Excitatory and Inhibitory Pathways in the Arm of Octopus

1963 ◽  
Vol 40 (2) ◽  
pp. 257-270
Author(s):  
C. H. FRASER ROWELL

1. The nervous system of isolated arms of Octopus vulgaris has been investigated with fine stimulating electrodes and lesions. The reflexes of the intact arm are in accordance with earlier reports. 2. The reflexes are abolished if the nerves from the medulla are cut. These nerves carry both sensory and motor signals, serving discrete areas of muscle and skin. The central mechanisms producing single-sucker reflexes are confined to the ventral ‘axial ganglia’. 3. Stimulation in the ventral medulla influences many suckers simultaneously or progressively, implying both through-pathways and polysynaptic pathways. 4. The nervous supply to the main longitudinal and oblique musculature remains obscure. Motor effects are produced by stimulating the median and central medulla, and require intact peripheral supply. The lateral nerve cords do not affect the main musculature. 5. The dermal musculature is affected by stimulation in the medulla and of its peripheral nerves. Only the subdermal muscle layer is excited by stimulation of the lateral nerve cords. 6. Normal expansion of the chromatophores depends on an intact nervous supply from the medulla, and is not due to autotonus of the chromatophore muscles. The final chromatophore nerves are probably medullar, not cerebral, and each controls only a few patches of skin over short lengths of the arm. 7. Through-pathways, affecting many or all of these chromatophore nerves, run in the dorsal medulla. They include local and general excitatory, general inhibitory and possibly local inhibitory channels. Their significance, and that of excitatory and inhibitory supplies to the sucker reflex mechanisms, is discussed.

Parasitology ◽  
1941 ◽  
Vol 33 (4) ◽  
pp. 373-389 ◽  
Author(s):  
Gwendolen Rees

1. The structure of the proboscides of the larva of Dibothriorhynchus grossum (Rud.) is described. Each proboscis is provided with four sets of extrinsic muscles, and there is an anterior dorso-ventral muscle mass connected to all four proboscides.2. The musculature of the body and scolex is described.3. The nervous system consists of a brain, two lateral nerve cords, two outer and inner anterior nerves on each side, twenty-five pairs of bothridial nerves to each bothridium, four longitudinal bothridial nerves connecting these latter before their entry into the bothridia, four proboscis nerves arising from the brain, and a series of lateral nerves supplying the lateral regions of the body.4. The so-called ganglia contain no nerve cells, these are present only in the posterior median commissure which is therefore the nerve centre.


1988 ◽  
Vol 73 (3) ◽  
pp. 481-488 ◽  
Author(s):  
T. Winkler ◽  
E. St�lberg

1981 ◽  
Vol 44 (4) ◽  
pp. 207-217 ◽  
Author(s):  
Don M. Long ◽  
Donald Erickson ◽  
James Campbell ◽  
Richard North

2013 ◽  
Vol 110 (5) ◽  
pp. 1180-1189 ◽  
Author(s):  
Gustaf M. Van Acker ◽  
Sommer L. Amundsen ◽  
William G. Messamore ◽  
Hongyu Y. Zhang ◽  
Carl W. Luchies ◽  
...  

High-frequency, long-duration intracortical microstimulation (HFLD-ICMS) applied to motor cortex is recognized as a useful and informative method for corticomotor mapping by evoking natural-appearing movements of the limb to consistent stable end-point positions. An important feature of these movements is that stimulation of a specific site in motor cortex evokes movement to the same spatial end point regardless of the starting position of the limb. The goal of this study was to delineate effective stimulus parameters for evoking forelimb movements to stable spatial end points from HFLD-ICMS applied to primary motor cortex (M1) in awake monkeys. We investigated stimulation of M1 as combinations of frequency (30–400 Hz), amplitude (30–200 μA), and duration (0.5–2 s) while concurrently recording electromyographic (EMG) activity from 24 forelimb muscles and movement kinematics with a motion capture system. Our results suggest a range of parameters (80–140 Hz, 80–140 μA, and 1,000-ms train duration) that are effective and safe for evoking forelimb translocation with subsequent stabilization at a spatial end point. The mean time for stimulation to elicit successful movement of the forelimb to a stable spatial end point was 475.8 ± 170.9 ms. Median successful frequency and amplitude were 110 Hz and 110 μA, respectively. Attenuated parameters resulted in inconsistent, truncated, or undetectable movements, while intensified parameters yielded no change to movement end points and increased potential for large-scale physiological spread and adverse focal motor effects. Establishing cortical stimulation parameters yielding consistent forelimb movements to stable spatial end points forms the basis for a systematic and comprehensive mapping of M1 in terms of evoked movements and associated muscle synergies. Additionally, the results increase our understanding of how the central nervous system may encode movement.


Author(s):  
Aaron Gilmour ◽  
Josef Goding ◽  
Ulises Aregueta Robles ◽  
Naomi Staples ◽  
Philip Byrnes-Preston ◽  
...  

1998 ◽  
Vol 275 (5) ◽  
pp. G964-G972 ◽  
Author(s):  
Zbigniew K. Krowicki ◽  
Nicole A. Nathan ◽  
Pamela J. Hornby

Insulin-binding sites exist in the lower brain stem of the rat, raising the possibility that the circulating hormone may have cardiovascular and gastric effects at this site. Therefore, we investigated the autonomic effects of applying rat insulin to the surface of the dorsal medulla (0.3 and 3 μU/rat) or microinjecting it into the dorsal vagal complex (DVC) (0.1–10 nU/site) in anesthetized rats. Application of rat insulin to the surface (3 μU/rat) and its microinjection into the DVC (1 and 10 nU/site) both evoked marked, albeit transient, increases in intragastric pressure, pyloric and greater curvature contractile activity, and blood pressure. Much higher doses of human (100 mU) and porcine insulin (3 mU) were needed to evoke modest changes in gastric motor and cardiovascular function when applied to the surface of the dorsal medulla. In addition, a 1,000-fold higher dose of porcine insulin (10 μU) in the DVC was not enough to mimic the autonomic effects of rat insulin microinjected into the same site. The excitatory gastric motor effects of rat insulin in the lower brain stem were abolished by vagotomy, whereas spinal cord transection blocked insulin-evoked increases in blood pressure. To test whether the gastric motor effects of rat insulin in the lower brain stem were caused by potential contamination with pancreatic polypeptide, we microinjected rat pancreatic polypeptide into the DVC at a single dose of 2 pmol. Only a modest increase in intragastric pressure in response to the hormone was observed. Thus it is likely that insulin, through its action in the lower brain stem, may be implicated in the pathogenesis of gastrointestinal and cardiovascular complications in hyperinsulinemia. In addition, species variations in the amino acid sequence of insulin may affect its biological activity in the brain of different species.


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