Drosophila melanogaster as a model to study drug addiction

Animal studies have been instrumental in providing knowledge about the molecular and neural mechanisms underlying drug addiction. Recently, the fruit fly Drosophila melanogaster has become a valuable system to model not only the acute stimulating and sedating effects of drugs but also their more complex rewarding properties. In this review, we describe the advantages of using the fly to study drug-related behavior, provide a brief overview of the behavioral assays used, and review the molecular mechanisms and neural circuits underlying drug-induced behavior in flies. Many of these mechanisms have been validated in mammals, suggesting that the fly is a useful model to understand the mechanisms underlying addiction.


Introduction
Drug addiction is a disorder characterized by excessive use of a drug to the point of compulsive drug seeking and consumption. The American Psychiatric Association (DMS-IV) diVerentiates between substance abuse, considered an earlier stage of addiction, and substance dependence. Substance abuse is deWned as continued drug use despite interpersonal problems, legal problems, failure to fulWll obligations, or physically hazardous situations. The criteria for substance dependence include physical symptoms, such as tolerance and withdrawal, as well as signs of uncontrolled use, which include giving up normal activities and continued use despite knowledge of self-harm and the desire to stop. These deWnitions highlight the fact that addiction is an exclusively human phenomenon. However, animal models have been used to study speciWc aspects of addiction, and have proved invaluable in understanding the underlying neural and molecular mechanisms.
Animal models allow the experimenter to focus on distinct components of the addiction process, ranging from simple, acute drug responses to more complex behaviors such as drug seeking, self-administration, and relapse. Each behavioral model has advantages and disadvantages. Whereas the more complex models likely have greater relevance to the human condition, assays for acute drug responses are simpler to perform and thus provide the potential for high-throughput analysis, facilitating the iden-tiWcation of the underlying mechanisms.
Although rodent models have provided crucial insights into the mechanisms underlying drug-related behaviors, they are not ideal for unbiased, forward genetic approaches aimed at identifying novel and unsuspected mechanisms. This is due primarily to the expense and time required for animal maintenance, breeding, and behavioral analyses. In contrast, the fruit Xy Drosophila melanogaster is one of the most genetically and experimentally accessible model organisms in biology. In this review the terms Drosophila and Xies will refer exclusively to this species. While for many years Xies were used primarily to identify the molecular and neural mechanisms regulating acute drug responses, the recent development of assays that measure drug self-administration and reward has allowed the analysis of these more complex behaviors.

Drosophila as a model system to study behavior
Drosophila has been used to gain insight into molecular, cellular, developmental, and disease processes that are conserved in mammals, including humans, as most of these fundamental biological mechanisms are shared throughout the animal kingdom. Although mammals have two to three times as many genes as Xies, they have approximately the same number of gene families (Holland 2003). About 75% of human disease genes have related sequences in Drosophila, suggesting that Xies can serve as an eVective model to study the function of a wide array of genes involved in human disease (Adams et al. 2000;Reiter et al. 2001). The nervous system of the Xy comprises approximately 300,000 neurons including a brain, ventral nerve cord (the equivalent of the spinal cord), and peripheral nervous system. Despite their relatively small number of neurons in comparison with mammals, Xies exhibit many complex behaviors such as associative learning, sensorimotor integration, and social behaviors (Quinn et al. 1974;Pick and Strauss 2005;Greenspan and Ferveur 2000;Chen et al. 2002).
The classical advantages of using Drosophila include factors such as cost, size, fecundity, and timescale. First, Xies are easy and inexpensive to rear in the laboratory using small vials or bottles and a yeast-based food medium. Due to their small size, thousands of genotypes of Xies can be maintained in a typical laboratory. Second, due to their high fecundity, hundreds of Xies can be obtained from a single female. Third, Xies have a rapid life cycle, requiring only 10 days at 25°C to develop from egg to mature adult.
For these reasons, Xies have long represented an ideal organism to conduct mutagenesis screens to isolate genes regulating a particular biological process of interest ("forward genetics", i.e. going from phenotype to gene). The advent of genetic transformation in the 1980s also allowed for "reverse genetics" (i.e. going from gene to phenotype) by allowing researchers to introduce speciWc genes of interest into a Xy (Rubin and Spradling 1982). The subsequent sequencing and annotation of the Drosophila genome have greatly facilitated both of these approaches (Adams et al. 2000).
In recent years, the generation of large collections of publicly available mutants and other transgenic tools has allowed for the functional study of nearly any Xy gene of interest. The traditional use of X-ray or chemical mutagenesis is becoming gradually supplanted by insertional mutagenesis, in which a transposable genetic element creates a mutation by inserting into a random genomic site, and the gene aVected can be easily identiWed by sequencing the Xanking DNA (Bingham et al. 1981). Several groups have now generated large mutant collections for which the insertion site in each mutant has been sequenced (Bellen et al. 2004;Thibault et al. 2004;Schuldiner et al. 2008). In addition, an RNA interference (RNAi) library has been generated in which each Xy line contains an inducible RNAi construct for silencing a single Xy gene, with nearly 90% of the Xy genome represented (Dietzl et al. 2007).
Some of the genetic tools developed in Drosophila have particular relevance to studying the relationship between genes, the brain, and behavior. For example, genetic tools in Xies allow one to manipulate the nervous system independently of other tissues in the body. Furthermore, because diVerent neural circuits may have distinct and perhaps opposing roles in behavior, one would ideally like to target speciWc sets of neurons within the brain. This cellular speciWcity can be accomplished by the bipartite Gal4/UAS system, in which the transcriptional activator Gal4 is expressed in a spatially restricted pattern and activates any gene placed downstream of the upstream activating sequence (UAS) (Brand and Perrimon 1993;Fig. 1a). The generation and characterization of thousands of Gal4 lines expressed in various patterns allow for manipulation of spe-ciWc brain regions or neuronal types (PfeiVer et al. 2008). This technique allows one to ask in which neurons a particular gene functions to regulate a behavioral response. These patterns can be further spatially reWned to very small subsets of neurons using the "split Gal4 system" in which the DNA-binding and transcriptional-activation domains of Gal4 are targeted to diVerent neuronal subsets using diVerent promoters; transcriptional activation of target genes occurs only in neurons expressing both domains (Luan et al. 2006). Temporal speciWcity can be achieved by using a temperature-sensitive Gal4 repressor called Gal80 ts and shifting the Xies from the permissive to the restrictive temperature during a particular time period (McGuire et al. 2003;Fig. 1b).
In addition to studying the function of genes within the nervous system, the Gal4/UAS system is well suited to studying neural circuit function. UAS lines are available in which proteins that inducibly control neuronal activity can be expressed, allowing one to activate or silence a particular set of neurons during a speciWc behavioral task. For example, neurons can be silenced using Shibire ts , a temperature-sensitive dynamin allele that blocks synaptic vesicle recycling (Fig. 1c), and neurons can be activated using TrpA1, a temperature-sensitive cation channel that causes neuronal depolarization (Fig. 1d) (Kitamoto 2001;Hamada et al. 2008). Furthermore, the development of a second binary system in addition to the Gal4/UAS system, the LexA/LexAop system (Lai and Lee 2006), allows for the independent manipulation of multiple neural circuits, such as activating some neurons while inhibiting others. Thus, Xies have now become a leading model organism for studying not only the molecular mechanisms but also the neural circuits that underlie behavior.

Models to study ethanol-related behaviors in Xies
Ethanol is the drug that has been by far the most intensively studied in Drosophila, and will therefore be the main focus of this review. Ethanol is a commonly abused psychoactive drug that can produce both short-term behavioral impairment as well as long-term addiction. Unlike other drugs such as cocaine and nicotine, ethanol does not act on a single molecular target but instead is thought to aVect a variety of molecules, including multiple ion channels (Koob 2004). Fruit Xies encounter ethanol in their natural environment since one of the main metabolites in fermenting fruit is ethanol. Ethanol can act as a long-distance signal to draw Xies to rotting fruit, as Xies are attracted to low concentrations of ethanol vapor (Dudley 2002;HoVmann and Parsons 1984). Female Xies prefer to lay their eggs in media containing up to 5% ethanol (McKenzie and Parsons 1972), and larvae eYciently metabolize ethanol and use it as a food source (Geer et al. 1993).
Despite this long-standing relationship between Drosophila and ethanol, the molecular underpinnings of the eVects of ethanol on Xy behavior were not investigated until relatively recently. Several types of ethanol-related behaviors have now been characterized in Xies, with the goal of using the abundant genetic tools in Drosophila to understand the underlying mechanisms. These behaviors range  (Brand and Perrimon 1993). The transcriptional activator Gal4 is expressed in a spatially restricted pattern and activates any gene placed downstream of the upstream activating sequence (UAS). b The TARGET system (McGuire et al. 2003). At the restrictive temperature (30°C), Gal80 ts is inactive, Gal4 is active and UAS-driven genes are expressed. At the permissive temperature (19°C), Gal80 ts is active, Gal4 is inhibited, and UAS-driven genes are not expressed.
c The Shibire ts system (Kitamoto 2001). At the restrictive temperature (30°C), but not the permissive temperature (19°C), Shi ts blocks neurotransmission by disrupting endocytosis and thereby depleting synaptic vesicles. d The TrpA1 system (Hamada et al. 2008;Pulver et al. 2009). At the restrictive temperature (27°C), but not the permissive temperature (19°C), cation Xow through the temperature-gated cation channel dTRPA1 causes neuronal depolarization from simple to complex: (1) acute locomotor responses to ethanol, (2) ethanol tolerance following an initial exposure, and (3) ethanol preference and conditioned preference behaviors that model speciWc facets of addiction.

Acute ethanol sensitivity
Flies exhibit acute responses to ethanol exposure that are quite similar to those of mammals, including humans (Morean and Corbin 2010). There is evidence in humans as well as mammalian models that sensitivity to acute ethanolinduced motor impairment correlates inversely with ethanol consumption and risk of abuse, and that the same genes can inXuence both types of behavior (Schuckit 1994;Morean and Corbin 2010;Kurtz et al. 1996;Thiele et al. 1998;Hodge et al. 1999). Studying these simpler ethanol responses, which are often easier to test in the laboratory, is therefore likely to provide insight into the mechanisms regulating more complex addiction-related behaviors as well.
To measure acute ethanol responses in Xies, ethanol is typically administered in the form of pure ethanol vapor mixed with air at a speciWed ratio, allowing one to control the ethanol concentration that the Xies receive (Wolf et al. 2002). Ethanol can also be administered to Xies by injection, though few studies have employed this technique (Dzitoyeva et al. 2003). Low to moderate concentrations of ethanol induce locomotor hyperactivity, which can be measured by Wlming the Xies and using tracking software to identify the Xies and calculate their locomotor speed (Wolf et al. 2002).
In contrast, high concentrations of ethanol elicit loss of postural control and eventually sedation (Moore et al. 1998;RothenXuh et al. 2006;Corl et al. 2009). Loss of postural control was initially assayed in the inebriometer, a vertical column containing mesh baZes (Weber 1988;Cohan and Graf 1985;Moore et al. 1998;Fig. 2a). Flies naturally exhibit negative geotaxis and therefore tend to remain at the top of the column, but as they lose postural control they gradually fall from one baZe to the next. Ethanol sensitivity can therefore be measured as the time required for the Xies to reach the bottom of the column. Negative geotaxis has also been directly assayed as a measure of ethanol sensitivity by quantifying the vertical distance that Xies climb after being knocked to the bottom of a vial (Bhandari et al. 2009). More recently, ethanol-induced loss of postural control (referred to more simply as "sedation") has been assayed manually using a loss-ofrighting reXex assay, in which one counts the number of Xies that fail to regain upright posture after being knocked over ( Fig. 2b) (RothenXuh et al. 2006;Corl et al. 2009).

Ethanol tolerance
In Xies, as in mammals, repeated exposure to ethanol induces tolerance, which is deWned as an acquired resis-tance to the eVects of the drug. Tolerance is one of the DSM-IV criteria for alcohol dependence (American Psychiatric Association 1994) and has been correlated with heavy drinking and alcohol abuse (Schuckit et al. 2008). In Xies, ethanol tolerance is assayed by measuring the decrease in sensitivity to ethanol-induced motor impairment after ethanol pre-exposure. This change in sensitivity can be assayed using the inebriometer (Scholz et al. 2000), the sedation assay (Berger et al. 2004), or negative geotaxis (Bhandari et al. 2009), and can be measured as a change in either the proportion of impaired Xies (Urizar et al. 2007), latency or duration of impairment (Dzitoyeva et al. 2003;Devineni et al. 2011), or the recovery time after sedation (Berger et al. 2004;Cowmeadow et al. 2005). Ethanol tolerance appears to be robust to variations in the tolerance protocol, as the studies cited above vary signiWcantly in the timing and concentration of ethanol exposure.
Two types of ethanol tolerance have been characterized in Xies, termed rapid and chronic. Rapid tolerance is induced by relatively brief exposure to a sedating concentration of ethanol, while chronic tolerance is induced by prolonged (»24 h) exposure to a low ethanol concentration that does not produce overt intoxication (Berger et al. 2004). Rapid and chronic tolerance are mediated by distinct mechanisms; for example, only chronic tolerance is dependent on protein synthesis (Berger et al. 2004).

Voluntary ethanol consumption
The behavioral assays described above were designed to study relatively simple behaviors associated with ethanol exposure, and much has been learned from these assays regarding the molecular mechanisms underlying the eVects of ethanol. However, in order to relate these discoveries to addiction-related processes, more complex assays that more closely mimic mammalian behavior are needed. A recently developed ethanol self-administration assay demonstrates that Xies prefer to consume ethanol-containing food over regular food and that this preference exhibits several features reminiscent of compulsive alcohol consumption (Ja et al. 2007;Devineni and Heberlein 2009).
Ethanol consumption can be measured in Xies using a two-choice assay similar to the two bottle choice assay used in rodent studies ( Fig. 2c) (Devineni and Heberlein 2009). Flies exhibit a robust, dose-dependent preference for food containing 5-25% ethanol. This ethanol preference cannot be entirely explained by either chemosensory or caloric attraction to ethanol; ethanol preference persists in the absence of olfactory or gustatory input, and preference is not altered by varying the relative caloric content of the solutions (Devineni and Heberlein 2009). Flies also show increased ethanol consumption over time, and, when food deprived, voluntarily consume ethanol to pharmacologically relevant concentrations. Importantly, Xies demonstrate two additional criteria of addiction-like behavior; they will overcome an aversive stimulus, the bitter-tasting compound quinine, in order to consume ethanol, and they rapidly return to high levels of ethanol consumption after ethanol deprivation, modeling a relapse-like eVect (Devineni and Heberlein 2009).

Conditioned preference for ethanol reward
To test directly whether intoxicating doses of ethanol are rewarding to Xies, a conditioned ethanol preference assay was recently developed (Kaun et al. 2011;Fig. 2d). In this assay, Xies are initially exposed to two neutral odor cues, one of which is paired with a moderately intoxicating exposure to ethanol vapor. Flies are later oVered a choice between the two odors, and preference for the ethanol-associated odor is measured. Similar to mammalian conditioned place preference (CPP) models, this assay uses conditioned preference to assess the rewarding properties of ethanol intoxication. This assay has some advantages over the ethanol self-administration assay: (1) the ethanol concentration that the Xies experience can be controlled by the experimenter and (2) the ethanol stimulus is removed during the test, allowing measurement of the rewarding value of the drug rather than immediate preference for the drug.  (Weber 1988;Moore et al. 1998). b The booz-o-mat allows for the measurement of ethanol-induced hyperactivity and sedation while streaming vaporized ethanol into horizontal tubes containing groups of Xies. Hyperactivity is measured by Wlming the Xies and using tracking software to calculate their locomotor speed. Sedation is measured by recording the time required for Xies to exhibit the loss-of-righting reXex (Wolf et al. 2002). c The two-choice CAFE assay measures consumption preference for food containing ethanol compared to normal food (Ja et al. 2007;Devineni and Heberlein 2009). d Conditioned ethanol preference is measured by training the Xies in a sealed container to associate a neutral odor with the presence of an intoxicating dose of ethanol, and later testing preference for that odor in the absence of ethanol using a Y-maze (Kaun et al. 2011)

Consumption
When Xies have been trained to associate an odor cue with ethanol intoxication, they show initial aversion to the cue, which, within 12-15 h, transforms into a long-lasting preference (Kaun et al. 2011). The development of conditioned preference is dependent on the ethanol concentration; preference is induced only by exposure to moderate ethanol doses that induce locomotor hyperactivity. Conditioned preference is not induced by lower ethanol concentrations that fail to elicit behavioral changes or higher concentrations that cause sedation. Thus, Xies seem to require an intoxicating, but not sedating, dose of ethanol for it to be remembered as rewarding. Remarkably, Xies will endure electric shock in order to attain the cue associated with ethanol, indicating that they are willing to tolerate punishment to seek the drug (or, in this case, a cue that predicts the presence of the drug) (Kaun et al. 2011). This response is reminiscent of compulsive behavior such as impaired response inhibition observed in mammalian studies of drug reward. Furthermore, Xies will endure a stronger shock intensity to attain a cue associated with ethanol than a cue associated with sugar, suggesting that the preference for ethanol is distinct from a preference for food reward (Kaun et al. 2011).

Molecular mechanisms underlying ethanol-induced behavior in Drosophila
As described above, an array of assays has been established to study various aspects of ethanol-induced behavior in Drosophila. All of these assays are relatively simple, robust, and high-throughput, allowing researchers to conduct forward genetic screens to identify the underlying mechanisms. The genes identiWed in these screens have led to the characterization of diverse molecular and cellular processes that mediate ethanol-induced behavior in Xies.

Molecular pathways
Several classical molecular signaling pathways have been implicated in regulating sensitivity to ethanol-induced motor impairment in Xies, including the epidermal growth factor receptor (EGFR), phosphoinositide 3-kinase (PI3K)/ Akt, and cyclic adenosine monophosphate (cAMP) pathways. Genetic and pharmacological evidence indicates that the EGFR and cAMP pathways promote resistance to ethanol sedation (Corl et al. 2009;Moore et al. 1998), while the PI3K/Akt pathway enhances ethanol sedation ). However, these pathways are likely to regulate ethanol sensitivity in more complex ways depending on factors such as the cell types in which they are expressed and the presence of multiple protein isoforms. For example, a mutation disrupting the function of the type II regulatory subunit of protein kinase A (PKA), a key eVector of cAMP signaling, causes the opposite eVect on ethanol sedation as expected from previous manipulations that disrupt overall PKA signaling (Park et al. 2000;Moore et al. 1998).
A genetic screen revealed that scabrous (sca), encoding a secreted protein that negatively regulates the Notch signaling pathway (Baker et al. 1990;Powell et al. 2001), is required for ethanol reward memory. Notch signaling is required for long-term memory formation in Xies, suggesting that sca may contribute generally to long-term memory processes (Presente et al. 2004;Ge et al. 2004). However, a mutation of sca that aVects ethanol reward memory does not aVect short-term memory (LaFerriere et al. 2008). Notch signaling has been shown to regulate migration, morphology, synaptic plasticity and survival of immature and mature neurons (Ables et al. 2011). It will be interesting to examine how sca and the Notch pathway aVect the neural plasticity underlying memory for ethanol reward.
Transcription and translation have been implicated in ethanol-induced behaviors. Two genes encoding putative transcriptional regulators, Drosophila LIM-domain only (dLmo) and hangover (hang), were identiWed as regulators of ethanol sedation and ethanol tolerance, respectively (Lasek et al. 2011a;Scholz et al. 2005). One likely target gene whose expression is regulated by dLmo, the Drosophila homolog of anaplastic lymphoma kinase (dAlk), has been identiWed and shown to regulate ethanol sedation (Lasek et al. 2011b).
A mutation in krasavietz (kra), which encodes a predicted translation initiation factor that inhibits protein translation in vitro (Lee et al. 2007), causes decreased sensitivity to ethanol-induced sedation, decreased rapid and chronic ethanol tolerance, and decreased ethanol consumption (Berger et al. 2008;Devineni and Heberlein 2009). Although protein synthesis is required for chronic tolerance, it is not required for the development of rapid tolerance and is unlikely to occur during the brief timescale of acute ethanol intoxication (»30 min; Berger et al. 2004). However, treating Xies with a protein synthesis inhibitor prior to ethanol exposure caused pronounced resistance to ethanol impairment (Berger et al. 2004), suggesting that some proteins that are constitutively synthesized in the absence of ethanol mediate naive ethanol sensitivity. The role of protein synthesis in ethanol consumption has not been directly tested.
Finally, molecular pathways involved in cellular stress responses have been implicated in ethanol tolerance. hang mutants, which show decreased ethanol tolerance, also show sensitivity to oxidative stress and decreased heat-ethanol cross-tolerance (i.e. tolerance to ethanol stimulated by heat shock stress instead of ethanol exposure; Scholz et al. 2005). The gene jwa, a retinoic acid-responsive gene whose product associates with the cytoskeleton, mediates oxidative and heat stress responses and also promotes ethanol tolerance (Li et al. 2008). Since high doses of ethanol induce cellular stress, which in some ways mimics oxidative and heat stress, it may not be surprising that common molecular pathways respond to ethanol as well as other stressors (e.g. Wu and Cederbaum 2009;Wilke et al. 1994;Piper 1995).

Cellular mechanisms
One of the key cellular processes that has been implicated in ethanol-induced behaviors in Xies is cytoskeletal dynamics. thousand and one (tao), which was identiWed as a critical regulator of ethanol-induced hyperactivity, implicated microtubule dynamics in the hyperactivity response (King et al. 2011). tao was shown to function through the conserved kinase PAR-1 (also called MARK in mammals) to regulate the microtubule-binding protein Tau during Xy brain development (Matenia and Mandelkow 2009;King et al. 2011). The mouse homolog of jwa, which promotes ethanol tolerance in Xies (see above), is also a microtubuleassociated protein (Li et al. 2008;Chen et al. 2007).
In addition to microtubule organization, the regulation of actin has been implicated in ethanol responses. Rho GTPase activator protein 18B (RhoGAP18B) regulates sensitivity to both ethanol-induced sedation and hyperactivity through diVerent protein isoforms (RothenXuh et al. 2006). RhoGAP18B is a GTPase activating protein that regulates ethanol sensitivity by functioning through Rho family GTPases, which are key regulators of actin dynamics (RothenXuh et al. 2006). Additionally, Kra (described above) interacts with the crosslinking protein Short stop to regulate actin organization, suggesting that that actin regulation may underlie some of its diverse eVects on ethanolinduced behavior (Lee et al. 2007;Sanchez-Soriano et al. 2009). However, it is important to note that changes in neither microtubule nor actin organization have been directly linked to altered ethanol responses in these mutants.
Finally, the integrin class of cell adhesion molecules has been implicated in ethanol-induced behaviors. Mutations in the alpha-integrin gene scab (scb) or the -integrin gene myospheroid (mys) cause increased ethanol sensitivity as well as increased tolerance (Bhandari et al. 2009). It will be interesting to determine the mechanisms by which disruptions in cytoskeletal organization or cell adhesion lead to altered ethanol responses.

Synaptic function and neuronal excitability
Synapse number has recently been implicated in ethanol sensitivity in Xies. Several genetic manipulations that lead to increased ethanol sedation sensitivity, such as mutations in arouser (aru) or amnesiac (amn) and overexpression of PI3K or Ras homolog enriched in brain (Rheb), also increase synapse number at the larval neuromuscular junction (NMJ) and/or the adult central brain ). An environmental manipulation, adult social isolation, which is known to reduce the number of synapses of a speciWc set of Xy brain neurons (Donlea et al. 2009), also reduces ethanol sensitivity ). Furthermore, social isolation concurrently restores normal synapse number and ethanol sensitivity to the ethanol-sensitive mutant aru . This correlation between synapse number and ethanol sedation sensitivity using multiple independent genetic and environmental manipulations suggests that increased synapse number may directly promote increased sensitivity to ethanol sedation.
In addition to providing a novel cellular mechanism by which ethanol behaviors can be regulated, these Wndings suggest the hypothesis that ethanol tolerance may result from a compensatory decrease in synapse number induced by the initial ethanol exposure. While this hypothesis has not been directly tested, hang, which promotes ethanol tolerance (see above), negatively regulates synapse number at the larval NMJ (Schwenkert et al. 2008). For both ethanol sensitivity and tolerance, it remains to be investigated whether increased synapse number translates into increased postsynaptic excitation (or inhibition), and whether ethanol sensitivity depends on increased synapse number generally throughout the nervous system or in speciWc neurons.
There is abundant evidence that synaptic transmission regulates ethanol-induced behaviors in Xies. Flies carrying a mutation in Syntaxin 1A (Syx1A) or shibire (shi, encoding Drosophila dynamin), which are, respectively, required for synaptic vesicle docking and recycling, show defects in ethanol sedation tolerance (Krishnan et al. 2011). Use of conditional mutations revealed that normal synaptic vesicle release is required immediately after initial ethanol exposure rather than after recovery from intoxication to promote tolerance (Krishnan et al. 2011). A diVerent study showed that Xies lacking Synapsin (Syn), encoding a presynaptic vesicle scaVolding protein, unexpectedly show increased ethanol tolerance (Godenschwege et al. 2004). This result may reXect the fact that Synapsin is involved not only in regulating neurotransmitter release but also in neurite growth, synaptic formation and maturation, and in segregating the reserve and readily releasable pools of vesicles (Cesca et al. 2010). Finally, Homer, a protein that interacts with postsynaptic scaVolding and signaling proteins, including metabotropic glutamate receptors, regulates both initial ethanol sensitivity and ethanol tolerance (Urizar et al. 2007).
The major regulators of neuronal excitability that have been implicated in ethanol-induced behaviors in Xies are the -aminobutyric acid B (GABA B ) receptors and the large conductance calcium-activated potassium (BK) channels. GABA B receptor activity promotes sensitivity to ethanol sedation but reduces rapid ethanol tolerance (Dzitoyeva et al. 2003). As in mammals, Drosophila GABA B receptors are metabotropically coupled to potassium channels, thereby inhibiting neuronal excitability due to potassium eZux (Mezler et al. 2001). The BK channel encoded by the gene slowpoke (slo) has also been implicated in rapid ethanol tolerance, but in the opposite direction. Expression of the Xy BK channel is upregulated by ethanol exposure and its function is required for the development of rapid ethanol tolerance; induction of BK channel expression is in fact suYcient to induce ethanol resistance, mimicking the tolerant state (Cowmeadow et al. 2005(Cowmeadow et al. , 2006. The fact that GABA B receptors and BK channels likely aVect neuronal excitability in the same direction, but regulate tolerance in opposite ways, suggests that they may function in diVerent subsets of neurons that exert opposing eVects on behavior. Alternatively, it has been proposed that BK channels may in fact enhance neuronal excitability by reducing the refractory period or enhancing Wring rates, allowing neurons to compensate for the depressant eVect of ethanol during sedation (Atkinson 2009).
In addition to classical neurotransmitters such as GABA, neuromodulators, including biogenic amines and neuropeptides, also regulate ethanol-induced behavior in Xies. Dopamine promotes ethanol hyperactivity through the D1-like receptor DopR (Bainton et al. 2000;Kong et al. 2010b) and is also required for conditioned ethanol preference (Kaun et al. 2011). Octopamine, a biogenic amine thought to be the invertebrate analog of norepinephrine, is essential for the development of rapid but not chronic ethanol tolerance (Scholz 2000;Berger et al. 2004). Two neuropeptides produced in the Xy brain, neuropeptide F (NPF) and insulin, have been shown to regulate ethanol sedation. NPF, the Xy homolog of neuropeptide Y, enhances ethanol sedation (Wen et al. 2005). Mutations in the insulin receptor (InR) cause increased sedation sensitivity, as does overexpression of the adaptor protein p60 to inhibit the coupling between the insulin receptor (InR) and PI3K, the main eVector of insulin signaling (Corl et al. 2005). These results indicate that insulin acts through PI3K to promote sedation resistance. However, a diVerent study (discussed earlier) using several more direct manipulations of the PI3K/Akt pathway demonstrated that this pathway promotes sedation sensitivity . PI3K may therefore have opposing roles in regulating ethanol sedation depending on the upstream molecule to which it is coupled and the cell type in which it is expressed. In general, the mechanisms by which these neuromodulators aVect postsynaptic and/or presynaptic cells have not yet been characterized. It thus remains an open question whether they directly aVect postsynaptic excitability or modulate other pre-or postsynaptic properties.

Genome-wide studies
The majority of the genes discussed above were identiWed using genetic screens in which mutants exhibiting abnormal behavior were isolated. However, an alternative approach is to use transcriptional proWling to compare gene expression under diVerent conditions. For example, one study identi-Wed genes diVerentially expressed in Xy strains selected for increased versus decreased sensitivity to ethanol, and con-Wrmed that mutations in many of these genes cause altered ethanol sensitivity (Morozova et al. 2007).
Three studies have identiWed genes whose expression is regulated by ethanol exposure, making them good candidates for mediating the development of tolerance. These studies used varying exposure protocols and collectively identiWed 1,669 candidate genes, 29 of which were common to all three studies and 229 of which were common to at least two out of three studies (Morozova et al. 2006;Urizar et al. 2007;Kong et al. 2010a). Many of these genes were functionally validated using mutant analysis (Morozova et al. 2006;Kong et al. 2010a), but in most cases the molecular and cellular mechanisms by which these genes function have not been determined.

Neural circuits underlying ethanol-induced behavior in Drosophila
Although the neural circuits mediating ethanol-induced behaviors in Drosophila have not been as extensively studied as the molecular mechanisms, new tools such as Gal4 lines to target particular neurons and transgenes to manipulate neuronal activity have made the study of circuits more accessible.
In mammals, dopamine is an important regulator of many ethanol-related behaviors (Soderpalm et al. 2009). In the Xy, dopamine is expressed in several clusters of neurons that project to a variety of brain regions (Nassel and Elekes 1992). As in mammals, many of these dopaminergic cells have been shown to play a role in ethanol-related behaviors. The function of dopamine in regulating ethanol hyperactivity was localized to a pair of dopaminergic neurons projecting to DopR-expressing neurons in the ellipsoid body of the central complex (Kong et al. 2010b), a region known to regulate visual and locomotor behavior, arousal, and memory (Martin et al. 1999;Wu et al. 2007;Neuser et al. 2008;Ofstad et al. 2011). The ellipsoid body is also the site of Homer function in the regulation of ethanol sedation sensitivity and tolerance (Urizar et al. 2007), though it is unknown whether Homer functions via DopR signaling, or in DopR-expressing neurons.
Dopamine neurons also mediate conditioned ethanol preference. Ethanol reward memory, like other forms of memory, can be divided into three phases: acquisition (memory formation during training), consolidation (the period between training and testing), and retrieval (expression of the memory during testing) (Krashes et al. 2007). Interestingly, silencing dopaminergic neurotransmission impairs retrieval, but not acquisition or consolidation, of ethanol reward memory (Kaun et al. 2011).
While some dopaminergic neurons innervate the ellipsoid body, others terminate in the mushroom body, a brain structure implicated in olfactory processing and learning (Davis 2011). Neurotransmission of mushroom body neurons is required for both ethanol-induced hyperactivity and conditioned ethanol preference (King et al. 2011;Kaun et al. 2011). Both behaviors are mediated by neurons in speciWc subregions within this structure, and distinct phases of conditioned ethanol preference are in fact localized to diVerent mushroom body neurons (King et al. 2011;Kaun et al. 2011). Together, these studies demonstrate that diVerent ethanol-induced behaviors can be mapped to distinct neural loci, and that some brain structures, such as the mushroom body, are important for multiple behaviors.

Mammalian validation of mechanisms underlying ethanol-induced behavior
Now that years of research have implicated many diVerent molecular and cellular pathways in mediating Xy responses to ethanol, it is important to ask whether these mechanisms function in mammals as well. In fact, many of the genes and molecular pathways implicated in Drosophila ethanol responses play a similar role in mammals (see Table 1). For example, the cAMP, EGFR, and NPF/NPY pathways all regulate ethanol sensitivity similarly in Xies and rodents (Moore et al. 1998;Wand et al. 2001;Corl et al. 2009;Wen et al. 2005;Thiele et al. 1998). Furthermore, these pathways regulate not only ethanol sensitivity but also ethanol consumption in rodents (Wand et al. 2001;Corl et al. 2009;Thiele et al. 1998). Thus, simple behavioral assays that are readily used for genetic screening in Xies can yield candidate genes that have homologous roles in rodent models. Moreover, an FDA-approved drug that inhibits the function of EGFR, a molecule Wrst shown to regulate ethanol-related behavior in the Xy, has been shown to be eVective in a preclinical rat model of ethanol addiction (Corl et al. 2009).
While most of the genes aVecting ethanol-induced behavior in Xies have not yet been tested for a role in humans, a few have already been associated with human ethanol-related behavior. Polymorphisms in the human ALK gene are correlated with multiple measures of ethanol sensitivity (Lasek et al. 2011b), and polymorphisms in one human homolog of hang, ZNF699, were found to be associated with alcohol dependence (Riley et al. 2006). Recently, a genome-wide meta-analysis revealed that polymorphisms in autism susceptibility candidate 2 (AUTS2) are associated with alcohol consumption (Schumann et al. 2011). Mice selected for high versus low alcohol consumption diVer in expression of AUTS2, and downregulation of the Xy homolog of AUTS2 leads to reduced ethanol sensitivity (Schumann et al. 2011). Given the signiWcant conservation of genes aVecting ethanol responses in Xies and rodents, it is likely that additional genes identiWed in Xies will be validated in rodents and humans, and vice versa.
In addition to molecular pathways, some of the cellular mechanisms implicated in Drosophila ethanol responses have also been studied in mammals. For example, the role of synapse function in ethanol-induced behavior is still an emerging Weld of study in Xies, while the eVects of ethanol at the synapse have been well studied in mammals. Ethanol acts on a variety of postsynaptic receptors, most notably GABA A and N-methyl-D-aspartic acid (NMDA) receptors, and also exerts presynaptic eVects on neurotransmitter release (Siggins et al. 2005). Whether changes in synapse number are associated with altered ethanol behaviors in mammals, as is the case in Xies  has not yet been studied.
While at the molecular level Xies and mammals share many features (Littleton and Ganetzky 2000;Lloyd et al. 2000), the anatomical organization of Xy and mammalian nervous systems is quite distinct. It is therefore diYcult to draw parallels between the neural circuits that regulate ethanol-induced behavior in Xies and mammals. In Xies, brain structures such as the ellipsoid body and the mushroom body have been implicated in various ethanol responses; it is unclear what the equivalent structures are in the mammalian brain. Nevertheless, certain conserved neurochemical systems function similarly in Xies and mammals. The mammalian mesolimbic dopamine pathway, including its target regions, is perhaps the most intensely studied neural circuit in the context of alcohol reward and addiction (Soderpalm et al. 2009). Dopamine neurons were similarly found to be required for ethanol hyperactivity and reward in Drosophila (Kong et al. 2010b;Kaun et al. 2011). Neuropeptidergic systems, such as the NPY/NPF system, also regulate ethanol responses similarly in Xies and rodents, as discussed above. Thus, the functions of neurochemically deWned neural pathways, rather than morphologically deWned brain regions, are likely to be conserved in regulating ethanol behaviors.

Study of other drugs of abuse in Drosophila
Drugs of abuse other than ethanol have not yet been studied extensively in Xies. This may be due in part to the fact that ethanol, in vapor or liquid form, can be delivered to Xies This table includes the genes referred to in the text, which represent many of the genes that have been functionally characterized as regulators of ethanol-induced behavior. We have not included every gene that has been identiWed, but we have made an eVort to include representative genes for each signaling pathway or general mechanism. Studies identifying a large number of genes with limited characterization of mechanism (e.g. Berger et al. 2008) have not been included. In cases where many genes in the same signaling pathway have been implicated, the gene initially identiWed is listed and the signaling pathway is described in the second column (e.g. aru, PI3K/Akt pathway). Unless otherwise speciWed, the ethanol-related phenotype described in the third column refers to the phenotype upon impairing the function of the gene product by mutation, RNAi, or pharmacology

Tbh
Octopamine synthesis Decreased tolerance Scholz et al. (2000) and Berger et al. (2004) TabakoV and Ritzmann (1977) InR Insulin signaling Increased sedation Corl et al. (2005) npf NPF signaling Decreased sedation Wen et al. (2005) Thiele et al. (1998 quite readily and in a reproducible manner; the same is not true for drugs such as cocaine and nicotine (McClung and Hirsh 1998;Bainton et al. 2000). Although there are assays to measure the locomotor eVects of some of these other drugs, there are currently no assays to investigate their rewarding and addiction-like properties. Nevertheless, several genes and molecular mechanisms regulating drug-induced behaviors have been discovered using simple locomotion assays (Table 2).

Cocaine
Cocaine is an addictive psychostimulant that causes enhanced locomotor activity and stereotypy (repetitive behavior) in mammals (Satel et al. 1991). When Xies are exposed to volatilized cocaine, they show similar behavioral eVects including continuous grooming at low doses, circling and aberrant walking behavior at intermediate doses, and fast, uncontrolled movements followed by body tremors and akinesia at high doses (McClung and Hirsh 1998). Repeated cocaine exposure causes Xies to become increasingly sensitive to the behavioral eVects of the drug, a process referred to as sensitization (McClung and Hirsh 1998). In addition to direct observation, other assays have been developed for greater control of drug delivery and simpler behavioral analysis. For example, the "crackometer" quantiWes the loss of negative geotaxis and positive phototaxis (two robust innate behaviors in Xies) under the inXuence of volatilized cocaine (Bainton et al. 2000). Semi-automation of this assay allows for high-throughput behavioral analysis (George et al. 2005). Finally, locomotor tracking systems allow for quantiWcation of locomotor speed and pattern (Bainton et al. 2000;Dimitrijevic et al. 2004). Unlike ethanol, cocaine acts primarily on a single class of molecular targets: it inhibits monoamine transporters, thereby increasing synaptic levels of monoamines including dopamine, serotonin, epinephrine, and norepinephrine. Inhibition of the dopamine transporter (DAT), in particular, is largely responsible for cocaine-induced locomotor hyperactivity in mammals (Giros et al. 1996). It is therefore not surprising that dopamine signaling is also required for cocaine-induced hyperactivity in Xies. A key role for the dopaminergic system in mediating the eVect of cocaine has been demonstrated through both pharmacological and genetic methods. Pharmacological reduction of dopamine levels or dopamine receptor function causes decreased locomotor hyperactivation by cocaine, suggesting that cocaine induces hyperactivity by increasing dopaminergic transmission (Bainton et al. 2000;Torres and Horowitz 1998;Yellman et al. 1998). However, genetic studies provide conXicting results: (1) overexpression of one isoform of the vesicular monoamine transporter (VMAT-A), which is expected to increase dopamine levels, decreases cocaine sensitivity (Chang et al. 2006), and (2) constitutive inhibition of dopaminergic transmission, predicted to block the eVects of cocaine, causes cocaine hypersensitivity . In both cases these initially counterintuitive results  Bainton et al. (2000) P r a d h a n ( 1983) Vmat (isoform A) Monoamine storage and release Reduced cocaine-induced hyperactivity Chang et al. (2006) Brown et al. (2001 per, Clk, cyc, and dco Regulation of circadian rhythms Reduced behavioral sensitization to cocaine Andretic et al. (1999) Abarca et al. (2002 and McClung et al. (2005) moody Development and permeability of blood-brain barrier Increased sensitivity to cocaine Bainton et al. (2005) and Schwabe et al. (2005) loco Functions with moody in development of blood-brain barrier Reduced sensitivity to cocaine Bainton et al. (2005) and Schwabe et al. (2005) Bishop et al. (2002) and Schwendt et al. (2007) RhoGAP18B Regulates actin cytoskeleton? Reduced sensitivity to cocaine and nicotine RothenXuh et al. (2006) dLmo Regulates dopamine receptor expression?
Reduced sensitivity to cocaine and nicotine King et al. (2011) could be explained by compensatory adaptations in postsynaptic dopamine signaling (Chang et al. 2006;Li et al. 2000). Drosophila studies have identiWed unanticipated genes and pathways regulating cocaine-induced behavior. For example, mutations in the circadian genes period (per), clock (Clk), cycle (cyc), and doubletime/discs overgrown (dco) reduce behavioral sensitization to cocaine (Andretic et al. 1999). These genes may regulate cocaine sensitization by aVecting dopaminergic signaling since cocaine-treated per mutants, unlike cocaine-treated wild-type Xies, do not increase locomotion in response to a dopamine receptor agonist (Andretic et al. 1999). Circadian genes similarly mediate cocaine-induced behaviors in mammals. The mammalian homologs of per have been shown to regulate cocaine sensitization and CPP in mice (Abarca et al. 2002). In addition, mice lacking a functional Clock gene display increased cocaine reward and dopamine neuron excitability in the midbrain (McClung et al. 2005).
moody, which encodes two G protein-coupled receptors (GPCRs), was identiWed in a genetic screen for cocaineinduced loss of negative geotaxis . moody mutant Xies show enhanced cocaine sensitivity, and moody was shown to function in glia to regulate bloodbrain barrier permeability Schwabe et al. 2005). loco, which encodes a regulator of G protein signaling (RGS) that terminates GPCR signaling, functions along with moody to regulate blood-brain barrier permeability . As predicted from its molecular function, loco regulates cocaine sensitivity in the opposite direction as moody (Granderath et al. 1999;Bainton et al. 2005). The mammalian homolog of loco, RGS4, has been implicated in psychostimulant use (Bishop et al. 2002;Gold et al. 2003;Schwendt et al. 2006Schwendt et al. , 2007. These studies suggest that blood-brain barrier permeability may play an important role in drug sensitivity and potentially addiction. Genetic screens have revealed overlap between genes that regulate ethanol and cocaine sensitivity. RhoGAP18B, tao, and dLmo, three genes that were identiWed in genetic screens and shown to regulate ethanol sensitivity (see previous section), also regulate cocaine sensitivity (RothenXuh et al. 2006;King et al. 2011;Tsai et al. 2004). Both Rho-GAP18B and tao mutants exhibit cocaine resistance, while dLmo mutants show increased cocaine sensitivity. dLmo regulation of cocaine sensitivity has been mapped to a subset of the pigment-dispersing factor (PDF) neurons (Tsai et al. 2004), the primary circadian pacemaker cells in Xies (Renn et al. 1999). The function of dLmo has been validated in mammals, as downregulation of one of the mammalian homologs, Lmo4, causes increased cocaine sensitivity and sensitization in mice (Lasek et al. 2010). Lmo4 may regulate cocaine sensitivity by acting through the dopamine D2 receptor (Drd2) or the GluR1 subunit of the AMPA receptor, both of which show decreased expression upon Lmo4 downregulation ).

Amphetamines
Amphetamines are psychostimulants that, like cocaine, increase monoaminergic transmission. Amphetamines cause monoamine transporters to function in reverse, transporting these transmitters into the synapse (Koob and Nestler 1997). A small number of studies have characterized the eVects of amphetamines in Drosophila, focusing on methamphetamine and 3,4-methylenedioxy-methamphetamine (MDMA, also known as ecstasy).
One study investigated the behavioral eVects of orally administering methamphetamine to adult Xies. Consistent with its stimulant eVects in mammals, methamphetamine increased locomotor activity of Xies, interrupted sleep, and also aVected male courtship (Andretic et al. 2005). Methamphetamine administration was also associated with changes in visually evoked neural activity, suggesting that it may aVect visual perception (Andretic et al. 2005). Methamphetamine showed interactions with the dopaminergic system in aVecting this type of neural activity, consistent with its mode of action in mammals (Andretic et al. 2005).
In a diVerent study, MDMA was orally administered to Drosophila larvae, which caused reduced feeding and locomotion (Dasari et al. 2007). It has not been determined whether MDMA also produces stimulant eVects on Drosophila behavior. Larvae fed MDMA did not show an acute diVerence in levels of dopamine or serotonin, but did contain higher levels of both transmitters as adults, suggesting that monoamine synthesis may be upregulated over time in response to MDMA-induced monoamine depletion (Dasari et al. 2007).

Nicotine
Nicotine, the major addictive component of tobacco, aVects mammalian behavior by activating nicotinic acetylcholine receptors (Nestler 2005). When exposed to volatilized nicotine, Xies exhibit locomotor hyperactivity and spasmodic movements leading to grooming at low doses and hypokinesis and akinesia at higher doses (Bainton et al. 2000). Similar to cocaine, nicotine exposure dose-dependently impairs negative geotaxis in Xies (Bainton et al. 2000). In mammals, the addictive properties of nicotine are thought to be mediated by both direct and indirect activation of dopaminergic neurons (Nestler 2005). The locomotor eVects of nicotine in Xies are similarly dependent on dopamine, as pharmacological depletion of dopamine reduces nicotine sensitivity (Bainton et al. 2000). Aside from dopamine, little is known about the molecular mechanisms mediating nicotine sensitivity in Xies. However, several genes known to mediate cocaine sensitivity in Xies have also been shown to regulate nicotine sensitivity: moody mutant Xies are sensitive to the eVects of both drugs, whereas RhoGAP18B and tao mutants are resistant RothenXuh et al. 2006;King et al. 2011). These genes suggest that certain shared mechanisms may regulate multiple types of drug addiction in Xies.

Conclusions and future directions
For many years Xies have been used as a model to study acute drug responses, with a particular focus on ethanol, and the mechanisms underlying these behaviors have turned out to be remarkably conserved from Xies to mammals. More recently, the development of new assays, in particular the voluntary ethanol consumption and conditioned ethanol preference assays, has demonstrated that Xies exhibit addiction-like behavior. Flies fulWll several of the criteria proposed for an animal model of alcohol addiction (Cicero 1979;McBride and Li 1998). The ethanol consumption assay reveals that (1) Xies voluntarily consume ethanol and can achieve pharmacologically relevant internal ethanol levels, (2) their consumption is not dependent on caloric or sensory properties of ethanol, and (3) they exhibit a relapse-like eVect (Devineni and Heberlein 2009). The conditioned preference assay further demonstrates that Xies Wnd ethanol intoxication rewarding (Kaun et al. 2011). In both assays Xies were willing to overcome negative stimuli (bitter-tasting compound or electric shock, respectively) in order to obtain ethanol or the ethanol-associated cue, suggesting compulsive-like behavior toward ethanol.
However, certain important criteria for addiction have not yet been met in Xies. For example, it has not been shown that voluntary ethanol consumption leads to ethanol tolerance, that ethanol removal causes withdrawal symptoms, or that Xies are willing to "work" in order to obtain ethanol. The latter criterion could be demonstrated by showing that Xies exhibit operant responding for ethanol, a paradigm that has not yet been developed in Drosophila.
In addition to developing new and more complex behavioral assays, many questions remain to be tested using the existing assays for ethanol consumption and reward. For example, Xies are typically trained in the conditioned preference assay for only 1 day; it is unknown whether this preference would be altered if Xies were trained intermittently over many days. Preliminary data suggest that such long-term ethanol exposures are still perceived as rewarding (K. Kaun and U. Heberlein, unpublished data). In addition, it is unknown whether Xies in the conditioned preference assay show behavior indicative of a relapse-like eVect, which could be demonstrated by showing that Xies exhibit reinstatement to the ethanol-associated cue following extinction.
While more complex assays improve the validity of Drosophila as a model system to study drug addiction, these assays are necessarily more cumbersome and time-consuming, thus making large-scale genetic screening diYcult. It is therefore important to understand how the simple and more complex assays for drug-induced behavior are related. Evidence in humans and rodent models is generally consistent with the notion that resistance to the acute eVects of ethanol predicts increased ethanol consumption and risk of abuse (Schuckit 1994;Schuckit and Smith 1996;Morean and Corbin 2010). While this association suggests that an overlapping set of genes regulates both simple and complex drug behaviors, several exceptions to this correlation exist (e.g. Colombo et al. 2000;Phillips et al. 1998;Boehm et al. 2004), indicating that factors other than acute drug sensitivity modulate drug intake.
A recent study analyzed the relationships between initial ethanol sensitivity, ethanol tolerance, and voluntary ethanol consumption in Xies. Ethanol consumption was positively correlated with the development of tolerance, but not with naive sensitivity to the sedating or hyperactivating eVects of ethanol (Devineni et al. 2011). These results suggest that complex behaviors such as voluntary ethanol consumption are not simply readouts of acute responses; they likely incorporate acute sensitivity and the development of tolerance in addition to other factors, such as experience and learning. Some genes have been found to regulate multiple ethanol-induced behaviors: for example kra regulates sedation sensitivity, tolerance, and voluntary ethanol consumption (Berger et al. 2008;Devineni and Heberlein 2009). In contrast, other genes regulate individual ethanol-induced behaviors: for instance sca mediates conditioned ethanol preference, but not acute ethanol sensitivity (Kaun et al. 2011;LaFerriere et al. 2008). Thus, while the simpler assays are ideal for rapidly identifying ethanol-related genes and have some predictive value for more complex behaviors, the development of high-throughput versions of the more complex assays will be necessary in order to apply the power of Drosophila genetics to the study of addictionlike behaviors.
Intriguingly, forward genetic screens in Xies have identi-Wed many diVerent and unexpected molecular mechanisms that regulate ethanol-related behavior. These mechanisms include signaling pathways such as the cAMP and PI3K pathways that have broad roles in regulating many diverse processes such as development, cell signaling, and neuronal plasticity. Many of the signaling pathways that have been identiWed can aVect each other in complex ways, so it is likely that some pathways may have a more direct role in regulating ethanol responses than others. In most cases it is unknown whether the molecules that have been implicated are direct targets of ethanol or are required downstream of ethanol binding.
One theme that emerges from this large number of pathways is the involvement of molecules aVecting molecular or cellular plasticity (e.g. cytoskeletal regulators, ion channels, synaptic molecules), which appear to be recruited to induce behavioral changes in response to ethanol. Much work remains to be done in uncovering how diVerent mechanisms interact to regulate ethanol-related behavior, and how the molecular and cellular changes induced by acute ethanol exposure are translated into addiction-like responses. For example, cytoskeletal changes caused by acute ethanol exposure may be required to induce changes in synapse number, which consequently may mediate ethanol tolerance and preference behaviors. Understanding the relationship between mechanisms mediating acute and long-term responses to ethanol is key to understanding the addictive properties of the drug. The Xy is ideally suited to this task due to the availability of tools to investigate these mechanisms with high spatial and temporal resolution.
The next decade should witness the discovery of many novel mechanisms underlying addiction-related behaviors in Xies as the number of tools available to study molecular and neural processes is expanding at a rapid rate. Based on what we have learned in the last 15 years from Drosophila addiction research, we expect that these novel mechanisms will be relevant to mammalian models and provide novel targets for the development of pharmacotherapies for drug addiction.
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