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Actions of hypoxia on catecholamine synthetic enzyme mRNA expression before and after development of adrenal innervation in the sheep fetus

机译:缺氧对绵羊胎儿肾上腺神经支配发生前后儿茶酚胺合成酶mRNA表达的影响

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class="enumerated" style="list-style-type:decimal">We have investigated adrenal mRNA expression of the catecholamine synthetic enzymes tyrosine hydroxylase (TH) and phenylethanolamine N-methyltransferase (PNMT) following acute hypoxia in fetal sheep before (< 105 days gestation, n = 20) and after (> 125 days gestation, n = 20) the development of adrenal innervation and following pretreatment with the nicotinic receptor anatgonist hexamethonium (n = 12).Total RNA was extracted from fetal adrenal glands collected at specific time points at 3-20 h after the onset of either hypoxia (∼50% reduction in fetal arterial oxygen saturation (SO2) for 30 min), or normoxia.Before 105 days, there was a decrease in adrenal TH mRNA expression at 20 h after hypoxia and adrenal TH mRNA expression was directly related to the changes in arterial PO2 measured during normoxia and hypoxia. After 125 days, adrenal TH mRNA levels were suppressed for up to 12 h following hypoxia.In both age groups, adrenal PNMT mRNA expression increased at 3-5 h after hypoxia and was inversely related to the changes in fetal arterial PO2 during normoxia or hypoxia.After 125 days, the administration of hexamethonium (25 mg kg−1, I. V.) reduced TH mRNA but not PNMT mRNA expression after normoxia. After hexamethonium pretreatment, there was no significant change in either adrenal TH or PNMT mRNA expression following hypoxia.We conclude that acute hypoxia differentially regulates adrenal TH and PNMT mRNA expression in the fetal sheep both before and after the development of adrenal innervation. After the development of adrenal innervation, however, the effect of acute hypoxia upon adrenal TH and PNMT mRNA expression is dependent upon neurogenic input acting via nicotinic receptors.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 我们调查了急性缺氧后胎儿绵羊缺氧前(<105天,n = 20)和之后(> 125天,n)儿茶酚胺合成酶酪氨酸羟化酶(TH)和苯乙醇胺N-甲基转移酶(PNMT)的肾上腺mRNA表达= 20)肾上腺神经支配的发展,并用烟碱样受体激动剂己六甲铵(n = 12)进行预处理。 从特定时间点采集的胎儿肾上腺在3-20小时后提取总RNA。缺氧(胎儿动脉血氧饱和度(SO2)降低约50%,持续30分钟)或常氧的发作。 在缺氧前105天,缺氧后20 h肾上腺TH mRNA表达降低肾上腺TH mRNA的表达与常氧和低氧时动脉PO2的变化直接相关。 125天后,缺氧后长达12 h肾上腺TH mRNA水平被抑制。 在两个年龄组中,缺氧后3-5 h肾上腺PNMT mRNA表达均升高,与肾上腺皮质激素的变化呈负相关。常氧或低氧时胎儿的动脉PO2。 在125天后,给予六甲铵(25 mg kg -1 ,IV)可使常氧后TH mRNA降低,但PNMT mRNA表达降低。六甲铵盐预处理后,缺氧后肾上腺TH或PNMT mRNA表达均无显着变化。 我们得出结论,急性缺氧对胎儿绵羊发育前后的肾上腺TH和PNMT mRNA表达有不同的调节作用。肾上腺神经支配。然而,在肾上腺神经支配发展之后,急性缺氧对肾上腺TH和PNMT mRNA表达的影响取决于通过烟碱受体发挥作用的神经源性输入。

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