Purpose: The aim of the present study was to investigate the changes occurring in leukocyte levels of reactive oxygen species (ROS) and total blood plasma antioxidant capacity (TAS) as a result of a marathon/half-marathon race.
Methods: Fourteen men participating in the Oslo Marathon 2000 and 8 women and 8 men participating in the Oslo Half-Marathon 2001 were recruited to the study. Flow cytometry and the ROS-sensitive probe dihydroethidium (DHE) were used to study the intracellular levels of ROS in circulating leukocytes. Both basal ROS levels as well as the capacity of leukocytes to respond with ROS synthesis upon a defined in vitro stimulus, i.e., phorbol myristate acetate (PMA) was assessed before and immediately after the races. TAS was measured using the ABTS+ reduction assay kit.
Results: The basal levels of ROS in leukocytes were either not significantly changed (men, 3-25% reduced) or reduced 33% (women, P < 0.01) as a result of the marathon/half-marathon race. After the marathon race, the capacity of leukocytes to produce ROS upon PMA stimulation was reduced, i.e., 6% (granulocytes) (P < 0.001) and 23% (monocytes) (P < 0.01) residual capacity compared with the prerace situation. A 22-30% reduction (P < 0.05) in monocyte ROS response was seen also as a result of the half-marathon race, whereas the granulocyte ROS response was maintained at the prerace level (19% (women) and 15% (men) reduction, NS)). TAS increased significantly (11-19%, P < 0.05) after both races.
Conclusions: The present results indicate an exhaustion of leukocyte ROS-generating mechanisms after prolonged strenuous exercise. This may partly explain the observation that athletes are more sensitive to attract infectious diseases if exposed to pathogenic micro-organisms during the immediate period after intensive physical activity.
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http://dx.doi.org/10.1249/01.MSS.0000106168.12113.95 | DOI Listing |
Inflamm Res
January 2025
Department of Otolaryngology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, China.
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de Duve Institute, Université catholique de Louvain, Brussels, Belgium. Electronic address:
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January 2025
Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands; Department of Immunology, Leiden University Medical Center, Leiden, The Netherlands; Oncode Institute, Utrecht, The Netherlands. Electronic address:
Neutrophils are pivotal in orchestrating tumor-induced systemic inflammation and are increasingly recognized for their critical involvement in both the initiation and progression of cancer. A fundamental facet of neutrophil biology is their migratory capacity, which enables them to extravasate and infiltrate tumors in other tissues, where they carry out essential effector functions. Unraveling the intricate mechanisms of neutrophil motility and migration is crucial for comprehending immune responses and inflammatory processes, shedding light on their substantial contribution to cancer progression.
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January 2025
Istituto per l'Endocrinologia e l'Oncologia Sperimentale "G. Salvatore", IEOS-CNR, Napoli, Italy.
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Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Early-onset (EOCC) and late-onset cervical cancers (LOCC) represent two clinically distinct subtypes, each defined by unique clinical manifestations and therapeutic responses. However, their immunological profiles remain poorly explored. Herein, we analyzed single-cell transcriptomic data from 4 EOCC and 4 LOCC samples to compare their immune architectures.
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