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Quadros, I. M. H.

Publications and source records attributed to Quadros, I. M. H..

2 recordsLinked to original sources

Alcohol or stress exposure during late adolescence impairs risk assessment later in life, disrupting the ethological structure of behavior in mice

BackgroundDecision-making is a key component of adaptive behavior and relies on risk assessment as a critical process that enables organisms to evaluate threats before exploring potentially dangerous areas. During adolescence, this process is particularly vulnerable to disruption by external factors such as stress and substance use, potentially leading to changes in the structure of defensive and exploratory behaviors, potentially leading to riskier choices. MethodsWe investigated whether repeated ethanol intoxication or pharmacological stress during late adolescence (7-8 weeks of age) alters overall behavioral structure, focusing on risk assessment behaviors, in adulthood. Male and female C57BL/6 mice received four intermittent injections of saline, ethanol (4.0 g/kg), or the 2-adrenergic antagonist yohimbine (2.0 mg/kg). In early adulthood (9th week), animals were tested in the Light-Dark Box and Elevated Plus Maze. In addition to traditional anxiety-like behavior and exploratory measures, risk assessment behaviors (stretches and head outs) were classified as NoGo (risk evaluation without entering the aversive area) or Go (risk evaluation followed by exploration), and behavioral organization was examined using first-order Markov chain analyses. ResultsBoth ethanol and yohimbine exposure produced persistent reductions in NoGo risk assessment behaviors in adulthood, in both sexes, with minimal effects on classical anxiety-like measures. Correlation and transition probability analyses revealed a reorganization of behavioral structure, characterized by reduced transitions toward risk assessment events and a bias toward risk-taking actions. ConclusionsThese findings indicate that repeated late adolescent alcohol intoxication and stress exposure induce long-lasting alterations in risk assessment and decision-making strategies.

animal behavior and cognition↗

Pursuing reconsolidation in ethanol-CPP: memory reactivation in different conditions did not trigger destabilization

Consolidated memories can return to a labile state during retrieval, through destabilization, and must be reconsolidated to persist. Associative memories of contextual cues paired with hedonic effects of drugs of abuse exert a pivotal role in maintaining maladaptive behaviors in addiction. Thus, impairment of reconsolidation of drug-associated memories may provide a potential strategy to reduce drug-seeking and relapse in addiction. It is critical to understand the conditions under which a consolidated memory becomes labile and may undergo reconsolidation. After inducing ethanol Conditioned Place Preference (CPP; 2 g/kg ethanol, i.p.) in male mice, we examined different parameters during the reactivation session that could turn memory susceptible to disruption by systemic injection of the protein synthesis inhibitor cycloheximide (CHX, 100 mg/kg, i.p.). Reactivation with free access to the apparatus (similarly to a Test session, for 10, 5, or 3 min) or Reactivation sessions restricted to ethanol-paired compartment with no ethanol (for 10 or 5 min), or with the administration of a low dose of ethanol (5 min session), failed to reduced ethanol-preference after CHX administration. These findings suggest that boundary conditions constraint memory in ethanol-CPP to undergo reconsolidation.

neuroscience↗