2021
DOI: 10.1016/j.tox.2021.152749
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Oral isoniazid causes oxidative stress, oocyte deterioration and infertility in mice

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Cited by 7 publications
(2 citation statements)
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“…Furthermore, an increase in the expression of key CRGs could lead to infertility in patients with EMT. Qiao et al showed that isoniazid activates the Keap1/Nrf2 signaling pathway by inducing oxidative stress and apoptosis, thereby impairing the reproductive system and reducing fertility in mammals [22]. Ivanov et al showed that melatonin could protect the developing embryo from oxidative stress by modulating NFE2L2, SOD1, and GPX1 expression [23].…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, an increase in the expression of key CRGs could lead to infertility in patients with EMT. Qiao et al showed that isoniazid activates the Keap1/Nrf2 signaling pathway by inducing oxidative stress and apoptosis, thereby impairing the reproductive system and reducing fertility in mammals [22]. Ivanov et al showed that melatonin could protect the developing embryo from oxidative stress by modulating NFE2L2, SOD1, and GPX1 expression [23].…”
Section: Discussionmentioning
confidence: 99%
“…The Kelch-like ECH-associated protein 1 (Keap1) counteracts the effect of NRF2 by contributing to its degradation by ubiquitin proteasomes [177]. In vitro exposure to isoniazid in mice oocytes led to an increase in ROS and to the activation of the OS-response pathway Keap1-NRF2 [178]. Similarly, in vitro exposure to OS resulted in an up-regulation of NRF2 expression and its downstream antioxidant genes in preimplantation bovine embryos at different times of development (8-cell, 16-cell, and blastocyst stage embryos).…”
mentioning
confidence: 99%