
Journal of Functional Foods, Journal Year: 2024, Volume and Issue: 122, P. 106531 - 106531
Published: Oct. 24, 2024
Language: Английский
Journal of Functional Foods, Journal Year: 2024, Volume and Issue: 122, P. 106531 - 106531
Published: Oct. 24, 2024
Language: Английский
Materials Today Bio, Journal Year: 2025, Volume and Issue: 32, P. 101750 - 101750
Published: April 17, 2025
Osteoporotic fractures typically exhibit delayed healing due to impaired cell recruitment, chronic inflammation, and disrupted neurovascular signaling. Sensory nerve signaling plays a crucial role in fracture repair, its deficiency is significant factor leading healing. Addressing these deficiencies overcoming the challenges associated with bone repair osteoporosis. In this study, smart composite hydrogel (denoted as OCS-MPC) was synthesized by embedding CGRP-functionalized polydopamine-coated MXene nanosheets (MXene/PDA/CGRP) into boronic acid-modified oxidized hyaluronic acid-crosslinked carboxymethyl chitosan (OHA-PBA/CMCS) loaded SDF-1. OCS-MPC enables controlled release of SDF-1 CGRP, aiming promote early callus formation late-stage remodeling osteoporotic fractures. Due dynamic crosslinking via imine borate ester bonds, exhibits rapid gelation, injectability, self-healing properties. vitro experiments demonstrated excellent osteogenic, angiogenic, neurogenic properties hydrogel. vivo studies using an femoral model showed that enhanced MSCs recruitment SDF-1/CXCR4 axis, significantly improving stages repair. Additionally, promoted mineralization later through enhancing CGRP Immunofluorescence analysis further confirmed increased expression TUBB3, CD31, indicating successful regeneration network. These findings highlight potential addressing both healing, providing promising therapeutic strategy for patients.
Language: Английский
Citations
0Journal of Orthopaedic Surgery and Research, Journal Year: 2025, Volume and Issue: 20(1)
Published: April 29, 2025
Language: Английский
Citations
0Biomolecules, Journal Year: 2025, Volume and Issue: 15(5), P. 682 - 682
Published: May 8, 2025
Melatonin (N-acetyl-5-methoxytryptamine) is a hormone associated with the regulation of biological rhythms. The indoleamine secreted by pineal gland during night, following circadian rhythm. highest plasmatic levels are reached whereas lowest achieved day. In addition to gland, other organs and tissues also produce melatonin, like, for example, retina, Harderian glands, gut, ovaries, testes, skin, leukocytes, or bone marrow. list extensive, including cerebellum, airway epithelium, liver, kidney, adrenals, thymus, thyroid, pancreas, carotid body, placenta, endometrium. At all these locations, availability melatonin intended local use. Interestingly, decline amplitude secretion occurs in old subjects comparison that found younger subjects. Moreover, genetic environmental factors primary causes diseases, oxidative stress key contributor most pathologies. Numerous studies exist show interesting effects different models disease. Impairment its might have deleterious consequences cellular physiology. this regard, natural compound carrier not yet completely known potential deserves consideration. Thus, has emerged as helpful ally could be considered guard powerful tools orchestrate homeostasis majorly based on antioxidant effects. review, we provide an overview widespread actions against diseases preferentially affecting elderly.
Language: Английский
Citations
0The FASEB Journal, Journal Year: 2025, Volume and Issue: 39(10)
Published: May 19, 2025
ABSTRACT While adipose‐derived stem cells (ADSCs) transplantation represents an appealing therapeutic strategy for bone defect repair, the osteogenic capacity of ADSCs is largely limited. Melatonin has been demonstrated to contribute marrow cell (BMSC) osteogenesis. However, its effect on differentiation not yet determined. This study aims identify whether melatonin exerts influences in rat ADSCs. Rat were isolated and identified. Subsequently, impact proliferation was examined. The effects phenotypic features as well marker genes proteins determined through use alkaline phosphatase (ALP) staining, ALP activity assay, alizarin red staining (ARS), RT‐qPCR, western blot cellular immunofluorescence assay. To investigate potential molecular mechanism which promotes ADSCs, RNA sequencing, MAPK signaling pathway blocking assay p38 mRNA interference carried out. results showed that at concentrations 0–100 μM safe nontoxic with concentration 100 exhibiting most pronounced Additionally, observed activate p38/MAPK Moreover, inhibitor (SB203580) siRNA targeting (p38 siRNA) found inhibit melatonin‐promoted In conclusion, this indicate activation pathway. light these findings, treatment effective promoting
Language: Английский
Citations
0Journal of Pineal Research, Journal Year: 2025, Volume and Issue: 77(3)
Published: April 1, 2025
ABSTRACT Human dental pulp stem cells (hDPSCs) exhibit amazing therapeutic abilities in a variety of diseases due to their remarkable self‐renewal capacity and multi‐differentiation potential. However, potential could be weakened by various factors such as oxidative stress cell survival microenvironment In Vivo. Here, we explored the protective effect mechanism melatonin (Mel) on hDPSCs transplanted type 1 diabetes mellitus (T1DM) rat model. Nicotinamide adenine dinucleotide (NAD + ) metabolism mitochondrial function were remarkably impaired T1DM rats caused stress, while combination Mel post‐hDPSCs transplantation rebalance NAD homeostasis through regulating NAMPT‐NAD ‐SIRT1 axis. Furthermore, significantly reduced intracellular reactive oxygen species, alleviated senescence apoptosis exposed hydrogen peroxide ameliorating depletion dysfunction. The role extremely essential tissue engineering regenerative medicine.
Language: Английский
Citations
0International Archives of Occupational and Environmental Health, Journal Year: 2024, Volume and Issue: 97(8), P. 855 - 864
Published: July 26, 2024
Language: Английский
Citations
3Composites Part B Engineering, Journal Year: 2024, Volume and Issue: 275, P. 111348 - 111348
Published: Feb. 28, 2024
Language: Английский
Citations
2International Immunopharmacology, Journal Year: 2024, Volume and Issue: 141, P. 112932 - 112932
Published: Aug. 17, 2024
Language: Английский
Citations
2Composites Part B Engineering, Journal Year: 2024, Volume and Issue: unknown, P. 112005 - 112005
Published: Nov. 1, 2024
Language: Английский
Citations
2Experimental Physiology, Journal Year: 2024, Volume and Issue: 110(2), P. 261 - 276
Published: Nov. 29, 2024
Osteoporosis (OP) is a prevalent bone disease characterized by reduced density and quality, increasing fragility fracture risk. Osteoclast (OC) activity circadian rhythm play role in the pathogenesis of OP. Melatonin regulator that affects metabolism, but its molecular mechanism has not been studied detail. This study aimed to identify relationship between melatonin-related genes OP through bioinformatics methods verify it experimentally.We analysed microarray data from GSE35959 dataset, identifying differentially expressed patients. Circadian rhythm-related intersect with these genes, highlighting CSNK1D central gene. Functional enrichment, correlation protein-protein interaction analyses were conducted. Experimental validation involved vitro differentiation assays using RAW264.7 cells vivo studies an ovariectomy-induced rat model evaluate osteoclastogenesis effect on Differential expression analysis revealed 272 significant identified as melatonin interplay. showed involvement OC inflammatory pathways. experiments confirmed upregulation during differentiation, small interfering RNA-mediated knockdown marker TRAP+ cell formation. vivo, associated loss rats. Melatonin-related promotes development These findings suggest potential therapeutic target for OP, offering insights into new treatment strategies integrating regulation.
Language: Английский
Citations
2