors

Compared with structural imaging techniques (e.g., MRI), PET images are blurred because of the limited resolution of the PET scanners (i.e., their limited ability to distinguish closely spaced regions of small dimensions). This limited resolution has two potential consequences:

• An apparent loss (or “spill–out”) of radioactivity signals from a small region of interest into the adjacent tissues owing to the size of the small brain region compared with the spatial resolution of the scanner

• A “spill–in” of radioactive signals into the region of interest from adjacent brain areas with different radioactive tracer concentrations.

These effects, which are known as “partial volume errors,” are more pronounced in alcoholics with alcohol–related brain shrinkage, where loss of signal because of partial volume errors could be confounded with an actual loss of tissue function (Rousset et al. 1998).

Several methods are available to correct for this problem. The most common approach is to perform both an MRI scan and a PET scan of a patient’s brain and then to combine the images using several available methods (see figure 1). Computer simulations then are used to mimic the effect of limited spatial resolution to characterize the partial volume effects for each brain region (Rousset et al. 1998). With this information, investigators then can apply correction factors to obtain more accurate estimates of the actual regional activity (e.g., regional blood flow or glucose metabolism).

THE FUTURE OF PET STUDIES IN ALCOHOLISM

Although researchers have been employing PET and other functional imaging techniques in the analysis of alcohol–induced changes in brain functioning, the full potential of these approaches has not yet been realized. For example, it might be useful to correlate functional imaging data with information on demographic traits of the subjects (Brašic 2003) as well as with behavioral measures, including questionnaires addressing psychological traits and the desire for alcohol. Demographic and psychological traits may identify biological subtypes of alcoholism detected by PET. Questionnaires to identify behavioral data could function as biological markers for the presence of distinct biological variants of alcoholism and could help identify the effects of potential therapeutic interventions targeted to the distinct variant (Wong et al. 2002). Other possible applications of PET include the following:

• Studies in humans and animals to characterize neurochemical processes associated with alcohol reinforcement and/or craving, such as the production, release, and transport of neurotransmitters or changes in receptor concentrations

• Identification of neural circuits that play a role in the cognitive deficits associated with acute alcohol intake as well as elucidation of the pathways through which functional deficits in specific neural circuits and the resulting cognitive deficits may contribute to excessive alcohol intake

• Analyses of neurobiological markers of vulnerability to alcohol abuse

• Combination with structural imaging techniques (e.g., MRI or CT) to obtain a fused image automatically (see figure 1)

• Development of new pharmaceutical agents to prevent and treat alcoholism (Wong et al. 2002).

SUMMARY

PET allows researchers to visualize in living human beings the damage to the brain that results from chronic excessive alcohol consumption. This technology has been used to analyze alcohol’s effects on various neurotransmitter systems as well as on glucose metabolism and regional blood flow in the brain. Such analyses have detected deficits in alcoholics, particularly in the frontal lobes, which control numerous cognitive functions, and in the cerebellum, which controls voluntary movements. In addition, PET is a promising tool for monitoring the effects of alcoholism treatment and abstinence on damaged portions of the brain. Finally, PET may be able to help researchers develop new medications targeted at correcting the chemical deficits found in the brains of people with alcohol dependence and alcohol abuse.

REFERENCES

BAKER, K.G.; HARDING, A.J.; HALLIDAY, G.M.; et al. Neuronal loss in functional zones of the cerebellum of chronic alcoholics with and without Wernicke’s encephalopathy. Neuroscience 91:429–438, 1999.

BASAVARAJAPPA, B.S., and HUNGUND, B.L. Neuromodulatory role of the endocannabinoid signaling system in alcoholism: An overview. Prostaglandins, Leukotrienes and Essential Fatty Acids 66:287–299, 2002.

BENCHERIF, B.; WAND, G.S.; MCCAUL, M.E.; et al. Mu–opioid receptor binding measured by [¹¹C]carfentanil positron emission tomography is related to craving and mood in alcohol dependence. Biological Psychiatry 55:255–262, 2004.

BERGGREN, U.; ERIKSSON, M.; FAHLKE, C.; and BALLDIN, J. Is long–term heavy alcohol consumption toxic for brain serotonergic neurons? Relationship between years of excessive alcohol consumption and serotonergic neurotransmission. Drug and Alcohol Dependence 65:159–165, 2002.

BIRON, D.; DAUPHIN, C.; and DI PAOLO, T. Effects of adrenalectomy and glucocorticoids on rat brain dopamine receptors. Neuroendocrinology 55(4):468–476, 1992.

BRAŠIC , J.R. Documentation of demographic data. Psychological Reports 93:151–152, 2003.

DEROCHE, V.; MARINELLI, M.; MACCARI, S.; et al. Stress–induced sensitization and glucocorticoids. I. Sensitization of dopamine–dependent locomotor effects of amphetamine and morphine depends on stress–induced corticosterone secretion. Journal of Neuroscience 15:7181–7188, 1995.

DE WITTE, P.; PINTO, E.; ANSSEAU, M.; and VERBANCK, P. Alcohol and withdrawal: From animal research to clinical issues. Neuroscience and Biobehavioral Reviews 27:189–197, 2003.

DODD, P.R.; KRIL, J.J.; THOMAS, G.J.; et al. Receptor binding sites and uptake activities mediating GABA neurotransmission in chronic alcoholics with Wernicke encephalopathy. Brain Research 710:215–228, 1996.

FAHLKE, C.; ENGEL, J.A.; ERIKSSON, C.J.; et al. Involvement of corticosterone in the modulation of ethanol consumption in the rat. Alcohol 11:195– 202, 1994.

FLANNERY, B.A.; ROBERTS, A.J.; COONEY, N.; et al. The role of craving in alcohol use, dependence, and treatment. Alcoholism: Clinical and Experimental Research 25(2):299–308, 2001.

GILMAN, S.; KOEPPE, R.A.; ADAMS, K.; et al. Positron emission tomographic studies of cerebral benzodiazepine receptor binding in chronic alcoholics. Annals of Neurology 40:163–171, 1996.

HEINZ, A.; JONES, D.W.; MAZZANTI, C.; et al. A relationship between serotonin transporter genotype and in vivo protein expression and alcohol neurotoxicity. Biological Psychiatry 47:643–649, 2000.

JOHNSON–GREENE, D.; ADAMS, K.M.; GILMAN, S.; et al. Effects of abstinence and relapse upon neuropsychological function and cerebral glucose metabolism in severe chronic alcoholism. Journal of Clinical and Experimental Neuropsychology 19(3): 378–385, 1997.

KALIVAS, P.W., and STEWART, J. Dopamine transmission in the initiation and expression of drug– and stress–induced sensitization of motor activity. Brain Research Reviews 16:223–244, 1991.

KATNER, S.N., and WEISS, F. Ethanol–associated olfactory stimuli reinstate ethanol–seeking behavior after extinction and modify extracellular dopamine levels in the nucleus accumbens. Alcoholism: Clinical and Experimental Research 23(11):1751–1760, 1999.

KATO, A.; SUZUKI, K.; KANETA, H.; et al. Regional differences in cerebral glucose metabolism in cirrhotic patients with subclinical hepatic encephalopathy using positron emission tomography. Hepatology Research 17(3): 237–245, 2000.

KOOB, G.F., and WEISS, F. Neuropharmacology of cocaine and ethanol dependence. Recent Developments in Alcohol 10:201–233, 1992.

KORPI, E.R.; GRÜNDER, G.; and LÜDDENS, H. Drug interactions at GABA_A receptors. Progress in Neurobiology 67:113–159, 2002.

MADEIRA, M.D., and PAULA–BARBOSA, M.M. Effects of alcohol on the synthesis and expression of hypothalamic peptides. Brain Research Bulletin 48(1):3–22, 1999.

MAINI, A.; WONG, D.F.; OSWALD, L.M.; et al. “Brain Dopamine Release Correlates With Neuroendocrine Stress Measures and Subjective Response: Implication for Alcoholism.” Abstracts, College on Problems of Drug Dependence, Sixty–Fifth Annual Scientific Meeting, June 14–19, 2003. Bal Harbour, FL, Abstract 413, p. 104. Available online at: http://www.cpdd.vcu.edu/images/2003abstracts.pdf.

MCCAUL, M.E.; WAND, G.S.; ROHDE, C.; and LEE, S.M. Serum 6–beta–naltrexol levels are related to alcohol responses in heavy drinkers. Alcoholism: Clinical and Experimental Research 24:1385–1391, 2000.

MODELL, J.G.; MOUNTZ, J.M.; and BERESFORD, T.P. Basal ganglia/limbic striatal and thalamocortical involvement in craving and loss of control in alcoholism. Journal of Neuropsychiatry and Clinical Neuroscience 2(2):123–144, 1990.

MONTEROSSO, J.R.; FLANNERY, B.A.; PETTINATI, H.M.; et al. Predicting treatment response to naltrexone: The influence of craving and family history. American Journal on Addictions 10:258–268, 2001.

MOSELHY, H.F.; GEORGIOU, G.; and KAHN, A. Frontal lobe changes in alcoholism: A review of the literature. Alcohol & Alcoholism 36:357–368, 2001.

NEVO, I., and HAMON, M. Neurotransmitter and neuromodulatory mechanisms involved in alcohol abuse and alcoholism. Neurochemistry International 26(4):305–336, 1995.

OSLIN, D.W.; BERRETTINI, W.; KRANZLER, H.R.; et al. A functional polymorphism of the μ–opioid receptor gene is associated with naltrexone response in alcohol–dependent patients. Neuropsychopharmacology 28(8):1546–1552, 2003.

OSWALD, L.M.; WONG, D.F.; MCCAUL, M.E.; et al. Subjective and cortisol responses to IV amphetamine correlate with ventral striatal dopamine release. Alcoholism: Clinical and Experimental Research 27 (Suppl. 5):21A, 2003.

PFEFFERBAUM, A., and SULLIVAN, E.V. Microstructural but not macrostructural disruption of white matter in women with chronic alcoholism. NeuroImage 15:708–718, 2002.

PIAZZA, P.V., and LE MOAL, M. Pathophysiological basis of vulnerability to drug abuse: Role of an interaction between stress, glucocorticoids, and dopaminergic neurons. Annual Review in Pharmacology and Toxicology 36:359–378, 1996.

PIAZZA, P.V.; DEMINIERE, J.–M.; LE MOAL, M.; and SIMON, H. Stress– and pharmacologically–induced behavioral sensitization increases vulnerability to acquisition of amphetamine self–administration. Brain Research 514:22–26, 1990.

PIAZZA, P.V.; MARINELLI, M.; JODOGNE, C.; et al. Inhibition of corticosterone synthesis by Metyrapone decreases cocaine–induced locomotion and relapse of cocaine self–administration. Brain Research 658:259–264, 1994.

ROMACH, M.K.; SELLERS, E.M.; SOMER, G.R.; et al. Naltrexone in the treatment of alcohol dependence: A Canadian trial. Canadian Journal of Clinical Pharmacology 9(3):130–136, 2002.

ROUSSET, O.G.; MA, Y.; and EVANS, A.C. Correction for partial volume effects in PET: Principle and validation. Journal of Nuclear Medicine 39(5):904–911, 1998.

SULLIVAN, E.V. Human brain vulnerability to alcoholism: Evidence from neuroimaging studies. In: Noronha, A.; Eckardt, M.; and Warren, K., eds. Review of NIAAA’s Neuroscience and Behavioral Research Portfolio. National Institute on Alcohol Abuse and Alcoholism Research Monograph No. 34. Bethesda, MD: National Institute on Alcohol Abuse and Alcoholism, 2000. pp. 473–508.

SULLIVAN, E.V., and PFEFFERBAUM, A. Diffusion tensor imaging in normal aging and neuropsychiatric disorders. European Journal of Radiology 45: 244–255, 2003.

TERENIUS, L. Alcohol addiction (alcoholism) and the opioid system. Alcohol 13(1):31–34, 1996.

VIOLA, A.; NICOLI, F.; CONFORT–GOUNY, S.; et al. Applications de la spectrométrie de résonance magnétique (SRM) à l’étude des perturbations métaboliques affectant le cerveau au cours de l’alcoolisme [Applications of magnetic resonance spectroscopy (MRS) to the investigation of the alterations in cerebral metabolism affecting the brain in the course of alcoholism]. Pathologie Biologie 49:718–725, 2001.

VOLKOW, N.D.; MULLANI, N.; GOULD, L.; et al. Effects of acute alcohol intoxication on cerebral blood flow measured with PET. Psychiatry Research 24:201–209, 1988.

VOLKOW, N.D.; HITZEMANN, R.; WANG, G.–J.; et al. Decreased brain metabolism in neurologically intact healthy alcoholics. American Journal of Psychiatry 149(8):1016–1022, 1992.

WAND, G.S.; MANGOLD, D.; EL DEIRY, S.; et al. Family history of alcoholism and hypothalamic opioidergic activity. Archives of General Psychiatry 55:1114–1119, 1998.

WANG, G.–J.; VOLKOW, N.D.; FOWLER, J.S.; et al. Alcohol intoxication induces greater reductions in brain metabolism in male than in female subjects. Alcoholism: Clinical and Experimental Research 27:909–917, 2003.

WONG, D.F., and BRAŠIC, J.R. In vivo imaging of neurotransmitter systems in neuropsychiatry. Clinical Neuroscience Research 1:35–45, 2001.

WONG, D.F.; POTTER, W.Z.; AND BRAŠIC, J.R. Proof of concept: Functional models for drug development in humans. In: Davis, K.L.; Charney, D.; Coyle, J.T.; and Nemeroff, C., eds. Neuropsychopharmacology: The Fifth Generation of Progress. Baltimore, MD: The American College of Neuropsychopharmacology and Lippincott Williams & Wilkins, 2002. pp. 457–473.

YOSHIMOTO, K.; UEDA, S.; KATO, B.; et al. Alcohol enhances characteristic release of dopamine and serotonin in the central nucleus of the amygdala. Neurochemistry International 37:369–376. 2000.

[ NIAAA Home Page | Site Map | Accessibility | Privacy statement | Disclaimer | Contact Us ] National Institute on Alcohol Abuse and Alcoholism (NIAAA) 5635 Fishers Lane, MSC 9304 Bethesda, MD 20892-9304 email: Web Sponsor (niaaaweb-r@exchange.nih.gov) National Institutes of Health Department of Health and Human Services