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毕业论文网 > 任务书 > 化学化工与生命科学类 > 药物制剂 > 正文

木犀草素对雷公藤甲素诱发睾丸支持细胞损伤的保护作用研究任务书

 2020-07-02 22:39:06  

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2. 参考文献

[1] Wan, H. T.; Mruk, D. D.; Wong, C. K.; Cheng, C. Y. Perfluorooctanesulfonate (PFOS) perturbs male rat Sertoli cell blood-testis barrier function by affecting F-actin organization via p-FAK-Tyr(407): an in vitro study. Endocrinology 155:249-262; 2014. [2] Cao, X. N.; Shen, L. J.; Wu, S. D.; Yan, C.; Zhou, Y.; Xiong, G.; Wang, Y. C.; Liu, Y.; Liu, B.; Tang, X. L.; Guo, M.; Liu, D. Y.; Long, C. L.; Sun, M.; He, D. W.; Lin, T.; Wei, G. H. Urban fine particulate matter exposure causes male reproductive injury through destroying blood-testis barrier (BTB) integrity. Toxicol Lett 266:1-12; 2017. [3] Aravindakshan, J.; Cyr, D. G. Nonylphenol alters connexin 43 levels and connexin 43 phosphorylation via an inhibition of the p38-mitogen-activated protein kinase pathway. Biol Reprod 72:1232-1240; 2005. [4] Carette, D.; Perrard, M. H.; Prisant, N.; Gilleron, J.; Pointis, G.; Segretain, D.; Durand, P. Hexavalent chromium at low concentration alters Sertoli cell barrier and connexin 43 gap junction but not claudin-11 and N-cadherin in the rat seminiferous tubule culture model. Toxicol Appl Pharmacol 268:27-36; 2013. [5] Zhou, D. R.; Zhou, Y. C.; Cui, G. H.; Guo, X.; Qin, J.; Gui, Y. T.; Cai, Z. M. Gossypol repressed the gap junctional intercellular communication between Sertoli cells by decreasing the expression of Connexin43. Toxicol In Vitro 22:1719-1725; 2008. [6] Li, N.; Mruk, D. D.; Chen, H.; Wong, C. K.; Lee, W. M.; Cheng, C. Y. Rescue of perfluorooctanesulfonate (PFOS)-mediated Sertoli cell injury by overexpression of gap junction protein connexin 43. Sci Rep 6:29667; 2016. [7] Yang, D.; Tan, X.; Lv, Z.; Liu, B.; Baiyun, R.; Lu, J.; Zhang, Z. Regulation of Sirt1/Nrf2/TNF-α signaling pathway by luteolin is critical to attenuate acute mercuric chloride exposure induced hepatotoxicity. Sci Rep 6:37157; 2016. [8] Xu, J.; Wang, H.; Ding, K.; Zhang, L.; Wang, C.; Li, T.; Wei, W.; Lu, X. Luteolin provides neuroprotection in models of traumatic brain injury via the Nrf2-ARE pathway. Free Radic Biol Med 71:186-195; 2014. [9] Hong, Z.; Cao, X.; Li, N.; Zhang, Y.; Lan, L.; Zhou, Y.; Pan, X.; Shen, L.; Yin, Z.; Luo, L. Luteolin is effective in the non-small cell lung cancer model with L858R/T790M EGF receptor mutation and erlotinib resistance. Br J Pharmacol 171:2842-2853; 2014. [10] Liu, C. W.; Lin, H. W.; Yang, D. J.; Chen, S. Y.; Tseng, J. K.; Chang, T. J.; Chang, Y. Y. Luteolin inhibits viral-induced inflammatory response in RAW264.7 cells via suppression of STAT1/3 dependent NF-κB and activation of HO-1. Free Radic Biol Med 95:180-189; 2016. [11] Bai, L.; Nong, Y.; Shi, Y.; Liu, M.; Yan, L.; Shang, J.; Huang, F.; Lin, Y.; Tang, H. Luteolin Inhibits Hepatitis B Virus Replication through Extracellular Signal-Regulated Kinase-Mediated Down-Regulation of Hepatocyte Nuclear Factor 4α Expression. Mol Pharm 13:568-577; 2016. [12] Hu, J.; Man, W.; Shen, M.; Zhang, M.; Lin, J.; Wang, T.; Duan, Y.; Li, C.; Zhang, R.; Gao, E.; Wang, H.; Sun, D. Luteolin alleviates post-infarction cardiac dysfunction by up-regulating autophagy through Mst1 inhibition. J Cell Mol Med 20:147-156; 2016. [13] Chu, Q.; Tian, X.; Lin, M.; Ye, J. Electromigration profiles of Cynomorium songaricum based on capillary electrophoresis with amperometric detection. J Agric Food Chem 54:7979-7983; 2006. [14] Qiu, L.; Zhang, X.; Zhang, X.; Zhang, Y.; Gu, J.; Chen, M.; Zhang, Z.; Wang, X.; Wang, S. L. Sertoli cell is a potential target for perfluorooctane sulfonate-induced reproductive dysfunction in male mice. Toxicol Sci 135:229-240; 2013. [15] Ma, B.; Qi, H.; Li, J.; Xu, H.; Chi, B.; Zhu, J.; Yu, L.; An, G.; Zhang, Q. Triptolide disrupts fatty acids and peroxisome proliferator-activated receptor (PPAR) levels in male mice testes followed by testicular injury: A GC-MS based metabolomics study. Toxicology 336:84-95; 2015. [16] Xu, L.; Qiu, Y.; Xu, H.; Ao, W.; Lam, W.; Yang, X. Acute and subacute toxicity studies on triptolide and triptolide-loaded polymeric micelles following intravenous administration in rodents. Food Chem Toxicol 57:371-379; 2013. [17] Ma, B.; Zhang, Q.; Wu, D.; Wang, Y. L.; Hu, Y. Y.; Cheng, Y. P.; Yang, Z. D.; Zheng, Y. Y.; Ying, H. J. Strontium fructose 1,6-diphosphate prevents bone loss in a rat model of postmenopausal osteoporosis via the OPG/RANKL/RANK pathway. Acta Pharmacol Sin 33:479-489; 2012. [18] Yang, Y.; Wang, W.; Xiong, Z.; Kong, J.; Qiu, Y.; Shen, F.; Huang, Z. Activation of SIRT3 attenuates triptolide-induced toxicity through closing mitochondrial permeability transition pore in cardiomyocytes. Toxicol In Vitro 34:128-137; 2016. [19] Hu, J.; Yu, Q.; Zhao, F.; Ji, J.; Jiang, Z.; Chen, X.; Gao, P.; Ren, Y.; Shao, S.; Zhang, L.; Yan, M. Protection of Quercetin against Triptolide-induced apoptosis by suppressing oxidative stress in rat Leydig cells. Chem Biol Interact 240:38-46; 2015. [20] Zhou, J.; Xi, C.; Wang, W.; Yang, Y.; Qiu, Y.; Huang, Z. Autophagy plays an important role in triptolide-induced apoptosis in cardiomyocytes. Toxicol Lett 236:168-183; 2015. [21] Zhou, J.; Xi, C.; Wang, W.; Fu, X.; Jinqiang, L.; Qiu, Y.; Jin, J.; Xu, J.; Huang, Z. Triptolide-induced oxidative stress involved with Nrf2 contribute to cardiomyocyte apoptosis through mitochondrial dependent pathways. Toxicol Lett 230:454-466; 2014. [22] Zhang, Y. C.; Gan, F. F.; Shelar, S. B.; Ng, K. Y.; Chew, E. H. Antioxidant and Nrf2 inducing activities of luteolin, a flavonoid constituent in Ixeris sonchifolia Hance, provide neuroprotective effects against ischemia-induced cellular injury. Food Chem Toxicol 59:272-280; 2013. [23] Kittiratphatthana, N.; Kukongviriyapan, V.; Prawan, A.; Senggunprai, L. Luteolin induces cholangiocarcinoma cell apoptosis through the mitochondrial-dependent pathway mediated by reactive oxygen species. J Pharm Pharmacol 68:1184-1192; 2016. [24] Stanton, P. G. Regulation of the blood-testis barrier. Semin Cell Dev Biol 59:166-173; 2016. [25] Gerber, J.; Weider, K.; Hambruch, N.; Brehm, R. Loss of connexin43 (Cx43) in Sertoli cells leads to spatio-temporal alterations in occludin expression. Histol Histopathol 29:935-948; 2014. [26] Li, M. W.; Mruk, D. D.; Lee, W. M.; Cheng, C. Y. Connexin 43 is critical to maintain the homeostasis of the blood-testis barrier via its effects on tight junction reassembly. Proc Natl Acad Sci U S A 107:17998-18003; 2010. [27] Kidder, G. M.; Cyr, D. G. Roles of connexins in testis development and spermatogenesis. Semin Cell Dev Biol 50:22-30; 2016. [28] Li, N.; Mruk, D. D.; Mok, K. W.; Li, M. W.; Wong, C. K.; Lee, W. M.; Han, D.; Silvestrini, B.; Cheng, C. Y. Connexin 43 reboots meiosis and reseals blood-testis barrier following toxicant-mediated aspermatogenesis and barrier disruption. FASEB J 30:1436-1452; 2016. [29] Chen, Z.; Xie, X.; Huang, J.; Gong, W.; Zhu, X.; Chen, Q.; Huang, J.; Huang, H. Connexin43 regulates high glucose-induced expression of fibronectin, ICAM-1 and TGF-β1 via Nrf2/ARE pathway in glomerular mesangial cells. Free Radic Biol Med 102:77-86; 2017.

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