• 其次毒性问题

    The second issue is that of lipotoxicity.

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  • 目的探讨针刺是否具有抑制毒性作用及其可能机制

    Objective to investigate if acupuncture has an inhibitory effect on fatty toxicity and its possible mechanism.

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  • 心脏质大量积聚可以引起心脏功能异常称之为脂毒性心肌病。

    Lipid accumulation in the heart may lead to cardiac dysfunction, which is called lipotoxic cardiomyopathy.

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  • 心肌游离肪酸摄入利用失协调导致心肌中积聚进而引起脂毒性心肌病

    Mismatches between myocardial fatty acid uptake and utilization lead to the accumulation of cardiotoxic lipid species, and cause lipotoxic cardiomyopathy.

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  • 结论针刺可以降低肥胖患者游离肪酸水平提高胰岛素敏感性,从而表现出抑制毒性效应

    Conclusion Acupuncture can lower the levels of free fatty acids in the patients and increase their sensitivity to insulin to inhibit the effect of fatty toxicity.

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  • 研究过氧化物酶体增殖剂活化受体脂毒性心肌病中的作用可以预防治疗脂毒性心肌病提供思路。

    Studies of the role of the peroxisome proliferators-activated receptor plays in lipotoxic cardiomyopathy will provide new strategies to prevent and cure lipotoxic cardiomyopathy.

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  • 吸收组织人体处理这种毒性一种途径

    Absorbing them into adipose tissue is one of the body's ways of dealing with that toxicity.

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  • 多糖绑定血浆白蛋白形成复合物增加LPS毒性以及LPS受体的亲和力

    LPS can bind to plasma proteins and form complexes that increase toxic activity of LPS and affinity of LPS to cell receptors.

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  • 提示过氧化可能毒性作用机制之一

    It indicates that lipid peroxidation may be one of the mechanisms of liver and brain injury in arsenic poisoning.

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  • 结论潜在致畸胚胎毒性,胚胎组织gsh活性和卵黄囊细胞膜流动性降低可能氟致胚胎发育毒性起重要作用

    Conclusions Fluoride could result in embryonic growth retardation and potential teratogenic toxicity. These effects might be due in part to decrease in GSH activity and membrane lipid fluidity.

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  • 润滑油毒性主要来源于添加剂填充物主要危害皮炎

    The toxicity of lubricating oil and grease 'chiefly stem from additives and stuff. Its main harm is dermatitis.

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  • 苯妥英缺血性脑损伤神经保护作用与其抑制自由基形成,减轻自由基介导毒性,抗过氧化反应以及扩张血管,增加局部流量有关。

    Phenytoin sodium may protect brain tissues from cerebral ischemic injury by inhibiting formation of free radical, anti-lipid peroxidation and improving regional cerebral blood flow.

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  • 结论微囊藻毒素- LR细胞毒性剂量下引起细胞的氧化应激,但尚不足以导致质过氧化。

    Conclusion The dose of MCLR that is not cytotoxic can induce hepatocyte oxidative stress, which can not be identified as lipid peroxidation yet.

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  • 目的探讨氯化对NRK细胞毒性作用过氧化影响

    Objective to investigate the effects of cadmium chloride on cytotoxicity and lipid - peroxidation reaction in NRK cells.

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  • 目的研究排毒胶囊长期毒性

    Objective to study the long-term toxicity of Paidu Qingzhi capsule in rats.

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  • 结论2 -氧基乙醇引起肝脏一氧化氮自由基增加诱发过氧化反应对肝脏发生毒性作用

    Conclusion the study demonstrated that 2 ethoxyethanol can increase the liver level of no free radicals and the lipid peroxidation may play an important role in 2 ethoxyethanol's liver toxicity.

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  • 目的:研究p选择高胆固醇血症小鼠肾脏表达探讨质肾毒性损伤机制

    Objective: to detect the expression of P-selectin in mice with hypercholesterolemia, and to explore the mechanism of toxic injury to the kidney induced by lipid.

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  • 目的研究及其子体对小鼠血液质过氧化以及骨髓毒性联合作用及其类型,进一步探讨二者联合毒作用的机理提供实验依据

    Objective: To study the joint effects of radon and benzene on the blood and bone marrow of mice to provide experimental data for further study.

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  • 阳离子质体毒性主要来自于小分子阳离子质分子。

    Cytotoxicity of cationic liposome is mainly engendered by cationic lipid.

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  • 过氧化反应产生产物mda具有细胞毒性所以可以通过测mda含量评价细胞质受损程度

    Produced by lipid peroxidation end products MDA cytotoxicity, so the content of MDA can be measured to assess the extent of the damage of cell plasma membrane.

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  • 通过药物组合物包含LL - 37的生长培养基包括双层性极性,具体为双乳糖基甘油二酯,降低LL - 37的细胞毒性作用

    The cytotoxic effect of LL-37 may be reduced by including a bilayer-forming polar lipid, especially a digalactosyldiacylglycerol, in pharmaceutical compositions and growth media comprising LL-37.

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  • 嗜热菌杀酵母素通过耗尽细胞诱导凋亡抑制白介素2依赖性小鼠毒性细胞增殖一种有效免疫抑制剂

    Myriocin induces apoptosis by depletion of cellular sphingolipids, inhibits proliferation of IL-2-dependent mouse cytotoxic cells and is a potent immunosuppressant.

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  • 嗜热菌杀酵母素通过耗尽细胞诱导凋亡抑制白介素2依赖性小鼠毒性细胞增殖一种有效免疫抑制剂

    Myriocin induces apoptosis by depletion of cellular sphingolipids, inhibits proliferation of IL-2-dependent mouse cytotoxic cells and is a potent immunosuppressant.

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