Tolfenamic Acid Prevents Amyloid β-induced Olfactory Bulb Dysfunction In Vivo
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Updated: Feb 14, 2026

Ex Vivo Preparations of the Intact Vomeronasal Organ and Accessory Olfactory Bulb
Published on: August 4, 2014
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.
Background:
Amyloid beta inhibits olfactory bulb function. The mechanisms involved in this effect must include alterations in network excitability, inflammation and the activation of different transduction pathways. Thus, here we tested whether tolfenamic acid, a drug that modulates several of these pathological processes, could prevent amyloid beta-induced olfactory bulb dysfunction.
Objective:
To test whether tolfenamic acid prevents amyloid beta-induced alterations in olfactory bulb network function, olfaction and GSK3β activity.
Method:
The protective effects of tolfenamic acid against amyloid beta-induced population activity inhibition were tested in olfactory bulb slices from adult mice, while tolfenamic acid and amyloid beta were bath-applied. We also tested the effects of amyloid-beta in slices obtained from animals pre-treated chronically (21 days) with tolfenamic acid. The effects of amyloid beta micro-injected into the olfactory bulbs were also tested, after two weeks, on olfactory bulb population activity and olfaction in control and tolfenamic acid chronically treated animals. Olfaction was assessed with the odor-avoidance and the habituation/cross-habituation tests. GSK3β activation was evaluated with Western-blot.
Results:
Acute bath application of tolfenamic acid does not prevent amyloid beta-induced inhibition of olfactory bulb network activity in vitro. In contrast, chronic treatment with tolfenamic acid renders the olfactory bulb resistant to amyloid beta-induced network activity inhibition in vitro and in vivo, which correlates with the inhibition of GSK3β activation and the protection against amyloid beta-induced olfactory dysfunction.
Conclusion:
Our data further support the use of tolfenamic acid to prevent amyloid beta-induced pathology and the early symptoms of Alzheimer Disease.
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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