Tolfenamic Acid Prevents Amyloid β-induced Olfactory Bulb Dysfunction In Vivo

Jose M Cornejo-Montes-de-Oca1, Rebeca Hernández-Soto1, Arturo G Isla1

  • 1Departamento de Neurobiología del Desarrollo y Neurofisiología, Instituto de Neurobiología, Universidad Nacional Autónoma de Mexico, Queretaro, Qro., 76230, Mexico.

Current Alzheimer Research
|February 24, 2018
PubMed
Abstract

Insights

Chronic treatment with tolfenamic acid protects the olfactory bulb from amyloid beta-induced dysfunction. This effect is linked to reduced GSK3β activation, offering potential for Alzheimer

Area of Science:

  • Neuroscience
  • Pharmacology

Background:

  • Amyloid beta (Aβ) accumulation in the olfactory bulb disrupts network excitability, inflammation, and signaling pathways.
  • Olfactory bulb dysfunction is an early indicator of neurodegenerative diseases like Alzheimer's Disease (AD).

Purpose of the Study:

  • To investigate whether tolfenamic acid can prevent Aβ-induced olfactory bulb dysfunction.
  • To assess the impact of tolfenamic acid on olfactory bulb network activity, olfaction, and GSK3β activity in the presence of Aβ.

Main Methods:

  • In vitro studies using mouse olfactory bulb slices exposed to tolfenamic acid and Aβ.
  • In vivo studies involving chronic tolfenamic acid treatment in mice before Aβ administration.
  • Assessment of olfactory function using odor-avoidance and habituation/cross-habituation tests.
  • Evaluation of GSK3β activation via Western blot analysis.

Main Results:

  • Acute tolfenamic acid application did not prevent Aβ-induced inhibition of olfactory bulb network activity.
  • Chronic tolfenamic acid treatment conferred resistance to Aβ-induced network activity inhibition both in vitro and in vivo.
  • Chronic treatment correlated with inhibited GSK3β activation and protected against Aβ-induced olfactory dysfunction.

Conclusions:

  • Chronic administration of tolfenamic acid effectively prevents Aβ-induced olfactory bulb pathology.
  • Tolfenamic acid shows promise in mitigating early AD symptoms associated with olfactory dysfunction.

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