2020
DOI: 10.1016/j.biopha.2019.109554
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γ-Oryzanol suppresses cell apoptosis by inhibiting reactive oxygen species-mediated mitochondrial signaling pathway in H2O2-stimulated L02 cells

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Cited by 34 publications
(39 citation statements)
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“…In this study, we showed that the EtOAc fraction significantly increased the cell viability, reduced LDH release, It is well-known that these critical antioxidant enzymes play a major role in ROS scavenging [26]. As already mentioned, extracts of D. moldavica L. could reduce the MDA level and increase the contents of SOD and CAT in diabetic rats [27].…”
Section: Discussionsupporting
confidence: 64%
“…In this study, we showed that the EtOAc fraction significantly increased the cell viability, reduced LDH release, It is well-known that these critical antioxidant enzymes play a major role in ROS scavenging [26]. As already mentioned, extracts of D. moldavica L. could reduce the MDA level and increase the contents of SOD and CAT in diabetic rats [27].…”
Section: Discussionsupporting
confidence: 64%
“…20 GO could suppress ROS accumulation and ROS-activated mitochondrial apoptotic pathway in a hepatic cell line. 19 However, the impact of GO on renal IRI-induced distant organ dysfunction has not been reported to our knowledge. In this study, the results pointed out the potential of GO to ameliorate extrarenal organ dysfunctions after IRI in vivo .…”
Section: Discussionmentioning
confidence: 88%
“…The anti-inflammatory and antioxidant effects of GO are reported in different studies. [17][18][19][20][21] Understanding the complex connections between renal and distant organs can result in the development of novel diagnostics and therapeutic strategies to recover outcomes in cases with AKI. In the present study, the effects of GO on I/R-induced oxidative stress in distant organs including brain, heart, and liver of rats were evaluated.…”
Section: Introductionmentioning
confidence: 99%
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“…The L02 cells were purchased from BeNa Culture Collection Company (BNCC, Beijing, China) and cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin–streptomycin solution at 37 °C under 5% CO 2 in a humidified incubator. The H 2 O 2 induced oxidative stress model of L02 cell was established according to the reported method with slight modifications [ 28 , 29 , 30 ]. Firstly, 120 µL L02 cell suspension (1 × 10 4 cells) was seeded in a 96-well plate and incubated for 24 h, followed by the addition of 15 µL PBS buffer (corresponding to the addition of tested samples).…”
Section: Methodsmentioning
confidence: 99%