首页> 外文期刊>Biological trace element research >The Association Between Thyroid Injury and Apoptosis, and Alterations of Bax, Bcl-2, and Caspase-3 mRNA/Protein Expression Induced by Nickel Sulfate in Wistar Rats
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The Association Between Thyroid Injury and Apoptosis, and Alterations of Bax, Bcl-2, and Caspase-3 mRNA/Protein Expression Induced by Nickel Sulfate in Wistar Rats

机译:硫酸镍大鼠硫酸镍诱导的甲状腺损伤和凋亡的关系,以及Bax,Bcl-2和Caspase-3 mRNA /蛋白表达的变化

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To study the toxicity induced by Nickel sulfate (NiSO4) on thyroid tissue, and investigate the role of apoptosis as the possible mechanism, thirty-two male Wistar rats were randomly divided into control group (normal saline, ip), low dose group (2.5 mg/kg day NiSO4, ip), middle dose group (5 mg/kg day NiSO4, ip), high dose group (10 mg/kg day NiSO4, ip). After 40 consecutive days of treatment, there were obvious pathological changes in the thyroids of high dose group. Free T-4 (FT4) and thyroid-stimulating hormone (TSH) were significantly lower in the NiSO4-treated groups than those in the control group (F = 4.992, p = 0.016; F = 4.524, p = 0.012). The mRNA expression of Caspase-3 was significantly higher (F = 10.259, p = 0.014) in all NiSO4-treated groups, and the mRNA expression of Bcl-2 was significantly lower (F = 9.225, p = 0.018) only in the high dose group. Both control group and the NiSO4-treated groups showed no changes in the mRNA expression of Bax gene. The ratio of Bcl-2/Bax decreased with the increase in exposure dose of NiSO4 (F = 13.382, p = 0.015). The mRNA expression of Fas went up in high dose group (F = 66.632, p < 0.001). The Caspase-3, Fas, and the Bax protein expressions measured by immunohistochemistry were consistent with the mRNA expression. The expression of Bcl-2 protein was significantly lower in the test groups than in the control group (F = 3.873, p = 0.025). NiSO4 as an Endocrine Disrupting Chemical may induce the thyroid injury through apoptosis and lead to hypothyroidism. Also, apoptosis in thyroid tissues was closely related to the alternations of Caspase-3, Bcl-2, and Fas mRNA and protein expression.
机译:为了研究硫酸镍(NISO 4)诱导的甲状腺组织诱导的毒性,并研究凋亡的作用作为可能的机制,将32只雄性Wistar大鼠随机分为对照组(正常盐水,IP),低剂量组(2.5 Mg / kg Day Niso4,IP),中剂量组(5mg / kg日Niso4,IP),高剂量组(10 mg / kg Day Niso4,IP)。连续40天治疗后,高剂量组甲状腺发生明显的病理变化。在NISO 4处理组中,游离T-4(FT4)和甲状腺刺激激素(TSH)显着低于对照组(F = 4.992,P = 0.016; F = 4.524,P = 0.012)。在所有NISO 4处理基团中,Caspase-3的mRNA表达显着更高(f = 10.259,p = 0.014),并且Bcl-2的mRNA表达仅在高处剂量组。对照组和NISO 4治疗组均显示BAX基因的mRNA表达没有变化。 Bcl-2 / Bax的比例随NISO 4的曝光剂量的增加而降低(F = 13.382,P = 0.015)。 FAS的mRNA表达在高剂量组(f = 66.632,p <0.001)中。通过免疫组织化学测量的Caspase-3,Fas和Bax蛋白表达与mRNA表达一致。测试组中Bcl-2蛋白的表达显着低于对照组(F = 3.873,P = 0.025)。 NISO4作为内分泌破坏化学物质可以通过凋亡诱导甲状腺损伤并导致甲状腺功能亢进。此外,甲状腺组织中的细胞凋亡与Caspase-3,Bcl-2和Fas mRNA和蛋白质表达的交替密切相关。

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