Malagon M, Vaudry H, Van Strien F, Pelletier G, Gracia-Navarro F, Tonon M C
European Institute for Peptide Research, CNRS URA 650, UA INSERM, University of Rouen, Mont-Saint-Aignan, France.
Neuroscience. 1993 Dec;57(3):777-86. doi: 10.1016/0306-4522(93)90023-9.
Benzodiazepine receptors are expressed very early in the brain during embryonic life, suggesting that endogenous ligands for these receptors may play an important role during ontogenesis in the central nervous system. In the present study, the distribution and characterization of diazepam-binding inhibitor-related peptides (endozepines) in the rat brain was investigated during embryonic and postnatal development using an antibody raised against the biologically active region of the precursor molecule. Immunohistochemical labelling showed that, in newborn rats, endozepine-like immunoreactivity was present in ependymal cells of the hypothalamus. Although the number of positive cells increased by day 5, the intensity of the immunoreaction in each cell diminished. In 15-day-old rats, both the number of endozepine positive cells and the intensity of the immunoreaction increased in the ependymal layer. At day 40, a dense accumulation of immunoreactive tanycytes and glial cells was observed in the median eminence and the arcuate nucleus. Endozepines were detected by radioimmunoassay in all regions of the brain as early as embryonic day 18. The concentration of endozepine-related peptides increased in the hypothalamus and olfactory bulb during late gestation. Between birth and postnatal day 5, the levels of endozepines decreased two- to four-fold in all brain regions studied. Thereafter, endozepine concentration increased gradually until day 25. Reversed-phase high-performance liquid chromatography analysis of tissue extracts revealed that the olfactory bulb, pituitary, hypothalamus and cerebellum contained only one immunoreactive peak eluting at 39 min (peak C). In the telencephalon two peaks were observed: peak C and a second one eluting at 34 min (peak B). Peak B was present as early as embryonic day 20 and the ratio peak B/peak C gradually increased until day 25. At day 25 peak B was also detected in hippocampus, medulla oblongata, cortex and striatum extracts. In any brain region, no immunoreactivity co-eluting with the octadecaneuropeptide was observed. Sephadex G-50 gel filtration of hypothalamus extracts of 25-day-old animals, confirmed the existence of only one immunoreactive compound with an apparent molecular weight of 10,000. In the telencephalon two major species were resolved, with apparent molecular weights of 10,000 and 8800, and a minor one of 6500 mol. wt. In conclusion, the present study shows that endozepines are expressed in the rat brain as early as embryonic day 18 and the amount of endozepine-like material increases rapidly during the two days preceding birth. The results also indicate that diazepam-binding inhibitor is processed to different molecular forms depending on the brain region.(ABSTRACT TRUNCATED AT 400 WORDS)
苯二氮䓬受体在胚胎期大脑中很早就有表达,这表明这些受体的内源性配体可能在中枢神经系统的个体发育过程中发挥重要作用。在本研究中,使用针对前体分子生物活性区域产生的抗体,研究了大鼠胚胎期和出生后发育过程中地西泮结合抑制剂相关肽(内源性苯二氮䓬)在大鼠脑中的分布和特性。免疫组织化学标记显示,在新生大鼠中,下丘脑室管膜细胞存在内源性苯二氮䓬样免疫反应性。虽然阳性细胞数量在第5天增加,但每个细胞中的免疫反应强度减弱。在15日龄大鼠中,室管膜层内源性苯二氮䓬阳性细胞数量和免疫反应强度均增加。在第40天,在正中隆起和弓状核中观察到免疫反应性伸长细胞和胶质细胞的密集聚集。早在胚胎第18天,通过放射免疫测定法就在大脑的所有区域检测到了内源性苯二氮䓬。在妊娠后期,下丘脑和嗅球中内源性苯二氮䓬相关肽的浓度增加。在出生至出生后第5天之间,所研究的所有脑区中内源性苯二氮䓬的水平下降了两到四倍。此后,内源性苯二氮䓬浓度逐渐增加直至第25天。对组织提取物进行反相高效液相色谱分析表明,嗅球、垂体、下丘脑和小脑中仅含有一个在39分钟洗脱的免疫反应峰(峰C)。在端脑中观察到两个峰:峰C和在34分钟洗脱的第二个峰(峰B)。峰B早在胚胎第20天就已出现,峰B/峰C的比值逐渐增加直至第25天。在第25天,在海马、延髓、皮质和纹状体提取物中也检测到了峰B。在任何脑区,均未观察到与十八肽共洗脱的免疫反应性。对25日龄动物下丘脑提取物进行葡聚糖G-50凝胶过滤,证实仅存在一种表观分子量为10,000的免疫反应性化合物。在端脑中分辨出两种主要成分,表观分子量分别为10,000和8800,还有一种次要成分的分子量为6500。总之,本研究表明内源性苯二氮䓬早在胚胎第18天就在大鼠脑中表达,并且在出生前的两天内,内源性苯二氮䓬样物质的量迅速增加。结果还表明,地西泮结合抑制剂根据脑区不同被加工成不同的分子形式。(摘要截短为400字)