Modular Neurosynaptic Structure for Configurable Spiking Dynamics

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Solution Overview

Problem

Existing neurosynaptic computational structures lack the flexibility and efficiency to capture complex spatio-temporal spiking behavior and plasticity in spiking neural networks, failing to accurately model diverse temporal dynamics of biological synapses.

Innovation Solution

A hierarchical, modular neurosynaptic structure with configurable synaptic elements, including AMPA, GABBA, NMDA, and other receptors, and feedback mechanisms, allowing dynamic weight adjustments and spatial-temporal concentration of signal processing to enhance efficiency and adaptability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If a generic synapse structure is used, then device complexity is reduced, but the ability to capture diverse temporal dynamics of biological synapses is lost

Engineering Contradiction:
Improvesynapse structure complexityVSAvoidtemporal dynamics modeling capability
Core Design Contradiction:
Device complexityVSAdaptability or versatility

Solution Approach 1:

The synapse is divided into multiple functional segments: AMPA receptors for fast excitatory transmission, NMDA receptors for slow excitatory transmission with voltage dependence, and GABA receptors for inhibitory transmission. Each segment is independently configurable to model different temporal dynamics, resolving the contradiction between structural simplicity and functional versatility.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The synapse structure incorporates dynamic configurability where receptor types, connection weights, and temporal characteristics can be adjusted in real-time. This allows the same physical structure to adapt its behavior to match diverse temporal dynamics of biological synapses, achieving versatility without permanent structural complexity.

Inventive Principle:
Principle #15Dynamics

2Measurement precision

If multiple receptor types are included in each synapse, then temporal dynamics accuracy is improved, but device complexity increases

Engineering Contradiction:
Improvetemporal dynamics accuracyVSAvoidreceptor configuration complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

A universal synapse structure is designed that can accommodate multiple receptor types (AMPA, NMDA, GABA) within a single configurable unit. The same physical infrastructure supports different receptor configurations, enabling accurate temporal dynamics modeling without proportionally increasing device complexity through dedicated structures for each receptor type.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

Instead of creating physically different structures for each receptor type, the invention uses parameter configuration to differentiate receptor behavior. Temporal characteristics, conductance values, and activation thresholds are adjusted as configurable parameters, allowing accurate modeling of diverse temporal dynamics while maintaining structural uniformity.

Inventive Principle:
Principle #35Parameter changes

3Device complexity

If neurosynaptic resources are allocated uniformly, then system simplicity is maintained, but efficiency is reduced due to wasteful excess capacity

Engineering Contradiction:
Improveresource allocation complexityVSAvoidsignal processing efficiency
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

The system implements non-uniform resource allocation where each synapse receives neurosynaptic resources (number of receptors, connection strength) matched to its specific needs. High-priority or high-frequency signals receive more resources, while low-priority signals receive fewer resources, optimizing overall system efficiency without requiring complex global resource management structures.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

Resource allocation is controlled through configurable parameters that can be dynamically adjusted based on signal characteristics and system state. This allows efficient resource distribution across different synapses and signals without hardwiring complex allocation logic into the system architecture.

Inventive Principle:
Principle #35Parameter changes

4Reliability

If signals are processed in distributed fashion, then system robustness is improved, but energy consumption increases due to longer transmission paths

Engineering Contradiction:
Improvesystem robustnessVSAvoidsignal transmission energy
Core Design Contradiction:
ReliabilityVSUse of energy by moving object

Solution Approach 1:

The invention combines multiple signal processing functions (reception, integration, weighting, and initial processing) at the synapse location before transmitting the processed signal to the neuron. This merging of functions reduces the distance and energy required for signal transmission while maintaining the distributed architecture's robustness, as failures in individual synapses still allow other pathways to function.

Inventive Principle:
Principle #5Merging (Combining)

Data Source

PatentUS20260044705A1System and method for reconfigurable modular neurosynaptic computational structure
Publication Date: 2026.02.12 INNATERA NANOSYSTEMS BV
  • US20260044705A1 patent drawing
  • US20260044705A1 patent drawing
  • US20260044705A1 patent drawing

AI summary

The present invention discloses a neurosynaptic structure for a spiking neural network, wherein the neurosynaptic structure comprises: one or more input ports, one or more synaptic elements, each synaptic element connected to at least one of the input ports and configured to receive an input signal and to output a weighted postsynaptic signal. Furthermore, the neurosynaptic structure comprises a neuron connected to the one or more synaptic elements. The neurosynaptic structure is provided with different feedback and control structures such as AMPA-, GABA-, and NMDA receptors, axon-, dendrite- and neuron back-propagation channels and/or an astrocytes structure.