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  4. Capsaicin inhibits collagen fibril formation and increases the stability of collagen fibers
 
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Capsaicin inhibits collagen fibril formation and increases the stability of collagen fibers

ISSN
01757571
Date Issued
2015-02-01
Author(s)
Perumal, Sathiamurthi
Dubey, Kriti
Badhwar, Rahul
George, Kodimattan Joseph
Sharma, Rakesh Kumar 
Department of Chemistry 
Bagler, Ganesh
Madhan, Balaraman
Kar, Karunakar
DOI
10.1007/s00249-014-1002-9
Abstract
Capsaicin is a versatile plant product which has been ascribed several health benefits and anti-inflammatory and analgesic properties. We have investigated the effect of capsaicin on the molecular stability, self-assembly, and fibril stability of type-I collagen. It was found that capsaicin suppresses collagen fibril formation, increases the stability of collagen fibers in tendons, and has no effect on the molecular stability of collagen. Turbidity assay data show that capsaicin does not promote disassembly of collagen fibrils. However, capsaicin moderately protects collagen fibrils from enzymatic degradation. Computational studies revealed the functions of the aromatic group and amide region of capsaicin in the collagen–capsaicin interaction. The results may have significant implications for capsaicin-based therapeutics that target excess collagen accumulation-linked pathology, for example thrombosis, fibrosis, and sclerosis.
Subjects
  • Capsaicin

  • Tendons

  • Triple-helix

  • Type-I collagen

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