Whisenton L R, Watson R D, Granger N A, Bollenbacher W E
Gen Comp Endocrinol. 1987 Apr;66(1):62-70. doi: 10.1016/0016-6480(87)90350-9.
A previous study of the role of 20-hydroxyecdysone in the regulation of juvenile hormone (JH) biosynthesis during pupal commitment in the last (fifth, V) larval instar of Manduca sexta revealed that the increase in the hemolymph edysteroid titer that elicits commitment also stimulates the corpora allata (CA) to synthesize JHs I and III and/or their acids. This stimulation is exerted indirectly via the brain-corpora cardiaca and results in the postcommitment increase in the JH titer that is important for the molt to a pupa. The possibility that a similar form of interendocrine regulation of JH biosynthesis by 20-hydroxyecdysone is involved in the control of larval molting in Manduca was investigated for the molt from the fourth (IV) to the V larval instar. During the IV instar, the increase in the hemolymph ecdysteroid titer and the capacity of the CA to synthesize JHs I and III in vitro correlated temporally in a manner suggestive of CA regulation by 20-hydroxyecdysone. With an in vitro approach, physiological concentrations of 20-hydroxyecdysone (greater than or equal to 1 microgram ml-1 hemolymph) were shown to have a dose-dependent trophic effect on CA activity, specifically stimulating JH I synthesis. Since neither basally active nor stimulated CA contained significant amounts of JH I, it appears that 20-hydroxyecdysone acts at the level of biosynthesis rather than at the level of release. The specificity of 20-hydroxyecdysone stimulation of JH I synthesis was demonstrated by the inability of the biologically inactive ecdysteroids 22-isoecdysone and 5 alpha-ecdysone to activate the glands.(ABSTRACT TRUNCATED AT 250 WORDS)
先前一项关于20-羟基蜕皮酮在烟草天蛾末(第五,V)龄幼虫化蛹过程中对保幼激素(JH)生物合成调节作用的研究表明,引发化蛹的血淋巴蜕皮甾体滴度升高也会刺激咽侧体(CA)合成JH I和III及其酸类。这种刺激是通过脑-心侧体间接施加的,导致化蛹后JH滴度升高,这对蜕皮变为蛹很重要。研究了20-羟基蜕皮酮对JH生物合成的类似内分泌调节形式是否参与烟草天蛾幼虫从第四(IV)龄到V龄蜕皮控制的可能性。在IV龄期间,血淋巴蜕皮甾体滴度的增加与CA体外合成JH I和III的能力在时间上相关,这表明CA受20-羟基蜕皮酮调节。通过体外实验方法,已证明生理浓度的20-羟基蜕皮酮(大于或等于1微克/毫升血淋巴)对CA活性具有剂量依赖性的营养作用,特别是刺激JH I的合成。由于基础活性的CA和受刺激的CA都不含大量的JH I,因此20-羟基蜕皮酮似乎作用于生物合成水平而非释放水平。生物活性不高的蜕皮甾体22-异蜕皮酮和5α-蜕皮酮无法激活腺体,这证明了20-羟基蜕皮酮对JH I合成刺激的特异性。(摘要截短于250字)