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Hypothyroidism and oxidative stress: Differential effect on the heart of virgin and pregnant rats

机译:甲状腺功能减退和氧化应激:对处女和怀孕大鼠心脏的差异作用

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摘要

The present study investigates the effects of hypothyroidism on both the redox state and the thyroid hormone receptors expression in the heart ventricle of virgin and pregnant rats. Hypothyroid state was induced by 6-n-propyl-2-thiouracil in drinking water given to Wistar rats starting 8 days before mating until day 21 of pregnancy or for 30 days in virgin rats. Serum paraoxonase-1 (PON-1) activity, serum and heart nitrites, and thiobarbituric acid-reactive substances (TBARS) were analyzed. Heart protein oxidation, as carbonyls, and copper-zinc superoxide dismutase (CuZnSOD), glutathione peroxidase (GPx), and catalase (CAT) activities, were determined. In addition, heart expressions of NADPH oxidase (NOX-2), CAT, SOD, GPx, and thyroid receptors (TRα and TRβ) mRNA were assessed by RT-PCR. Inducible and endothelial Nitric Oxide Synthase (iNOS and eNOS) were determined by Western blot. Hypothyroidism in the heart of virgin rats decreased TRα and TRβ expressions, and induced oxidative stress, leading to a decrease of nitrites and an increase of carbonyls, NOX-2 mRNA, and GPx activity. A decreased PON-1 activity suggested low protection against oxidative stress in blood circulation. Pregnancy reduced TRα and TRβ mRNA expressions and induced oxidative stress by increasing nitrite and TBARS levels, SOD and CAT activities and NOX-2, eNOS and iNOS expressions, while hypothyroidism, emphasized the decreases of TRα mRNA levels and did not alter the redox state in the heart. TR expressions and redox balance of rat hearts depend on the physiological state. Pregnancy per se seems to protect the heart against oxidative stress induced by hypothyroidism.
机译:本研究调查了甲状腺功能低下对处女和怀孕大鼠心室中氧化还原状态和甲状腺激素受体表达的影响。在交配前8天至妊娠第21天或初次大鼠中,在Wistar大鼠饮用饮用水中的6-n-丙基-2-硫氧嘧啶诱导甲状腺功能减退状态。分析了血清对氧磷酶-1(PON-1)活性,血清和心脏亚硝酸盐以及硫代巴比妥酸反应性物质(TBARS)。确定了心脏蛋白的氧化形式(羰基),铜锌超氧化物歧化酶(CuZnSOD),谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)活性。另外,通过RT-PCR评估NADPH氧化酶(NOX-2),CAT,SOD,GPx和甲状腺受体(TRα和TRβ)mRNA的心脏表达。通过蛋白质印迹法测定诱导型和内皮型一氧化氮合酶(iNOS和eNOS)。处女大鼠心脏的甲状腺功能减退会降低TRα和TRβ的表达,并诱导氧化应激,导致亚硝酸盐的减少和羰基,NOX-2 mRNA和GPx活性的增加。 PON-1活性降低表明对血液循环中的氧化应激的保护作用很低。怀孕通过增加亚硝酸盐和TBARS水平,SOD和CAT活性以及NOX-2,eNOS和iNOS的表达降低TRα和TRβmRNA的表达并诱导氧化应激,而甲状腺功能减退症则强调TRαmRNA的降低且不改变氧化还原状态。心。大鼠心脏的TR表达和氧化还原平衡取决于生理状态。怀孕本身似乎可以保护心脏免受甲状腺机能减退引起的氧化应激的影响。

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