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生长激素和甲状旁腺激素可刺激老年雌性大鼠肠道对钙的吸收。

Growth hormone and parathyroid hormone stimulate intestinal calcium absorption in aged female rats.

作者信息

Fleet J C, Bruns M E, Hock J M, Wood R J

机构信息

U.S. Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts.

出版信息

Endocrinology. 1994 Apr;134(4):1755-60. doi: 10.1210/endo.134.4.8137740.

Abstract

Aged (16-month-old) female rats (n = 8/treatment) were injected for 12 days with GH (100 micrograms/100 g x day), PTH (8 micrograms/100 g x day), GH plus PTH, or vehicle (V) in an experiment designed to determine the effects of these hormones on intestinal mineral absorption in senescent rats. PTH and GH increased fractional net calcium absorption to a similar extent (PTH, 1.6-fold; GH, 1.4-fold) even though PTH increased serum 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] 3.7-fold, and GH had no significant effect. GH plus PTH caused no further increase in serum 1,25-(OH)2D3 above that caused by PTH alone, but resulted in an additive effect on net calcium absorption (2.3-fold increase). PTH and GH also had statistically independent effects on phosphate absorption; magnesium absorption was elevated only by PTH. Duodenal calbindin-D9k levels were increased by GH (from 3.79 +/- 0.72 to 6.98 +/- 0.73 micrograms/mg protein) and PTH (from 3.23 +/- 0.46 to 7.55 +/- 0.75 micrograms/mg protein); PTH plus GH treatment resulted in an additive effect on calbindin-D9k levels. Additional in vitro transport studies in the human intestinal cell line Caco-2 showed that 72 h of pretreatment with the local mediator of GH action, insulin-like growth factor-I (at 10 and 100 ng/ml), stimulated transcellular calcium transport (22% and 44%, respectively) regardless of concomitant 1 nM 1,25-(OH)2D3 pretreatment (80% increase). Our findings suggest a 1,25-(OH)2D3-mediated mechanism for PTH-induced changes in calcium and phosphorus absorption. In contrast, the effects of GH in the senescent rat are independent of changes in circulating 1,25-(OH)2D3 and our data suggest that these effects may be mediated by insulin-like growth factor-I.

摘要

在一项旨在确定这些激素对衰老大鼠肠道矿物质吸收影响的实验中,对16月龄雌性大鼠(每组8只)连续12天注射生长激素(GH,100微克/100克体重/天)、甲状旁腺激素(PTH,8微克/100克体重/天)、生长激素加甲状旁腺激素或溶剂(V)。尽管甲状旁腺激素使血清1,25 - 二羟维生素D3 [1,25-(OH)2D3]升高了3.7倍,而生长激素无显著影响,但甲状旁腺激素和生长激素使钙净吸收分数增加的程度相似(甲状旁腺激素为1.6倍;生长激素为1.4倍)。生长激素加甲状旁腺激素使血清1,25-(OH)2D3升高的幅度并未超过单独使用甲状旁腺激素时,但对钙净吸收产生了相加作用(增加2.3倍)。甲状旁腺激素和生长激素对磷吸收也有统计学上的独立作用;仅甲状旁腺激素使镁吸收升高。十二指肠钙结合蛋白-D9k水平因生长激素(从3.79±0.72微克/毫克蛋白增至到6.98±0.73微克/毫克蛋白)和甲状旁腺激素(从3.23±0.46微克/毫克蛋白增至7.55±0.75微克/毫克蛋白)而升高;甲状旁腺激素加生长激素处理对钙结合蛋白-D9k水平产生了相加作用。在人肠细胞系Caco-2中进行的额外体外转运研究表明,用生长激素作用的局部介质胰岛素样生长因子-I(10和百100纳克/毫升)预处理72小时,无论是否同时用1纳摩尔1,25-(OH)2D3预处理(增加80%),均刺激跨细胞钙转运(分别增加22%和44%)。我们的研究结果提示了一种1,25-(OH)2D3介导的甲状旁腺激素诱导钙和磷吸收变化的机制。相比之下,生长激素在衰老大鼠中的作用独立于循环中1,25-(OH)2D3的变化,我们的数据表明这些作用可能由胰岛素样生长因子-I介导。

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