Evidence map›Paper›PMID 41135876›Full record

ArticleJournal of advanced research2026

Modeling homosynaptic and heterosynaptic plasticity with a single neuromemristive synapse.

Zubaer Ibna Mannan, Sami Azam, Ram Kaji Budhathoki, M D Nur Alam, Hyongsuk Kim

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Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zubaer Ibna MannanDepartment of Computer Science and Engineering, East West University, Jahurul Islam Ave., Dhaka 1212, Bangladesh. Electronic address: zubaer.mannan@ewubd.edu.
Sami AzamFaculty of Science and Technology, Charles Darwin University, NT 0810, Australia. Electronic address: Sami.Azam@cdu.edu.au.
Ram Kaji BudhathokiDepartment of Electrical and Electronics Engineering, School of Engineering, Kathmandu University, Dhulikhel, Kavre, 45200, Nepal. Electronic address: ram.budhathoki@ku.edu.np.
M D Nur AlamDepartment of Artificial Intelligence, Kyungdong University Global, Geosong, Gangwon-do 46(4)-24764, the Republic of Korea. Electronic address: na@kduniv.ac.kr.
Hyongsuk KimDivision of Electronics Engineering, and Intelligent Robot Research Center, Jeonbuk National University, Jeonju, Jollabuk-do 567-54896, the Republic of Korea. Electronic address: hskim@jbnu.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEfforts are being made to design a brain-like intelligence due to its robustness, synaptic modification (i.e., learning and memory), analog synaptic multiplication, multi-state storage, ultra-low power consumption, and parallel computation. However, current bioelectronic and biomedical technologies have yet to fully replicate brain-like intelligence. In particular, devices that can emulate both homosynaptic and heterosynaptic plasticity remain extremely limited.

objectivesThis work presents a neuromemristive synapse capable of replicating key biological features, including homosynaptic and heterosynaptic plasticity. The proposed synapse uses a memristor, a promising candidate for achieving bio-realistic features of synapse due to its low power consumption, multi-state operation, analog behavior, high data storage durability, and CMOS compatibility.

methodsThe artificial synapse is designed as a composite 1-port structure consisting of a memristor (M) and a controlled capacitor (CCon). The memristor is responsible for emulating synaptic plasticity in response to distinct brainwave patterns, while the capacitor modulates the discharge rate through the memristor. During the active input phase (synaptic potentiation), the composite 1-port charges up. During the inactive phase (synaptic depression), CCon governs the discharging of the memristor, enabling full or partial discharging through memory fading or homosynaptic and heterosynaptic depression pathways.

resultsWe designed the proposed synapse in SPICE and validated its bio-functionalities through various simulations. The proposed synapse demonstrates low power consumption and replicates key neurobiological processes for learning and memory such as heterosynaptic homeostasis, modular input specificity, associativity, and homosynaptic long-term and short-term potentiation and depression (LTP, LTD, STF, STD), along with memory fading effect (MFE), and strong stimulation (SST).

conclusionThe proposed synapse bio-realistically mimics synaptic plasticity, neurotransmitter dynamics, and neuronal responses. Implemented using off-the-shelf components, it supports both volatile and non-volatile modes, making it suitable for CMOS integration. This enables advancements in spiking neural networks, brain function analysis, and scalable neuromorphic computing systems.

Indexed as

Models, NeurologicalNeuronal PlasticitySynapsesHumansArtificial synapseAssociativityHomeostaticLong-term depression (LTD)Long-term potentiation (LTP)Memristor and memristive systemModular input-specificNeuromorphic circuitShort-term depression (STD)Short-term facilitation (STF)Synapse

Identifiers

PMID41135876
PMCPMC13316508

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.