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Updated: Jul 18, 2026

Investigating Long-term Synaptic Plasticity in Interlamellar Hippocampus CA1 by Electrophysiological Field Recording
Published on: August 11, 2019
Is hippocampal atrophy a future drug target?
Vikas Dhikav1, Kuljeet Singh Anand
1Department of Pharmacology, All India Institute of Medical Sciences, New Delhi 110029, India. vikasdhikav@hotmail.com
Hippocampal atrophy, common in neurological and psychiatric disorders, may precede symptoms. Several drugs show potential in preventing atrophy, raising questions about therapeutic targets for conditions like Alzheimer's disease.
Area of Science:
- Neuroscience
- Neurology
- Psychiatry
Background:
- Hippocampal atrophy is a hallmark of numerous neurological and psychiatric conditions, including Alzheimer's disease, depression, and schizophrenia.
- This atrophy can precede symptom onset or correlate with disease progression, impacting memory and cognition.
- Factors such as stress, glucocorticoids, and neurotransmitters contribute to hippocampal structural changes.
Purpose of the Study:
- To explore the role of hippocampal atrophy in the development and progression of various neurological and psychiatric disorders.
- To investigate the potential of pharmacological interventions in preventing or reversing hippocampal atrophy.
- To assess the clinical utility of targeting hippocampal atrophy as a therapeutic strategy.
Main Methods:
- Review of existing literature on hippocampal atrophy in neurological and psychiatric disorders.
- Analysis of studies investigating the effects of various drugs on hippocampal structure and plasticity.
- Examination of the relationship between hippocampal atrophy and disease symptomatology and progression.
Main Results:
- Hippocampal atrophy is consistently observed across a spectrum of brain disorders and aging.
- Multiple drug classes, including antidepressants, anticonvulsants, and antipsychotics, demonstrate the ability to prevent hippocampal atrophy.
- These drugs exhibit diverse mechanisms, affecting structural plasticity, neuroprotection, and neurogenesis.
Conclusions:
- Hippocampal atrophy is a significant pathological feature with implications for disease genesis and progression.
- Pharmacological prevention of atrophy holds promise as a therapeutic avenue, necessitating further research into optimal drug selection, dosage, and timing.
- Targeting hippocampal atrophy could offer a novel strategy for managing neurological and psychiatric conditions, potentially improving patient outcomes.
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