Watts A G
Neural Systems Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.
Neuroscience. 1992;46(4):859-79. doi: 10.1016/0306-4522(92)90190-d.
The response of six mRNAs (for prepro-corticotropin-releasing hormone, prepro-enkephalin, prepro-vasoactive intestinal polypeptide/peptide histidine isoleucine, prepro-neurotensin/neuromedin N, prepro-cholecystokinin, and prepro-tyrosine hydroxylase) was measured in the hypothalamic paraventricular and supraoptic nuclei after increasing periods of osmotic stimulation caused by the replacement of regular drinking water with hypertonic saline (up to five days) or by forced dehydration (up to three days). In addition, hematocrits and concentrations of corticosterone were determined after the different periods of osmotic stimulation and correlated with the effects on the content of the various mRNAs. The temporal response of the mRNAs within the paraventricular and supraoptic nuclei to osmotic stimulation was different within the three compartments of these nuclei. First, in response to overnight osmotic stimulation, magnocellular neurosecretory neurons increased their mRNA content for two molecules (prepro-corticotropin-releasing hormone and tyrosine hydroxylase). As the stimulus was maintained over the next two to four days, these cells accumulated the mRNAs for at least three other peptides (cholecystokinin, vasoactive intestinal polypeptide/peptide histidine isoleucine and enkephalin). Second, the response of peptide-coding mRNAs in parvicellular neurosecretory neurons of the paraventricular nucleus appeared to be slower; no changes could be measured after overnight stimulation. However, after a further two- to four-days of continued osmotic stimulation, the content of the mRNA coding for corticotropin-releasing hormone markedly decreased while that for cholecystokinin increased. No change in the content of the mRNAs coding for prepro-vasoactive intestinal polypeptide/peptide histidine isoleucine, enkephalin, and prepro-neurotensin/neuromedin N could be seen at any time after osmotic stimulation in parvicellular neurosecretory neurons. Third, increases in the content of mRNA coding for corticotropin-releasing hormone in the parvicellular neurons that provide descending projections from the paraventricular nucleus could only be detected after longer periods of osmotic stimulation. The effect of osmotic stimulation on plasma corticosterone concentrations was quickly apparent; plasma corticosterone concentrations were significantly elevated on the first morning after the beginning of salt-loading, and demonstrated the rapid effects of osmotic stimulation on the mechanisms controlling corticosterone release. These results show that the synthetic capability of cells in all three compartments of the paraventricular and supraoptic nuclei are modified by osmotic stimulation over different time scales, thereby allowing differential modulation of the neuroendocrine, autonomic, and behavioral components of the animal's response to disturbances in fluid homeostasis.(ABSTRACT TRUNCATED AT 400 WORDS)
用高渗盐水替代常规饮水(长达五天)或强制脱水(长达三天),造成不同时长的渗透刺激后,检测下丘脑室旁核和视上核中六种信使核糖核酸(前促肾上腺皮质激素释放激素原、脑啡肽原、血管活性肠肽/组氨酸异亮氨酸肽原、神经降压素/神经介素N原、胆囊收缩素原和酪氨酸羟化酶原)的反应。此外,在不同时长的渗透刺激后测定血细胞比容和皮质酮浓度,并将其与对各种信使核糖核酸含量的影响相关联。室旁核和视上核内的信使核糖核酸对渗透刺激的时间反应在这些核的三个区域内有所不同。首先,对过夜渗透刺激的反应中,大细胞神经分泌神经元增加了两种分子(前促肾上腺皮质激素释放激素和酪氨酸羟化酶)的信使核糖核酸含量。随着刺激在接下来的两到四天持续,这些细胞积累了至少其他三种肽(胆囊收缩素、血管活性肠肽/组氨酸异亮氨酸肽和脑啡肽)的信使核糖核酸。其次,室旁核小细胞神经分泌神经元中肽编码信使核糖核酸的反应似乎较慢;过夜刺激后未检测到变化。然而,在持续渗透刺激另外两到四天后,促肾上腺皮质激素释放激素编码信使核糖核酸的含量显著下降,而胆囊收缩素的则增加。在渗透刺激后的任何时间,室旁核小细胞神经分泌神经元中血管活性肠肽/组氨酸异亮氨酸肽原、脑啡肽原和神经降压素/神经介素N原编码信使核糖核酸的含量均未出现变化。第三,只有在更长时间的渗透刺激后,才能检测到从室旁核发出下行投射的小细胞神经元中促肾上腺皮质激素释放激素编码信使核糖核酸含量的增加。渗透刺激对血浆皮质酮浓度的影响很快显现;在开始盐负荷后的第一个早晨,血浆皮质酮浓度显著升高,表明渗透刺激对控制皮质酮释放机制具有快速影响。这些结果表明,室旁核和视上核所有三个区域的细胞合成能力在不同时间尺度上受到渗透刺激的影响,从而使动物对液体稳态紊乱的反应中神经内分泌、自主和行为成分得到不同调节。(摘要截选至400字)