scholarly journals The control of anterior foregut motility during a larval molt of the moth Manduca sexta involves the modulation of presynaptic activity

2006 ◽  
Vol 209 (20) ◽  
pp. 4000-4010 ◽  
Author(s):  
J. E. Bestman ◽  
R. Booker
Keyword(s):  
1984 ◽  
Vol 167 (3) ◽  
pp. 568-578 ◽  
Author(s):  
LOUIS SAFRANEK ◽  
CARROLL M. WILLIAMS

2000 ◽  
Vol 227 (2) ◽  
pp. 481-494 ◽  
Author(s):  
Rosalie E Langelan ◽  
Jeffrey E Fisher ◽  
Kiyoshi Hiruma ◽  
Subba Reddy Palli ◽  
Lynn M Riddiford

1996 ◽  
Vol 199 (8) ◽  
pp. 1757-1769 ◽  
Author(s):  
A Novicki ◽  
J C Weeks

Each larval molt of Manduca sexta culminates in the sequential performance of pre-ecdysis (cuticle loosening) and ecdysis (cuticle shedding) behaviors. Both behaviors are thought to be triggered by the release of a peptide, eclosion hormone (EH), from brain neurons whose axons extend the length of the nervous system. EH bioactivity appears in the hemolymph at the onset of pre-ecdysis behavior, and EH injection can trigger pre-ecdysis and ecdysis behaviors prematurely. The present study examined the effects of removing or disconnecting portions of the central nervous system prior to the time of EH release on the initiation of pre-ecdysis and ecdysis behaviors at the final larval molt. We found that the initiation of pre-ecdysis abdominal compressions at the appropriate time required the terminal abdominal ganglion (AT) but not the brain; the initiation of pre-ecdysis proleg retractions at the appropriate time required neither the AT nor the brain; the initiation of ecdysis at the appropriate time usually required the brain but did not require the AT; and premature pre-ecdysis (but not ecdysis) could be elicited in isolated abdomens by injection of EH. Finally, pre-ecdysis behavior performed by brainless larvae was not associated with the normal elevation of EH bioactivity in the hemolymph or the normal loss of EH immunoreactivity from peripheral neurohemal release sites.


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.


1990 ◽  
Vol 265 (1) ◽  
pp. 546-552
Author(s):  
R O Ryan ◽  
R Van Antwerpen ◽  
D J Van der Horst ◽  
A M Beenakkers ◽  
J H Law
Keyword(s):  

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