Juvenile hormone regulates the steroidogenic competence of Manduca sexta prothoracic glands

1988 ◽  
Vol 57 (3) ◽  
pp. 251-259 ◽  
Author(s):  
R.D. Watson ◽  
W.E. Bollenbacher
1985 ◽  
Vol 117 (1) ◽  
pp. 45-68 ◽  
Author(s):  
O. S. Dominick ◽  
J. W. Truman

Removal of the prothoracic glands early during the 5th instar of Manduca sexta prevented the larvae from wandering and from further development. Infusion of 20-hydroxyecdysone (20-HE) into these larvae induced wandering behaviour. In intact larvae, induction of precocious wandering behaviour required a 20-HE infusion lasting longer than 5 h. Infused 20-HE induced maximal response (90%) when delivered at a rate of 0.06 micrograms g-1 body weight h-1. At considerably higher concentrations (0.25 micrograms g-1 h-1 larvae performed brief, erratic behaviour or omitted wandering entirely. The latency between appearance of 20-HE and the onset of wandering was dose-dependent with a minimum of 11 h following infusion at 0.1 micrograms g-1 h-1. Latency was not affected by the duration of 20-HE infusion. The duration of induced wandering behaviour was proportional to the duration of 20-HE infusion. Minimal wandering behaviour lasted 2 h following 20-HE infusions at 5 h, while infusions lasting 11 h induced 9 h of wandering behaviour. Several lines of evidence suggest that the effects of 20-HE accumulate over time and directly determine the duration of wandering behaviour. Many larvae exhibited a series of temporally distinct locomotor periods following various 20-HE infusion protocols, suggesting that a series of separate exposures to 20-HE can result in corresponding serial bouts of locomotion. Responsiveness to 20-HE appeared to be principally modulated by juvenile hormone. Allatectomy of 2nd, 3rd and 4th instar larvae removed juvenile hormone (JH) precociously from these stages and was followed several days later by precocious wandering behaviour. Likewise, application of the JH mimic, EGS, prior to 20-HE exposure or at the start of it, could prevent the behavioural induction. During the 5th instar, 20-HE became increasingly effective in inducing wandering as larvae grew larger than 5 g, the size at which JH normally begins to disappear from the haemolymph. Allatectomized 5th instar larvae responded directly to 20-HE a day sooner than larvae with normal JH titres, but before day 2 the effects of 20-HE on wandering behaviour appear to be indirect, requiring a latency greater than 24 h. Several processes, of which the elimination of JH is the last, appear to be required before 20-HE can induce wandering behaviour.(ABSTRACT TRUNCATED AT 400 WORDS)


1986 ◽  
Vol 120 (1) ◽  
pp. 41-58 ◽  
Author(s):  
D. B. Rountree ◽  
W. E. Bollenbacher

Pupal development is elicited early in the last larval instar of the tobacco hornworm, Manduca sexta (Johannson), by a precise temporal and quantitative increase in the haemolymph titre of 20-hydroxyecdysone. This increase in the titre is referred to as the pupal commitment peak, and it occurs once the titre of juvenile hormone (JH) has dropped. If the haemolymph titre of JH remains elevated at this time due to topical application of the hormone or of its analogue ZR512, commitment is delayed or inhibited in a dose-dependent manner. This delay or inhibition is due to the curtailment of the commitment peak in the ecdysteroid titre, which results from a failure of the prothoracic glands (PG) to increase the synthesis/secretion of the premoulting hormone, ecdysone. Since the PG from ZR512- and JH 1-treated larvae are capable of being activated in vitro by the prothoracicotropic hormone (PTTH), the effect of JH on the PG does not involve suppression of gland sensitivity to PTTH. The locus of the JH effect was determined to be the brain-retrocerebral complexes (Br-CC-CA), on the basis of experiments which tested the effect of implanted Br-CC-CA from pre-commitment larvae treated with JH on the occurrence of pupal commitment in head-ligated larval hosts. The implanted, JH-treated Br-CC-CA exhibited a delayed release of PTTH, and the effect was at concentrations of JH that were physiological. These results argue that JH functions to control the time during the last larval instar when pupal commitment occurs by dictating when PTTH will undergo gated release.


Author(s):  
Ji-da Dai ◽  
M. Joseph Costello ◽  
Lawrence I. Gilbert

Insect molting and metamorphosis are elicited by a class of polyhydroxylated steroids, ecdysteroids, that originate in the prothoracic glands (PGs). Prothoracicotropic hormone stimulation of steroidogenesis by the PGs at the cellular level involves both calcium and cAMP. Cell-to-cell communication mediated by gap junctions may play a key role in regulating signal transduction by controlling the transmission of small molecules and ions between adjacent cells. This is the first report of gap junctions in the PGs, the evidence obtained by means of SEM, thin sections and freeze-fracture replicas.


1988 ◽  
Vol 34 (7) ◽  
pp. 571-576 ◽  
Author(s):  
J.T. Warren ◽  
S. Sakurai ◽  
D.B. Rountree ◽  
L.I. Gilbert

1989 ◽  
Vol 35 (3) ◽  
pp. 259-274 ◽  
Author(s):  
István Ujváry ◽  
György Matolcsy ◽  
Lynn M. Riddiford ◽  
Kiyoshi Hiruma ◽  
Kathleen L. Horwath

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