2021
DOI: 10.1016/j.fct.2021.111972
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Aflatoxin B1 disrupts blood-testis barrier integrity by reducing junction protein and promoting apoptosis in mice testes

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Cited by 41 publications
(26 citation statements)
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“…MAPK signaling pathway is the key mediator that controls the phosphorylation of many downstream effectors, leading to modulate different cellular functions, including cell proliferation, differentiation, and migration ( Joerger-Messerli et al, 2021 ). Oxidative stress-mediated p38 MAPK signaling pathway was associated with the blood-testis barrier-related junction protein and promoting apoptosis in mice testes ( Huang et al, 2021 ). Moreover, activation of the MAPK signaling pathway was involved in the molecular mechanism of apoptosis in spermatogonia cells ( Park et al, 2020 ).…”
Section: Discussionmentioning
confidence: 99%
“…MAPK signaling pathway is the key mediator that controls the phosphorylation of many downstream effectors, leading to modulate different cellular functions, including cell proliferation, differentiation, and migration ( Joerger-Messerli et al, 2021 ). Oxidative stress-mediated p38 MAPK signaling pathway was associated with the blood-testis barrier-related junction protein and promoting apoptosis in mice testes ( Huang et al, 2021 ). Moreover, activation of the MAPK signaling pathway was involved in the molecular mechanism of apoptosis in spermatogonia cells ( Park et al, 2020 ).…”
Section: Discussionmentioning
confidence: 99%
“…Our study indicated that T-2 toxin caused structural damage and osteogenesis dysfunction along with oxidative stress in mouse femur. Oxidative stress is the pathological mechanism of many mycotoxins, 30,31 and involved in bone pathogenesis including osteoporosis, arthritis, diabetes-induced bone complications, and other [32][33][34] In this study, T-2 toxin exposure increased ROS generation and lipid peroxidation, but decreased the activity of T-AOC in mouse femur. On the one hand, ROS directly inhibits osteoblast function.…”
Section: Discussionmentioning
confidence: 59%
“…The presence of EHS was also detected in brain and gonadal tissues, indicating that EHS could cross the blood-brain barrier and blood-testis barrier and increase the risk of neurotoxicity and transgenerational toxicity. 48,49 Similar to gill tissue, skin tissue can also be in direct contact with the exposure solution, while the mucus layer secreted on the skin surface becomes the main resistance to the enrichment of target pollutants, resulting in a lower level of occurrence. 50 Muscle is the tissue with the lowest cumulative concentration of EHS, possibly because EHS is lipophilic and muscle tissue has a low fat content, which leads to a low affinity between EHS and muscle tissue.…”
Section: Resultsmentioning
confidence: 99%