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  • 1
    UID:
    (DE-627)174273877X
    Format: 11
    ISSN: 1662-5153
    Content: Drug related cue-induced reactivity plays a significant role in maintaining drug use and relapse in addicted individuals. The activation of dorsal lateral striatum -sensorimotor system (DLS-SM) has been suggested as an important route through which drug cues may induce automatic drug using behavior. The current study used fMRI to investigate the reactivity of heroin abstinent individuals to different types of cues, to clarify the characteristics of the cues that induce the activation of the sensorimotor area. 40 heroin-dependent abstinent individuals and 29 healthy subjects were recruited to perform the heroin cue-reactivity task during fMRI. The participants’ subjective craving and physical signs were evaluated before and after scanning. Whole-brain analysis showed that compared to drug use tool and drug cues, cues related to drug use action were more likely to activate bilateral middle temporal cortex, bilateral calcarine and bilateral inferior parietal cortex. Left insula, bilateral caudate and right putamen were significantly activated in neural interactions among subjects group, cue category and cue type. These areas are involved in motor preparation and output, indicating that the DLS-SM area is also an important neural basis of craving and automatic drug using behavior, and may mediate craving and drug seeking behavior. Our findings thus suggest that cues related to drug using action may induce automatic drug seeking behavior more than cues related only to the drug itself.
    Note: Gesehen am 14.12.2020
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 12(2018) Artikel-Nummer 123, 11 Seiten, 1662-5153
    In: volume:12
    In: year:2018
    In: extent:11
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 2
    UID:
    (DE-627)1669344851
    Format: 16
    ISSN: 1662-5153
    Content: Social affiliation is essential for many species and gains significant importance during adolescence. Disturbances in social affiliation, in particular social rejection experiences during adolescence, affect an individual’s well-being and are involved in the emergence of psychiatric disorders. The underlying mechanisms are still unknown, partly because of a lack of valid animal models. By using a novel animal model for social peer-rejection, which compromises adolescent rats in their ability to appropriately engage in playful activities, here we report on persistent impairments in social behavior and dysregulations in the endocannabinoid system. From postnatal day (pd) 21 to pd 50 adolescent female Wistar rats were either reared with same-strain partners (control) or within a group of Fischer 344 rats (inadequate social rearing, ISR), previously shown to serve as inadequate play partners for the Wistar strain. Adult ISR animals showed pronounced deficits in social interaction, social memory, processing of socially transmitted information, and decreased pain sensitivity. Molecular analysis revealed increased CB1 receptor protein levels and CP55,940 stimulated [35S]GTPγS binding activity specifically in the amygdala and thalamus in previously peer-rejected rats. Along with these changes, increased levels of the endocannabinoid anandamide and a corresponding decrease of its degrading enzyme fatty acid amide hydrolase were seen in the amygdala. Our data indicate lasting consequences in social behavior and pain sensitivity following peer-rejection in adolescent female rats. These behavioral impairments are accompanied by persistent alterations in CB1 receptor signaling. Finally, we provide a novel translational approach to characterize neurobiological processes underlying social peer-rejection in adolescence.
    Note: Gesehen am 17.07.2019
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 10(2016) Artikel-Nummer 203, 16 Seiten, 1662-5153
    In: volume:10
    In: year:2016
    In: extent:16
    Language: English
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  • 3
    UID:
    (DE-627)1866116649
    ISSN: 1662-5153
    Content: The question of how individual differences related to self-regulation interact with alcohol use patterns to predict intimate partner aggression (IPA) is examined. We hypothesized that excessive drinking will be related to partner aggression among those who have low self-regulation. In addition, we explored the extent to which differences in self-regulation in one partner may moderate the relationship between alcohol use and partner aggression. A sample of married or cohabitating community couples (N = 280) ages 18–45 was recruited according to their classification into four drinking groups: heavy drinking in both partners (n = 79), husband only (n = 80), wife only (n = 41), by neither (n = 80), and interviewed annually for 3 years. IPA, drinking, and scores on measures of negative affect, self-control, and Executive Cognitive Functioning (ECF) were assessed for both members of the couple. The Actor Partner Interdependence Model (APIM) was used to analyze longitudinal models predicting the occurrence of IPA from baseline alcohol use, negative affect, self-control and ECF. Actor self-control interacted with partner self-control such that IPA was most probable when both were low in self-control. Contrary to prediction, actors high in alcohol use and also high on self-control were more likely to engage in IPA. Partner alcohol use was predictive of actor IPA when the partner was also high in negative affect. Low partner ECF was associated with more actor IPA. These findings suggest that self-regulatory factors within both members of a couple can interact with alcohol use patterns to increase the risk for relationship aggression
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, (2018), 1662-5153
    In: year:2018
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
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  • 4
    UID:
    (DE-627)1733865454
    Format: 10
    ISSN: 1662-5153
    Content: Viral transduced gene expression is the current standard for cell-type specific labelling and cell tacking in experimental neuroscience. To achieve widespread gene expression, a viral delivery method to neonatal rodents was introduced more than two decades ago. Most of those neonatal virus-injection based gene transduction methods in mice have used deep hypothermia for anesthesia, which was reported to be associated with behavioral impairments in respective animals. To explore other options for neonatal viral applications, we applied a combination of Medetomidine, Midazolam and Fentanyl (MMF), each of which can be antagonized by a specific antagonist. Later in their adulthood, drug treated, virus injected mice and naïve mice showed a similar performance in all behavioral tasks tested, including motor coordination tasks, anxiety-related tasks and spatial memory tasks, demonstrating MMF anesthesia could be safely applied to mice for neonatal viral transduction at postnatal day 2.
    Note: Gesehen am 28.09.2020
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 14(2020) Artikel-Nummer 115, 10 Seiten, 1662-5153
    In: volume:14
    In: year:2020
    In: extent:10
    Language: English
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  • 5
    UID:
    (DE-627)1830658441
    Format: 13
    ISSN: 1662-5153
    Content: The radial arm maze (RAM) is a common behavioral test to quantify spatial learning and memory in rodents. Prior attempts to refine the standard experimental setup have been insufficient. Previously, we demonstrated the feasibility of a fully automated, voluntary, and stress-free eight-arm RAM not requiring food or water deprivation. Here, we compared this newly developed refined RAM to a classic manual experimental setup using 24 female 10-12 weeks old C57BL/6J mice. We used a lipopolysaccharide (LPS)-induced model of systemic inflammation to examine long-term cognitive impairment for up to 13 weeks following LPS injection. Both mazes demonstrated robust spatial learning performance during the working memory paradigm. The refined RAM detected spatial learning and memory deficits among LPS-treated mice in the working memory paradigm, whereas the classic RAM detected spatial learning and memory deficits only in the combined working/reference memory paradigm. In addition, the refined RAM allowed for quantification of an animal’s overall exploratory behavior and day/night activity pattern. While our study highlights important aspects of refinement of the new setup, our comparison of methods suggests that both RAMs have their respective merits depending on experimental requirements.
    Note: Gesehen am 10.01.2023
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 16(2022), Artikel-ID 1013624, Seite 1-13, 1662-5153
    In: volume:16
    In: year:2022
    In: elocationid:1013624
    In: pages:1-13
    In: extent:13
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 6
    UID:
    (DE-627)1789981905
    Format: 6
    ISSN: 1662-5153
    Content: Autobiographical memory (ABM) comprises memories of one’s own past that are characterized by a sense of subjective time and autonoetic awareness. Although ABM deficits are among the primary symptoms of patients with major psychiatric conditions such as mild cognitive impairment (MCI) and Alzheimer Disease (AD) or chronic schizophrenia large clinical studies are scarce. We therefore summarize and discuss the results of our clinical studies on ABM deficits in the respective conditions. In these studies ABM was assessed by using the same instrument - i.e., the Erweitertes Autobiographisches Gedächtnis Inventar (E-AGI) - thus allowing a direct comparison between diagnostic groups. Episodic ABM, especially the richness of details was impaired already in MCI and in beginning AD. Semantic memories were spared until moderate stages, indicating a dissociation between both memory systems. A recency effect was detectable in cognitively unimpaired subjects and vanished in patients with AD. A similar pattern of deficits was found in patients with chronic schizophrenia but not in patients with major depression. These ABM deficits were not accounted for by gender, or education level and did not apply for the physiological ageing process in otherwise healthy elderly. In conclusion, ABM deficits are frequently found in AD and chronic schizophrenia and primarily involve episodic rather than semantic memories. This dissociation corresponds to the multiple trace theory which hypothesized that these memory functions refer to distinct neuronal systems. The semi-structured interview E-AGI used to discern ABM changes provided a sufficient reliability measures, moreover potential effects of a number of important confounders could be falsified so far. These findings underline the relevance of ABM-assessments in clinical practice.
    Note: Gesehen am 17.02.2022
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 7(2013), Artikel-ID 194, Seite 1-6, 1662-5153
    In: volume:7
    In: year:2013
    In: elocationid:194
    In: pages:1-6
    In: extent:6
    Language: English
    URL: Volltext  (lizenzpflichtig)
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  • 7
    UID:
    (DE-627)1865866709
    Format: 13
    ISSN: 1662-5153
    Content: Predicting the consequences of one’s own decisions is crucial for organizing future behavior. However, when reward contingencies vary frequently, flexible adaptation of decisions is likely to depend on the situation. We examined the effects of an instructed threat context on choice behavior (i.e., reversal learning) and its electrocortical correlates. In a probabilistic decision-making task, 30 participants had to choose between two options that were either contingent on monetary gains or losses. Reward contingencies were reversed after reaching a probabilistic threshold. Decision-making and reversal learning were examined with two contextual background colors, which were instructed as signals for threat-of-shock or safety. Self-report data confirmed the threat context as more unpleasant, arousing, and threatening relative to safety condition. However, against our expectations, behavioral performance was comparable during the threat and safety conditions (i.e., errors-to-criterion, number of reversal, error rates, and choice times). Regarding electrocortical activity, feedback processing changed throughout the visual processing stream. The feedback-related negativity (FRN) reflected expectancy-driven processing (unexpected vs. congruent losses and gains), and the threat-selective P3 component revealed non-specific discrimination of gains vs. losses. Finally, the late positive potentials (LPP) showed strongly valence-specific processing (unexpected and congruent losses vs. gains). Thus, regardless of contextual threat, early and late cortical activity reflects an attentional shift from expectation- to outcome-based feedback processing. Findings are discussed in terms of reward, threat, and reversal-learning mechanisms with implications for emotion regulation and anxiety disorders.
    Note: Gesehen am 17.10.2023
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 16(2022), Artikel-ID 908454, Seite 1-13, 1662-5153
    In: volume:16
    In: year:2022
    In: elocationid:908454
    In: pages:1-13
    In: extent:13
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
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  • 8
    UID:
    (DE-627)1778263682
    Format: 12
    ISSN: 1662-5153
    Content: Depression is a major neuropsychiatric disorder, decreasing the ability of hundreds of millions of individuals worldwide to function in social, academic, and employment settings. Beyond the alarming public health problem, depression leads to morbidity across the entire age including adolescence and adulthood. Modeling depression in rodents has been used to understand the pathophysiological mechanisms behind this disorder and create new therapeutics. Although women are two times more likely to be diagnosed with depression compared to men, behavioral experiments on rodent models of depression are mainly performed in males based on the assumption that the estrous cycles in females may affect the behavioral outcome and cause an increase in the intrinsic variability compared to males. Still, the inclusion of female rodents in the behavioral analysis is mandatory to establish the origin of sex bias in depression. Here, we investigated the baseline depression-like behaviors in male and female mice of three adolescent wild-type inbred strains, C57BL/6N, DBA/2, and FVB/N, that are typically used as background strains for mouse models of neuropsychiatric disorders. Our experiments, performed at two different developmental stages during adolescence (P22-P26 and P32-P36), revealed strain but no sex differences in a set of depression-related tests, including tail suspension, sucrose preference and forced swim tests. Additionally, the 10-day interval during this sensitive period uncovered a strong impact on the behavioral outcome of C57BL/6N and FVB/N mice, highlighting a significant effect of maturation on behavioral patterns. Since anxiety-related behavioral tests are often performed together with depression tests in mouse models of neuropsychiatric disorders, we extended our study and included hyponeophagia as an anxiety test. Consistent with a previous study revealing sex differences in other anxiety tests in adolescent mice, male and females mice behaved differently in the hyponeophagia test at P27. Our study gives insight into the behavioral experiments assessing depression and stresses the importance of considering strain, age and sex when evaluating neuropsychiatric-like traits in rodent models.
    Note: Gesehen am 22.11.2021
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 15(2021), Artikel-ID 759574, Seite 1-12, 1662-5153
    In: volume:15
    In: year:2021
    In: elocationid:759574
    In: pages:1-12
    In: extent:12
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 9
    UID:
    (DE-627)169467701X
    Format: 10
    ISSN: 1662-5153
    Content: DREADDs (Designer Receptors Exclusively Activated by Designer Drugs) are popular tools used to manipulate the activity of defined groups of neurons. Recent work has shown that DREADD effects in the brain are most likely not mediated by the proposed ligand clozapine-N-oxide but its metabolite clozapine. However, it is not known whether low doses of clozapine required to activate DREADDs already have DREADD-independent effects on behavior as described for higher clozapine doses used in previous preclinical studies. To close this gap, we compared effects of acute systemic (i.p.) clozapine treatment vs. vehicle in a wide range of behavioral tests in male wild-type rats. We found that clozapine doses as low as 0.05-0.1 mg/kg significantly affected locomotion, anxiety and cognitive flexibility but had no effect on working memory or social interaction. These results highlight the need for careful controls in future chemogenetic experiments and show that previous results in studies lacking clozapine-N-oxide/clozapine controls may require critical re-evaluation.
    Note: Gesehen am 16.04.2020
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 12(2018) Article 173, 10 Seiten, 1662-5153
    In: volume:12
    In: year:2018
    In: extent:10
    Language: English
    URL: Volltext  (lizenzpflichtig)
    URL: Volltext  (lizenzpflichtig)
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  • 10
    UID:
    (DE-627)1571022023
    Format: 13
    ISSN: 1662-5153
    Content: The endocannabinoid system possesses neuromodulatory functions by influencing the release of various neurotransmitters, including γ-aminobutyric acid (GABA) and glutamate. A functional interaction between endocannabinoids and the serotonergic system has already been suggested. Previously, we showed that cannabinoid type 1 (CB1) receptor mRNA and protein are localized in serotonergic neurons of the raphe nuclei, implying that the endocannabinoid system can modulate serotonergic functions. In order to substantiate the physiological role of the CB1 receptor in serotonergic neurons of the raphe nuclei, we generated serotonergic (5-HT) neuron-specific CB1 receptor-deficient mice, using the Cre/loxP system with a tamoxifen-inducible Cre recombinase under the control of the regulatory sequences of the tryptophan hydroxylase 2 gene (TPH2-CreERT2), thus, restricting the recombination to 5-HT neurons of the central nervous system. Applying several different behavioral paradigms, we revealed that mice lacking the CB1 receptor in serotonergic neurons are more anxious and less sociable than control littermates. Thus, we were able to show that functional CB1 receptor signaling in central serotonergic neurons modulates distinct behaviors in mice.
    Note: Gesehen am 13.03.2018
    In: Frontiers in behavioral neuroscience, Lausanne : Frontiers Research Foundation, 2007, 9(2015) Artikel-Nummer 235, 13 Seiten, 1662-5153
    In: volume:9
    In: year:2015
    In: extent:13
    Language: English
    URL: Volltext  (kostenfrei)
    URL: Volltext  (kostenfrei)
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