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Related Concept Videos

Brain Imaging01:14

Brain Imaging

Brain imaging technologies provide critical insights into both the structure and function of the human brain, enabling medical professionals and researchers to diagnose, study, and treat neurological disorders or psychiatric disorders more effectively.
These technologies include computerized axial tomography (CAT or CT scans), positron-emission tomography (PET scans),  magnetic resonance imaging (MRI),  functional magnetic resonance imaging (fMRI), and Transcranial Magnetic Stimulation (TMS).
Cognitive Enhancers: Cholinesterase Inhibitors and NMDA Receptor Antagonists01:30

Cognitive Enhancers: Cholinesterase Inhibitors and NMDA Receptor Antagonists

Cognitive enhancers, also known as "smart drugs," are substances used to enhance memory, mental alertness, and concentration. These can be natural or synthetic and improve cognition in conditions like Alzheimer's disease (AD) and other neurodegenerative diseases. Some common examples include caffeine, amphetamines, methylphenidate, modafinil, arecoline, donepezil, vortioxetine, and piracetam. These enhancers work on the principle of synaptic plasticity and altered circuit function. They...
Antidepressant Drugs: MAOIs and Other Agents01:23

Antidepressant Drugs: MAOIs and Other Agents

Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
Drugs Affecting Neurotransmitter Release or Uptake01:21

Drugs Affecting Neurotransmitter Release or Uptake

Certain drugs can affect how neurotransmitters called catecholamines, are released or taken back up in the adrenergic neuron. They can have different effects on the body's sympathetic transmission. Reserpine, a natural compound found in the Rauwolfia shrub, blocks a transporter called vesicular monoamine transporter (VMAT), which leads to a buildup of catecholamines in the cell and reduces sympathetic transmission. Another drug called guanethidine works in multiple ways, including blocking...
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein01:20

Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein

Antiepileptic drugs, such as levetiracetam (Keppra) and brivaracetam (Briviact), have emerged as crucial tools in managing epilepsy. These medications exert their therapeutic effects by targeting the synaptic vesicle protein SV2A, a transmembrane glycoprotein primarily found in the brain.
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
Transducer Mechanism: Nuclear Receptors01:31

Transducer Mechanism: Nuclear Receptors

Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:

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Related Experiment Video

Updated: Jun 6, 2026

Focused Ultrasound Induced Blood-Brain Barrier Opening for Targeting Brain Structures and Evaluating Chemogenetic Neuromodulation
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Focused Ultrasound Induced Blood-Brain Barrier Opening for Targeting Brain Structures and Evaluating Chemogenetic Neuromodulation

Published on: December 22, 2020

Selective estrogen receptor modulators as brain therapeutic agents.

María Angeles Arevalo1, María Santos-Galindo, Natalia Lagunas

  • 1Instituto Cajal, CSIC, Avenida Doctor Arce 37, E-28002 Madrid, Spain.

Journal of Molecular Endocrinology
|November 13, 2010
PubMed
Summary

Selective estrogen receptor modulators (SERMs) show neuroprotective effects, reducing neural damage in various brain conditions. Novel SERMs targeting neurons and glial cells offer potential new brain therapies.

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Protocol for Studying Extinction of Conditioned Fear in Naturally Cycling Female Rats
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Protocol for Studying Extinction of Conditioned Fear in Naturally Cycling Female Rats

Published on: February 23, 2015

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Last Updated: Jun 6, 2026

Focused Ultrasound Induced Blood-Brain Barrier Opening for Targeting Brain Structures and Evaluating Chemogenetic Neuromodulation
08:37

Focused Ultrasound Induced Blood-Brain Barrier Opening for Targeting Brain Structures and Evaluating Chemogenetic Neuromodulation

Published on: December 22, 2020

Protocol for Studying Extinction of Conditioned Fear in Naturally Cycling Female Rats
09:07

Protocol for Studying Extinction of Conditioned Fear in Naturally Cycling Female Rats

Published on: February 23, 2015

Area of Science:

  • Neuroscience
  • Pharmacology
  • Endocrinology

Background:

  • Selective estrogen receptor modulators (SERMs) are clinically used for breast cancer, osteoporosis, and menopausal symptoms.
  • SERMs exert effects beyond reproductive tissues, including the central nervous system.
  • Emerging evidence suggests SERMs possess neuroprotective properties.

Purpose of the Study:

  • To review the neurobiological effects of SERMs.
  • To explore the potential of SERMs in treating neurological and psychiatric disorders.
  • To highlight the therapeutic promise of novel SERMs for brain health.

Main Methods:

  • Literature review of preclinical and clinical studies on SERMs and the nervous system.
  • Analysis of experimental models for neural trauma, neuroinflammation, neurodegeneration, cognitive impairment, and affective disorders.
  • Examination of the molecular mechanisms underlying SERM neuroprotection.

Main Results:

  • Certain SERMs demonstrate neuroprotective effects across diverse experimental models.
  • SERMs have shown efficacy in reducing neural damage and improving outcomes in models of brain injury and disease.
  • Specific SERMs modulate neuronal and glial cell functions.

Conclusions:

  • SERMs represent a class of drugs with significant potential for treating a range of brain disorders.
  • Targeting specific neuronal and glial pathways with novel SERMs could lead to innovative therapeutic strategies.
  • Further research into SERM neurobiology is warranted to optimize their clinical application in neurology and psychiatry.