The fact that adolescents commonly initiate drug use in social settings is well established. Both clinical and preclinical research has investigated how social interaction is altered by a variety of drugs of abuse. What is less understood is how the rewarding value of drugs of abuse is affected by the presence of social peers. This dissertation aimed to investigate the interaction of morphine and social play on conditioned place preference (CPP) in adolescent male Sprague Dawley rats, using both behavioral and immunohistochemistry (IHC) methods. Rats were exposed to morphine (0, 1, or 3 mg/kg; s.c.), social interaction, or a combination of both and tested in a modified CPP procedure. Behavioral results indicate that, while doses of morphine used produced only weak CPP across experiments, they were sufficient to reduce the rewarding effect of social interaction. IHC results suggest that this finding may be due to reduced activation in NAc shell. Taken together, the results of this dissertation may help to provide an explanation as to why persons with opioid use disorder spend less time interacting with social peers, compared to non-dependent persons.

Addiction is a chronic disease that characterize as habitual or compulsive involvement in an activity despite it¡¦s bring negative consequences. Some of psystimulants such as cocaine or amphetamine cause a strong reinforcing effects even after prolonged abstinence periods. Such illegal drugs not only hurt on the adult health but also result in fetal physiological damage. For example, that babies born to mothers who abuse with cocaine bring prematurely delivered, low birth weights, smaller head circumferences and increased heart disease in adult offspring. Mesolimbic dopamine system include nucleus accumbens (NAc) and ventral tegmental area (VTA) are critical regions for the neural adaptations that contribute to addiction. VTA that receives inputs from a large number of brain regions. For example, it receives glutamatergic inputs from prefrontal cortex, or GABAergic inputs from NAc. It has been known that VTA play a major role in the acquisition and expression of learned addictive behaviors. Results from many neuropharmacological studies in animal models indicate that exposure to cocaine or some other drugs of abuse seems to induce long-term potentiation (LTP) ¢w like changes of synaptic plasticity among neurons in VTA region. LTP was first described in hippocampus, a region that associated with memory formation, and were found widespread events in many mammalian brain sites. In the present time, theories and investigation indicated that memory and addiction might shared the similar neural circuitry and signal pathways. In general, LTP can be separate into two main phases : induction and maintenance phases. Many of molecules participate in induction phase such as calcium/calmodulin-dependent protein kinase II (CaMKII), cyclic AMP (cAMP), phosphatidylinositol 3-kinases (PI3K) and protein kinase C (PKC). However, until now there was only one molecule has been found associated with LTP maintenance¡Xprotein kinase M£a (PKM£a). PKM£a is a brain specific, constitutively active form of PKC that does not need Ca2+ or diacylglycerol (DAG) for its activation. Molecular evidences showed that PKM£a is translated uniquely by PKM£a mRNA which is generated under the control of an internal promoter in the PKC£a gene. Recently, investigators introduced a PKM£a selective inhibitor¡XZIP, to hippocampus or insular cortex both successful to eliminate long-term spatial memory or conditioned taste aversion (CTA) behavior, respectively, on rat. Therefore, exclude PKM£a by specific inhibitors and then result in abolish long-term synaptic potentiation which had already established seem to be a leading candidate for cure addiction. Here we showed that blocked of PKM£a activity in VTA dopaminergic neuron eliminated mEPSCs or AMPAR/NMDAR ratio increment elicited by cocaine. Otherwise, our results also presented that myristoylatedinhibitory peptide¢wZIP had no effect on spike timing-dependent long-term potentiation in rats previously injected with saline but remarkably restored spike timing-dependent long-term potentiation in VTA dopamine neurons in slices prepared from rats that received single or multiple cocaine exposure. Furthermore, our western blot analyses showed that both single and five consecutive cocaine injections induced a significant increase in PKM£a level in VTA or NAc. Moreover, our ex vivo cocaine incubation results indicated that multiple kinases activation or de novo protein synthesis was required for PKM£a increment. The most important, our data provided the first physiological evidence between PKM£a and drug addiction when intracranial administered specific PKM£a inhibitors to VTA reversed cocaine-induced conditioned-place preference (CPP) behavior. Finally, we investigated the behavioral effect of cocaine-induced locomotor sensitization in an open field apparatus. Our data showed that peri-adolescent (P21) rats exhibited prominently increased in either acute or repeated cocaine-induced locomotor activity than mid-adolescent (P28) and post-adolescent (P41). Interestingly, applied to high dosage cocaine (30 mg/kg) rescued the acute locomotor response in P28 rats but not behavioral sensitization. We further examined the locomotion on rats that were exposed to cocaine in utero after single or multiple cocaine injection. However, cocaine-induced increase in locomotor activity was lower in P21 rats which exposed to cocaine during pregnancy but no significantly difference in P28 rats. Surprisingly, single high dose cocaine treatment caused a marked reduction in locomotor activity on P21 rats prenatally exposed to cocaine. Otherwise, we also provided the first evidences that repeated cocaine injection in pregnant rats induced a significant decreased to KCC2 level in PFC regions prepared from P20 rat. In conclusion, results from our current studies demonstrate for the first time that persistently active PKM£a is necessary in (1) mEPSC facilitation induced by single cocaine exposure; (2) cocaine-induced enhancement in AMPAR/NMDAR ratio; (3) single or repeated cocaine-induced LTP but not in LTP induced by spike-timing stimulation; and (4) cocaine conditioned place preference in the VTA. In addition, our results also present evidence that the expression of PKM£a is increased by either single or repeated cocaine exposure. Furthermore, our behavioral or Western blotting consequence of cocaine treatment in utero was reflected by the diminishion in the sensitivity of locomotor activity in postnatal rats to cocaine and KCC2 level in PFC regions.

The salience of natural or drug-associated reward is mediated by phasic dopamine (DA) release in the nucleus accumbens (NAc) arising from DAergic cells in the ventral tegmental area (VTA). Circulating sex steroid hormones can modulate reward associated with drugs of abuse; yet, it still remains unclear which brain regions are responsible for this modulation. The medial preoptic area (mPOA) is a hypothalamic brain area involved in the expression of naturally rewarding behaviors as well as the regulation and reception of circulating sex steroid hormones in female rats. Considering its role in regulating naturally rewarding behaviors, its well-established anatomical connectivity with the VTA, and its responsiveness to circulating sex steroid hormones, the mPOA is an ideal neural node through which hormones could modulate the rewarding facets of drugs of abuse. Here I show that preoptotegmental efferents to the VTA are primarily GABAergic, that they appose putative DAergic cell bodies in the VTA that project to the NAc, and that they are capable of responding to sex steroid hormones and changes in DA release. Furthermore, cocaine influences neural activity in mPOA efferents that project to the VTA. Removal of the mPOA also enhanced cocaine-induced locomotion, Fos-immunoreactivity in the mesolimbic reward system, DA release in the NAc, and augmented conditioned place preference. Together these findings suggest that the mPOA modulates the release of DA in the mesolimbic reward circuitry via inhibitory connections with DA neurons residing in the VTA, and sex steroid hormones, in turn, may act in the mPOA to modulate response to cocaine. / text

Adolescence is a period of development that is associated with increased risk taking behaviors and experimenting with drugs of abuse, including alcohol and nicotine. Early onset of use of these agents may be associated with long-term changes in behavior and enhanced sensitivity to the subsequent effects of alcohol in adulthood. The present experiment was designed to assess the long-term behavioral alterations that occur due to adolescent exposure to ethanol and nicotine, either alone or in combination, on adulthood responsivity to the rewarding properties of environmental cues paired with ethanol. It was hypothesized that adolescent rats exposed to the combination of ethanol and nicotine would exhibit enhanced novelty seeking behaviors in adulthood. When assessing the rewarding properties of environmental cues paired with ethanol in adulthood using the CPP paradigm, it was hypothesized that adolescent rats exposed to the combination of a moderate dose of alcohol (0.75 g/kg) and nicotine (0.4 mg/kg) would more readily acquire a CPP in adulthood as compared to animals exposed to either drug alone. However, no changes in novelty seeking behaviors or conditioned place preference in adulthood were observed due to exposure to ethanol and/or nicotine during adolescence .Methodological considerations are discussed. Currently, other experiments are being conducted to assess the effects of nicotine on voluntary ethanol treatment in adolescent and adult male rats.

During adolescent brain maturation, there are likely sensitive periods where environmental conditions, including drug exposure, may influence development by modifying neuronal connections. Altering neuronal function may produce different phenotypes than expected under normal conditions that may influence subsequent responding to drugs of abuse after the brain is fully mature. Experiment one investigated the relationship between novelty preference and cocaine place preference in adolescent and adult rats. High responding adolescent rats displaying greater free choice novelty exploration (but not forced novelty locomotion) expressed decreased cocaine place conditioning compared to low responding rats. No relationship was found in adult rats. Experiment two evaluated novelty-induced behaviors in adulthood after adolescent cocaine exposure. Repeated cocaine administration produced greater stress and anxiogenic behavioral responses to novelty in adult rats. Repeated alcohol administration produced less-inhibited novelty-induced behaviors in adulthood. Experiment three and four evaluated the consequence of developmental cocaine exposure on the rewarding efficacy of cocaine in adolescence and adulthood. Additionally, the interaction of D2 receptors and the rewarding efficacy of cocaine were investigated. After developmental cocaine exposure, adolescent and adult rats demonstrate decreased rewarding efficacy to cocaine. Importantly, blockade of the D2 receptor prevents cocaine-induced neurochemical changes, potentially regulating the behavioral and neurochemical alterations that occur after repeated drug use that increases the likelihood of dependence. Together, these data implicate both short and long-term behavioral adaptations that occur after developmental cocaine exposure that may result in a predisposition to develop adulthood drug dependence.

Binge eating disorder is characterized by excessive consumption of highly palatable food within short periods of time accompanied by loss of control over eating. Extensive evidence provides support for the consideration of binge eating disorder as an addiction-like disorder. In this study, we wanted to determine whether rats undergoing an operant binge-like eating procedure could develop maladaptive forms of conditioned feeding behaviors. For this purpose, we trained male rats to self-administer either a sugary, highly palatable diet (Palatable rats) or a chow diet (Chow rats) for 1 hour/day. Following escalation and stabilization of palatable food intake, we tested both Chow and Palatable rats in a i) conditioned place preference, a ii) second-order schedule of reinforcement and, finally, a iii) cue-induced suppression of feeding. In the conditioned place preference task, Palatable rats spent significantly more time in the compartment which was paired with the palatable food when compared to Chow controls. Furthermore, in the second-order schedule of reinforcement task, Palatable rats exhibited active lever responding 4- to 6-fold higher than Chow control rats. Finally, in the conditioned suppression of feeding test, while Chow control subjects reduced responding by one-third in the presence of the conditioned punishment, Palatable rats persevered in responding despite the aversive cue. These results further characterize our animal model of binge-like eating and provide additional evidence for the addictive properties of highly palatable food.

abstract: Social influences are important determinants of drug initiation in humans, particularly during adolescence and early adulthood. My dissertation tested three hypotheses: 1) conditioned and unconditioned nicotine and social rewards elicit unique patterns of neural signaling in the corticolimbic neurocircuitry when presented in combination versus individually; 2) play behavior is not necessary for expression of social reward; and 3) social context enhances nicotine self-administration. To test the first hypothesis, Fos protein was measured in response to social and nicotine reward stimuli given alone or in combination and in response to environmental cues associated with the rewards in a conditioned place preference (CPP) test. Social-conditioned environmental stimuli attenuated Fos expression in the nucleus accumbens core. A social partner elevated Fos expression in the caudate-putamen, medial and central amygdala, and both nucleus accumbens subregions. Nicotine decreased Fos expression in the cingulate cortex, caudate-putamen, and the nucleus accumbens core. Both stimuli combined elevated Fos expression in the basolateral amygdala and ventral tegmental area, suggesting possible overlap in processing both rewards in these regions. I tested the second hypothesis with an apparatus containing compartments separated by a wire mesh barrier that allowed limited physical contact with a rat or object. While 2 pairings with a partner rat (full physical contact) produced robust CPP, additional pairings were needed for CPP with a partner behind a barrier or physical contact with an object (i.e., tennis ball). The results demonstrate that physical contact with a partner rat is not necessary to establish social-reward CPP. I tested the third hypothesis with duplex operant conditioning chambers separated either by a solid or a wire mesh barrier to allow for social interaction during self-administration sessions. Nicotine (0.015 and 0.03 mg/kg, IV) and saline self-administration were assessed in male and female young-adult rats either in the social context or isolation. Initially, a social context facilitated nicotine intake at the low dose in male rats, but suppressed intake in later sessions more strongly in female rats, suggesting that social factors exert strong sex-dependent influences on self-administration. These novel findings highlight the importance of social influences on several nicotine-related behavioral paradigms and associated neurocircuitry. / Dissertation/Thesis / Doctoral Dissertation Psychology 2015

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Drug addiction has exerted a considerable impact on society, resulting in one of the biggest public health problems reaching different ethnic groups and social classes worldwide. Brazil is the largest consumer of opioid analgesics in South America, presenting, from a clinical point of view, a problematic situation, because the continuous administration could lead to tolerance and dependence. In this sense, the conditioned preference place protocol (CPP) has been widely used to evaluate the addition related to drug abuse. According to the World Health Organization (2010), stress is recognized by its chronicity, being identified as the evil of the XXI century. Its effects are directly related to the quality of life of the individual, family and society. This study was performed to evaluate the influence of stress exposure in different early life periods (fetal and neonatal) on anxiety-like symptoms and emotionality, and its consequences on addiction parameters after young animals' exposure to morphine. Animals exposed to post-NS showed lesser anxiety in different behavioral paradigms as well as increased exploratory behavior, and no preference for morphine in CPP. In contrast, animals exposed to pre-NS showed increased corticosterone plasma levels together with anxiety symptoms and greater preference for morphine following three days of drug withdrawal. Our findings indicate that the prenatal period is critical for stress, whose effects may be manifest throughout life. Although data demonstrate that the post -NS can develop chronic stress or adverse experiences, we can see from our results that the post -NS can trigger neuroadaptations able to overcome emotional consequences of early life. We hypothesized that pre-NS is able to modify responses to opioids along adulthood, which may facilitate development of addiction to these drugs. / A adição apresenta um impacto considerável na sociedade, resultando em um dos maiores problemas de saúde pública, uma vez que assola diferentes etnias e classes sociais em todo o mundo. O Brasil é o maior consumidor de analgésicos opioides da América do Sul, apresentando, sob o ponto de vista clínico, uma situação problemática, pois a administração contínua pode levar a tolerância e dependência. Nesse sentido, o protocolo de preferência condicionada de lugar (do inglês conditioned place preference-CPP) tem sido amplamente utilizado para avaliar a adição relacionada à drogas de abuso. Segundo a Organização Mundial da Saúde (2010), o estresse é reconhecido por sua cronicidade, sendo identificado como o mal do século XXI. Suas repercussões estão diretamente associadas à qualidade de vida do indivíduo, da família e da sociedade. Assim, esse estudo objetivou investigar a influência de diferentes períodos de estresse (fetal e neonatal) sobre parâmetros comportamentais e de dependência à morfina em ratos jovens adultos. Animais expostos ao Post-NS mostraram menor grau de ansiedade, comportamento mais exploratório sem mostrar preferência por morfina. Em contrapartida, animais expostos ao protocolo de Pre-NS mostraram maiores níveis de corticosterona e menor ganho de peso, junto com maiores sintomas de ansiedade e preferência por morfina após três dias de abstinência. Nossos resultados indicam que o período pré-natal é mais susceptível ao estresse, cujos efeitos podem ser manifestar ao longo da vida. Embora dados demonstrem que o post-NS possa desenvolver estresse crônico ou experiências adversas, podemos verificar a partir dos nossos resultados que o post-NS pode desencadear neuroadaptações capazes de superar as consequências emocionais da vida precoce. Assim, nós hipotetizamos que o Pre-NS é capaz de modificar as respostas aos opioides ao longo da vida adulta, o que poderia facilitar o desenvolvimento de dependência a esses fármacos.

The effects of dopamine D1 and D2 antagonists on conditioned place preference (CPP) and locomotor activity were assessed. A total of three experiments were conducted. In each experiment there were two conditioning days followed by a test day. The results indicate that DA D1 and D2 receptors have distictly different roles in the mediation of behavior.

No description available.