2018
DOI: 10.1016/j.cbi.2018.09.012
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The inhibition of heme oxigenase-1 (HO-1) abolishes the mitochondrial protection induced by sesamol in LPS-treated RAW 264.7 cells

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Cited by 11 publications
(10 citation statements)
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“…Sesamin is another prominent compound reported in SO that possesses significant protective effects against oxidative stress in animal model including through ameliorate SOD, GPx, reduction of malondialdehyde and elevated different liver marker, TBARS, and lipid peroxidation as well as reduction of superoxide production (Ahmad et al, ; Chen, Ying, Chen, Zhang, & Zhang, ; Hou, Chang, & Jeng, ; Hsieh et al, ; Jeng & Hou, ; Jnaneshwari et al, ; Nakai et al, ; Tian & Guo, ; Zhang et al, ). In vitro studies of sesamin especially in neuronal cell line (PC12), it showed reduction of reactive oxygen species (ROS) generation especially NO production (Cao et al, ; Duarte, Chenet, de Almeida, Andrade, & de Oliveira, ; Lee et al, ; Yashaswini, Rao, & Singh, ). However, Hou et al () reported that 10‐μM sesamin derivative, 3‐bis (3‐methoxybenzyl) butane‐1, 4‐diol, inhibits lactate dehydrogenase, lipid peroxidation, and apoptosis as well as increases ACh release and also prevents cell damage, scavenges ROS, and attenuates the elevation of intracellular free Ca 2+ ion on Aβ‐stressed PC12 cells (Hou et al, ).…”
Section: Resultsmentioning
confidence: 99%
“…Sesamin is another prominent compound reported in SO that possesses significant protective effects against oxidative stress in animal model including through ameliorate SOD, GPx, reduction of malondialdehyde and elevated different liver marker, TBARS, and lipid peroxidation as well as reduction of superoxide production (Ahmad et al, ; Chen, Ying, Chen, Zhang, & Zhang, ; Hou, Chang, & Jeng, ; Hsieh et al, ; Jeng & Hou, ; Jnaneshwari et al, ; Nakai et al, ; Tian & Guo, ; Zhang et al, ). In vitro studies of sesamin especially in neuronal cell line (PC12), it showed reduction of reactive oxygen species (ROS) generation especially NO production (Cao et al, ; Duarte, Chenet, de Almeida, Andrade, & de Oliveira, ; Lee et al, ; Yashaswini, Rao, & Singh, ). However, Hou et al () reported that 10‐μM sesamin derivative, 3‐bis (3‐methoxybenzyl) butane‐1, 4‐diol, inhibits lactate dehydrogenase, lipid peroxidation, and apoptosis as well as increases ACh release and also prevents cell damage, scavenges ROS, and attenuates the elevation of intracellular free Ca 2+ ion on Aβ‐stressed PC12 cells (Hou et al, ).…”
Section: Resultsmentioning
confidence: 99%
“…Studies have shown that sesamol could induce apoptosis in cancer cells and inhibit the effects of proliferation and autophagy in lung cancer and colon cancer [11]. We and other research groups also discovered that sesamol could inhibit the secretion of inflammatory cytokines and reduce oxidative damage caused by inflammatory macrophages [12,23]. Other studies found that sesamol could ameliorate the effects of oxidative stress and inflammation in focal cerebral ischemia/reperfusion injury in the rat brain [24].…”
Section: Discussionmentioning
confidence: 96%
“…Next, mice inhaled 2% OVA administered with an ultrasonic nebulizer for 30 min to induce asthma symptoms (DeVilbiss Pulmo-Aide 5650D, United States) on days 14, 17, 20, 23, and 27. Then, for 2 weeks (days [14][15][16][17][18][19][20][21][22][23][24][25][26][27], in addition to their regular diet, each mouse group received a daily dose of saline (N and OVA groups), sesamol (S10 and S30 groups), or prednisolone (P group). On day 28, we calculated the AHR in all mice; then, on day 29, we sacrificed mice to investigate the asthma pathology, immune regulation, inflammation, and oxidative stress.…”
Section: Establishment Of An Asthma Model and Sesamol Administrationmentioning
confidence: 99%
“…SML has been previously tested on different cell lines as an antioxidant to protect them against the damaging effect of cancer therapy. [36]. Sesamol could reduce the oxidative damage and the toxicity to H9c2 cardiomyoblasts caused by doxorubicin [37].…”
Section: Discussionmentioning
confidence: 99%