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Brain networks associated with mood regulation represent a complex system of integrated neural circuits responsible for the generation, processing, and modulation of emotional states. These networks primarily involve the cortico-limbic circuit, including key nodes such as the prefrontal cortex, amygdala, hippocampus, and anterior cingulate cortex, which coordinate to balance bottom-up emotional triggers with top-down cognitive control [8, 11]. Dysregulation within these networks—characterized by aberrant functional connectivity or impaired neuroplasticity—is a central feature of psychiatric disorders like major depressive disorder and bipolar disorder [3, 7]. Pharmacological treatments, such as SSRIs and ketamine, work by modulating neurotransmitter systems (serotonin, glutamate) to restore healthy network dynamics and promote synaptic growth [15, 19]. Additionally, these networks serve as direct targets for neuromodulation therapies like Transcranial Magnetic Stimulation (TMS), which aim to recalibrate electrical activity in specific cortical regions to alleviate mood symptoms [6, 10]. Understanding these systems is vital for the development of precision medicine approaches that target the specific neural substrates of emotional dysfunction.
Drugs modulate neurotransmitter signaling (e.g., serotonin, glutamate) and activate intracellular pathways (e.g., mTOR, BDNF) to enhance synaptic plasticity and normalize functional connectivity between cortical and limbic regions [3, 15].
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