Boer G J, Feenstra M G, Botterblom M J, Korse V, Te Riele P
Graduate School Neurosciences Amsterdam, Netherlands Institute for Brain Research.
Int J Dev Neurosci. 1995 Apr;13(2):63-74. doi: 10.1016/0736-5748(95)00023-a.
The course of postnatal development of noradrenaline (NA) and its unconjugated free metabolite 3-methoxy-4-hydroxyphenylglycol (MHPG), as well as the influence on early chronic vasopressin treatment, were investigated in various brain regions of the hereditary vasopressin-deficient (homozygous di/di) Brattleboro rat. In addition, the densities of the adrenergic receptor subtypes were measured in adult brain. Brain NA levels of di/di pups appeared enhanced already at 7 days of age when compared with data of heterozygous (+/di) controls. This was also seen in areas not known to receive a vasopressinergic input, e.g. the frontal cortex. Levels of MHPG also differed between genotypes, but changes were slight and either a decrease or increase, depending on age and region tested. Saturation analyses of alpha 1-, alpha 2-, and beta-adrenoceptor binding on crude membrane preparations of some brain regions revealed no differences in adulthood. Chronic treatment with vasopressin between 6 and 13 days of age reduced the enhanced NA brain levels throughout the brain of the di/di Brattleboro pups. The known vasopressin-mediated enhancement of NA turnover in adult brain was also measurable in +/di pups of this neonatal period (MHPG/NA ratios), indicating the early maturation of the interaction of vasopressinergic and NAergic systems. However, the dose-response in the di/di Brattleboro rat was biphasic with a decrease at a low dose of vasopressin. Since changes were found throughout the brain, it was concluded that vasopressin deficiency had altered the maturation of NA neurons of the locus coeruleus which may be due to the absence of a presumed inhibitory control of vasopressin on synthesis and storage mechanisms at the perikaryal level.
研究了遗传性抗利尿激素缺乏(纯合子di/di)的布拉德福德大鼠不同脑区中去甲肾上腺素(NA)及其未结合的游离代谢物3-甲氧基-4-羟基苯乙二醇(MHPG)的产后发育过程,以及早期慢性抗利尿激素治疗的影响。此外,还测量了成年大脑中肾上腺素能受体亚型的密度。与杂合子(+/di)对照的数据相比,di/di幼崽在7日龄时脑内NA水平就已升高。在已知未接受抗利尿激素能输入的区域,如额叶皮质,也观察到了这种情况。MHPG水平在不同基因型之间也存在差异,但变化较小,且根据所测试的年龄和区域,要么降低,要么升高。对一些脑区粗制膜制剂上的α1、α2和β肾上腺素能受体结合进行的饱和分析显示,成年期无差异。在6至13日龄期间用抗利尿激素进行慢性治疗,可降低di/di布拉德福德幼崽全脑升高的脑内NA水平。在这个新生儿期的+/di幼崽中,也可测量到成年大脑中已知的抗利尿激素介导的NA周转率增强(MHPG/NA比值),这表明抗利尿激素能系统和NA能系统相互作用的早期成熟。然而,di/di布拉德福德大鼠的剂量反应呈双相性,低剂量抗利尿激素时会降低。由于在全脑均发现了变化,得出的结论是,抗利尿激素缺乏改变了蓝斑NA神经元的成熟,这可能是由于在胞体水平上抗利尿激素对合成和储存机制缺乏假定的抑制性控制所致。