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ObjectiveTo elucidate the role of decorin, a small leucine‐rich proteoglycan, in the degradation of cartilage matrix during the progression of post‐traumatic osteoarthritis (OA). MethodsThree‐month–old decorin‐null (Dcn−/−) and inducible decorin‐knockout (DcniKO) mice were subjected to surgical destabilization of the medial meniscus (DMM) to induce post‐traumaticOA. TheOAphenotype that resulted was evaluated by assessing joint morphology and sulfated glycosaminoglycan (sGAG) staining via histological analysis (n = 6 mice per group), surface collagen fibril nanostructure via scanning electron microscopy (n = 4 mice per group), tissue modulus via atomic force microscopy–nanoindentation (n = 5 or more mice per group) and subchondral bone structure via micro–computed tomography (n = 5 mice per group). Femoral head cartilage explants from wild‐type and Dcn−/−mice were stimulated with the inflammatory cytokine interleukin‐1β (IL‐1β) in vitro (n = 6 mice per group). The resulting chondrocyte response toIL‐1β and release ofsGAGs were quantified. ResultsIn both Dcn−/−and DcniKOmice, the absence of decorin resulted in acceleratedsGAGloss and formation of highly aligned collagen fibrils on the cartilage surface relative to the control (P< 0.05). Also, Dcn−/−mice developed more salient osteophytes, illustrating more severeOA. In cartilage explants treated withIL‐1β, loss of decorin did not alter the expression of either anabolic or catabolic genes. However, a greater proportion ofsGAGs was released to the media from Dcn−/−mouse explants, in both live and devitalized conditions (P< 0.05). ConclusionIn post‐traumaticOA, decorin delays the loss of fragmented aggrecan and fibrillation of cartilage surface, and thus, plays a protective role in ameliorating cartilage degeneration.
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This content will become publicly available on April 11, 2026
Characterization of weakened Haematococcus pluvialis encapsulated in alginate‐based hydrogel
Abstract BACKGROUNDHaematococcus pluvialis(Hp), a freshwater chlorophyte microalga, is a major natural source of astaxanthin (ASX), a potent antioxidant with anti‐inflammatory, anticarcinogenic and muscle pigmentation properties. However,ASXbioavailability is limited by the rigid cyst wall and, although cell wall rupture improves bioavailability, the free form is unstable under high temperatures,pHextremes, light or oxygen. Encapsulation techniques improveASXstability, making it suitable for functional foods and aquaculture, especially in salmonid feeds where natural pigments are preferred. The present study evaluates the stability of weakenedHp(Hpw) biomass encapsulated in alginate (ALG) via ionic gelation. RESULTSEncapsulation utilizingALGachieved high efficiency (97 ± 2.63%) and loading capacity (32 ± 0.90%), confirming its suitability as a wall material.ALG‐Hpwhydrogels displayed significant color intensity, enhancing potential feed or food hues. Low bulk density (0.59 ± 0.01 g cm−3), moisture content (11.97 ± 0.20%) and water activity (0.28 ± 0.00) suggest minimized oxidation processes. Hydrogels measured 1.30 ± 0.06 mm with a uniform sphericity factor of 0.058 ± 0.03. Confocal laser scanning microscopy confirmed uniformHpwdistribution andscanning electron microscopyrevealed fissure‐free surfaces, ensuring minimal permeability. DPPH (i.e. 2,2‐diphenyl‐1‐picrylhydrazyl) scavenging activity was similar betweenHpwextract (38.32 ± 2.30% to 96.32 ± 0.88%) andALG‐Hpwhydrogels (33.20 ± 1.55% to 93.30 ± 0.44%).ALGIncreasedHpwdecomposition temperature by 40.97 °C. Encapsulation ofHpwinALGsignificantly enhanced the bioaccessibility ofASX. TheALG‐based encapsulation effectively preservedASXstability, retaining over 90% of its content under storage conditions. CONCLUSIONALGis a suitable biopolymer for encapsulatingHpw, preserving antioxidant activity, and enhancing thermal properties, making it valuable for broader applications. © 2025 Society of Chemical Industry.
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- PAR ID:
- 10599482
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Journal of the Science of Food and Agriculture
- ISSN:
- 0022-5142
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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