


Learn the science behind constant dopamine release within daily life influencing teen impulsivity behavior.
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Natural sugar is replaced with
Artificial sweeteners in Zero Sugar Coke

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Increasing impulsive suicide rates in teenagers
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Increasing consumption of zero sugar beverages
Potential correlation between consumption of zero sugar beverages and impulsive suicides in teenagers

Methodology



FoxP
Shaker
BTBD9
Neuropsychological Biomarker Genes
1. FoxP - Functioning of the nervous system (e.g. decision- making)
2. Shaker - Neuronal excitability and muscle contraction (e.g. sleep deprivation, performance decline)
3. BTBD9 - Iron metabolism (e.g. restless legs syndrome)
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3. Neuropsychological Biomarker Genes
1. Total RNA Extraction
1. Impulsivity Behavior Test
4. Gel electrophoresis

Image J software
Chemidoc
Exposure through food
Exposure through cotton lids of test tubes
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Propionic Acid
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Cinnamon Extract
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Heat
Deterrent
Stimulus
2. Drosophila Reproduction & Development
Impulsivity
Self control
Heat (>32C) - LED strap
Newly emerged flies were counted through empty pupa cases

2. cDNA synthesis
3. PCR
Results
1. Impulsivity Behavior Test - 1st generation
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2. Drosophila Reproduction and Development - 2nd generation

3. Neuropsychological Biomarker Genes
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2nd generation
1st generation
1st generation
exposed to artificial sweeteners
2nd generation
impulsivity
Conclusion


Examining the generational impulsiveness from Zero Sugar Drinks
and exploring preventive strategies through psychobiotics
Artificial sweeteners (AS), widely used as sugar substitutes in beverages, have been increasingly associated with gut microbiome imbalance and elevated depression risk. Given their growing prevalence in modern diets, particularly through zero-sugar beverages, concerns have emerged regarding their potential effects on behavior and cognitive function. Notably, the surge in zero-sugar beverage consumption since 2018 coincides with rising impulsive suicide rates among adolescents, suggesting a possible causal relationship between AS exposure and impulsivity. This research investigates the effects of two prevalent artificial sweeteners, sucralose and acesulfame potassium, commonly found in beverages like Coke Zero and Sprite Zero Sugar, on impulsivity-related behaviors in Drosophila melanogaster across two generations, utilizing neuropsychological biomarker gene expression to assess cognitive impact. Flies were exposed to varying AS concentrations, and their behavioral responses were quantified under stimuli designed to elicit impulsive versus self-controlled behaviors. Reproductive and developmental parameters were also monitored. Additionally, psychobiotics specifically Lactobacillus acidophilus and Levilactobacillus brevis were evaluated as potential interventions. Research demonstrated that AS exposure significantly increased impulsive behavior, evidenced by greater tendency to engage in risk-taking behaviors under thermal stress conditions with cinnamon and propionic acid serving as behavioral stimulants. Gene expression analysis revealed notable upregulation of neuropsychological biomarkers, specifically BTBD9 and Shaker, which are associated with depression and neural excitability, respectively. Critically, the introduction of psychobiotics in the parental generation normalized these elevated expression levels in the offspring, suggesting transgenerational prevention and a therapeutic avenue for mitigating the adverse effects of AS consumption. Overall, this study demonstrates that artificial sweeteners can induce heritable impulsivity, as a psychological stimulant, while psychobiotics may counteract these effects across generations. These findings establish a foundation for future investigations into gut-brain axis interactions and their implications for dietary recommendations, with relevance to public health policies regarding artificial sweetener consumption in human diets.
Title

Susceptible dopamine exposure from prevalent SNS usage
Homicides perpetrated by juveniles
jumped 65% from 2016 to 2022

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Most Risky Env
Typical Env
Most Protective Env
The dopaminergic system is related to delinquent behavior among adolescents

Methodology
1. Drosophila melanogaster
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2. Human Brain Cells
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3. Neuropsychological Biomarker Genes
1. Total RNA Extraction
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2. cDNA synthesis
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3. PCR

4. Gel electrophoresis


Image J software
Chemidoc



FoxP
Shaker
BTBD9
Neuropsychological Biomarker Genes
1. FoxP - Functioning of the nervous system (e.g. decision- making)
2. Shaker - Neuronal excitability and muscle contraction (e.g. sleep deprivation, performance decline)
3. BTBD9 - Iron metabolism (e.g. restless legs syndrome)
Results
1.1 Drosophila - Generational Dopamine Exposure
1.2 Drosophila - Natural Product Intervention
2.1 Human Brain Cell (without LPS)







2.2 Human Brain Cell (with LPS)
Conclusion
Transgenerational dopamine-activated genes linked to delinquent behavior and the therapeutic potential of natural products
Delinquent behavior emerges from complex interactions between genetic predisposition and environmental factors, with dopamine–a neurotransmitter central to reward processing and decision-making–playing a key regulatory role. The proliferation of technology and social media has exacerbated dopamine dysregulation, particularly among Generation Z, contributing to heightened impulsivity, addictive behaviors, and mental health disorders. While dopamine imbalance is increasingly recognized as a significant factor in the manifestation of delinquent behaviors, the genetic mechanisms underlying this relationship remain poorly understood. This study examines the expression of neuropsychological biomarker genes associated with dopamine-mediated behavior across two generations, employing both Drosophila melanogaster and human brain nerve cells, with particular emphasis on intergenerational inheritance and lipopolysaccharide (LPS)-induced inflammatory models. Drosophila were exposed to dopamine alongside phytogenic compounds such as turmeric, ashwagandha, and cinnamon, to assess their capacity to reverse dopamine-induced dysregulation of key biomarker genes including BDNF, SERT, and DAT1. Findings revealed notable intergenerational amplification of gene dysregulation, indicating that chronic dopamine exposure alters epigenetic mechanisms and compounds behavioral and cognitive deficits across generations. Natural products demonstrated efficacy in modulating dopamine signaling through antioxidative and epigenetic pathways, with significant normalization of gene expression patterns associated with impulsivity and risk-taking behaviors. However, certain compounds produced effects exceeding baseline levels, underscoring the critical need for precise dosage optimization in therapeutic applications. LPS-induced inflammation further revealed compensatory and maladaptive neural responses, adding complexity to the dopamine-delinquency pathway. These findings establish dopamine as a key mediator of both immediate behavior dysregulation and hereditary vulnerabilities, providing a foundation for biologically informed interventions that bridge genetic susceptibility and behavioral resilience in at-risk populations.