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Peer-reviewedCC BY 4.0Frontiers in Pharmacology

Trans-anethole attenuates streptozotocin-induced cognitive dysfunction by modulating oxidative stress and cholinergic activity

  1. 1Department of Pharmacology, NGSM Institute of Pharmaceutical Sciences (NGSMIPS), Nitte (Deemed to be University)
  2. 2Silicon Script Sciences Pvt. Ltd.

Abstract

Introduction: Cognitive impairment is a neurological disorder defined as an inability to learn, think, judge, remember, and make decisions. The primary cause of chronic, age- related cognitive decline is Alzheimer’s disease (AD), which is frequently studied as a representative model. The current therapies for AD provide only symptomatic relief, which necessitates the need for safer, multi-target treatments. Trans- anethole, the primary constituent of Illicium verum , Pimpinella anisum , and Foeniculum vulgare , is an aromatic molecule that possesses several pharmacological activities, including anti-inflammatory and antioxidant effects, which may have neuroprotective benefits.

Methods: The current study integrated in silico , in vitro , and in vivo approaches to examine the neuroprotective potential of trans- anethole. In silico studies were carried out to find out the potential molecular targets and pathways associated with the effects of trans-anethole against AD- related cognitive dysfunction. Cytotoxicity, antioxidant activity, and cholinesterase inhibition were assessed in vitro on BV2 cells. Intracerebroventricular (ICV) administration of streptozotocin (STZ: 3 mg/kg) in rats induces an insulin-resistant brain state leading to progressive cognitive and memory impairment, a condition that closely relates to sporadic Alzheimer’s disease. ICV-STZ-induced Wistar rats were used to assess the effect of trans- anethole on AD-related cognitive dysfunction through behavioral, biochemical, and histopathological assessments.

Results: A total of 174 common targets were identified, enriching pathways including apoptosis, AGE-RAGE, TNF, and PI3K- Akt signaling. Stable interactions were observed in molecular docking and molecular dynamics simulations. Trans-anethole demonstrates moderate cholinesterase inhibition and antioxidant activity in BV2 cells. Comparing STZ- treated rats to disease control, trans-anethole at doses of 100 mg/kg and 400 mg/kg significantly reduced lipid peroxidation, restored antioxidant enzyme levels, and attenuated cholinergic dysfunction. Histopathological findings showed qualitative preservation of hippocampal neuronal morphology.

Discussion: Overall, these findings suggest that trans-anethole may represent a potential neuroprotective preclinical candidate for further investigation in Alzheimer’s disease-related cognitive dysfunction.

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BibTeX
@article{mole2026transanethole,
  title = {{Trans-anethole attenuates streptozotocin-induced cognitive dysfunction by modulating oxidative stress and cholinergic activity}},
  author = {Shruti S. Mole and Prarambh S. R. Dwivedi and Wilona Loren Lobo and C. S. Shastry and Pukar Khanal},
  journal = {Frontiers in Pharmacology},
  year = {2026},
  month = oct,
  doi = {10.3389/fphar.2026.1954658},
  url = {https://www.frontiersin.org/articles/10.3389/fphar.2026.1954658/full},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Trans-anethole attenuates streptozotocin-induced cognitive dysfunction by modulating oxidative stress and cholinergic activity
AU  - Shruti S. Mole
AU  - Prarambh S. R. Dwivedi
AU  - Wilona Loren Lobo
AU  - C. S. Shastry
AU  - Pukar Khanal
PY  - 2026
DA  - 2026/10/16
JO  - Frontiers in Pharmacology
DO  - 10.3389/fphar.2026.1954658
UR  - https://www.frontiersin.org/articles/10.3389/fphar.2026.1954658/full
AB  - Introduction: Cognitive impairment is a neurological disorder defined as an inability to learn, think, judge, remember, and make decisions. The primary cause of chronic, age- related cognitive decline is Alzheimer’s disease (AD), which is frequently studied as a representative model. The current therapies for AD provide only symptomatic relief, which necessitates the need for safer, multi-target treatments. Trans- anethole, the primary constituent of Illicium verum , Pimpinella anisum , and Foeniculum vulgare , is an aromatic molecule that possesses several pharmacological activities, including anti-inflammatory and antioxidant effects, which may have neuroprotective benefits.  Methods: The current study integrated in silico , in vitro , and in vivo approaches to examine the neuroprotective potential of trans- anethole. In silico studies were carried out to find out the potential molecular targets and pathways associated with the effects of trans-anethole against AD- related cognitive dysfunction. Cytotoxicity, antioxidant activity, and cholinesterase inhibition were assessed in vitro on BV2 cells. Intracerebroventricular (ICV) administration of streptozotocin (STZ: 3 mg/kg) in rats induces an insulin-resistant brain state leading to progressive cognitive and memory impairment, a condition that closely relates to sporadic Alzheimer’s disease. ICV-STZ-induced Wistar rats were used to assess the effect of trans- anethole on AD-related cognitive dysfunction through behavioral, biochemical, and histopathological assessments.  Results: A total of 174 common targets were identified, enriching pathways including apoptosis, AGE-RAGE, TNF, and PI3K- Akt signaling. Stable interactions were observed in molecular docking and molecular dynamics simulations. Trans-anethole demonstrates moderate cholinesterase inhibition and antioxidant activity in BV2 cells. Comparing STZ- treated rats to disease control, trans-anethole at doses of 100 mg/kg and 400 mg/kg significantly reduced lipid peroxidation, restored antioxidant enzyme levels, and attenuated cholinergic dysfunction. Histopathological findings showed qualitative preservation of hippocampal neuronal morphology.  Discussion: Overall, these findings suggest that trans-anethole may represent a potential neuroprotective preclinical candidate for further investigation in Alzheimer’s disease-related cognitive dysfunction.
SN  - 1663-9812
ER  -