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器官培养中的下丘脑-神经垂体复合体:代谢抑制剂、生物制剂及药理制剂的作用

The hypothalamo-neurohypophysial complex in organ culture: effects of metabolic inhibitors, biologic and pharmacologic agents.

作者信息

Pearson D, Shainberg A, Malamed S, Sachs H

出版信息

Endocrinology. 1975 Apr;96(4):994-1003. doi: 10.1210/endo-96-4-994.

Abstract

Organ cultures of the guinea pig hypothalamo-neurohypophysial complex synthesize the octapeptide hormone, vasopressin, a specific product of the neurosecretory cells of the supraoptic nucleus. Inhibitors of both protein and RNA synthesis (cycloheximide and bromotubercidin respectively) were found to block vasopressin biosynthesis. In the presence of bromotubercidin, the apparent half-time of decline in the rate of hormone biosynthesis was about 28 h. Colchicine inhibited the distal transport of vasopressin into the posterior pituitary. Ultrastructural studies on colchicine-treated cultures indicated the neuronal stalks were intact and that neurotubules were still present. The narcotic drug, levorphanol at 10-7 M and 10-9 M was found to inhibit RNA synthesis by 20 percent. At these concentrations it had no demonstrable effect on vasopressin synthesis. Cultures established from animals that had been rendered tolerant to narcotics also had no observable alterations in vasopressin biosynthesis, although the initial pituitary vasopressin content of these cultures was reduced by about 35 percent. Various pharmacologic and biologic compounds were tested for their effects on vasopressin biosynthesis in organ cultures. Dibutyryl cyclic AMP, estradiol-17beta, nicotine, nerve growth factor (NGF), and pineal extract all had no effects under the present experimental regimen. Medium conditioned by the presence of fetal hypothalami of 40-55 days gestation produced a 2-4 fold increase in vasopressin biosynthesis in cultures established from adult animals. Medium conditioned by fetal cerebral cortex, liver, or hypothalamic tissue from fetuses of less than 33 days gestation did not have this stimulatory effect.

摘要

豚鼠下丘脑 - 神经垂体复合体的器官培养物可合成八肽激素——血管加压素,它是视上核神经分泌细胞的一种特定产物。已发现蛋白质和RNA合成抑制剂(分别为环己酰亚胺和溴杀结核菌素)可阻断血管加压素的生物合成。在溴杀结核菌素存在的情况下,激素生物合成速率下降的表观半衰期约为28小时。秋水仙碱抑制血管加压素向垂体后叶的远端转运。对经秋水仙碱处理的培养物进行的超微结构研究表明,神经柄完整且仍存在神经微管。发现浓度为10⁻⁷M和10⁻⁹M的麻醉药左啡诺可抑制RNA合成20%。在这些浓度下,它对血管加压素合成没有明显影响。从对麻醉药产生耐受性的动物建立的培养物,其血管加压素生物合成也没有可观察到的变化,尽管这些培养物最初的垂体血管加压素含量降低了约35%。测试了各种药理和生物化合物对器官培养物中血管加压素生物合成的影响。在当前实验方案下,二丁酰环磷腺苷、雌二醇 - 17β、尼古丁、神经生长因子(NGF)和松果体提取物均无作用。由妊娠40 - 55天的胎儿下丘脑存在所调节的培养基,可使成年动物建立的培养物中血管加压素生物合成增加2 - 4倍。由妊娠小于33天的胎儿的大脑皮质、肝脏或下丘脑组织调节的培养基没有这种刺激作用。

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