Melatonin Rescues the Dendrite Collapse Induced by the Pro-Oxidant Toxin Okadaic Acid in Organotypic Cultures of Rat Hilar Hippocampus

Autor: Aline Domínguez-Alonso, Eduardo Calixto, Jesús Argueta, Marcela Valdés-Tovar, Héctor Solís-Chagoyán, Gloria Benítez-King, Zuly A Sánchez-Florentino
Rok vydání: 2020
Předmět:
hippocampus
education
Pharmaceutical Science
melatonin
DNA fragmentation
Hippocampal formation
medicine.disease_cause
Article
Analytical Chemistry
lcsh:QD241-441
Melatonin
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
lcsh:Organic chemistry
okadaic acid
Drug Discovery
medicine
Animals
hilus
dendrite complexity
DAPI
Physical and Theoretical Chemistry
Cognitive decline
030304 developmental biology
0303 health sciences
TUNEL assay
Organic Chemistry
Neurodegeneration
neurodegeneration
Dendrites
Okadaic acid
Oxidants
medicine.disease
Immunohistochemistry
humanities
Rats
Cell biology
Organoids
Oxidative Stress
Neuroprotective Agents
chemistry
Chemistry (miscellaneous)
Molecular Medicine
Reactive Oxygen Species
Oxidation-Reduction
030217 neurology & neurosurgery
Oxidative stress
medicine.drug
Zdroj: Molecules, Vol 25, Iss 5508, p 5508 (2020)
Molecules
Volume 25
Issue 23
ISSN: 1420-3049
Popis: The pro-oxidant compound okadaic acid (OKA) mimics alterations found in Alzheimer&rsquo
s disease (AD) as oxidative stress and tau hyperphosphorylation, leading to neurodegeneration and cognitive decline. Although loss of dendrite complexity occurs in AD, the study of this post-synaptic domain in chemical-induced models remains unexplored. Moreover, there is a growing expectation for therapeutic adjuvants to counteract these brain dysfunctions. Melatonin, a free-radical scavenger, inhibits tau hyperphosphorylation, modulates phosphatases, and strengthens dendritic arbors. Thus, we determined if OKA alters the dendritic arbors of hilar hippocampal neurons and whether melatonin prevents, counteracts, or reverses these damages. Rat organotypic cultures were incubated with vehicle, OKA, melatonin, and combined treatments with melatonin either before, simultaneously, or after OKA. DNA breaks were assessed by TUNEL assay and nuclei were counterstained with DAPI. Additionally, MAP2 was immunostained to assess the dendritic arbor properties by the Sholl method. In hippocampal hilus, OKA increased DNA fragmentation and reduced the number of MAP2(+) cells, whereas melatonin protected against oxidation and apoptosis. Additionally, OKA decreased the dendritic arbor complexity and melatonin not only counteracted, but also prevented and reversed the dendritic arbor retraction, highlighting its role in post-synaptic domain integrity preservation against neurodegenerative events in hippocampal neurons.
Databáze: OpenAIRE
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