Bambuterol: A New Hope for Alzheimer’s Disease?


Newsletter # 128


In vivo studies


Bambuterol, a long-acting β₂-adrenergic agonist widely used in respiratory medicine, has recently attracted interest as a candidate in the field of neurodegenerative disease. Originally developed as a bronchodilator, Bambuterol is gaining scientific interest for its potential to enhance cognition and protect neurons, thanks to its effects on adrenergic signaling, cholinergic modulation, and anti-inflammatory pathways. Drug repurposing using established medicines for new therapeutic indications offers a faster, lower-risk path to innovation in Alzheimer’s disease (AD). Bambuterol’s established human safety profile, oral bioavailability, and blood–brain barrier permeability makes it particularly well-suited for rapid translation. Its dual-action potential combining cognitive enhancement with neuroprotection further strengthens its appeal as a next-generation AD candidate.
Our recent preclinical study utilized a scopolamine-induced model to evaluate Bambuterol’s impact on cognitive performance. Scopolamine disrupts cholinergic signaling, leading to deficits comparable to those seen in Alzheimer’s disease. In this model, Bambuterol produced a dose-dependent reversal of these impairments, restoring cognitive performance to near-baseline levels.

Importantly, these results build on previously published preclinical evidence [DOI: 10.1038/s42003-025-07599-7]) showing Bambuterol’s neuroprotective effects in amyloid-related models. Together, these independent lines of research strengthen the scientific rationale for its repurposing in Alzheimer’s disease.
While further investigation is required, Bambuterol’s strong safety record, pharmacological versatility, and demonstrated cognitive benefits highlight its potential as a transformative therapy for Alzheimer’s and related disorders. As research advances, this familiar respiratory drug could support new avenues of therapeutic exploration in memory related cognitive health.


  • **, p≤0.01, ***p≤0.001, vs scopolamine + placebo (red column).
  • The graph illustrates mice’s cognitive performance measured through spontaneous alternation in the T-maze, a widely used test for assessing rodent cognition in a single session. In cognitively intact mice (Saline/Placebo, white column), a high rate of alternation is observed as they naturally prefer to explore a novel arm over one recently visited. Administration of 1 mg/kg scopolamine induces a cognitive deficit, reducing alternation to levels below 50%. This indicates the emergence of stereotypy (repetitive behavior) and thus cognitive deficit (red column).





Bambuterol administration shows a dose-dependent restoration of alternation performance (red vs. blue columns), demonstrating its potent cognitive-enhancing potential.

If you are interested in these models and would like to learn more about them or other models and assays available at NEUROFIT, please visit our website : THERAPEUTIC AREA or TESTS sections


NEUROFIT offers a range of validated in vitro and in vivo screening tests for psychiatry and neurology.

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