1971
DOI: 10.2170/jjphysiol.21.529
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The Effects of Tetrodotoxin on the Slow Potential and Spikes in the Cardiac Ganglion of a Crab, Eriocheir Japonicus

Abstract: Summary The effects of tetrodotoxin on the electrical components slow potential and spikes have been studied in the crab cardiac ganglion cell.

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Cited by 27 publications
(7 citation statements)
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“…The present investigation was inspired by a molecular study of the CG of C. borealis in which mRNA transcripts of LCs that encode for ion channel proteins were measured, revealing correlations between transcript numbers for many genes (Tobin et al, 2009). The CG network model was developed from biological CG data, especially the comprehensive studies performed by Tazaki and Cooke (Tazaki, 1971; Tazaki and Cooke, 1979a,b,c, 1983a,b, 1986, 1990; Cooke, 2002), and this model reproduced many features of the CG output, in particular the driver potential response of the LC, spontaneous bursting of the synaptically coupled large and small cells, and various essential features of both types of output. In addition to thoroughly characterizing the contribution of each ionic current to the properties of the driver potential, we varied the maximal conductances of the ionic currents in the LC soma and investigated relationships between the maximal conductances that preserved the form of the LC driver potential.…”
Section: Discussionmentioning
confidence: 99%
“…The present investigation was inspired by a molecular study of the CG of C. borealis in which mRNA transcripts of LCs that encode for ion channel proteins were measured, revealing correlations between transcript numbers for many genes (Tobin et al, 2009). The CG network model was developed from biological CG data, especially the comprehensive studies performed by Tazaki and Cooke (Tazaki, 1971; Tazaki and Cooke, 1979a,b,c, 1983a,b, 1986, 1990; Cooke, 2002), and this model reproduced many features of the CG output, in particular the driver potential response of the LC, spontaneous bursting of the synaptically coupled large and small cells, and various essential features of both types of output. In addition to thoroughly characterizing the contribution of each ionic current to the properties of the driver potential, we varied the maximal conductances of the ionic currents in the LC soma and investigated relationships between the maximal conductances that preserved the form of the LC driver potential.…”
Section: Discussionmentioning
confidence: 99%
“…In Eriocheir cells the slow potential remains after the spike potentials are abolished by addition of tetrodotoxin to the medium (Tazaki, 1971). During the burst period the slow potential of Squilla and Eriocheir neurons and the first derivative of the relaxation oscillator slowly decreases from a point of maximum depolarization at the start of the burst period, and, as one might expect from this, the frequency of spikes slowly declines during the burst period in each of these cardiac ganglia (Watanabe et al, 1967;Tazaki, 1971;Maynard, 1955;Hartline and Cooke, 1969). Also, during the silent period membrane potential slowly becomes more positive in each case.…”
Section: Discussionmentioning
confidence: 99%
“…Two additional procedures were utilized in order to demonstrate direct effects of proctolin on the large anterior cells: (1) application of tetrodotoxin (TTX, 3-6 x 10-7M) was used to eliminate spike mediated interactions between small and large cells (see Tazaki, 1971; ;…”
Section: Effects Of Proctolin On Isolated Large Cellsmentioning
confidence: 99%
“…Meanwhile, detailed transection and pharmacological experiments led several investigators to stress the endogenous nature of motorneuron rhythm and burst generation (Matsui, 1955;Watanabe, 1958;Connor, 1969;Matsui, Arinobu, and Naohiro, 1972;Tazaki, 1973;. The demonstration of TTXresistant, Ca' +-dependent driver potentials in motorneurons (Tazaki, 1971;Tazaki and Cooke, 1979b) led to the current view that rhythmic motor pattern generation results from a combination of integrated small cell inputs with the regenerative driver potential of large cells ; see also review by Hartline, 1979). Ganglionic rhythmicity is attributed to ramp or pacemaker potentials which have been recorded in small cells (Tameyasu, 1976;Tazaki and Cooke, 1979a).…”
Section: Network Architecture and Rhythmic Pattern Generation: A N Almentioning
confidence: 99%