» Articles » PMID: 32132227

Anatomy and Function of the Fornix in the Context of Its Potential As a Therapeutic Target

Overview
Date 2020 Mar 6
PMID 32132227
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

The fornix is a white matter bundle located in the mesial aspect of the cerebral hemispheres, which connects various nodes of a limbic circuitry and is believed to play a key role in cognition and episodic memory recall. As the most prevalent cause of dementia, Alzheimer's disease (AD) dramatically impairs the quality of life of patients and imposes a significant societal burden on the healthcare system. As an established treatment for movement disorders, deep brain stimulation (DBS) is currently being investigated in preclinical and clinical studies for treatment of memory impairment in AD by modulating fornix activity. Optimal target and stimulation parameters to potentially rescue memory deficits have yet to be determined. The aim of this review is to consolidate the structural and functional aspects of the fornix in the context of neuromodulation for memory deficits. We first present an anatomical and functional overview of the fibres and structures interconnected by the fornix. Recent evidence from preclinical models suggests that the fornix is subdivided into two distinct functional axes: a septohippocampal pathway and a subiculothalamic pathway. Each pathway's target and origin structures are presented, followed by a discussion of their oscillatory dynamics and functional connectivity. Overall, neuromodulation of each pathway of the fornix is discussed in the context of evidence-based forniceal DBS strategies. It is not yet known whether driving fornix activity can enhance cognition-optimal target and stimulation parameters to rescue memory deficits have yet to be determined.

Citing Articles

Neuronal Network Activation Induced by Forniceal Deep Brain Stimulation in Mice.

Tang B, Wu Z, Wang Q, Tang J Genes (Basel). 2025; 16(2).

PMID: 40004540 PMC: 11855867. DOI: 10.3390/genes16020210.


Disproportional smaller fornix with altered microstructure in pediatric multiple sclerosis shown by high-resolution fluid-suppressed diffusion tractography.

Weber C, Wilbur C, Blevins G, Beaulieu C Mult Scler J Exp Transl Clin. 2025; 11(1):20552173251315161.

PMID: 39895880 PMC: 11783520. DOI: 10.1177/20552173251315161.


Lateral hypothalamic area high-frequency deep brain stimulation rescues memory decline in aged rat: behavioral, molecular, and electrophysiological study.

Hussein A, Abouelnaga A, Obydah W, Saad S, Abass M, Yehia A Pflugers Arch. 2025; 477(3):371-391.

PMID: 39836224 PMC: 11825635. DOI: 10.1007/s00424-024-03059-z.


Genome-wide association study unravels mechanisms of brain glymphatic activity.

Huang S, Ge Y, Ren P, Wu B, Gong W, Du J Nat Commun. 2025; 16(1):626.

PMID: 39805841 PMC: 11730627. DOI: 10.1038/s41467-024-55706-9.


Sex-specific hypothalamic neuropathology and glucose metabolism in an amyloidosis transgenic mouse model of Alzheimer's disease.

Qi G, Tang H, Gong P, Liu Y, He C, Hu J Cell Biosci. 2024; 14(1):120.

PMID: 39272160 PMC: 11395863. DOI: 10.1186/s13578-024-01295-5.


References
1.
Wood E, Dudchenko P, Eichenbaum H . The global record of memory in hippocampal neuronal activity. Nature. 1999; 397(6720):613-6. DOI: 10.1038/17605. View

2.
Bozoki A, Korolev I, Davis N, Hoisington L, Berger K . Disruption of limbic white matter pathways in mild cognitive impairment and Alzheimer's disease: a DTI/FDG-PET study. Hum Brain Mapp. 2011; 33(8):1792-802. PMC: 6870438. DOI: 10.1002/hbm.21320. View

3.
Rowland N, Sammartino F, Tomaszczyk J, Lozano A . Deep Brain Stimulation of the Fornix: Engaging Therapeutic Circuits and Networks in Alzheimer Disease. Neurosurgery. 2016; 63 Suppl 1:1-5. DOI: 10.1227/NEU.0000000000001254. View

4.
Bloom G . Amyloid-β and tau: the trigger and bullet in Alzheimer disease pathogenesis. JAMA Neurol. 2014; 71(4):505-8. DOI: 10.1001/jamaneurol.2013.5847. View

5.
La Joie R, Visani A, Baker S, Brown J, Bourakova V, Cha J . Prospective longitudinal atrophy in Alzheimer's disease correlates with the intensity and topography of baseline tau-PET. Sci Transl Med. 2020; 12(524). PMC: 7035952. DOI: 10.1126/scitranslmed.aau5732. View