Effects of electrocoagulation of cerebral neurosecretory cells and implantation of corpora allata on oöcyte development in Locusta migratoria

The implantation of active corpora allata into intact Locusta females during growth accelerates pre-vitellogenic oöcyte growth and vitellogenesis. Localised stimulation of yolk deposition follows the implantation of active corpora allata between the ovarioles demonstrating a gonadotrophic rôle for the corpus allatum hormone. Electrocoagulation of the median neurosecretory cells of the brain prevents vitellogenesis whilst pre-vitellogenic oöcyte growth occurs normally. Implantation of active corpora allata into females with ablated cerebral neurosecretory cells promotes vitellogenesis in a proportion of test animals although mature oöcytes are never produced.It is suggested that the rôle of the median neurosecretory cells during egg development in Locusta is primarily concerned with the activation and maintenance of activity of the corpora allata. The corpus allatum hormone acts both metabolically and gonadotrophically.     

Phase polymorphism in Schistocerca gregaria: Assessment of juvenile hormone synthesis in relation to vitellogenesis

Juvenile hormone (JH) synthesis by the corpora allata of gregarious and solitarious phase females of Schistocerca gregaria was determined in vitro during the penultimate and last stadia as well as during the first gonotrophic period of adults. Generally, the corpora allata of solitarious females showed higher rates of JH synthetic activity. In addition, in adult females there was a temporal difference between the corpora allata activities of gregarious and solitarious locusts, the latter exhibiting relatively higher rates of JH synthesis early in the first gonotrophic period. The corpus allatum volumes of solitarious females were also generally larger than those of their gregarious counterparts; there was no synchrony between fluctuations in JH synthetic activity and changes in corpus allatum volume in either phase.The early onset of relatively high JH synthetic rates in solitarious females was correlated with the early detection, by rocket immunoelectrophoresis, of vitellogenin in the haemolymph and vitellin in the oöcytes. Vitellogenin appeared in the haemolymph on day 4 in solitarious females and on day 6 in gregarious females and vitellin appeared in the oöcytes on days 6 and 8 respectively. Oöcyte length at which vitellogenesis was first detected was 1.8 mm for gregarious and 1.3 mm for solitarious females. However, despite the accelerated onset of both vitellogenin synthesis and uptake, oöcyte maturation time of solitarious females was longer. In both gregarious and solitarious females, vitellogenin titres increased until oöcytes reached a length of about 4 mm and declined thereafter. Vitellin content of ovaries increased proportionately to oöcyte growth until they attained a length of 5.0 mm. The subsequent increase in length of oöcytes to maturity is attributed to postvitellogenic growth, possibly by hydration.     

Evidence that the ovaries of Musca domestica do not maintain cyclicity by regulating the corpus allatum.

When the female housefly retains eggs, vitellogenesis in the penultimate oöcytes is suppressed during continued protein feeding. Allatectomy of gravid females or of females with developing oöcytes did not prevent maturation of a second batch of eggs. This result does not support the claim of Adams (1970) that an oöstatic hormone, produced by ovaries with retained eggs, inactivates the corpus allatum (CA) and thereby prevents development of the next batch of eggs.The report of Adams and Hintz (1969) that the CA regulates egg maturation depends on their removal of ring gland, which they incorrectly refer to as ‘allatectomy’. In the present report, removal of the ring gland from 1 day old females suppressed egg development, whereas removal of the CA alone did not. Therefore, sufficient CA hormone for reproduction was secreted within 24 hr of emergence, and it was the removal of the corpus cardiacum, and not the CA, that had prevented egg development in the experiments of Adams and Hintz.     

Controle neuroendocrine du fonctionnement du corpus allatum chez Rhodnius prolixus

Cauterization of the dorsal portion of the protocerebrum effected immediately after cessation of feeding in adult females blocks vitellogenesis. The growth of the oöcytes can be re-established by the implantation of corpora allata or by the application of juvenile hormone analogue, and it is suggested that the protocerebrum has a corpus allatum stimulating influence. The corpus allatum deprived of all its cerebral nervous connexions by cutting the aorta just behind the corpora cardiaca induces abundant vitellogenesis. Females with denervated corpora allata or pars intercerebralis cauterized 24 hr after a meal show a phase of vitellogenesis more active than that in normal female adults. This suggests the existence of a cerebral inhibitory centre: its activity through a nervous or endocrine path is discussed.     

Endocrine control of vitellogenin synthesis and vitellogenesis in Triatoma protracta.

The corpus allatum (CA) is required for vitellogenesis in the blood-sucking reduviid, Triatoma protracta, as seen by the total lack of yolk deposition in allatectomized females. Normally the CA becomes active within a day after emergence. After a period of activity during which unfed virgins may mature a few eggs, the CA is inhibited via its neural connectives from the brain. The CA is activated by mating, while a blood meal provides an additional stimulus for vitellogenesis. If the ventral nerve cord (VNC) is severed within 48 hr after copulation, the mating stimulus does not get through. However, the pathway of the feeding stimulus does not involve the VNC. The brain does not have any allatotropic or gonadotropic function in this species.A female-specific protein (vitellogenin) was identified by immunoelectrophoresis in the haemolymph of egg-maturing females. This protein is taken up by the oöcytes immunologically unaltered and forms the bulk of the yolk. Allatectomy at emergence prevents the appearance of the vitellogenin, and the topical application of JH_III to allatectomized females led to its synthesis de novo, as shown by the incorporation of labelled precursors into vitellogenin. From its mobility in polyacrylamide gels of different concentrations, the molecular weight of the yolk protein is estimated to be 4.37 × 10⁵ daltons.     

Oöcyte resorption during ovarian development in the blowfly Lucilia cuprina

Nulliparous females of a normal anautogenous strain of Lucilia cuprina mature all of their primary oöcytes after feeding ad lib on sheep's liver. Females fed measured inadequate amounts of protein-rich materia either fail to mature any oöcytes or mature less than their full complement. These mature oöcytes are smaller than in ad lib fed females. In females maturing no oöcytes, ovarian development ceases with all oöcytes in a pre-vitellogenic or early vitellogenic stage. When females mature only some of their oöcytes, the remainder are resorbed in early vitellogenesis. Few females mature less than 100 oöcytes, if they mature any at all.     

Factors responsible for the initiation of a second oöcyte maturation cycle in the ovoviviparous cockroach Nauphoeta cinerea

The factors responsible for the initiation of a second oöcyte maturation cycle were investigated by measuring oöcyte growth, vitellogenin titre, and corpus allatum activity after injection of juvenile hormone and/or removal of the egg-case from pregnant females and by performing ovary and corpus allatum transplant experiments.Egg-case removal in late pregnancy results in immediate oöcyte growth, whereas in early pregnancy oöcyte growth is resumed only after a lapse of time, even after injection of juvenile hormone. This, however, induces an immediate increase in the haemolymph vitellogenin titre. A single injection of 2 or 10 μg of juvenile hormone II first stimulates some oöcyte growth after this lapse of time and later activates the corpora allata, which in turn leads to completion of oöcyte maturation. A repeat injection of 10 μg stimulates continuous oöcyte growth without activating the corpora allata. In the presence of an egg case, activation of the corpora allata is suppressed, even after injection of 2 μg of juvenile hormone III, and the oöcytes do not grow. Injection of higher doses stimulates oöcyte growth and leads to expulsion of the egg case in up to 95% of the females. This, however, is not a direct consequence of the increase in size of the ovaries. Ovary transplant experiment show that in young pregnant females the second generation of oöcyte is not yet competent for growth and that ovaries which are competent can mature in young pregnant females, treated with juvenile hormone, whose egg case has been removed.The results are summarized in a model demonstrating the various factors involved in regulating corpus allatum activity in oöcyte maturation and pregnancy and after application of juvenile hormone. We prepose that the corpus allatum activating effect of exogenous juvenile hormone is mediated by the growing oöcyte and that this activation can be suppressed by the continuous presence of exogenous juvenile hormone.     

Endocrine control of oögenesis in the housefly,Musca domestica vicina

The endocrine system involved in the control of oögenesis in the housefly, Musca domestica vicina, was investigated. Allatectomy, decapitation, and starvation of newly emerged females resulted in inhibition of oögenesis, showing a close relationship between enlargement of the corpus allatum and growth of follicles during the first oögenesis. Histological observation of sexually matured females showed active secretion of the corpus allatum and the medial neurosecretory cells of pars intercerebralis. Topical application of juvenile hormone analogues (JHA) to the allatectomized fly induced the growth of ovary, and critical doses of methoprene and methyl-7, 11-diethyl-juvenate for the maturation of the ovary were determined. JHA stimulated initiationof oögenesis in the starved or decapitated flies as well as vitellogenesis in the sugar-fed one; subsequently it was found that juvenile hormone acted not only as a gonadotropin but also as a regulator of vitellogenesis. Furthermore, JHA stimulated cell lysis in pupal fat body of female flies, indicating a possible influence of juvenile hormone upon the process of releasing vitellogenin.     

Effects of food and water availability,and of NCA-1 section,upon juvenile hormone biosynthesis and oöcyte development in adult female Periplaneta americana

The combined stimuli from feeding, drinking, mating and crowding are required for the highest rates of oöcyte development in maturing adult female Periplaneta americana. A graded series of “sexually suppressed” females can be produced by withholding one or more of these stimuli, and this stepwise retardation of ovarian development appears to be achieved by a progressive increase in corpus allatum restrain. It seems that all of these environmental cues are centrally integrated such that juvenile hormone-dependent processes can proceed at an appropriate pace. Water availability is evidently the most important factor. Water-deprived females are sexually unreceptive, and are found to have very low rates of juvenile hormone biosynthesis and ovarian development. This holds true even when they are provided with food. In contrast, 75% of starved females are sexually receptive if allowed free access to drinking water. At the same time they have enhanced corpus allatum activity, and show significant oöcyte growth.The mode of regulation of corpus allatum function in adult female P. americana appears to be significantly different to the model proposed for the cockroaches Leucophaea maderae and Diploptera punctata. Allatotropic signals may be more important than inhibitory signals in the former species. The glands continue to be moderately active in fed, mated female P. americana after NCA-1 section (although a major peak of corpus allatum activity is not obvious), and the rate of oöcyte development is not greatly reduced. However, NCA-1 mediated inhibition of juvenile hormone biosynthesis is less readily demonstrated. We could observe no enhancement of corpus allatum activity nor stimulation of oöcyte growth after unilateral NCA-1 section when the operation was performed on starved virgins, and the same result was found after bilateral NCA-1 section when starvation or virginity were separately enforced. A slight stimulation of juvenile hormone biosynthesis, together with a small increase in oöcyte development, could only be demonstrated after both NCA-1 were cut in starved virgins.We conclude that neurally mediated corpus allatum inhibition in has yet to be adequately verified, and that the available evidence does not contradict the theory that juvenile hormone biosynthesis in adult females could be regulated predominantly by chemicals released into the haemolymph.     

Corpus allatum activity during overlapping cycles of oöcyte growth in adult female Melanoplus sanguinipes

Cycles of oögenesis in Melanoplus sanguinipes overlap to the extent that there are always 2 and occasionally 3 sets of vitellogenic oöcytes in the ovarioles at any one time. Three phases of vitellogenic oöcyte development can be distinguished: (1) An initial 24-hour phase of slow development (1.0–1.2 mm, 0.05–0.10 mm³). (2) A phase of rapid oöcyte growth (1.2–3.5 mm, 0.1–1.3 mm³). The duration of this phase is 2 days in the first cycle and 3 days in subsequent cycles. (3) A final phase of rapid oöcyte growth and maturation (3.5–4.5 mm, 1.3–2.8 mm³). Including the time taken for oviposition the duration of this latter phase is 3 days. Phases 1, 2 and 3 of cycles n + 2, n + 1 and n, respectively, overlap entirely. Activity of the corpora allata was measured using a radio-biosynthetic technique. A period of increased corpus allatum activity coincides with the initial part of phase 2 in each cycle. Each set of oöcytes is, thus, subject to 2 and occasionally 3 peaks of corpus allatum activity during development. Using these data a model of the control of oöcyte development has been devised     

Precocene I and II inhibition of vitellogenic oöcyte development in Drosophila melanogaster

Adult female Drosophila melanogaster were exposed to precocene I and II, antiallatropin compounds which result in juvenile hormone deficiency in many insects. The presence of juvenile hormone in Drosophila adults was evaluated by examining vitellogenic oöcyte development, a process regulated by juvenile hormone in these flies. Both precocenes reduced the number of vitellogenic oöcytes present 43 hr after exposure in a dose-dependent manner. Precocene I was effective when applied to either newly eclosed females prior to vitellogenic oöcyte development or to gravid females. Precocene I was also effective in decapitated females, indicating that the action of the compound is not mediated by the brain. Corpus allatum volume, presumably a reflection of secretory activity, increased between 0 and 24 hr after eclosion in control females but not in precocene-treated females even after 48 hr. However, when females were removed from precocene medium, gland volumes increased within 48 hr to approximately those of control flies. This result is consistent with the reversibility of the precocene effect on Drosophila adults. These results suggest that precocene acts on the corpus allatum of Drosophila adult females to produce juvenile hormone deficiency.     

Determinants of oöcyte degeneration in Drosophila melanogaster

During normal oögenesis in many insects some of the oöcytes fail to mature; instead they degenerate and are resorbed. In this work oöctte degeneration was investigated in Drosophila melanogaster females and found to be limited to early vitellogenic stages (stages 8–10). Even when retained for up to 18 days by females, mature (stage 14) oöcytes showed unaltered protein patterns after separation by SDS polyacrylamide electrophoresis, indicating that protein breakdown, which is characteristic of degeneration, does not occur in chorionated oöcytes.A number of environmental parameters were shown to influence the percentage of degenerating oöcytes in females. Strong responses as reflected by increased stage-8 and 9 oöcyte degeneration were found in females subjected to suboptimal (but not starvation) medium, virgin females, females mechanically unable to oviposit, and females unable to locate suitable oviposition sites. Little or no response was seen in females subjected to crowding, however, since all of these environmental parameters except adult crowding have been shown to decrease fecundity, and therefore the rate of oöcyte production, it is suggested that oöcyte degeneration is a strategy for decreasing the rate of oöcyte production in Drosophila.     

Actions of the juvenile hormone, 20-hydroxy-ecdysone,and the oöstatic hormone during oögenesis in the flies Phormia regina and Sarcophaga bullata

Application of juvenile hormone (JH) to sugar-fed Phormia flies leads to full ovarian development, i.e. the flies become autogenous. Application of JH to sugar + liver-fed Phormia leads to the simultaneous development of primary, secondary and tertiary oöcytes, suggesting the role of the oöstatic hormone is to shut off the action of the JH. This is consistent with the notion that the oöstatic hormone may act on the corpus allatum either directly or through the neurosecretory system. Application of 20-hydroxy-ecdysone to Phormia or Sarcophaga, when primary oöcytes have started to develop (stage 4A), causes the primary oöcytes to degenerate, with concomitant development of the secondary oöcytes.     

Oöcyte activation in Xyleborus ferrugineus by bacterial symbionts

In both virgin and mated Xyleborus ferrugineus females, the oöcytes in the ovarioles are activated in the presence of bacterial symbionts. Streptomycin sulphate and chlorotetracycline-HCl incorporated in a sodium benzoate-, or in a sorbic acid-based meridic diet, significantly reduced oviposition by, and number of progeny of, ectosymbiotic fungus-free virgin females. ‘G’-potassium penicillin was effective only when combined with a sodium benzoate-based diet. All antibiotic-treated reproductively sterilized females regained fertility upon being transferred to an antibiotic-free diet, and eggs laid by such females contained large numbers of transovarially transmitted symbionts. Bacteria were not found in primary oöcytes of antibiotic-treated females that did not oviposit. It is concluded that the observed symbionts are involved in oöcyte activation, and thus enable the beetle to reproduce asexually.     

Synthesis and deposition of yolk protein in adult Drosophila melanogaster

Newly eclosed Drosophila melanogaster females contain only previtellogenic stage oöcytes and no immunologically detectable female specific haemolymph protein. During the subsequent 48 hr the concentration of female specific protein in the haemolymph rises to a plateau value of 21 μg/μl; at this time yolk protein represents about one third of the total haemolymph protein in adult females. The first mature (stage 14) oöcytes are observed at 48 hr post eclosion. The female specific haemolymph protein and the major protein from mature oöcytes are electophoretically and immunologically the same or very similar. Injection of alpha amanitin into newly eclosed females inhibits the development of mature oöcytes and the degree of inhibition depends on the age of the female at the time of injection. Phenocopies of non-vitellogenic mutants result when alpha amanitin is injected into newly eclosed females; after 36 hr post eclosion no visible inhibition of vitellogenesis (as observed morphologically at 72 hr post eclosion) can be produced by alpha amanitin.     

Haemolymph ecdysteroid levels in female tsetse fly Glossina fuscipes (Diptera) during the first reproductive cycle: A comparison between virgin and mated females

The fluctuations in haemolymph ecdysteroid levels were recorded by radioimmunoassay during the first two ovarian cycles of the tsetse fly, Glossina fuscipes. During the first ovarian cycle, the patterns of ecdysteroid levels are similar in virgin and mated females. In virgins, the first oöcyte is not ovulated and ecdysteroid levels during the second vitellogenesis remain low. In mated females, vitellogenesis of the second oöcyte is concomitant with growth of the first larva in the mother's uterus and ecdysteroid levels are higher than during the first cycle. Two ecdysteroid increases were recorded in mated females and not in virgins. One coincides with vitellogenesis of the second oöcyte and the other occurs at the end of pregnancy and finishes after larviposition. The roles of ecdysteroids in the regulation of vitellogenesis, ovulation, pregnancy and larviposition are discussed.     

Influence de modifications des conditions lumineuses sur les rythmes circadiens de vitellogenese et d'ovulation chez Drosophila melanogaster

Under photoperiodic conditions (LD 12:12), a rhythm was observed in the frequencies of ovarian egg chambers and of mature oöcytes. Females reared and kept in permanent darkness (DD) did not show any rhythm. After a transition from LD 12:12 to DD, the rhythm of vitellogenesis remained almost unchanged for at least 5 days while the rhythm of oöcytes retention disappeared.Suppression of a suitable oviposition substrate resulted in an accumulation of mature oöcytes in the ovaries. When a conveneint medium was given again, the egg-laying proved to be highly dependent on the light conditions. Most of the oöcytes remained in retention during the light phase. Significant egg-laying only occurred after the beginning of darkness. In such conditions females can lay one egg every 3 min.The egg-laying rhythm observed under cyclic light conditions thus arises from two separate physiological processes: oöcyte production (vitellogenesis) which has a circadian, endogenous rhythm and oviposition which is directly dependent on the light conditions.     

The role of endocrines in flight-muscle degeneration in Dysdercus cingulatus (Heteroptera: Pyrrhocoridae)

In Dysdercus cingulatus, extirpation of the median neurosecretory cells inhibits flight-muscle breakdown. However, implantation of median neurosecretory cells or corpus allatum into females lacking these neurosecretory cells induces muscle histolysis. Median neurosecretory cells stimulate the corpus allatum to produce juvenile hormone which in turn induces muscle degeneration. Topical application of kinoprene induces muscle breakdown, even in males and starved virgin females. The direct participation of juvenile hormone in muscle degeneration is further confirmed by observations on the effect of precocene II which inhibits muscle histolysis in many individuals. The endocrine basis of vitellogenesis and flight-muscle degeneration could be identical; vitellogenesis however appears to require a higher threshold concentration of juvenile hormone.     

Vitellogenic and embryogenic activity of the microtubule disruptor vinblastine following ingestion by the wasp Bracon hebetor

The reproductive performance of Bracon hebetor females was adversely affected by the consumption of sub-lethal doses of vinblastine. While all oögenic cell types present in the gonads at the time of treatment displayed various degrees of fecundity and/or fertility depression, the transitional cells proved to be the least susceptible to vinblastine damage. Vitellogenically active oöcytes were most sensitive to vinblastine. In these oöcytes development was blocked at or prior to the terminal growth phase. Oviposited eggs which did arise from the exposed vitellogenic oöcytes were few in number and characterized by aberrant morphology. Embryogenic effects were predominantlydue to pre-blastoderm formation damage and most pronounced in oöcytes exposed during the most advanced stages of gonadal development, late vitellogenesis through meiotic metaphase I. Reduced egg hatchability also occurred in exposed undifferentiated oögonial cells but the effect was less severe than that seen in the more mature oögenic cells. All observed effects could be accounted for by vinblastine's selective interference with microtubule-dependent processes. Fecundity effects were most closely associated with oöcyte cortex and possibly follicular cell damage which prevented vitellogenic growth beyond the terminal growth phase. Fertility effects were caused by the inhibition of early embryonic karyokinesis with the most plausible target being mitotic spindle formation.     

The effects of starvation and subsequent feeding on juvenile hormone synthesis and oöcyte growth in Schistocerca americana gregaria

The effect of starvation on the synthesis of C₁₆ juvenile hormone (JH) and the growth of terminal oöcytes was assessed in Schistocerca americana gregaria at two times during adult life: before activation of the corpora allata and during the first gonotrophic cycle. In both groups, starvation resulted in a decline in JH synthesis within 2–3 days and rates of synthesis remained low throughout the experimental period. The growth rate of oöcytes which were not vitellogenic at the time of starvation was depressed whereas the percentage of resorption of vitellogenic oöcytes increased dramatically with starvation. Although the percentage of resorption increased in animals with vitellogenic oöcytes, some mature oöcytes were produced, particularly in animals in which the oöcytes were greater than 5 mm in length at the time of starvation. This suggests that oöcyte maturation can be divided into two distinct phases—an early phase of vitellogenesis associated with high rates of JH synthesis and a late phase, in oöcytes greater than 5 mm, associated with much lower rates of JH synthesis.Stimulation of JH synthesis by farnesenic acid in 5-day starved animals resulted in high rates of JH synthesis, indicating that starvation did not appreciably alter the enzymic activities of the final two stages in JH synthesis. Thus rate limitation did not occur at these stages.Feeding of 5-day starved animals resulted in a transient increase in the rate of JH synthesis. However, rates of JH synthesis and oöcyte growth remained subnormal throughout the observation period, suggesting that the effects of starvation cannot be entirely reversed by feeding. Thus starvation may decrease the reproductive potential of the females.