首页> 外文期刊>Pediatric Research >27 THYROXIN (T4) EFFECTS ON GROWTH AND HEPATIC EPIDERMAL GROWTH FACTOR RECEPTOR (EGF) ONTOGENY IN MICE WITH CONGENITAL HYPOTHYROIDISM (CH)
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27 THYROXIN (T4) EFFECTS ON GROWTH AND HEPATIC EPIDERMAL GROWTH FACTOR RECEPTOR (EGF) ONTOGENY IN MICE WITH CONGENITAL HYPOTHYROIDISM (CH)

机译:27甲状腺素(T4)对先天性甲状腺功能低下症(CH)小鼠生长和肝表皮生长因子受体(EGF)的影响

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The effects of thyroid hormones on growth and development are probably mediated by specific growth factors as EGF. We have studied the effects of thyroxine on growth and hepatic EGF receptor ontogeny in a mouse strain with an inherited form of CH.Hypothyroid mice (h/h) were treated with T4 between day 20 and day 40 postnatally, h/h nontreated mice and euthyroid (+/+) mice served as controls. Animals were killed at day 20 or day 40 postnatally. Serum thyroxine was measured by RIA and EGF receptor binding in a liver plasma-membrane homogenate. Up to 20 days of age all mice showed the same weight gain and EGF hepatic receptor binding were low and not significantly different between h/h and +/+ mice. From day 20 h/h mice had a significantly lower growth rate than +/+ mice, a growth retardation that were normalised by T4 treatment.Early postnatal growth (day 0-20) in mice is thyroid hormone independent and resembles in that respect late prenatal growth in humans. In contrast, between day 20 and 40 postnatally thyroid hormone is necessary for normal growth and for the increase in hepatic EGF binding observed in mice. Our results indicate that an altered ontogeny of Epidermal Growth Factor receptors might be involved in the growth and developmental retardation found in CH.
机译:甲状腺激素对生长和发育的影响可能是由特定的生长因子如EGF介导的。我们已经研究了甲状腺素对具有CH遗传形式的小鼠品系中生长和肝EGF受体发育的影响。甲状腺功能低下的小鼠(h / h)在出生后第20天到第40天之间用T4处理,h / h未治疗的小鼠和正常(+ / +)小鼠作为对照。在出生后第20天或第40天处死动物。通过RIA和EGF受体结合在肝血浆膜匀浆中测量血清甲状腺素。到20天龄时,所有小鼠均表现出相同的体重增加,而EGF肝受体结合率低,并且在h / h和+ / +小鼠之间无显着差异。从第20 h / h天起,小鼠的生长速度明显低于+ / +小鼠,生长迟缓已通过T4处理得以恢复。小鼠的出生后早期生长(第0-20天)与甲状腺激素无关,在这方面与晚期相似人类的产前生长。相反,在小鼠出生后第20天到40天之间,甲状腺激素对于正常生长和肝EGF结合增加是必需的。我们的结果表明,表皮生长因子受体的个体发生改变可能与CH中的生长发育迟缓有关。

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