Prepupal regulation of juvenile hormone esterase through direct induction by juvenile hormone

The regulation of the prepupal peak of juvenile hormorne esterase activity was investigated and found to be directly induced by juvenile hormone. Allatectomy and reimplanation as well as juvenile hormone application experiments all indicated that the appearance of prepupal juvenile hormone esterase activity was in response to a prepupal burst of juvenile hormone. Implantation experiments indicated that the effect of juvenile hormone is not mediated through the isolated brain or subesophageal ganglion.     

Central nervous system actions of growth hormone on brain monoamine levels and behavior of juvenile rainbow trout

Growth hormone (GH) has been demonstrated to alter the behavior of juvenile salmonids. However, the mechanisms behind this action are not yet understood. In mammals and birds, peripheral GH treatment has been shown to affect monoaminergic activity in the central nervous system, which may be a mechanism whereby GH alters behavior. To investigate if GH may influence behavior directly at the central nervous system, juvenile rainbow trout were injected with GH into the third ventricle of the brain, whereupon physical activity and food intake were observed during 2 h. Thereafter, brains were sampled and the content of serotonin, dopamine, and noradrenaline and their metabolites were measured in hypothalamus, telencephalon, optic tectum, and brainstem. The GH-treated fish increased their swimming activity relative to sham-injected controls, while appetite remained unchanged, compared with sham-injected controls. Analysis of brain content of monoamines revealed that the GH treatment caused a decrease in the dopamine metabolite homovanillic acid in the hypothalamus, indicating a lowered dopaminergic activity. It is concluded that GH may alter behavior by acting directly on the central nervous system in juvenile rainbow trout. Furthermore, GH seems to alter the dopaminergic activity in the hypothalamus. Whether this is a mechanism whereby GH affects swimming activity remains to be clarified.     

Morphogenetic effects of juvenile hormone and juvenile hormone mimics on adult development of Drosophila

The morphogenetic effects of t,t-farnesol, Law-Williams juvenile hormone analogue, dichlorofarnesenic acid ethyl ester (DFAEE), and a syntetic racemic or isomeric mixture of C₁₈ juvenile hormone (JH), when applied topically to pharate pupae and adults of D. melanogaster have been studied. Of these various agents tested, only DFAEE and JH affected adult development and eclosion and the pharate pupae were the most sensitive to these agents. The racemic mixture of JH induced the secretion, in the abdomen, of a supernumerary cuticle indistinguishable from that of the pupa; it, in addition, retarded the synthesis of brown eye pigments, general body pigmentation, and affected the differentiation of various internal organs and cuticular structures of the abdomen. By comparing the effects of JH with those of Minute (M) and bobbed (bb) mutations on the adult development, it is suggested that JH, by retarding genetic translation mimics M or bb.     

The ovicidal effects of a juvenile hormone and a juvenile hormone analogue on the fleshfly, Sarcophaga bullata

Egg fertility was reduced in adult females of Sarcophaga bullata treated topically with a juvenile hormone (Cecropia JH-1) or a juvenile hormone analogue, ZR-515 (isopropyl-11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoate), the effect was most noticeable when the flies were treated on the day of ovulation. Depending on the time of treatment, JH and JHA affected different stages of development. Treatment on the day before ovulation produced a high percentage of embryonic arrest; when the flies were treated on the day of ovulation a major proportion of fully developed embryos failed to hatch. Treatment at the early stages of embryogenesis caused mortality of larvae before molting to third instar. There was no delayed mortality after the third instar.

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Résumé Les effets ovicides d'une hormone juvénile (Cecropia JH-1) et d'un analogue d'hormone juvénile (ZR-515) ont été examinés par application locale sur des femelles adultes de Sarcophaga bullata à différents stades du dévelopement des ufs.Le traitement des mouches le jour de l'ovulation est très efficace et empèche les embryons totalement développés d'éclore et de donner des larves de premier stade.L'application de ces produits un jour avant l'ovulation provoque l'arrêt de l'embryogenèse; quand les mouches sont traitées un jour après l'ovulation, la mortalité est plus tardive et une proportion importante de larves meurt avant la mue donnant le troisième stade.

     

Activity of juvenile hormone and juvenile hormone analogues on the growth of Trypanosoma cruzi

The effects of juvenile hormone-III (JH-III) and the juvenile hormone analogues (JHA) methoprene and fenoxycarb on the growth and macromolecular biosynthesis in Trypanosoma cruzi were studied in vitro. It was observed that JH-III and JHA blocked growth and ³H-thymidine incorporation without killing the cells within certain concentrations (≤1 × 10⁻⁴M), but they caused cellular death at concentrations over 1 × 10⁻³M. The inhibitory effect on growth was partially reversible. On the other hand, the inhibitory action of JH-III, methoprene and fenoxycarb was an unspecific effect according to the results obtained with Leishmania mexicana mexicana (promastigotes) and human peripheral blood lymphocytes. The JHA have a good possibility of being used in the control of trypanosomiasis.     

Comparison of two juvenile hormone radioimmunoassays

Juvenile hormone from the hemolymph of adult worker honey bees of known age and behavioral status was extracted and analyzed by two different radioimmunoassays in two independent laboratoies. The assays are different in hapten attachment, radiolabeled tracer, and the method by which bound and unbound hormone are separated. Despite these differences in the methods, hormone determinations were in excellent agreement at lower levels (0–50 ng/ml) but diverged as the hormone concentrations increased (> 50 ng/ml). The relative changes are in good agreement, with a correlation coefficient of 0.97. © 1993 Wiley-Liss, Inc.     

保幼激素的分子作用机制研究

保幼激素(juvenile hormone,JH)和蜕皮激素(20-hydroxyecdysone,20E)是协同调控昆虫发育、变态与生殖的两个重要激素。由于20E的主要分子作用机制已经比较明了,揭示JH的分子作用机制成为过去20多年来昆虫学领域研究的一个重点和难点。国内外多个研究团队利用赤拟谷盗Tribolium castaneum、果蝇Drosophilamelanogaster、烟草天蛾Manduca sexta等为模式,在JH受体的鉴定、JH在昆虫发育变态和生殖中的分子调控机制以及JH与20E在分子水平上的交互作用等方面开展了大量的研究工作,本文就近几年在这些方面取得的主要研究进展作一个综述。     

Comparison of effects of juvenile hormone mimic and synthetic juvenile hormone I on the bug Lygaeus kalmii

ABSTRACT. The possibility that JH mimics cause artifactual responses was investigated by comparing one such mimic (JH-M) and a 'true' JH (JH I) in the effects of each upon L.kalmii larval colouring and development. Post-blastokinesis treatment with synthetic JH I affected larval colour pattern in the same way as JH-M, but higher hormone concentrations were required. JH I also caused higher larval mortality. JH-M and JH I were equally effective in producing supernumerary instars.     

Tissue-specific regulation of juvenile hormone esterase gene expression by 20-hydroxyecdysone and juvenile hormone in Bombyx mori

Juvenile hormone esterase (JHE) is the primary juvenile hormone (JH) metabolic enzyme in insects and plays important roles in the regulation of molt and metamorphosis. We investigated its mRNA expression profiles and hormonal control in Bombyx mori larvae. JHE mRNA was expressed at the end of the 4th and 5th (last) larval instars in the midgut and in all the three (anterior, middle, posterior) parts of the silk gland. In the fat body, JHE expression peaked twice in the 5th instar, at wandering and before pupation, while it gradually decreased through the 4th instar. When 20-hydroxyecdysone (20E) was injected into mid-5th instar larvae, JHE mRNA expression was induced in the anterior silk gland but suppressed in the fat body. Topical application of a juvenile hormone analog fenoxycarb to early-5th instar larvae induced JHE expression in both tissues. In the anterior silk gland, JHE expression was accelerated and strengthened by 20E plus fenoxycarb treatments compared with 20E or fenoxycarb single treatment, indicating positive interaction of 20E and JH. JHE mRNA is thus expressed in tissue-specific manners under the control of ecdysteroids and JH.     

Nutrient-mediated juvenile hormone secretion in mosquitoes

Our objective was to determine whether environmental conditions affect the juvenile hormone (J.H.) regulated phase of ovarian development of mosquitoes. Primary ovarian follicles of nutrient-deprived adult Aedes aegypti reared in non-crowded cultures remain in an early, teneral stage of development. After a meal of sucrose or blood, follicles of crowded mosquitoes develop to a stage competent to deposit yolk directly following blood ingestion; a topically-applied analogue of J.H. stimulates the ovaries to develop to a similar stage. A. aegypti collected in nature are of a size suggesting that their follicles would remain in the teneral stage when adults are nutrient-deprived.     

Perturbation of phospholipid membranes by juvenile hormone

The effects of juvenile hormone and its analogs Altozar 4E and ZR-777 5E on the phase properties of liposomes prepared from dipalmitoyl phosphatidyl-choline (DPPC) have been examined by differential scanning calorimetry. Each of these compounds reduced the co-operativity of the gel to liquid-crystalline phase transition, which is manifest as a distinct broadening of the main transition endotherm, and split the transition into two distinguishable components centered at 34 and 37°C. However, there was no significant change in enthalpy of the main phase transition, suggesting that juvenile hormone and its analogs perturb the bilayer primarily in the vicinity of the phospholipid headgroups. Moreover, this perturbation does not appear to influence bilayer permeability since the osmotic swelling rates of liposomes prepared from either phosphatidylcholine or dipalmitoyl phosphatidylcholine that contained up to 33 mol% juvenile hormone were not significantly different from the swelling rates of corresponding liposomes containing no juvenile hormone. Splitting of the transition endotherm into two peaks appeared to be peculiar to compounds possessing juvenile hormone activity. A mixture of fatty acid methyl esters broadened the main transition of DPPC, but did not split the endotherm or shift the transition midpoint, and the insect hormone ecdysone had no discernible effect on the DPPC transition apart from eliminating the pretransition. The data indicate that juvenile hormone and its analogs can modulate the physical properties of phospholipid bilayers, and raise the prospect that some of the physiological effects of this hormone may be achieved through its influence on the molecular organization of membrane lipid.     

The substrate specificity of juvenile hormone esterase from Manduca sexta haemolymph

Haemolymph of $\text{Manduca sexta}$ fifth instar larvae contains a high esterase activity capable of hydrolyzing $\text{Hyalophora cecropia}$ C₁₈ juvenile hormone (JH). In an attempt to characterize the substrate specificity of the enzyme (s) involved, dilute haemolymph was incubated $\text{in vitro}$ with a series of JH-analogs. Ethyl esters with or without the 10,11-epoxide group were hydrolyzed readily but isopropyl esters and the (2Z)-isomer of JH were not affected. Indirect evidence was obtained for the hydrolysis of aziridine analogs of JH. Correlations of these results to biological activities are discussed.     

Effects of juvenile hormone on polysome integrity

Juvenile hormone inhibits protein and RNA synthesis in cell cultures from Trichoplusia ni and in the testicular germinal cysts of Hyalophora cecropia pupae in vitro. Sucrose gradient analyses revealed that the polysomes of both the T. ni cells and the germinal cysts were disaggregated almost immediately after the addition of juvenile hormone in vitro with a corresponding dose-dependent increase in monosomes. It is suggested that previous reports revealing juvenile hormone inhibition of ecdysone stimulated RNA and protein synthesis may be due to polysome disaggregation. Further studies demonstrated that the effect is not restricted to insect cells and can be elicited by several other lipids devoid of juvenile hormone morphogenetic activity. Experiments with broken cell preparations and isolated polysomes suggest the necessity of cell membrane integrity for the effect on the polysomes. Several probing studies utilizing cycloheximide, ribonuclease, and high K⁺ concentrations were conducted on the means by which juvenile hormone and other lipids may elicit polysome disaggregation.     

Comparative metabolism of the Cecropia juvenile hormone

The in vivo and in vitro metabolism of ³H-Cecropia C18-juvenile hormone (JH) was studied in representative species of eight orders of insects. In all orders the major metabolites were found to be the JH-acid, the JH acid-diol, and conjugated polar metabolites thought to be glucosides or glucuronides. The JH-diol was also present in both Tenebrio and Saturniid pupae. In vitro studies revealed two additional metabolites produced by tissue homogenates in the presence of NADPH. On the basis of chromatographic evidence these are tentatively identified as the JH-tetrol metabolite in Cecropia, Thermobia, and Drosophila, and the JH-bisepoxide in Drosophila.