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Digestion begins with a cephalic phase that prepares the digestive system to receive food. When our brain processes visual or olfactory information about food, it triggers impulses in the cranial nerves innervating the salivary glands and stomach to prepare for food.
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Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and microglia. Abnormal...
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Related Experiment Video

Updated: May 16, 2026

Real-Time Fluorescent Measurement of Synaptic Functions in Models of Amyotrophic Lateral Sclerosis
08:59

Real-Time Fluorescent Measurement of Synaptic Functions in Models of Amyotrophic Lateral Sclerosis

Published on: July 16, 2021

Neuroproteomics: an insight into ALS.

D M F Mendonça1, L Pizzati, K Mostacada

  • 1Departamento de Biociências, Universidade Federal de Sergipe, Sergipe, Brazil. deise_mendonca@ufs.br

Neurological Research
|November 14, 2012
PubMed
Summary
This summary is machine-generated.

Researchers identified novel protein biomarkers in cerebrospinal fluid (CSF) for amyotrophic lateral sclerosis (ALS). Proteins involved in iron, zinc binding, and the ubiquitin-proteasome pathway were found in ALS patients, offering new diagnostic possibilities.

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Area of Science:

  • Neuroscience
  • Biochemistry
  • Proteomics

Background:

  • Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with unknown causes.
  • Current ALS diagnosis relies on clinical examination and exclusion of other conditions, lacking definitive biomarkers.
  • The ubiquitin-proteasome system and metal ion homeostasis are implicated in ALS pathogenesis.

Purpose of the Study:

  • To identify differentially expressed proteins in cerebrospinal fluid (CSF) of ALS patients compared to controls.
  • To discover a panel of potential protein biomarkers for ALS diagnosis.
  • To investigate the role of identified proteins in ALS pathophysiology.

Main Methods:

  • Proteomic analysis of CSF samples from ALS patients and healthy controls.
  • Two-dimensional (2D) electrophoresis to separate proteins.
  • Matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry for protein identification.

Main Results:

  • Several differentially expressed proteins were identified in ALS CSF.
  • Proteins including parkin-like and various iron and zinc binding proteins were found at altered levels.
  • These findings suggest potential links between protein dysregulation, metal ion metabolism, and the ubiquitin-proteasome system in ALS.

Conclusions:

  • The identified proteins represent potential biomarkers for ALS diagnosis.
  • Findings contribute to understanding the molecular mechanisms underlying ALS.
  • Further research into these proteins may advance ALS diagnostics and therapeutics.