Lakshmanan J, Landel C P
Pediatr Res. 1986 Jul;20(7):587-92. doi: 10.1203/00006450-198607000-00002.
We examined long-term effects of neonatal hyperthyroidism on salivary secretions of nerve growth factor and epidermal growth factor in male and female mice at the age of 31 days. Hyperthyroidism was induced by thyroxine (T4) injections (0.4 microgram/g body weight/day) during days 0-6. Littermate control mice were treated with vehicle. T4 treatment did not alter the amounts of protein secreted into saliva but hormone administration induced alteration in the types of protein secreted. T4 treatment decreased the contents of both nerve growth factor and epidermal growth factor secreted into the saliva. A Sephadex G-200 column chromatographic profile revealed the presence of two distinct nerve growth factor immunoreactive peaks, while epidermal growth factor immunoreactivity predominantly eluted as a single low molecular weight form. T4 treatment did not alter the molecular nature of their secretion, but the treatment decreased their contents. These results indicate an impairment in salivary secretion of nerve growth factor and epidermal growth factor long after T4 treatment has been discontinued.
我们研究了新生期甲状腺功能亢进对31日龄雄性和雌性小鼠唾液中神经生长因子和表皮生长因子分泌的长期影响。在出生后0至6天期间,通过注射甲状腺素(T4,0.4微克/克体重/天)诱导甲状腺功能亢进。同窝对照小鼠接受赋形剂处理。T4处理并未改变唾液中分泌的蛋白质总量,但激素给药导致分泌的蛋白质类型发生改变。T4处理降低了唾液中神经生长因子和表皮生长因子的含量。葡聚糖G - 200柱色谱图谱显示存在两个不同的神经生长因子免疫反应峰,而表皮生长因子免疫反应性主要以单一低分子量形式洗脱。T4处理并未改变它们分泌的分子性质,但降低了它们的含量。这些结果表明,在停止T4处理很久之后,神经生长因子和表皮生长因子的唾液分泌仍存在损害。