Effects of a juvenile hormone analogue on the metamorphic changes of the foregut and midgut in Tenebrio molitor L. (Insecta, Coleoptera)

1988 ◽  
Vol 66 (2) ◽  
pp. 421-426 ◽  
Author(s):  
Yao Tano ◽  
Jean François ◽  
Cécile Noirot-Timothée

During normal Tenebrio metamorphosis, the smooth pupal foregut cuticle is replaced by a thicker adult cuticle with spines. The pupal midgut epithelium includes regenerative cells organized into nests that proliferate during pupal life, protruding as crypts into the general cavity. At high levels of treatment with juvenoid (Methoprène), some adult characteristics of the foregut cuticle were observed: the foregut cuticle apolysed soon after ecdysis, and the duration of cuticular secretion was shortened. Differentation of the pupal midgut into the adult form was either stopped or delayed by the juvenoid; the growth of the crypts was often inhibited in supernumerary pupae and in other cases could be observed 10 days later than in controls.

1973 ◽  
Vol 28 (7-8) ◽  
pp. 456-459
Author(s):  
Peter Schmialek ◽  
Marina Borowski ◽  
Astrid Geyer ◽  
Verena Miosga ◽  
Michael Nündel ◽  
...  

A receptor protein was isolated from the epidermis cells of the pupae of Tenebrio molitor L. The affinity constant of the complex of this receptor protein and a juvenile hormone analogue was found to be 4.4 · 1010 l/mole. Its molecular weight is about 3.5·105. The isoelectric point is 4.4.


1971 ◽  
Vol 61 (2) ◽  
pp. 293-297 ◽  
Author(s):  
B. R. Critchley ◽  
D. G. Campion

The result of treating Tenebrio molitor L. pupae with synthetic juvenile hormone (JH) or a juvenile hormone analogue, methyl farnesoate dihydrochloride (DMF), is to arrest pupal development, producing pupal/adult intermediates. Both substances induced approximately 50% pupal/adult intermediates at a topically applied dose of 1 μg. The activity was greatly affected by the age of the pupa at the time of treatment, one- and two-day-old pupae being the most sensitive. Applied to four-day-old and older pupae complete metamorphosis to the adult was possible at a dose of 8 μg of synthetic JH and up to 200 μg for DMF. Doses above these levels merely increased toxicity without juvenilising activity.


1973 ◽  
Vol 28 (3-4) ◽  
pp. 173-177 ◽  
Author(s):  
Peter Schmialek ◽  
Marina Borowski ◽  
Astrid Geyer ◽  
Verena Miosga ◽  
Michael Nündel ◽  
...  

In vivo tests give evidence that the epidermis is the target organ for the juvenile hormone of insects. A study of the distribution of injected 10,11-epoxy-6,7-trans-2,5-trawi-farnesyl-propenylether and of its metabolic products in epidermis, lymphae, and other organs demonstrated that the unaltered ether accumulates in the epidermis against a concentration gradient and is more slowly metabolised there than in the non-target organs.


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