Cholinergic Neurotransmission from Mechanosensory Afferents to Giant Interneurons in the Terminal Abdominal Ganglion of the Cricket Gryllus bimaculatus

2008 ◽  
Vol 25 (5) ◽  
pp. 517-525 ◽  
Author(s):  
Oak Yono ◽  
Hitoshi Aonuma
2018 ◽  
Author(s):  
Keisuke Naniwa ◽  
Yasuhiro Sugimoto ◽  
Koichi Osuka ◽  
Hitoshi Aonuma

AbstractFeces contain information about the donor and potentially attracts both conspecifics and predators and parasites. The excretory system must be coordinated with other behaviors in insects. We found that crickets start walking forward following excretion of feces. Most intact crickets walked around the experimental arena, stopped at a particular site and raised up their body with a slight backward drift to excrete feces. After the feces dropped on the floor, the animal started walking with a random gait pattern away from the feces, and then changed the gait pattern to a tripod gait. Headless cricket also showed walking following excretion. In more than half of excretion events, headless crickets walked backward before excretion. The posture adopted during excretion was similar to that of intact crickets, and post-excretory forward walking was also observed. The occurrence rate of post-excretory walking was more than that of intact crickets. The gait pattern during forward walking was random and never transitioned to a tripod gait in the headless crickets. In animals whose abdominal nerve cords were cut, in any position, pre- or post-excretion walking was not shown in both intact and headless crickets, although they excreted feces. These results indicate that ascending signals from the terminal abdominal ganglion initiate leg movement through the neuronal circuits within thoracic ganglia, and that descending signals from the brain must regulate leg the motor circuit to express the appropriate walking gait.


1998 ◽  
Vol 201 (17) ◽  
pp. 2529-2541 ◽  
Author(s):  
P Kloppenburg ◽  
M Hörner

The electrophysiological properties of cultured giant interneurons isolated from the terminal ganglion of adult crickets (Gryllus bimaculatus) were investigated using whole-cell patch-clamp techniques. To allow for unequivocal identification of these interneurons in cell culture, a protocol for fast and selective labeling of their cell bodies was established. Prior to cell dissociation, the giant interneurons were backfilled through their axons in situ with a fluorescent dye (dextran tetramethylrhodamine). In primary cell cultures, the cell bodies of giant interneurons were identified among a population of co-cultured neurons by their red fluorescence. Action potentials were recorded from the cell bodies of the cultured interneurons suggesting that several types of voltage-activated ion channels exist in these cells. Using voltage-clamp recording techniques, four voltage-activated currents were isolated and characterized. The giant interneurons express at least two distinct K+ currents: a transient current that is blocked by 4-aminopyridine (4x10(-3 )mol l-1) and a sustained current that is partially blocked by tetraethylammonium (3x10(-2 )mol l-1) and quinidine (2x10(-4 )mol l-1). In addition, a transient Na+ current sensitive to 10(-7 )mol l-1 tetrodotoxin and a Ca2+ current blocked by 5x10(-4 )mol l-1 CdCl2 have been characterized. This study represents the first step in an attempt to analyze the cellular and ionic mechanisms underlying plasticity in the well-characterized and behaviorally important giant interneuron pathway in insects.


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