Free Radical Biology and Medicine, Journal Year: 2024, Volume and Issue: 227, P. 570 - 581
Published: Dec. 10, 2024
Language: Английский
Free Radical Biology and Medicine, Journal Year: 2024, Volume and Issue: 227, P. 570 - 581
Published: Dec. 10, 2024
Language: Английский
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Journal Year: 2024, Volume and Issue: 1870(7), P. 167446 - 167446
Published: July 29, 2024
Language: Английский
Citations
5Frontiers in Physiology, Journal Year: 2024, Volume and Issue: 15
Published: Oct. 15, 2024
Recently, chronic intermittent inhalation of low-dose carbon monoxide (CO) has been postulated as a practice to increase total hemoglobin mass with potential beneficial effects on endurance performance. In this perspective article, we discuss the performance enhancing capabilities well safety concerns, which include individual variability in CO response, and acute health effects. It is also important note that according World-Anti-Doping-Agency (WADA), could fall under “ M1. Manipulation Blood Components therefore be considered prohibited method if used non-diagnostic tool.
Language: Английский
Citations
4Science China Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 8, 2025
Language: Английский
Citations
0European Journal of Neuroscience, Journal Year: 2025, Volume and Issue: 61(2)
Published: Jan. 1, 2025
ABSTRACT Traumatic brain injury is one of the most common cerebral incidences worldwide. Repetitive mild traumatic injuries occurring, for example, in athletes or victims abuse, can cause chronic neurodegeneration due to neuroinflammation, which crosstalk between reactive astrocytes and activated microglia crucial modulating neuronal damage. The inducible enzyme heme oxygenase‐1 its product carbon monoxide are known be ascribed neuroprotective anti‐inflammatory properties. We caused repetitive wild‐type mice compared without microglial expression. Additionally, were treated daily with either air exogenously. In mice, we observed enhanced activation astrogliosis as well vasodilation after trauma. knockout at baseline pretrauma a lack an adequate inflammatory response injury. However, led NF‐κB IFNγ expression post‐trauma period. Carbon exerted neuroprotection, suggested by reduced wake‐up times beneficially altering inflammation post‐traumatic This study further underlines role oxygenase‐1/carbon system modulation damage associated neuroinflammatory
Language: Английский
Citations
0Bioorganic & Medicinal Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 118092 - 118092
Published: Jan. 1, 2025
Language: Английский
Citations
0Pharmaceuticals, Journal Year: 2025, Volume and Issue: 18(3), P. 344 - 344
Published: Feb. 27, 2025
Age-related oxidative stress is a critical factor in vascular dysfunction, contributing to hypertension and atherosclerosis. Smooth muscle cells endothelial are particularly susceptible damage, which exacerbates aging through cellular senescence, chronic inflammation, arterial stiffness. Gasotransmitters—hydrogen sulfide (H2S), nitric oxide (NO), carbon monoxide (CO)—are emerging as promising therapeutic agents for counteracting these processes. This review synthesizes findings from recent studies focusing on the mechanisms by H2S, NO, CO influence smooth cell function. Therapeutic strategies involving exogenous gasotransmitter delivery systems combination therapies were analyzed. H2S enhances mitochondrial bioenergetics, scavenges ROS, activates antioxidant pathways. NO improves function, promotes vasodilation, inhibits platelet aggregation. exhibits cytoprotective anti-inflammatory effects modulating heme oxygenase activity ROS production. In preclinical studies, gasotransmitter-releasing molecules (e.g., NaHS, SNAP, CORMs) targeted show significant promise. Synergistic with lifestyle modifications further enhance their potential. conclusion, gasotransmitters hold promise combat age-related cells. Their multifaceted innovative approaches make them potential candidates treating dysfunction promoting healthy aging. Further research needed translate into clinical applications.
Language: Английский
Citations
0Small, Journal Year: 2025, Volume and Issue: unknown
Published: April 7, 2025
Abstract A number of polymeric sulfur dioxide (SO 2 )‐releasing nanomedicines have demonstrated promise in cancer treatment by enabling controlled SO release, triggered endogenous (redox) stimuli. However, the heterogeneous distribution these stimuli across different organs presents a significant challenge to clinical translation. To overcome this limitation, developing donors that respond exogenous triggers offers promising strategy for therapeutic advancement. Herein, an stimuli‐responsive is presented generating from series amphiphilic block copolymers ( BCPx ) under visible light irradiation (427 nm) biological environment, aiming evaluate their potential therapy. The coumarin‐based, water‐soluble polymers form well‐defined nanostructures BCPxNs aqueous media, releasing 70–85% theoretical within 4 h. Moreover, exhibit self‐reporting behavior upon release. In vitro cellular assays with BCP2Ns demonstrate enhanced antiproliferative effect cervical carcinoma HeLa cells nm), IC 50 value 0.3 mg mL −1 . Investigations using confocal microscopy and flow cytometry confirm ‐induced cell death. Overall, underscores light‐responsive spatiotemporal control
Language: Английский
Citations
0Medicinal Chemistry Research, Journal Year: 2025, Volume and Issue: unknown
Published: April 9, 2025
Language: Английский
Citations
0Pharmacological Research, Journal Year: 2025, Volume and Issue: unknown, P. 107741 - 107741
Published: April 1, 2025
Language: Английский
Citations
0Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 142342 - 142342
Published: April 1, 2025
Language: Английский
Citations
0