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Biomedical Research Projects

Representing work conducted as a Graduate Researcher in Dr. Torres Laboratory Specializing in Molecular Pharmacology & Neuroscience

Loyola Stritch School of Medicine - Center for Translational Research

Profiling Drug Mediated SERT activity with False Fluorescent Neurotransmitters

Our team developed a preliminary drug screening assay aimed at investigating serotonin (5-HT) transport through the serotonin transporter (SERT). This assay utilizes False Fluorescent Neurotransmitter 246 (FFN-246) to precisely measure the uptake of 5-HT, providing valuable insights into SERT activity. By incorporating FFN-246, a photosensitive fluorescent probe, we achieved enhanced resolution and accuracy in characterizing serotonin transport dynamics. This approach not only advances our collective understanding of SERT function but also holds potential for identifying novel pharmacological agents to modulate serotonin pathways, offering new avenues for therapeutic intervention in neuropharmacological research.

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False Fluorescent Neurotransmitters

False Fluorescent Neurotransmitters (FFNs) are synthetic compounds engineered to mimic natural neurotransmitters while incorporating fluorescent properties. These compounds enable researchers to study neurotransmitter dynamics and interactions with high precision. By fluorescing under specific light conditions, FFNs allow for real-time visualization and tracking of neurotransmitter activity ex vivo and in vitro

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Synaptic Neurotransmission

Monoamine neurotransmission occurs within the synaptic cleft, where serotonin is released and binds to the postsynaptic receptor, promoting signal transduction. The serotonin transporter (SERT) reuptakes serotonin after release, regulating 5-HT levels and maintaining balance. Understanding the functionality of SERT with FFN246 is crucial for addressing novel therapeutic pathways for mental health disorders associated with serotonin signaling dysfunction.

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Serotonergic Pathways

Serotonergic pathways in the brain, originating primarily from the raphe nuclei, project to diverse regions including the cortex, limbic system, and spinal cord. These pathways play a critical role in regulating mood, emotion, and cognition. Disruptions in these pathways are linked to disorders such as depression and anxiety, emphasizing serotonin’s significance in brain function.

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