Cellular accumulation of amines and amino acids in the central ganglia of a gastropod mollusc,Planorbis corneus: An autoradiographic study

1978 ◽  
Vol 7 (6) ◽  
pp. 759-776 ◽  
Author(s):  
J. D. Turner ◽  
G. A. Cottrell
1975 ◽  
Vol 62 (3) ◽  
pp. 797-803
Author(s):  
M. S. Berry ◽  
V. W. Pentreath

Several investigators of the molluscan nervous system have used TEA, injected into presynptic neurones, to determine whether the connexions made by these neurones are monosynaptic. The increase in spike duration produced by the TEA causes an increase in transmitter release, and hence an increase in the amplitude of the postsynaptic potential if the connexion is direct. If the connexion is indirect, the spike in an intercalated neurone will not be affected by the TEA, and the postsynaptic response will remain constant. Experiments described here show that TEA can cross electrotonic junctions in the gastropod mollusc Planorbis corneus. They also show that each TEA-prolonged presynaptic impulse may produce more than one postsynaptic impulse. A larger postsynaptic potential could therefore be produced by presynaptic injection of TEA in the case of an indirect connexion. This indicates that care must be taken when interpreting the results of experiments using TEA to test for monosynaptic connexions.


1978 ◽  
Vol 56 (1) ◽  
pp. 7-18 ◽  
Author(s):  
J. F. MacDonald ◽  
M. S. Berry

Intracellular recordings from neurones, receiving monosynaptic contacts from a dopamine-containing (DA-containing) neurone in the central ganglia of the gastropod mollusc Planorbis corneus, revealed that there are at least three DA-mediated responses. These are 'fast' excitatory postsynaptic potentials (EfPSPs) (200 ms), 'slow' excitatory postsynaptic potentials (EsPSPs) (900 ms), and inhibitory postsynaptic potentials (IPSPs) (200–900 ms). Various combinations of these synaptic potentials were recorded from postsynaptic neurones: EsPSPs, EfPEPs, EsEfPSPs, or EfIPSPs. Neurones receiving such connections also responded appropriately to iontophoresized DA with a 'fast' depolarization (EfPSPs), a 'slow' depolarization (EsPSPs), or a hyperpolarization (IPSPs). These responses could be distinguished on the basis of function (excitation or inhibition), duration, rate of desensitization, and sensitivity to apomorphine, D-LSD, and tubocurarine. The neuroleptic drugs (DA antagonists) haloperidol, fluphenazine, and metoclopramide reduced both excitatory and inhibitory DA transmission. This investigation strongly supports the hypothesis that DA is the transmitter mediating multiple synaptic responses in Planorbis.


1965 ◽  
Vol 25 (2) ◽  
pp. 19-39 ◽  
Author(s):  
William B. Kinter ◽  
T. Hastings Wilson

Autoradiographs were prepared from frozen sections of everted sacs of hamster jejunum which had been incubated in vitro with C14- or H3-labeled sugars and amino acids. When such tissue was incubated in 1 mM solutions of L-valine or L-methionine, columnar absorptive cells at tips of villi accumulated these amino acids to concentrations ranging from 5 to 50 millimoles per liter of cells. Quantitative data were obtained by microdensitometry of C14 autoradiographs. Similar, though less striking, results were obtained with the sugars: galactose, 3-0-methylglucose, α-methylglucoside, and 6-deoxyglucose. In all cases the marked "step-up" in concentration occurred near the brush border of the cell, and a "step-down" in concentration occurred at the basal pole of the cell. Known inhibitors of intestinal absorption, e.g., phlorizin in the case of sugars, blocked the concentrative step at the luminal border of the absorptive cell. It is inferred from these data that active transport systems for sugars and amino acids reside in the brush border region of the cell. Additional evidence suggests that the basal membrane of the cell may be the site of both a diffusion barrier and a weak transport system directed into the cell.


1953 ◽  
Vol 11 ◽  
pp. 303-304 ◽  
Author(s):  
Thomas R. Riggs ◽  
Barbara Coyne ◽  
Halvor N. Christensen

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