Comparison of structurally analogous allatotoxins on the molting and morphogenesis of Rhodnius prolixus,and the reversal of ecdysial stasis by ecdysone

The allatotoxic effect of 3-ethoxy-4-methoxy-6-iso-pentenylphenol on nymphal molting and metamorphosis of Rhodnius prolixus was examined. Continuous contact treatment with IPP induced the formation of precocious adults and retarded molting or initiated a permanent ecdysial stasis. Insects treated with 7-ethoxy-6-methoxy-2,2-dimethylchrornene were similarly affected. Ecdysone given orally counteracted the ecdysial stasis and also reduced the duration of the molting delay caused by IPP.     

Metabolism and hepatotoxicity of the naturally occurring benzo[b]pyran precocene I

The in vitro metabolism of precocene I by liver microsomes from control and treated rats and the effects of precocene I on the function and histology of the rat liver were examined. The major metabolites (80-90% of total metabolites) from all microsomal preparations were the cis and trans 3,4-diols of precocene I produced with a cis/trans isomer ratio of 1:2. These diols appear to arise mainly by spontaneous hydrolysis of precocene I 3,4-oxide. (+)-(3R,4R)-cis- and (-)-(3R,4S)-trans-precocene I 3,4-diols were the predominant enantiomers of the 3,4-diol formed. The enantiomeric excess of these diols (2-50%) is dependent on the microsomal preparation, with microsomes from control rats exhibiting the highest stereoselectivity and microsomes from phenobarbital-treated rats the least. 6-Hydroxyprecocene I was the next major metabolite and was formed to the extent of 5% (control), 10% and 17% (phenobarbital and 3-methylcholanthrene treatment, respectively) of total metabolites. Treatment of rats with a single i.p. dose of precocene I (300 mg/kg) resulted in extensive hepatic damage as evidenced by a marked increase of plasma glutamic pyruvic transaminase levels and histologic observation in liver sections of severe centrolobular necrosis. Although phenobarbital treatment of rats increased the rate of liver microsomal metabolism of precocene I by approximately 50% (nmol products/nmol cytochrome P-450/min) compared to liver microsomes from control rats, hepatic damage caused by precocene I was not significantly affected. Depletion of glutathione levels in the rats with diethyl maleate prior to precocene I treatment dramatically increased the severity of hepatic insult, whereas treatment of the rats with the mixed function oxidase inhibitor piperonyl butoxide prior to treatment with precocene I blocked hepatic damage. Treatment of rats with cysteamine prior to treatment with precocene I protected the animals against the toxic effects. Neither cis nor trans precocene I 3,4-diol nor 3,4-dihydroprecocene I elicited impaired liver function or cellular damage. The above results are consistent with the view that precocene I 3,4-oxide is the metabolite responsible for the hepatotoxic effects observed when precocene I is injected into rats.     

Proximate factors influencing soldier development in the basal termite <Emphasis Type="Italic">Cryptotermes secundus</Emphasis> (Hill)

Summary Regulation of soldier development in termites at the endocrinological and social scale was intensively studied in the 60s and 70s, but conclusive results are still scanty. In termites, the presence of soldiers inhibits further soldier differentiation, but the mechanism is not well understood. Secretions from the frontal glands seem to be important, but dry- and dampwood termites do not have frontal glands. We investigated the influence of precocene I, a JH-antagonist, and of soldier head extracts on the development of soldiers in the drywood termite, Cryptotermes secundus (Hill). Soldierless colonies produced fewer soldiers when treated with precocene I or soldier head extract than control colonies. Furthermore, colonies treated with precocene I had produced worker-nymph intercastes, last stage nymphs and alates by the end of the experiment (after six months) which were not present in control colonies. Hence, both treatments inhibited soldier development while precocene I simultaneously promoted the development of adult traits, probably by reducing (directly or indirectly) the JH level. The inhibition effect of the soldier head extract indicates that at least in termites without a frontal gland, other sources of material in the head have a regulatory function.     

A possible therapy by juvenile hormone I to Spodoptera littoralis (Boisd.) larvae previously treated by precocene II

An effective constant dose (55 μg) of precocene II (PII) was topically tested against the last three instars of Spodoptera littoralis (Boisd.) larvae. Application of PII induced morphogenetic abnormalities typical of juvenile hormone (JH) excess. The resultant imperfect insects included larval‐pupal mosaic and partial or severe cases of untanned pupae. The sixth‐instar larvae were more sensitive to PII administration than the two preceding instars. However, sensitivity of the last larval instar to PII varied with the timing of dose application relative to the developmental status of the larvae. Whereas the newly ecdysed (0‐day old) larvae were more sensitive, the older larvae of the same sixth‐instar showed sharp decrease in their sensitivity to PII with a concomitant increase of their age. Application of a single dose (5 μg) of JH I to PII pre‐treated larvae significantly (P < 0.001) reduced the production of imperfect insects where many PH‐treated larvae developed successfully to apparent normal pupae. Although a single dose of PII was more effective on S. littoralis larvae than repeated daily doses, the effectiveness of JHI‐therapy to PH pre‐treated larvae by repeated doses was less effective in producing perfect insects than JH‐therapy to PII pre‐treated larvae by single doses. The reversal of any of these by applied JHI is quite interesting but the mechanisms remain to be unraveled.     

外用保幼激素与早熟素对丽斗蟋翅二型个体飞行与生殖发育间生理权衡的影响（英文）

为探讨丽斗蟋Velarifictorus ornatus翅二型个体飞行与生殖发育间生理权衡的内分泌控制机理, 本研究调查了外用保幼激素Ⅲ(JH-III)与早熟素Ⅰ(P-I)对丽斗蟋翅二型个体飞行肌与生殖发育的影响。结果表明： 成虫羽化后当日分别注射1, 5, 10和25 μg保幼激素7 d后, 显著促进了丽斗蟋长翅雌虫卵巢发育, 卵巢重量分别从对照组的16.8±11.4 mg/♀增加到43.9±10.7, 33.6±14.0, 56.8±7.6和 39.3±30.7 mg/♀; 但对卵巢内怀卵量无显著影响。相反, 外用保幼激素则诱发飞行肌降解, 1, 5和10 μg JH-III处理组飞行肌重量分别下降为12.9±4.7, 11.7±4.8和8.8±0.8 mg/♀, 显著低于对照组飞行肌重量(17.7±1.6 mg)。对短翅雌虫注射P-I时, 当注射的剂量超过50 μg/♀时, 能够显著抑制卵巢发育, 而低于50 μg/♀时则对卵巢发育无明显影响。外用JH-III对丽斗蟋长翅雄虫飞行肌、 精巢、 附腺的发育无明显影响; 外用P-I对短翅型雄虫精巢与附腺的发育也无明显影响。因此, 丽斗蟋翅二型雌虫与雄虫的飞行肌与生殖器官的内分泌控制机理可能存在差异。     

Methyl farnesoate and juvenile hormone III in normal and precocene treated embryos of the ovoviviparous cockroach Nauphoeta cinerea

Summary

Titers of juvenile hormone III and methyl farnesoate, its unepoxidized precursor, were measured throughout embryonic development using a gas-chromatographic method and it was revealed that both substances are undetectable before dorsal closure. Thereafter they both reach similarly high concentrations (800 ng/g) until a few days before hatching, when their titers begin to decrease. Application of the precocene analogue, 7-ethoxy-6-methoxy-2,2-dimethyl-chromene, to egg-cases at dorsal closure results in very low or undetectable titers of juvenile hormone III, depending on the dose applied, whereas methyl farnesoate is seen to reach high levels similar to those seen in the controls. The severe developmental disturbances observed suggest that juvenile hormone III is very important for normal development and formation of the 1st instar larva.     

Lepidopteran anti-juvenile hormones: Effects on development of Apanteles congregatus in Manduca sexta

Parasitism by the braconid wasp Apanteles congregatus decreases the effectiveness of the anti-juvenile hormone agents ETB (ethyl 4-[2-{ittert-butyl carbonyloxy}bytoxy]benzoate) and fluoromevalonolactone (FMev) in inducing precocious metamorphosis of Manduca sexta larvae. Topical application of 1–200 μg ETB to parasitized third-instar larvae had no effect on either host or parasite development, whereas doses of 50μg or more ETB applied to unparasitized third-instar larvae caused formation of larval-pupal intermediates after the fourth instar. Parasitism also decreased the effectiveness of 100–200 μg FMev in causing metamorphosis at the moult following its application. In contrast to ETB, FMev disrupted development of the parasitoids. No wasps emerged when preterminal stage hosts were treated with FMev and the hosts formed larval-pupal intermediates. After treatment of terminal stage hosts with FMev, the number of emerging parasitoids was reduced by one-third. Precocene II (100 μg per larvae) had no effect on development of either M. sexta or A. congregatus.     

Hormonal control of vitellogenin synthesis in Oncopeltus fasciatus

Previous work indicated the existence of two vitellogenins (A and B) in the haemolymph of Oncopeltus fasciatus, and that vitellogenin B was juvenile hormone (JH)-dependent whereas A was not (Kelly and Telfer, 1977). We have extended these results using several electrophoretic techniques in combination with limited proteolysis of key proteins to show that (1) vitellogenin B is present in eggs in a modified form while vitellogenin A cannot be detected in eggs. (2) Vitellogenin A may be a precursor of B since it has a molecular weight of 200,000D, approximately three times that of vitellogenin B (68,000D) and analysis by limited proteolysis shows that two proteins to be nearly identical. (3) Neither ovariectomy nor treatment with the anti-allatotropin, precocene II prohibits the appearance of vitellogenins A and B in the haemolymph. (4) Injection of ecdysone or 20-hydroxyecdysone into adult, male Oncopeltus fasciatus induces the appearance of both vitellogenin A and B in the haemolymph, suggesting the possible involvement of ecdysteroids in the control of vitellogenin synthesis in this species. (5) We have no evidence for JH control of the synthesis of vitellogenin, however, the ratio of vitellogenin A to B in the haemolymph is higher in the precocene-treated females.     

Effects of precocene I and II on flight behaviour in Oncopeltus fasciatus, the migratory milkweed bug

Treatment of newly emerged adult Oncopeltus fasciatus with the corpus allatum inhibitors. 7-methoxy-2,2-dimethyl chromene or 6,7-dimethoxy-2,2-dimethyl chromene (preocene I and II) results in an inhibition of long-term flight (presumed migratory) behaviour in both males and females and inhibition of oögenesis in females. Treatment of reproductive females with precocene briefly stimulates flight behaviour (which ceases in such females as oviposition begins) and then subsequently inhibits it. Oviposition also ceases in such females and oöcyte resorption occurs. Topical application or injections of JH III to precocenetreated animals results in immediate restoration of the tendency to make long tethered flights while corpora cardiaca extract injections, corpora cardiaca implantation, sham implantation, sham injections and sham topical applications were ineffective in restoring prolonged flight behaviour to precocene-treated animals.Restoration of flight by JH III injection was observed within 1 hr after treatment with the hormone. These results indicate that JH is necessary for prolonged flight and presumably migratory behaviour in this species and its stimulatory effect on flight behaviour is immediate. Possible mechanisms of action of the hormone on flight behaviour are discussed.     

Effects of juvenile hormone I and precocene I & II on Microplitis rufiventris when administered via its host, Spodoptera littoralis

We investigated the effect of juvenile hormoneI (JHI) and precocene I & II (PI & PII) onthe endo-developmental stages, reproductiveperformance and longevity of Microplitisrufiventris Kok. after topical treatment ofhost larvae of Spodoptera littoralis(Boisd.). Host larvae were treated with each ofthe test compounds by a single dose 2–4 h afterparasitization or 1 day prior to parasitoidemergence, or by repeated daily applications 2–4 h after parasitization to parasitoid emergence.JHI-treatments increased parasitoiddevelopmental time, induced developmentalabnormalities and inhibition of parasitoidegression. Interestingly, one of the causal factorsthat inhibited the parasitoid egression was themoulting of some parasitoid larvae into asupernumerary instar. Applications of PI or PIIto parasitized S. littoralis larvae didnot affect parasitoid developmental time, butsome developmental abnormalities were noted.Melanin formation in host's blood was greaterin PI-treatments than in PII-treatments.PII-treatments arrested development of somefirst instar parasitoid larvae typical of JHIexcess. Adult female wasps that emerged fromJHI-treated hosts lived for significantlylonger periods than control females, but didnot produce more offspring. The longevity andreproductive capacity of females whichdeveloped in hosts treated by precocenes werereduced compared with the females emerged fromcontrol hosts. Even the small number ofadult wasps from PII-treated hosts which livedfor the same period as control wasps, showed asignificant reduction in their reproductiveperformance. Repeated daily applications of thetest compounds reduced wasp fecundity andlongevity to a significantly greater degreethan the single applications, except for a lowdose of JHI (1 µg). The study demonstratesthat growth disrupters, such as JHs andprecocenes have a delayed developmental effect onM. rufiventris and points out the need tobe aware of these effects in implementingcontrol strategies of S. littoralis innatural habitats.