Research Overview
Origin of the bioregulator family
The peptide bioregulator programme began with peptide fractions extracted from animal organs — thymus, pineal, cartilage, vessel wall — which were later analysed to identify the short sequences thought to carry the activity. Cartalax belongs to the second, fully synthetic generation of that work: defined tripeptides made by solid-phase synthesis rather than tissue extracts of uncertain composition. Its relationship to Sigumir is exactly that of a synthetic single sequence to a natural mixture.
The proposed mechanism
- Chondrocyte culture models, with reported effects on expression of cartilage matrix components including collagen type II and aggrecan
- Cellular senescence markers in serially passaged connective-tissue cell lines
- Comparative studies across the tripeptide family, testing whether single residue substitutions redirect apparent tissue specificity
- DNA-binding and molecular-docking studies examining sequence preference of short acidic peptides
- Aged-animal models reporting changes in connective-tissue histology