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阿拉廷抑制素,一种烟草天蛾中保幼激素生物合成的神经激素抑制剂。

Allatinhibin, a neurohormonal inhibitor of juvenile hormone biosynthesis in Manduca sexta.

作者信息

Bhaskaran G, Dahm K H, Barrera P, Pacheco J L, Peck K E, Muszynska-Pytel M

机构信息

Department of Biology, Texas A&M University, College Station 77843.

出版信息

Gen Comp Endocrinol. 1990 Apr;78(1):123-36. doi: 10.1016/0016-6480(90)90053-o.

Abstract

The corpora allata (CA) of Manduca sexta larvae become incapable of synthesizing juvenile hormone (JH) early in the wandering stage of the last larval stadium. They then switch to the synthesis and release of JH acids. This change in CA activity is induced by an inhibitory factor--allatinhibin (AI)--from the brain. AI activity is present in the fifth (Vth) instar hemolymph from about Day 4 (day of wandering) until Day 7 (early prepupa). CA of early fifth instar larvae (uninhibited) incubated in vitro with brain-corpora cardiaca-corpora allata (Br-CC-CA) complexes or brain alone from wandering larvae are inhibited as demonstrated by bioassay. On the basis of these observations, an in vitro-in vivo assay for AI was developed. Br-CC-CA or Br alone were first incubated in tissue culture medium overnight. Day 0 (0d) Vth instar CA incubated for 16 hr in such medium will lose the ability to induce a larval molt in allatectomized 0d IVth instar larvae if the medium contained AI activity. The highest AI activity was exhibited by the medium obtained from incubations of brain from wandering larvae whereas the medium from incubation of 0d Vth and 0d pupal brains showed no AI activity. Dose-response data show that AI is active at 0.03 brain equivalents/200 microliters medium. CA must be exposed to AI for 12-16 hr for manifestation of inhibition. AI causes a stable inhibition of CA. AI is heat-labile, protease sensitive, has a molecular size between 1.0 and 3.5 kDa, and is clearly distinct from the allatostatins described by others.

摘要

烟草天蛾幼虫的咽侧体(CA)在最后一龄幼虫的化蛹前期早期就无法合成保幼激素(JH)。然后它们转而合成并释放保幼激素酸。CA活性的这种变化是由来自大脑的一种抑制因子——保幼激素抑制素(AI)诱导的。AI活性存在于五龄幼虫的血淋巴中,从大约第4天(化蛹前期)持续到第7天(早期蛹期)。如生物测定所示,用来自化蛹前期幼虫的脑 - 心侧体 - 咽侧体(Br - CC - CA)复合体或单独的脑在体外培养早期五龄幼虫(未受抑制)的CA时,CA会受到抑制。基于这些观察结果,开发了一种用于AI的体外 - 体内测定方法。首先将Br - CC - CA或单独的Br在组织培养基中孵育过夜。如果培养基含有AI活性,在这种培养基中孵育16小时的第0天(0d)五龄CA将失去诱导去咽侧体的0d四龄幼虫进行幼虫蜕皮的能力。来自化蛹前期幼虫脑孵育的培养基表现出最高的AI活性,而来自0d五龄和0d蛹脑孵育的培养基则没有AI活性。剂量 - 反应数据表明,AI在0.03脑当量/200微升培养基时具有活性。CA必须暴露于AI 12 - 16小时才能表现出抑制作用。AI对CA产生稳定的抑制作用。AI对热不稳定,对蛋白酶敏感,分子大小在1.0至3.5 kDa之间,并且与其他人描述的咽侧体抑制素明显不同。

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