Constancies in the neuronal architecture of the suboesophageal ganglion at metamorphosis in the beetleTenebrio molitor L.

1991 ◽  
Vol 266 (1) ◽  
pp. 173-190 ◽  
Author(s):  
Olaf Breidbach
Keyword(s):  
Suboesophageal Ganglion

The internal anatomy of the woodlouse, Metoponorthus pruinosus (Brandt), (Porcellionidae, Peracarida)

1968 ◽  
Vol 46 (3) ◽  
pp. 321-327 ◽  
Author(s):  
M. A. Alikhan
Keyword(s):  
Nervous System ◽  
Digestive System ◽  
Circulatory System ◽  
Reproductive Organs ◽  
The Body ◽  
Internal Anatomy ◽  
Suboesophageal Ganglion ◽  
Digestive Tube ◽  
Thoracic Ganglia ◽  
Digestive Glands

Tbe circulatory system, lying in the mid-dorsal line of the body, consists of an oval heart, the opthalmic artery, and a dorsal abdominal artery.The digestive system comprises a wide, large alimentary tube and two pairs of digestive glands. An oesophagus, a proventriculus, midgut, and a short proctodacum or hindgut form the digestive tube. The digestive glands are very well developed and are beaded in form; each pair lies on either side of the alimentary canal.The reproductive organs are well developed in both sexes: in the male they consist of paired testes and their vas deferentia, and in the female paired bilobed ovaries and oviducts.A cerebral or supraoesophageal ganglion, a suboesophageal ganglion, and seven thoracic ganglia form the nervous system. The supraoesophageal ganglion is united with the suboesophageal ganglion by means of the circumoesophageal commissures, whereas the thoracic ganglia and suboesophageal ganglia are linked with each other by paired connectives.The gills and the tracheae are the organs of respiration. The gills are borne of the bases of the pleopods and are enclosed in the branchial chamber. The tracheae are located on the lateral lobes of the first two pleopods only.

Levels of tryptophan, 5-hydroxytryptamine, and dopamine in some tissues of the cockroach Periplaneta americana

1986 ◽  
Vol 64 (12) ◽  
pp. 2669-2673 ◽  
Author(s):  
B. Duff Sloley ◽  
Roger G. H. Downer ◽  
Cedric Gillott
Keyword(s):  
Nervous Tissue ◽  
High Performance ◽  
Periplaneta Americana ◽  
Corpora Allata ◽  
Suboesophageal Ganglion ◽  
Corpora Cardiaca ◽  
Thoracic Ganglia ◽  
Frontal Ganglion ◽  
Low Levels ◽  
Immunohistochemical Studies

Tryptophan, 5-hydroxytryptamine, and dopamine were measured in the frontal ganglion, corpora cardiaca, corpora allata, nerves of the suboesophageal ganglion, nerves of the thoracic ganglia, gut, testes, and ovaries of the cockroach Periplaneta americana using high performance liquid chromatography with electrochemical detection. 5-Hydroxytryptamine was demonstrated in the frontal ganglion, corpora cardiaca, corpora allata, and nerves of the suboesophageal ganglion but not in the gut, testes, ovaries, or nerves of the thoracic ganglia. These results quantitatively confirm immunohistochemical studies of 5-hydroxytryptamine in neurohaemal and nonneuronal tissues of the cockroach. Dopamine was found in all neurohaemal and nervous tissue examined. Dopamine was also found at low levels in the rectum. Tryptophan was found in all tissues examined.

Hormonal Control of the Malpighian Tubules of the Stick Insect, Carausius Morosus

1970 ◽  
Vol 52 (3) ◽  
pp. 653-665 ◽  
Author(s):  
DIANA E. M. PILCHER
Keyword(s):  
Stick Insect ◽  
Hormonal Control ◽  
The State ◽  
Malpighian Tubules ◽  
Suboesophageal Ganglion ◽  
Carausius Morosus ◽  
Corpora Cardiaca ◽  
Diuretic Hormone ◽  
The Brain

1. Urine secretion by isolated Malpighian tubules of Carausius is accelerated by a diuretic hormone which can be extracted from the brain, corpora cardiaca and suboesophageal ganglion. 2. The level of this hormone in the haemolymph varies according to the state of hydration of the insect. 3. The hormone is inactivated by the tubules, and a mechanism is proposed whereby the tubules might be controlled by the hormone in vivo.

A Suboesophageal Ganglion Cell Innervates Heart and Retrocerebral Glandular Complex in the Locust

1991 ◽  
Vol 156 (1) ◽  
pp. 567-582
Author(s):  
PETER BRÄUNIG
Keyword(s):  
Pancreatic Polypeptide ◽  
Nerve Cord ◽  
Sagittal Plane ◽  
Locusta Migratoria ◽  
Neurosecretory Cells ◽  
Double Labelling ◽  
Suboesophageal Ganglion ◽  
Migratory Locust ◽  
Bovine Pancreatic Polypeptide ◽  
Thoracic And Abdominal

The suboesophageal ganglion of the migratory locust Locusta migratoria contains a pair of large neurosecretory cells located posteriorly, close to the sagittal plane. By means of double labelling, it is shown that the cells are immunoreactive to bovine pancreatic polypeptide. Using a combination of electrophysiological, neuroanatomical and immunocytochemical methods, it is shown that the neurones project into the corpora cardiaca with ascending anterior axons and into the lateral cardiac nerve cords with posterior axons that descend into the thoracic and abdominal nerve cord.

Studies on the Mode of Action of the Diapause Hormone in the Silkworm, BOMBYX MORI L.,

1963 ◽  
Vol 40 (3) ◽  
pp. 517-530
Author(s):  
KINSAKU HASEGAWA
Keyword(s):  
Low Temperature ◽  
Juvenile Hormone ◽  
Bombyx Mori ◽  
Mode Of Action ◽  
Adult Emergence ◽  
Suboesophageal Ganglion ◽  
Bombyx Mori L ◽  
Diapause Hormone ◽  
The Brain ◽  
Silkworm Bombyx Mori

1. The action of the diapause hormone has been studied by injecting extracts of the heads of male moths or of the brain-suboesophageal ganglion complexes of pupae into pupae expected to produce non-diapause eggs. 2. The effect of the injection of hormone upon young oocytes is to make them develop into diapause eggs. Older oocytes, which have already acquired non-diapause characters, are not affected. 3. The hormone is almost completely inactivated when injected on the day of pupation. The hormone is most effective when injected into pupae 2-3 days old, at which stage the ovarioles have started to grow vigorously. It is ineffective 1-2 days before adult emergence, by which time all the oocytes have acquired non-diapause characters. 4. The hormone is inactivated in all pupae irrespective of whether they are destined to produce diapause eggs or non-diapause eggs. Inactivation of diapause hormone (in contrast to that of juvenile hormone) is partially relieved by exposure to low temperature or by simultaneous injection of indian ink. 5. The extracts prepared as in (1) above do not serve as a stimulant for the brain causing the suboesophageal ganglion to produce diapause hormone. The action of the extract faithfully reflects the function of the diapause hormone which originates in the suboesophageal ganglion.

Cholinergic activation of stridulatory behaviour in the grasshopper Omocestus viridulus (L.)

1997 ◽  
Vol 200 (9) ◽  
pp. 1327-1337 ◽  
Author(s):  
R Heinrich ◽  
B Hedwig ◽  
N Elsner
Keyword(s):  
Rapid Onset ◽  
Suboesophageal Ganglion ◽  
Male And Female ◽  
Ach Receptors ◽  
Cholinergic Activation

When acetylcholine (ACh) and its agonists are injected into neuropile regions of the protocerebrum and the suboesophageal ganglion of male and female grasshoppers of the species Omocestus viridulus (L.), they elicit stridulation in a pattern no different from that of natural song. Stridulation can even be evoked in mated females which normally do not sing. By choosing suitable ACh agonists, nicotinic and muscarinic ACh receptors can be activated selectively. Activation of nicotinic ACh receptors produces individual song sequences with rapid onset; the stridulation induced by activation of the muscarinic ACh receptors begins after a longer latency, increases slowly in intensity and is maintained for many minutes. The sites within the cephalic ganglia where song can be initiated pharmacologically coincide with regions in which descending stridulatory command neurones arborize.

Reconfiguration of the Respiratory Network at the Onset of Locust Flight

1998 ◽  
Vol 80 (6) ◽  
pp. 3137-3147 ◽  
Author(s):  
Jan-Marino Ramirez
Keyword(s):  
Respiratory Activity ◽  
Respiratory Rhythm ◽  
Quiescent State ◽  
Suboesophageal Ganglion ◽  
Rhythm Generator ◽  
Locust Flight ◽  
Respiratory Network ◽  
Intracellular Stimulation ◽  
Tonic Stimulation ◽  
Stimulation Of

Ramirez, Jan-Marino. Reconfiguration of the respiratory network at the onset of locust flight. J. Neurophysiol. 80: 3137–3147, 1998. The respiratory interneurons 377, 378, 379 and 576 were identified within the suboesophageal ganglion (SOG) of the locust. Intracellular stimulation of these neurons excited the auxillary muscle 59 (M59), a muscle that is involved in the control of thoracic pumping in the locust. Like M59, these interneurons did not discharge during each respiratory cycle. However, the SOG interneurons were part of the respiratory rhythm generator because brief intracellular stimulation of these interneurons reset the respiratory rhythm and tonic stimulation increased the frequency of respiratory activity. At the onset of flight, the respiratory input into M59 and the SOG interneurons was suppressed, and these neurons discharged in phase with wing depression while abdominal pumping movements remained rhythmically active in phase with the slower respiratory rhythm (Fig. 9 ). The suppression of the respiratory input during flight seems to be mediated by the SOG interneuron 388. This interneuron was tonically activated during flight, and intracellular current injection suppressed the respiratory rhythmic input into M59. We conclude that the respiratory rhythm generator is reconfigured at flight onset. As part of the rhythm-generating network, the interneurons in the SOG are uncoupled from the rest of the respiratory network and discharge in phase with the flight rhythm. Because these SOG interneurons have a strong influence on thoracic pumping, we propose that this neural reconfiguration leads to a behavioral reconfiguration. In the quiescent state, thoracic pumping is coupled to the abdominal pumping movements and has auxillary functions. During flight, thoracic pumping is coupled to the flight rhythm and provides the major ventilatory movements during this energy-demanding locomotor behavior.

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