Anagenix and CytoSolve Build an Integrative Systems Architecture Explaining Kiwifruit-Derived Supplement Synergy on Gut Motility Mechanisms
Anagenix Group develops wholefood-based nutritional supplements, including Actazin™ and Livaux™, derived from green and gold kiwifruit, respectively. Their products are supported by clinical and experimental evidence in digestive health, with a focus on translating food-based bioactives into measurable physiological benefits.
Challenge
Clinical and experimental studies indicate that Actazin™ and Livaux™ positively impact digestive health, yet the molecular mechanisms driving these effects—both for individual ingredients and their combinations—were not fully characterized. Gut motility is regulated by multiple interacting biological systems, and conventional approaches often struggle to connect multi-ingredient supplement composition to system-level physiological outcomes.
To enable rational formulation, dosing, and mechanistic substantiation, Anagenix needed a comprehensive, testable systems architecture that could integrate the molecular pathways governing gut motility and evaluate potential synergy across multiple bioactive compounds.
How CytoSolve Helped
CytoSolve supported Anagenix by transforming a broad evidence base into a mechanistic, integrated in silico model of gut motility:
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Systematic Literature Review to Define Mechanism Space
A structured review identified molecular pathways implicated in gut motility and the biological processes most consistently supported by published evidence.
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Pathway-to-Model Conversion with Validation
The relevant gut motility pathways were translated into individual mathematical models, each validated prior to integration to ensure mechanistic and quantitative integrity.
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Dynamic Model Integration Using CytoSolve® Systems Architecture
CytoSolve enabled the plurality of validated pathway models to be integrated into an integrative gut motility model, capturing interactions and feedback across systems rather than treating mechanisms independently.
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In Silico Testing of Real-World Combinations and Doses
The complete set of bioactive molecules at recommended dose levels was tested computationally to evaluate synergy and predict multi-pathway impact.
A structured review identified molecular pathways implicated in gut motility and the biological processes most consistently supported by published evidence.
The relevant gut motility pathways were translated into individual mathematical models, each validated prior to integration to ensure mechanistic and quantitative integrity.
CytoSolve enabled the plurality of validated pathway models to be integrated into an integrative gut motility model, capturing interactions and feedback across systems rather than treating mechanisms independently.
The complete set of bioactive molecules at recommended dose levels was tested computationally to evaluate synergy and predict multi-pathway impact.
Key Benefits Realized
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Unified Mechanistic Explanation for Multi-Ingredient Effects
Converted fragmented pathway evidence into a single integrative model linking ingredient bioactives to gut motility biology.
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Synergy Quantification Across Core Biological Systems
Demonstrated system-level synergy consistent with enhanced motility through coordinated modulation of multiple mechanisms.
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Actionable, Evidence-Grounded Framework for Formulation Strategy
Provided a reproducible architecture to explore ingredient interactions, dose logic, and combined effects without relying on trial-and-error alone.
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Mechanism-Based Differentiation for Digestive Health Claims
Enabled mechanistic substantiation by connecting supplement bioactives to validated molecular pathways governing motility outcomes.
Converted fragmented pathway evidence into a single integrative model linking ingredient bioactives to gut motility biology.
Demonstrated system-level synergy consistent with enhanced motility through coordinated modulation of multiple mechanisms.
Provided a reproducible architecture to explore ingredient interactions, dose logic, and combined effects without relying on trial-and-error alone.
Enabled mechanistic substantiation by connecting supplement bioactives to validated molecular pathways governing motility outcomes.