12 results on '"Sang, Xuezi"'
Search Results
2. Neurotoxic characteristics of spatial recognition damage of the hippocampus in mice following subchronic peroral exposure to TiO2 nanoparticles.
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Ze, Yuguan, Sheng, Lei, Zhao, Xiaoyang, Ze, Xiao, Wang, Xuecen, Zhou, Qiuping, Liu, Jialiang, Yuan, Yifei, Gui, Suxin, Sang, Xuezi, Sun, Qingqing, Hong, Jie, Yu, Xiaohong, Wang, Ling, Li, Bingyan, and Hong, Fashui
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NEUROTOXICOLOGY , *HIPPOCAMPUS physiology , *TITANIUM dioxide , *METAL nanoparticles , *GENE expression , *LABORATORY mice - Abstract
Highlights: [•] TiO2 NPs exposure resulted in hippocampus injury and decreased spatial recognition of mice. [•] TiO2 NPs exposure resulted in decreased long-term potentiation. [•] TiO2 NPs exposure caused down-regulation of NR2A and NR2B expression in hippocampus. [•] TiO2 NPs decreased expression of CaMKIV, CREB-1 and FosB/DFosB. [Copyright &y& Elsevier]
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- 2014
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3. Oxidative stress in the kidney injury of mice following exposure to lanthanides trichloride.
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Zhao, Haiquan, Hong, Jie, Yu, Xiaohong, Zhao, Xiaoyang, Sheng, Lei, Ze, Yuguan, Sang, Xuezi, Gui, Suxin, Sun, Qingqing, Wang, Ling, and Hong, Fashui
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OXIDATIVE stress , *KIDNEY injuries , *RARE earth metals , *KIDNEY function tests , *ANTIOXIDANTS , *LABORATORY mice - Abstract
Highlights: [•] Exposure to lanthanides impaired renal function in mice. [•] Exposure to lanthanides induced cell necrosis in kidney. [•] Exposure to lanthanides promoted ROS accumulation in kidney. [•] Exposure to lanthanides caused the reduction of antioxidant capacity in kidney. [•] The order of kidney damages was Ce exposure>Nd exposure>La exposure. [Copyright &y& Elsevier]
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- 2013
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4. Molecular mechanism of titanium dioxide nanoparticles-induced oxidative injury in the brain of mice.
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Ze, Yuguan, Zheng, Lei, Zhao, Xiaoyang, Gui, Suxin, Sang, Xuezi, Su, Junju, Guan, Ning, Zhu, Liyuan, Sheng, Lei, Hu, Renping, Cheng, Jie, Cheng, Zhe, Sun, Qingqing, Wang, Ling, and Hong, Fashui
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BRAIN injuries , *NANOMEDICINE , *TITANIUM dioxide , *OXIDATIVE stress , *LABORATORY mice , *GENETIC regulation , *CELL proliferation , *REACTIVE oxygen species , *PHYSIOLOGY - Abstract
Abstract: Numerous studies have demonstrated that the brain is one of the target organs in acute or chronic titanium dioxide (TiO2) nanoparticles (NPs) toxicity, and oxidative stress plays an important role in this process. However, whether brain oxidative injury responds to TiO2 NPs by activating the P38-nuclear factor-E2-related factor-2 (Nrf-2) pathway is not fully understood. The present study aimed to examine activation of the P38-Nrf-2 signaling pathway associated with oxidative stress in the mouse brain induced by intranasal administration of TiO2 NPs for 90 consecutive days. Our findings indicate that TiO2 NPs caused overproliferation of spongiocytes and hemorrhage in the mouse brain. Furthermore, TiO2 NPs significantly activated p38, c-Jun N-terminal kinase, nuclear factor kappa B, Nrf-2 and heme oxygenase-1 expression in the brain, which in turn, led to increased production of reactive oxygen species, as well as lipid, protein and DNA peroxidation. These findings suggest that TiO2 NPs-induced oxidative damage in the mouse brain may occur via the p38-Nrf-2 signaling pathway. Therefore, application of TiO2 NPs in the environment should be performed with caution. [Copyright &y& Elsevier]
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- 2013
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5. Titanium dioxide nanoparticle-induced testicular damage, spermatogenesis suppression, and gene expression alterations in male mice.
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Gao, Guodong, Ze, Yuguan, Zhao, Xiaoyang, Sang, Xuezi, Zheng, Lei, Ze, Xiao, Gui, Suxin, Sheng, Lei, Sun, Qingqing, Hong, Jie, Yu, Xiaohong, Wang, Ling, Hong, Fashui, and Zhang, Xueguang
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TITANIUM dioxide nanoparticles , *TESTICULAR diseases , *SPERMATOGENESIS , *GENE expression , *LABORATORY mice , *SEX hormones , *SPERM motility - Abstract
Highlights: [•] Exposure to TiO2 NPs could cross blood–testis barrier and be accumulated in testis. [•] Exposure to TiO2 NPs caused testis and sperm lesions in male mice. [•] Exposure to TiO2 NP decreased sperm numbers and sperm motility in male mice. [•] Exposure to TiO2 NP resulted in imbalance of sex hormones in male mice. [•] Exposure to TiO2 NP caused alteration of 142 genes expression of known function in testis. [ABSTRACT FROM AUTHOR]
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- 2013
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6. Gene-Expression Changes in Cerium Chloride-Induced Injury of Mouse Hippocampus.
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Cheng, Zhe, Zhao, Haiquan, Ze, Yuguan, Su, Junju, Li, Bing, Sheng, Lei, Zhu, Liyuan, Guan, Ning, Gui, Suxin, Sang, Xuezi, Zhao, Xiaoyang, Sun, Qingqing, Wang, Ling, Cheng, Jie, Hu, Renping, and Hong, Fashui
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HIPPOCAMPUS injuries , *GENE expression , *CERIUM , *NEUROTOXIC agents , *OXIDATIVE stress , *APOPTOSIS , *INFLAMMATION , *CELLULAR signal transduction - Abstract
Cerium is widely used in many aspects of modern society, including agriculture, industry and medicine. It has been demonstrated to enter the ecological environment, is then transferred to humans through food chains, and causes toxic actions in several organs including the brain of animals. However, the neurotoxic molecular mechanisms are not clearly understood. In this study, mice were exposed to 0.5, 1, and 2 mg/kg BW cerium chloride (CeCl3) for 90 consecutive days, and their learning and memory ability as well as hippocampal gene expression profile were investigated. Our findings suggested that exposure to CeCl3 led to hippocampal lesions, apoptosis, oxidative stress and impairment of spatial recognition memory. Furthermore, microarray data showed marked alterations in the expression of 154 genes involved in learning and memory, immunity and inflammation, signal transduction, apoptosis and response to stress in the 2 mg/kg CeCl3 exposed hippocampi. Specifically, the significant up-regulation of Axud1, Cdc37, and Ube2v1 caused severe apoptosis, and great suppression of Adcy8, Fos, and Slc5a7 expression led to impairment of mouse cognitive ability. Therefore, Axud1, Cdc37, Ube2v1, Adcy8, Fos, and Slc5a7 may be potential biomarkers of hippocampal toxicity caused by CeCl3 exposure. [ABSTRACT FROM AUTHOR]
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- 2013
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7. Nanosized TiO2-Induced Reproductive System Dysfunction and Its Mechanism in Female Mice.
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Zhao, Xiaoyang, Ze, Yuguan, Gao, Guodong, Sang, Xuezi, Li, Bing, Gui, Suxin, Sheng, Lei, Sun, Qingqing, Cheng, Jie, Cheng, Zhe, Hu, Renping, Wang, Ling, and Hong, Fashui
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FEMALE reproductive organs , *OVARIES , *TITANIUM dioxide , *CYTOKINES , *GENE expression , *SERUM , *SEX hormones , *LABORATORY mice , *WOUNDS & injuries - Abstract
Recent studies have demonstrated nanosized titanium dioxide (nano-TiO2)-induced fertility reduction and ovary injury in animals. To better understand how nano-TiO2 act in mice, female mice were exposed to 2.5, 5, and 10 mg/kg nano-TiO2 by intragastric administration for 90 consecutive days; the ovary injuries, fertility, hormone levels, and inflammation-related or follicular atresia-related cytokine expression were investigated. The results showed that nano-TiO2 was deposited in the ovary, resulting in significant reduction of body weight, relative weight of ovary and fertility, alterations of hematological and serum parameters and sex hormone levels, atretic follicle increases, inflammation, and necrosis. Furthermore, nano-TiO2 exposure resulted in marked increases of insulin-like growth factor-binding protein 2, epidermal growth factor, tumor necrosis factor-α, tissue plasminogen activator, interleukin-1β, interleukin -6, Fas, and FasL expression, and significant decreases of insulin-like growth factor-1, luteinizing hormone receptor, inhibin α, and growth differentiation factor 9 expression in mouse ovary. These findings implied that fertility reduction and ovary injury of mice following exposure to nano-TiO2 may be associated with alteration of inflammation-related or follicular atresia-related cytokine expressions, and humans should take great caution when handling nano-TiO2. [ABSTRACT FROM AUTHOR]
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- 2013
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8. Molecular Mechanisms of Nanosized Titanium Dioxide–Induced Pulmonary Injury in Mice.
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Li, Bing, Ze, Yuguan, Sun, Qingqing, Zhang, Ting, Sang, Xuezi, Cui, Yaling, Wang, Xiaochun, Gui, Suxin, Tan, Danlin, Zhu, Min, Zhao, Xiaoyang, Sheng, Lei, Wang, Ling, Hong, Fashui, and Tang, Meng
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MOLECULAR biology , *TITANIUM dioxide , *DRUG side effects , *LUNG injuries , *PHOSPHATES , *CELLULAR signal transduction , *CELL proliferation , *LABORATORY mice - Abstract
The pulmonary damage induced by nanosized titanium dioxide (nano-TiO2) is of great concern, but the mechanism of how this damage may be incurred has yet to be elucidated. Here, we examined how multiple genes may be affected by nano-TiO2 exposure to contribute to the observed damage. The results suggest that long-term exposure to nano-TiO2 led to significant increases in inflammatory cells, and levels of lactate dehydrogenase, alkaline phosphate, and total protein, and promoted production of reactive oxygen species and peroxidation of lipid, protein and DNA in mouse lung tissue. We also observed nano-TiO2 deposition in lung tissue via light and confocal Raman microscopy, which in turn led to severe pulmonary inflammation and pneumonocytic apoptosis in mice. Specifically, microarray analysis showed significant alterations in the expression of 847 genes in the nano-TiO2-exposed lung tissues. Of 521 genes with known functions, 361 were up-regulated and 160 down-regulated, which were associated with the immune/inflammatory responses, apoptosis, oxidative stress, the cell cycle, stress responses, cell proliferation, the cytoskeleton, signal transduction, and metabolic processes. Therefore, the application of nano-TiO2 should be carried out cautiously, especially in humans. [ABSTRACT FROM AUTHOR]
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- 2013
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9. Ovarian dysfunction and gene-expressed characteristics of female mice caused by long-term exposure to titanium dioxide nanoparticles
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Gao, Guodong, Ze, Yuguan, Li, Bing, Zhao, Xiaoyang, Zhang, Ting, Sheng, Lei, Hu, Ringhu, Gui, Suxin, Sang, Xuezi, Sun, Qingqing, Cheng, Jie, Cheng, Zhe, Wang, Ling, Tang, Meng, and Hong, Fashui
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GENE expression , *TITANIUM dioxide nanoparticles , *OVARIAN physiology , *SEX hormones , *OXIDATIVE stress , *GENETIC regulation , *PROGESTERONE , *LABORATORY mice - Abstract
Abstract: Although numerous studies have described the accumulation of titanium dioxide nanoparticles (TiO2 NPs) in the liver, kidneys, lung, spleen, and brain, and the corresponding damage, it is unclear whether or not TiO2 NPs can be translocated to the ovary and cause ovarian injury, thus impairing fertility. In the current study, ovarian injury and gene-expressed characteristics in female mice induced by intragastric administration of TiO2 NPs (10mg/kg) for 90 consecutive days were investigated. Our findings indicated that TiO2 NPs can accumulate in the ovary and result in ovarian damage, cause an imbalance of mineral element distribution and sex hormones, decrease fertility or the pregnancy rate and oxidative stress in mice. Microarray analysis showed that in ovaries from mice treated with TiO2 NPs compared to controls, 223 genes of known function were up-regulated, while 65 ovarian genes were down-regulated. The increased expression of Cyp17a1 following TiO2 NPs treatment suggested that the increase in estradiol biosynthesis may be a consequence of increased TiO2 NPs. In addition, the elevated expression of Akr1c18 implied that progesterone metabolism was accelerated, thus causing a decrease in the progesterone concentration. Taken together, the apparent regulation of key ovarian genes supports the hypothesis that TiO2 NPs directly affects ovarian function. [Copyright &y& Elsevier]
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- 2012
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10. Pulmotoxicological effects caused by long-term titanium dioxide nanoparticles exposure in mice
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Sun, Qingqing, Tan, Danning, Ze, Yuguan, Sang, Xuezi, Liu, Xiaorun, Gui, Suxin, Cheng, Zhe, Cheng, Jie, Hu, Renping, Gao, Guodong, Liu, Gan, Zhu, Min, Zhao, Xiaoyang, Sheng, Lei, Wang, Ling, Tang, Meng, and Hong, Fashui
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INFLAMMATION , *TITANIUM dioxide nanoparticles , *LABORATORY mice , *PULMONARY artery , *LIPID peroxidation (Biology) , *CYCLOOXYGENASE 2 , *CYTOKINES , *WOUNDS & injuries - Abstract
Abstract: Exposure to titanium dioxide nanoparticles (TiO2 NPs) has been demonstrated to result in pulmonary inflammation in animals; however, very little is known about the molecular mechanisms of pulmonary injury due to TiO2 NPs exposure. The aim of this study was to evaluate the oxidative stress and molecular mechanism associated with pulmonary inflammation in chronic lung toxicity caused by the intratracheal instillation of TiO2 NPs for 90 consecutive days in mice. Our findings suggest that TiO2 NPs are significantly accumulated in the lung, leading to an obvious increase in lung indices, inflammation and bleeding in the lung. Exposure to TiO2 NPs significantly increased the accumulation of reactive oxygen species and the level of lipid peroxidation, and decreased antioxidant capacity in the lung. Furthermore, TiO2 NPs exposure activated nuclear factor-κB, increased the levels of tumor necrosis factor-α, cyclooxygenase-2, heme oxygenase-1, interleukin-2, interleukin-4, interleukin-6, interleukin-8, interleukin-10, interleukin-18, interleukin-1β, and CYP1A1 expression. However, TiO2 NPs exposure decreased NF-κB-inhibiting factor and heat shock protein 70 expression. Our results suggest that the generation of pulmonary inflammation caused by TiO2 NPs in mice is closely related to oxidative stress and the expression of inflammatory cytokines. [Copyright &y& Elsevier]
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- 2012
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11. Titanium dioxide nanoparticles relieve biochemical dysfunctions of fifth-instar larvae of silkworms following exposure to phoxim insecticide
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Li, Bing, Hu, Rengping, Cheng, Zhe, Cheng, Jie, Xie, Yi, Gui, Suxin, Sun, Qingqing, Sang, Xuezi, Gong, Xiaolan, Cui, Yaling, Shen, Weide, and Hong, Fashui
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TITANIUM dioxide , *NANOPARTICLES , *INSECTICIDES , *SILKWORMS , *INSECT pests , *ASPARTATE aminotransferase , *MALATE dehydrogenase - Abstract
Abstract: Phoxim insecticide is widely used in agriculture, which is toxic to insect pests and nontarget organisms. The phoxim poisoning is hard to prevent for silkworms. TiO2 NPs have been widely applied in whitening, brightening foods, toothpaste or sunscreens, and orally-administered drugs. However, whether TiO2 NPs can increase resistance of silkworm to phoxim poisoning has not been reported. The results demonstrated that added TiO2 NPs significantly decreased reduction of protein, glucose and pyruvate contents, lactate dehydrogenase, succinate dehydrogenase and malate dehydrogenase activities, and attenuated increases of free amino acids, urea, uric acid and lactate levels, activities of protease, alanine aminotransferase and aspartate aminotransferase in the hemolymph of silkworms caused by phoxim exposure. From the present study, it is clearly evident that added TiO2 NPs may relieve toxic impacts of phoxim insecticide on silkworm metabolism, which in turn may result in an increase in silk yield. [Copyright &y& Elsevier]
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- 2012
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12. Molecular mechanism of kidney injury of mice caused by exposure to titanium dioxide nanoparticles
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Gui, Suxing, Zhang, Zengli, Zheng, Lei, Cui, Yaling, Liu, Xiaorun, Li, Na, Sang, Xuezi, Sun, Qingqing, Gao, Guodong, Cheng, Zhe, Cheng, Jie, Wang, Ling, Tang, Meng, and Hong, Fashui
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KIDNEY injuries , *LABORATORY mice , *TITANIUM dioxide , *NANOPARTICLES , *KIDNEY diseases , *NF-kappa B , *TUMOR necrosis factors , *GENE expression , *INTERLEUKINS , *TRANSFORMING growth factors , *METABOLIC detoxification - Abstract
Abstract: Numerous studies have demonstrated that damage of kidney of mice can be caused by exposure to titanium dioxide nanoparticles (TiO2 NPs). However, the molecular mechanism of TiO2 NPs-induced nephric injury remains unclear. In this study, the mechanism of nephric injury in mice induced by an intragastric administration of TiO2 NPs was investigated. The results showed that TiO2 NPs were accumulated in the kidney, resulting in nephric inflammation, cell necrosis and dysfunction. Nucleic factor-κB was activated by TiO2 NPs exposure, promoting the expression levels of tumor necrosis factor-α, macrophage migration inhibitory factor, interleukin-2, interleukin-4, interleukin-6, interleukin-8, interleukin-10, interleukin-18, interleukin-1β, cross-reaction protein, transforming growth factor-β, interferon-γ and CYP1A1, while heat shock protein 70 expression was inhibited. These findings implied that TiO2 NPs-induced nephric injury of mice might be associated with alteration of inflammatory cytokine expression and reduction of detoxification of TiO2 NPs. [Copyright &y& Elsevier]
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- 2011
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