A complex glyconutritional (GN) mixture of mono-, di-and polysaccharides was investigated to assess its capacity to protect two different types of rodent cells, rat hepatocytes and mouse splenocytes, from depletion of glutathione by a sulfhydryl-reactive mycotoxin, patulin, or by coxsackievirus B3 (CVB3) infection, respectively. Rat hepatocytes were treated with the GN mixture in vitro or received carrier medium only prior to treatment with patulin. When treated with the GN mixture prior to patulin exposure hepatocytes demonstrated protection against depletion of intracellular reduced glutathione (GSH). Cells treated with the GN for up to 15 hours prior to patulin exposure showed no increase in protection of GSH above that demonstrated by cells treated for 3 hours. Mice were infected with CVB3 and one treatment group was injected intraperitoneally with the GN once a week. Animals were splenectomized each month over a ten month treatment for analysis of spleen monocytic cells. Splenocytes from mice treated with the GN mixture did not show the virally-associated depletion of intracellular GSH or damage to pancreatic acini observed in CVB3 inoculated but non-GN-treated mice. Animals from which spleen cells were taken for analysis showed no decrease in anti-CVB3 antibodies and no decrease in viral titers to accompany or explain the normal levels of intracellular GSH. These data strongly suggest that a complex mixture of exogenous saccharides exerts a protective effect on liver cells in vitro in that the cells are protected from chemically initiated depletion of intracellular GSH, and on spleen cells in vivo in that the cells are protected against a CVB3-initiated decrease in intracellular GSH and increase in pancreatic acini damage.
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http://dx.doi.org/10.1007/s11357-999-0018-z | DOI Listing |
ACS Biomater Sci Eng
March 2025
Weifang Key Laboratory of Respiratory Tract Pathogens and Drug Therapy, School of Life Science and Technology, Shandong Second Medical University, Weifang 261000 P. R. China.
Improvements in tumor therapy require a combination of strategies where targeted treatment is critical. We developed a new versatile nanoplatform, MA@E, that generates high levels of reactive oxygen species (ROS) with effective photothermal conversions in the removal of tumors. Enhanced stability liposomes were employed as carriers to facilitate the uniform distribution and stable storage of encapsulated gold nanorods (AuNRs) and Mn-MIL-100 metal-organic frameworks, with efficient delivery of MA@E to the cytoplasm.
View Article and Find Full Text PDFNano Lett
March 2025
Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Zhejiang Key Laboratory of Organosilicon Material Technology, College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 311121, Zhejiang, China.
Allosteric modulation of protein function, which involves effector binding triggering distant conformational changes, is crucial for cellular and metabolic control. However, achieving tunable control, structural diversity, and precise intracellular regulation remains challenging. Here, we designed dynamic supramolecular protein assemblies driven by enzyme-substrate interactions for antioxidant regulation in cells.
View Article and Find Full Text PDFJ Mol Histol
March 2025
Students Research Committee, Faculty of Pharmacy, Ardabil University of Medical Sciences, Ardabil, Iran.
Mechanistic studies have been suggested that adverse effect of bleomycin is attributed to formation of free radicals, mitochondria damages, oxidative stress and inflammation in lung tissue. Mitochondria act as central regulators in the oxidative stress and inflammatory responses in lung tissue, then it can be a promising approach for management bleomycin-induced pneumotoxicity. In the current study, we aim to investigated the injection of exogenous mitochondria into blood as one of the most promising pharmacological approaches to reduce bleomycin-induced lung toxicity in rats.
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March 2025
Department of Oncology, The First People's Hospital of Zunyi (The Third Affiliated Hospital of Zunyi Medical University), China.
Radiotherapy resistance is a major cause of recurrence and metastasis in colorectal cancer (CRC). We established radiotherapy-resistant cell lines to explore the molecular mechanisms of radiotherapy resistance in CRC. HT29 and HCT116 cells were subjected to repeated irradiation at 2 Gy to establish these lines.
View Article and Find Full Text PDFEur J Med Chem
February 2025
School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, PR China. Electronic address:
In this work, we have carefully designed and synthesized two Ru(II) metal complexes: [Ru(phen)(HMPIP)](PF) (6a, where phen = 1,10-phenanthroline, HMPIP = 2-(2-hydroxy-3-methylphenyl-1H-imidazo[4,5-f][1,10]phenanthroline) and [Ru(bpy)(HMPIP)](PF) (6b, where bpy = 2,2'-bipyridine). Using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) to explore the cytotoxicity of 6a and 6b towards HepG2, B16, A549, SGC-7901, HCT116 and non-cancer LO2. The complexes exhibited cytotoxicity activity against HepG2 cells.
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