Glutathione improves testicular spermatogenesis through inhibiting oxidative stress, mitochondrial damage, and apoptosis induced by copper deposition in mice with Wilson disease.
暂无分享,去创建一个
Dan Zhao | Xiang Liu | Limin Wu | Hui Han | Luyao Wang | Kuiyu Chen | Fang Tan | Jiabo Liu | Qianzhuo Liu | Xinru Fang
[1] Xiang Liu,et al. Copper deposition in Wilson’s disease causes male fertility decline by impairing reproductive hormone release through inducing apoptosis and inhibiting ERK signal in hypothalamic-pituitary of mice , 2022, Frontiers in Endocrinology.
[2] Keli Chen,et al. Long-term copper exposure promotes apoptosis and autophagy by inducing oxidative stress in pig testis , 2021, Environmental Science and Pollution Research.
[3] Wenlan Yu,et al. Protective effects of curcumin on ATO-induced nephrotoxicity in ducks in relation to suppressed autophagy, apoptosis and dyslipidemia by regulating oxidative stress. , 2021, Ecotoxicology and environmental safety.
[4] R. Vallone,et al. Reproductive function of long-term treated patients with hepatic onset of Wilson's disease: a prospective study. , 2020, Reproductive biomedicine online.
[5] A. Calogero,et al. Mitochondrial Membrane Potential Predicts 4-Hour Sperm Motility , 2020, Biomedicines.
[6] Ying-hua Jin,et al. Picrasma quassioides Extract Elevates the Cervical Cancer Cell Apoptosis Through ROS-Mitochondrial Axis Activated p38 MAPK Signaling Pathway , 2020, In Vivo.
[7] A. Agarwal,et al. Causes and consequences of sperm mitochondrial dysfunction , 2020, Andrologia.
[8] V. Sobhani,et al. Evaluation of the effects of different intensities of forced running wheel exercise on oxidative stress biomarkers in muscle, liver and serum of untrained rats , 2020, Lab Animal.
[9] N. Eskandari,et al. Curcumin protects the testis against cadmium-induced histopathological damages and oxidative stress in mice , 2019, Human & experimental toxicology.
[10] N. Qiao,et al. Copper-induced apoptosis and autophagy through oxidative stress-mediated mitochondrial dysfunction in male germ cells. , 2019, Toxicology in vitro : an international journal published in association with BIBRA.
[11] Vijay Kumar,et al. Heavy metal toxicity: An update of chelating therapeutic strategies. , 2019, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.
[12] P. Grzmil,et al. Functional iron deficiency in toxic milk mutant mice (tx-J) despite high hepatic ferroportin: a critical role of decreased GPI-ceruloplasmin expression in liver macrophages. , 2019, Metallomics : integrated biometal science.
[13] Zhuowei Zhang,et al. Copper induces oxidative stress and apoptosis through mitochondria-mediated pathway in chicken hepatocytes. , 2019, Toxicology in vitro : an international journal published in association with BIBRA.
[14] H. Zischka,et al. The exceptional sensitivity of brain mitochondria to copper. , 2018, Toxicology in vitro : an international journal published in association with BIBRA.
[15] M. Xing,et al. Arsenic and/or copper caused inflammatory response via activation of inducible nitric oxide synthase pathway and triggered heat shock protein responses in testis tissues of chicken , 2018, Environmental Science and Pollution Research.
[16] S. Abarikwu,et al. Rutin, an antioxidant flavonoid, induces glutathione and glutathione peroxidase activities to protect against ethanol effects in cadmium‐induced oxidative stress in the testis of adult rats , 2017, Andrologia.
[17] J. Kalita,et al. Memory and Learning Dysfunction Following Copper Toxicity: Biochemical and Immunohistochemical Basis , 2017, Molecular Neurobiology.
[18] P. Hedera. The Application of Clinical Genetics Dovepress Update on the Clinical Management of Wilson's Disease , 2022 .
[19] P. Dušek,et al. Pathogenesis of Wilson disease. , 2017, Handbook of clinical neurology.
[20] Nathan Bandow,et al. Methanobactin reverses acute liver failure in a rat model of Wilson disease. , 2016, The Journal of clinical investigation.
[21] Sudipta Basu,et al. Nanoparticle-Mediated Mitochondrial Damage Induces Apoptosis in Cancer. , 2016, ACS applied materials & interfaces.
[22] F. Jin,et al. Gallic acid induces apoptosis and enhances the anticancer effects of cisplatin in human small cell lung cancer H446 cell line via the ROS-dependent mitochondrial apoptotic pathway. , 2016, Oncology reports.
[23] J. Kalita,et al. Relationship of antioxidant and oxidative stress markers in different organs following copper toxicity in a rat model. , 2016, Toxicology and applied pharmacology.
[24] J. Kalita,et al. A Study on Apoptosis and Anti-apoptotic Status in Wilson Disease , 2016, Molecular Neurobiology.
[25] J. Kalita,et al. Role of Oxidative Stress in the Worsening of Neurologic Wilson Disease Following Chelating Therapy , 2015, NeuroMolecular Medicine.
[26] S. Sankhwar,et al. Differential Genes Expression between Fertile and Infertile Spermatozoa Revealed by Transcriptome Analysis , 2015, PloS one.
[27] S. Kaler,et al. Wilson's disease and other neurological copper disorders , 2015, The Lancet Neurology.
[28] K. Kuča,et al. Redox- and non-redox-metal-induced formation of free radicals and their role in human disease , 2015, Archives of Toxicology.
[29] R. Konwar,et al. A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings , 2014, Journal of Neuroimmunology.
[30] B. Mohit,et al. Importance of adequate decoppering in Wilson's disease , 2014, Movement disorders : official journal of the Movement Disorder Society.
[31] S. Sollott,et al. Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. , 2014, Physiological reviews.
[32] J. Kalita,et al. Worsening of Wilson Disease following Penicillamine Therapy , 2013, European Neurology.
[33] T. Rebai,et al. Wilson disease, genotype and infertility: is there a correlation? , 2013, Endocrine.
[34] A. Boveris,et al. The acute toxicity of iron and copper: biomolecule oxidation and oxidative damage in rat liver. , 2012, Journal of inorganic biochemistry.
[35] A. Kerkeni,et al. Impact of seminal trace element and glutathione levels on semen quality of Tunisian infertile men , 2012, BMC Urology.
[36] J. Martinou,et al. Mitochondria in apoptosis: Bcl-2 family members and mitochondrial dynamics. , 2011, Developmental cell.
[37] Nathan Bandow,et al. Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease. , 2011, The Journal of clinical investigation.
[38] D. Loo,et al. In situ detection of apoptosis by the TUNEL assay: an overview of techniques. , 2011, Methods in molecular biology.
[39] Michihiko Shibata,et al. Excess copper chelating therapy for Wilson disease induces anemia and liver dysfunction. , 2011, Internal medicine.
[40] A. Agarwal,et al. The role of antioxidant therapy in the treatment of male infertility , 2010, Human fertility.
[41] A. Mahdi,et al. Mitochondria, spermatogenesis and male infertility. , 2010, Mitochondrion.
[42] Sajal Gupta,et al. Female Infertility and Antioxidants , 2010 .
[43] G. Coticchio,et al. Ultrastructural markers of quality in human mature oocytes vitrified using cryoleaf and cryoloop. , 2009, Reproductive biomedicine online.
[44] A. Fischer,et al. Hematoxylin and eosin staining of tissue and cell sections. , 2008, CSH protocols.
[45] M. Finegold,et al. Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice. , 2006, The American journal of pathology.
[46] A. Agarwal,et al. A placebo-controlled double-blind randomized trial of the use of combined l-carnitine and l-acetyl-carnitine treatment in men with asthenozoospermia. , 2004, Fertility and sterility.
[47] J. Freedman,et al. Copper-inducible transcription: regulation by metal- and oxidative stress-responsive pathways. , 2004, American journal of physiology. Cell physiology.
[48] S. Salvioli,et al. Flow Cytometric Analysis of Mitochondrial Membrane Potential Using JC‐1 , 2000, Current protocols in cytometry.
[49] A. Means,et al. Spermiogenesis and exchange of basic nuclear proteins are impaired in male germ cells lacking Camk4 , 2000, Nature Genetics.
[50] A. Członkowska,et al. Procreation ability in Wilson's disease , 2000, Acta neurologica Scandinavica.
[51] A. Agarwal,et al. Relationship between oxidative stress, semen characteristics, and clinical diagnosis in men undergoing infertility investigation. , 2000, Fertility and sterility.
[52] F. Ursini,et al. Dual function of the selenoprotein PHGPx during sperm maturation. , 1999, Science.
[53] Diane W. Cox,et al. 3 Wilson disease , 1998 .
[54] I. Sternlieb,et al. Wilson disease and idiopathic copper toxicosis. , 1996, The American journal of clinical nutrition.
[55] J. Hansen,et al. Selenium and Fertility in Animals and Man–A Review , 1996, Acta Veterinaria Scandinavica.
[56] A. Lenzi,et al. Placebo-controlled, double-blind, cross-over trial of glutathione therapy in male infertility. , 1993, Human reproduction.
[57] I. Sternlieb. Fraternal concordance of types of abnormal hepatocellular mitochondria in Wilson's disease , 1992, Hepatology.
[58] C. Pfeiffer,et al. Wilson's disease. , 2007, Archives of neurology.
[59] G. Feldmann,et al. Effects of anticopper therapy on hepatocellular mitochondria in patients with Wilson's disease: an ultrastructural and stereological study. , 1976, Gastroenterology.