Further investigations were carried out into the formation mechanism of nitrosyl complexes of non-heme iron (complexes 2.03) in rat liver and blood at intrauterine injection of aqueous solutions of nitrosyl complexes of iron with cysteine, thiosulphate, phosphate, ATP and hydroxyl, as well as at keeping the animals on nitrite and iron diet. It has been found that 5-6 hours after the injection of iron nitrosyl complexes with cysteine/the shape of ESR signal with gav = 2.03 in the liver becomes identical to the shape of the signal obtained after adding nitrite and iron to the animal food. Therefore it is assumed that in spite of different methods of induction, the 2.03 complexes formed in these experiments are identical in structure and localization. The assumption was proved as to initial formation of Fe-NO in the blood with subsequent transition to SH-groups of liver proteins. It is suggested that complexes 2.03 in vivo are concerned with a specific type of protein.
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Front Aging
January 2025
Molecular Medicine, NSW Health Pathology, John Hunter Hospital, Newcastle, NSW, Australia.
Aging is a complex process marked by various changes at both cellular and systemic levels, impacting the functioning and lifespan of organisms. Over time, researchers have pinpointed several significant hallmarks of aging that lead to the gradual deterioration of tissue function, regulation, and homeostasis associated with aging in humans. Despite this, the intricate interactions and cumulative effects of these hallmarks are still mostly uncharted territory.
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Bronchopulmonary dysplasia is a prevalent respiratory disorder posing a significant threat to the quality of life in premature infants. Its pathogenesis is intricate, and therapeutic options are limited. Besides genetic coding, protein post-translational modification plays a pivotal role in regulating cellular function, contributing complexity and diversity to substrate proteins and influencing various cellular processes.
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