保幼激素类似物对粘虫飞行能力及能源物质含量的调控(英文)

本文报道了保幼激素类似物methoprene(JHM)对粘虫Mythimnaseparata(Walker)飞行能力及飞行能源物质含量的影响。总体而言 ,用JHM (30 μg/蛾 )处理过的成虫飞行能力比对照 (丙酮处理 )的弱 ,但因性别及处理后的时间变化而异 :处理雌蛾的飞行能力在处理后的 1d到 3d与对照没有显著差异 ,但在4d到 6d则显著低于对照 ;处理雄蛾的飞行能力一直比对照的强 ,尽管差异不显著。处理过的雌蛾飞行个体比对照的少 ,而处理过的雄蛾比对照的多。究其原因 ,主要是JHM处理过的雌蛾甘油酯含量在处理后的 3d后明显下降 ,而处理过的雄蛾甘油酯含量一直比对照的高。但无论是雌蛾还是雄蛾 ,处理的与对照的糖元含量均没有明显的差异。这些结果表明 ,作用于成虫体内甘油酯含量是保幼激素影响粘虫飞行能力的主要原因之一。最后 ,对保幼激素影响粘虫飞行能力的其它可能原因也进行了讨论     

一日龄饥饿对粘虫成虫卵巢发育和飞行能力的影响

为了明确羽化后0～24 h (1日龄)饥饿处理对迁飞型粘虫Mythimna separata (Walker)生殖系统和飞行系统发育的影响,对1日龄饥饿处理后粘虫的卵巢发育级别、产卵前期、飞行肌和飞行能力进行了系统研究。结果表明, 1日龄饥饿对粘虫成虫卵巢发育级别、产卵前期、中胸背纵肌干重、飞行能力等均有显著的影响。饥饿后成虫卵巢发育级别显著高于对照,产卵前期显著短于对照。成虫中胸背纵肌干重从饥饿后96 h开始下降,至120 h时饥饿粘虫(5.1 mg)显著低于对照(5.86 mg)。成虫飞行能力从饥饿后96 h开始显著低于对照,此时饥饿处理粘虫蛾的飞行距离平均为22.03 km,飞行时间平均为4.07 h,显著低于同时期的对照粘虫的飞行距离(42.3 km)和飞行时间(7.99 h),尽管在饥饿后72 h内差异不显著。实验结果显示,1日龄饥饿可以显著抑制粘虫飞行系统的发育,加速飞行向生殖的转变。     

粘虫飞行对生殖及寿命的影响

该文报道了粘虫Mythimna separata（Walker）成虫飞行后产卵、交配及寿命的研究结果。1日龄成虫飞行6 h、12 h、18 h、24 h后的产卵前期均显著短于对照的,其中飞行6 h、12 h的比对照的短2天以上,产卵量均比对照的高。对1～5日龄成虫分别飞行23.5 h后的研究结果表明,1日龄飞行的产卵前期和上述结果相一致。2～4日龄飞行的与对照的没有显著差异,但产卵量则随飞行日龄的延迟而逐渐减少。5日龄飞行的产卵前期显著延长,产卵量已不到对照的一半。所有经过飞行的成虫产卵高峰日比对照的早1天。不同日龄成虫飞行时间、距离与成虫产卵量的关系为：1～3日龄飞行时间、距离长的个体产卵量也高;但4～5日龄的成虫飞行时间与距离越长,其产卵量越少,表现出明显的卵子发生飞行拮抗症(oogenesis-flight syndrome)。除了5日龄飞行的成虫交配率有所下降以外,所有经过飞行的成虫产卵历期、交配率及寿命与对照的没有显著差异。最后,根据这些结果,对粘虫迁飞的起飞时期,迁飞在粘虫生殖、种群动态及成灾规律中的作用进行了讨论。     

棉铃虫及粘虫肠中咽侧体静止激素样活性物质对咽侧体活性的影响

利用放射化学的方法分别检测了棉铃虫Helicoverpaarmigera、粘虫Mythimnaseparata幼虫和成虫肠中咽侧体静止激素 (allatostatin ,AS)样的活性物质。发现在棉铃虫、粘虫幼虫和成虫肠中均存在的AS样活性物质 ,可以在体外抑制咽侧体 (corporaallata,CA)的保幼激素 ( juvenilehormone,JH)的生物合成。生物测定的结果表明 ,粘虫幼虫肠中AS样活性物质的含量较棉铃虫的高 ;粘虫 1个幼虫肠当量对CA的JH合成的抑制率达 4 3% ,而棉铃虫幼虫肠只有 2 6%。无论是棉铃虫还是粘虫 ,雌成虫中肠对CA的抑制比雄成虫中肠的高 ,后肠对CA的JH合成的抑制明显的低于中肠对CA的抑制。中肠对CA的JH合成的抑制是可回复的。中肠粗提物经蛋白酶水解后对CA合成JH的抑制率降低 ,表明肠中AS样的活性物质是肽或蛋白质     

粘虫飞行肌中与能量代谢有关的酶活性研究

该文报道粘虫Mythimna separata (Walker ) 蛹及不同日龄成虫飞行肌中与3 种代谢途径有关的5 种酶,即3-磷酸甘油醛脱氢酶(GAPDH)、3-磷酸甘油脱氢酶(GDH)、乳酸脱氢酶(LDH)、3-羟酰辅酶A 脱氢酶(HOAD)、柠檬酸合成酶(CS)活性的变化。成虫羽化后,这5 种酶的活性大多数都高于蛹期,表明成虫飞行肌与能量代谢有关的活动比蛹期高。不同日龄成虫飞行肌的能量代谢特点为：成虫羽化后糖酵解循环的活性增加;1 日龄进行糖酵解的能力较强,2 日龄即具备较强的脂肪代谢能力,2～5日龄糖及脂肪代谢的能力基本相当,但7日龄脂肪代谢的能力较强。1～7日龄粘虫蛾飞行肌具有较高的GDH 和LDH活性,这既是粘虫蛾飞行肌能进行高度有氧代谢的重要标志,也是其具有一定无氧代谢能力的最好说明,而飞行肌中较高的CS活性则是粘虫蛾具有较强飞行能力的重要保证。对成虫GAPDH∶HOAD 活性进行分析比较的结果还显示,粘虫蛾持续飞行的能源物质既有脂类也有糖类,而不仅仅只限于脂类。     

棉铃虫及粘虫肠中咽侧体静止激素样活性物质对咽侧体活性的影响

利用放射化学的方法分别检测了棉铃虫Helicoverpa armigera、粘虫Mythimna separata幼虫和成虫肠中咽侧体静止激素（allatostatin, AS）样的活性物质。发现在棉铃虫、粘虫幼虫和成虫肠中均存在的AS样活性物质,可以在体外抑制咽侧体（corpora allata, CA）的保幼激素（juvenile hormone, JH）的生物合成。生物测定的结果表明,粘虫幼虫肠中AS样活性物质的含量较棉铃虫的高;粘虫1个幼虫肠当量对CA的JH合成的抑制率达43%,而棉铃虫幼虫肠只有26%。无论是棉铃虫还是粘虫,雌成虫中肠对CA的抑制比雄成虫中肠的高,后肠对CA的JH合成的抑制明显的低于中肠对CA的抑制。中肠对CA的JH合成的抑制是可回复的。中肠粗提物经蛋白酶水解后对CA合成JH的抑制率降低,表明肠中AS样的活性物质是肽或蛋白质。     

粘虫咽侧体静止激素的初步分离纯化

用放射化学的方法,检测粘虫Mythimna separata幼虫脑提取物中咽侧体静止激素(Allatostatin,AS)样的活性物质。发现粘虫幼虫脑中含有AS样的活性物质,可抑制离体咽侧体(Corporaallata,CA)的保幼激素(Juvenile hormone,JH)的生物合成。用1个脑当量的幼虫脑提取物,对CA的JH合成的抑制率达51%。幼虫脑提取物经胰蛋白酶水解后,AS活性显著降低,表明幼虫脑中的活性物质是肽类或蛋白质类物质。幼虫脑提取物用Sep-Pak柱初步纯化,有活性的组分经高压液相色谱(HPLC)分离,洗脱组分的AS活性测定表明,有AS活性的组分主要集中在组分1～20和组分30～60,其中对离体CA的JH合成的抑制大于50%的组分有3、5、11、40、54和60。     

一些因子对七星瓢虫咽侧体活性的影响(英文)

七星瓢虫(Coccmella septimpunctata)为了适应环境的变化,通过咽侧体产生保幼激素的活动调节其生殖作用。为了探索内外因素对咽侧体活动的影响,应用放射化学法及免疫电泳测定了食物、卵巢发育、脑神经肽、保幼激素类似物对卵黄发生期成虫保幼激素生物合成及血淋巴中卵黄原蛋白含量的影响。结果表明咽侧体活性受上述各种因子的影响。咽侧体活性与卵黄原蛋白含量及卵母细胞生长密切相关,说明有反馈作用。食物的质与量影响着咽侧体活性的变化。低剂量外源保幼激素类似物处理成虫则可促使咽侧体活性的变化。脑分泌的神经肽(allatotropin)可活化咽侧体。这些结果表明雌瓢虫保幼激素的生产主要是受起源于脑的促咽侧体信号的调节作用。     

一日龄粘虫不同时长吊飞对生殖及寿命的影响

【目的】本研究旨在阐明羽化后1日龄粘虫Mythimna separata(Walker)的飞行潜力以及飞行对成虫生殖和寿命的影响,从而进一步解析粘虫的迁飞行为特征。【方法】利用室内昆虫飞行磨计算机数据采集系统,研究了羽化后1日龄粘虫吊飞6、9和12 h的飞行能力差异,以及不同时长吊飞后粘虫的生殖参数和成虫寿命的变化情况。【结果】结果表明,1日龄雌雄蛾均具有一定的飞行能力,但当吊飞时间超过9 h之后,成虫的飞行时间、距离和速度均不再显著上升。除吊飞12 h成虫的飞行速度外,其它处理雌雄蛾的飞行能力之间无显著差异。羽化后1日龄不同时长吊飞对粘虫的生殖均有显著的促进作用,但随着吊飞时间的延长,这种促进作用显著降低。6、9和12 h吊飞处理均导致成虫产卵前期显著缩短,但仅吊飞6和9 h成虫的产卵量和产卵历期显著高于对照。吊飞12 h成虫的产卵量和产卵历期则显著低于吊飞6和9 h的成虫,并和对照差异不显著。吊飞12 h后,雌雄成虫寿命均显著缩短。【结论】羽化后1日龄飞行显著促进粘虫的生殖,但随着飞行时间的延长,飞行对生殖的促进效应显著减弱。     

成虫滞育的主要特点及神经内分泌调控

成虫滞育的主要特点是生殖受到了抑制,其调控涉及到咽侧体、脑和前胸腺的作用,但主要以咽侧体的作用为主.滞育期间,咽侧体的活性很低,分泌的保幼激素量极微,而咽侧体的活性高低直接受脑所分泌的神经激素所调控.     

REGULATION OF FLIGHT CAPACITY AND CONTENTS OF ENERGY SUBSTANCES BY METHOPRENE IN THE MOTHS OF ORIENTAL ARMYWORM,MYTHIMNA SEPARATA*

Abstract The flight capacity and contents of energy substances in the moths of migratory Oriental armyworm, Mythimna separata (Walker)dosed with juvenile hormone analogue methoprene(JHM) were compared with the normal moth through day‐1 to day‐6 after the treatment. The flight capacity of JHM‐treated moths, as determined by a 12‐hours tethered‐flight test, was significantly lower than that of the controls, although it might differ with their age and sex. The moth's flight capacity between the treatments was insignificantly different from the first to 3rd day after the treatment but was significantly different from the 4th to 6th day either in the mean flight duration or in distance. Evaluation of the long fliers at the same stages between the treatments also supported this finding. Flight capacity of the JHM‐treated moths also differed with the sex. The JHM‐treated female did not fly less than the control from day‐1 to day‐3, but did significantly less from day‐4 to day‐6 after the treatment. The flight capacity of the JHM‐treated males, however, was not weaker than that of the control throughout the test period. Comparison of the levels of energy substances in the JHM‐treated adults and the controls showed that JHM may directly acted on metabolism of glyceride, which in turn affected flight capacity. Furthermore, higher levels of glyceride in the treated male adults raised their flight capacity to a stronger levels than the control in most of the days of tethered‐flight test period. Contents of glycogen, however, were insignificantly affected by JHM in both male and female adults. In might therefore be concluded that levels of JH is a critical factor regulationg migratory behavior in the army worm moth. In addition to affect metabolism of glyceride, other possible physiological roles that JH played in determining migrattory behavior are also discussed.     

The effect of l-methionine concentration on juvenile hormone biosynthesis by corpora allata of the cockroach Diploptera punctata

The effect of varying l-methionine (l-met) concentration on rates of juvenile hormone (JH) biosynthesis/release by corpora allata of females of the viviparous cockroach Diploptera punctata has been studied using a radiochemical assay. Both high activity glands (corpora allata from day 5 females) and low activity glands (corpora allata from day 11 females) were used to study the dose dependence of JH biosynthesis on l-met concentrations, under both de novo (spontaneous) conditions of JH biosynthesis and stimulated conditions (in the presence of the exogenous JH III precursor farnesoic acid). Maximal rates of JH biosynthesis/release were observed at l-met concentration of 20 μM (spontaneous) and 40 μM (stimulated). Below these concentrations, rates of JH biosynthesis declined linearly with decreasing l-met concentration. Optimal concentration of l-met appeared to be similar for both high and low activity corpora allata, under spontaneous and stimulated conditions of biosynthesis. Above 40 μM l-met, no increase in rates of JH biosynthesis was observed. It appears that the corpora allata of D. punctata are efficient scavengers of l-met and are able to utilize even low concentrations of the substrate for JH biosynthesis. The corpora allata of D. punctata may prove useful for the biosynthesis of authentic JH III, radiolabelled in the methyl position using as methyl donor, l[methyl-³H]met of high specific activity.     

Activity of the corpora allata of adult female Leucophaea maderae: effects of mating and feeding

Juvenile hormone III biosynthesis by corpora allata of adult female Leucophaea maderae was measured by an in vitro radiochemical assay. In fed females, JH III synthesis increases more than 20-fold after mating to a peak of 55 pmol/pair/h on day 9 and then rapidly declines. This increase in JH III synthesis concomitant with rapid oocyte growth in mated females is not observed in virgin females. The corpora allata from starved, virgin females appear to be inactive. The addition of 150 microM 2E,6E-farnesol (a) JH III precursor) to the incubation medium stimulates the corpora allata from starved, virgin females less than the corpora allata from starved, mated females. Both feeding and mating are necessary for the expression of a normal cycle of JH III synthesis in this cockroach.     

Enhancement by farnesol and farnesoic acid of juvenile-hormone biosynthesis in induced low-activity locust corpora allata

Exogenous farnesol or farnesoic acid (FA) stimulates juvenile hormone III (JH III) biosynthesis by isolated corpora allata from Locusta migratoria in a dose-dependent manner. Farnesol and FA also stimulate a dose-dependent accumulation of substantial amounts of methyl farnesoate (MF), identified by gas chromatography-mass spectroscopy (GCMS) analysis, in the corpora allata. Lower quantities of MF were found in the incubation medium. Corpora allata, denervated 2 days prior to assay, showed low spontaneous rates of JH biosynthesis which were stimulated by farnesol and FA. The dose-response curves for control and denervated corpora allata were similar. During oocyte maturation the rate of farnesol and FA stimulation of JH biosynthesis increased gradually. However, after transection of nervus corporis allati 1 (NCA-1), the rate of stimulated JH synthesis was maintained at preoperative levels. Although the spontaneous rate of JH biosynthesis decreased rapidly after NCA-1 transection, denervated glands could still be stimulated by farnesol or FA to produce large amounts of JH. These results suggest that the low spontaneous rate of JH biosynthesis in denervated corpora allata is not caused by inhibition of the final steps of JH biosynthesis.     

Control of C-16 juvenile hormone biosynthesis in active corpora allata of female African locusts

Summary

Corpora allata from 8-day-old female Locusta migratoria, during the phase of yolk deposition, exhibit high rates of C-16 juvenile hormone (JH) biosynthesis. The effect of different potential factors which may be involved in the regulation of corpora allata activity is reported. The biosynthetic activity of corpora allata was determined by radiochemical assay.

In maturing females, no changes in corpora allata activity are detected during one daily cycle. Starvation reduces JH biosynthesis only 3 days after the beginning of the food deprivation. Suppression of the median neurosecretory material by electrocoagulation of the internal cardiaca tract (TCC-I) does not disturb JH biosynthesis whereas the transection of the allata I nerve fibres (NCA-I) or the electrocoagulation of the lateral neurosecretory pericarya results in a rapid decline of JH biosynthesis. These data indicate that the median and lateral allatotropins are different, and that only the lateral neurosecretory material exerts an allatostimulating action on corpora allata at the time of vitellogenesis. The corpora allata response to the median allatotropin changes during oocyte growth. C-16 JH and/or 20-hydroxyecdysone treatments in vitro (addition in the culture medium) and in vivo (injection in female) do not influence JH production in our experimental conditions.     

Juvenile hormone biosynthesis in the fall armyworm, Spodoptera frugiperda (Lepidoptera, Noctuidae)

The in vitro production of juvenile hormones (JH) was investigated by using corpora allata (CA) of larvae and corpora cardiaca-corpora allata (CC-CA) complexes of adult females of the fall armyworm Spodoptera frugiperda. In female moths, JH release was high compared to that in 5th and 6th instar larvae. Concentrations of 0.11-0.12 mM methionine, 180-200 mM Na(+), 5.8-8.3 mM K(+), 10-50 mM Ca(2+) and a pH range of 5.7-6.3 yielded optimal incorporation of L-[methyl-(3)H] methionine in vitro by CC-CA complexes. The highest hourly incorporation occurred during a 9-h incubation period following a 1.5-h lag-phase. JH release from CC-CA complexes of adult females was shown to be age-dependent with a peak value on day 2 (approx. 4 pmol h(-1) CA(-1)). By a combination of reversed phase (RP)- and normal phase (NP)-high performance liquid chromatography (HPLC), two major labelled products released by the complex were separated. One compound co-migrated with chemically synthesized JH II diol, the second compound with JH III diol. Only traces of JH II and III could be detected in some samples. Gland extracts also contained both the major radiolabelled products. Double labelling experiments using [3H]methionine and [14C]acetate confirmed their de novo synthesis in CC-CA complexes of female moths. The nature of chemically synthesized reference JH III diol was proved by LC-MS (ESI mass spectrometry) and 1H-NMR (nuclear magnetic resonance spectroscopy).