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首页> 外文期刊>Biology of Sex Differences >Sex-specific phenotypes of hyperthyroidism and hypothyroidism in aged mice
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Sex-specific phenotypes of hyperthyroidism and hypothyroidism in aged mice

机译:老年小鼠甲状腺功能亢进和甲状腺功能减退的性别特异性表型

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Sex and age play a role in the prevalence of thyroid dysfunction (TD), but their interrelationship for manifestation of hyper- and hypothyroidism is still not well understood. Using a murine model, we asked whether sex impacts the phenotypes of hyper- and hypothyroidism at two life stages. Hyper- and hypothyroidism were induced by i.p. T4 or MMI/ClO4-/LoI treatment over 7?weeks in 12- and 20-months-old female and male C57BL/6N mice. Control animals underwent PBS treatment (n?=?7–11 animals/sex/treatment). Animals were investigated for impact of sex on body weight, food and water intake, body temperature, heart rate, behaviour (locomotor activity, motor coordination and strength) and serum thyroid hormone (TH) status. Distinct sex impact was found in eu- and hyperthyroid mice, while phenotypic traits of hypothyroidism were similar in male and female mice. No sex difference was found in TH status of euthyroid mice; however, T4 treatment resulted in twofold higher TT4, FT4 and FT3 serum concentrations in adult and old females compared to male animals. Hyperthyroid females consistently showed higher locomotor activity and better coordination but more impairment of muscle function by TH excess at adult age. Importantly and in contrast to male mice, adult and old hyperthyroid female mice showed increased body weight. Higher body temperature in female mice was confirmed in all age groups. No sex impact was found on heart rate irrespective of TH status in adult and old mice. By comparison of male and female mice with TD at two life stages, we found that sex modulates TH action in an organ- and function-specific manner. Sex differences were more pronounced under hyperthyroid conditions. Importantly, sex-specific differences in features of TD in adult and old mice were not conclusively explained by serum TH status in mice.
机译:性别和年龄在甲状腺功能障碍(TD)的患病率中起一定作用,但对于甲状腺功能亢进和甲状腺功能减退的表现之间的相互关系仍不甚了解。使用鼠模型,我们询问性别在两个生命阶段是否会影响甲亢和甲状腺功能减退症的表型。 i.p.诱发甲亢和甲状腺功能减退。在12和20个月大的雌性和雄性C57BL / 6N小鼠中,在7周内进行了T4或MMI / ClO4- / LoI处理。对照动物接受PBS处理(n?=?7-11动物/性别/处理)。研究了动物的性别对体重,食物和水的摄入量,体温,心率,行为(运动能力,运动协调能力和强度)和血清甲状腺激素(TH)状态的影响。在正常和甲状腺功能亢进的小鼠中发现了明显的性别影响,而雌雄小鼠的甲状腺功能减退症的表型特征相似。正常甲状腺小鼠的TH状态未发现性别差异;然而,与雄性动物相比,T4处理导致成年和成年雌性的TT4,FT4和FT3血清浓度高出两倍。甲亢女性一贯表现出较高的运动能力和更好的协调性,但成年后TH过量会导致更多的肌肉功能受损。重要的是,与雄性小鼠相比,成年和老年甲状腺功能亢进的雌性小鼠体重增加。在所有年龄组中均确认雌性小鼠体温升高。不论成年和成年小鼠的TH状态如何,均未发现对心律有性别影响。通过比较处于两个生命阶段的TD的雄性和雌性小鼠,我们发现性别以器官和功能特异性方式调节TH作用。在甲状腺功能亢进的条件下,性别差异更为明显。重要的是,成年和成年小鼠中TD的性别特异性差异并不能通过小鼠血清中的TH状态来得出结论。

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