Zusammenfassung
1. Aktive synaptische Stellen auf Endplatten von Nerv-Muskel-Präparaten (meistens M. cutaneus pectoris) des Frosches wurden durch extracelluläre Ableitung von min.e.p.p. identifiziert. Zur Lokalisation der Endigungen wurde ein stark vergrößerndes Präpariermikroskop und durchfallende Beleuchtung benützt.
2. Das präsynaptische Nervenaktionspotential (PNAP) konnte nach orthodromer Reizung von aktiven synaptischen Stellen als kleine Potentialschwankung vor dem e.p.p. abgeleitet werden. Das PNAP war nahe dem markhaltigen Motoaxon triphasisch, positiv-negativ-positiv, mit einem überwiegend negativen Anteil, während es gegen das Ende der marklosen Fasern mehr und mehr einphasisch positiv wurde.
3. Die Leitungsgeschwindigkeit des PNAP hatte ihren kleinsten Wert am Übergang vom markhaltigen Axon zu den marklosen Zweigen und nahm dann im Verlauf der marklosen Fasern wieder zu. Die durchschnittliche Leitungsgeschwindigkeit im Verlauf der gesamten Endplatte betrug etwa 30 cm/sec.
4. Während tetanischer Reizung mit mehr als 5 Hz war das PNAP fast immer kleiner als sein Kontrollwert bei 1 Hz, während das e.p.p. die erwartete Zunahme zeigte. Die jeweilige Größe des PNAP hing ab von: der Reizfrequenz, der Zahl der vorhergegangenen Reize und von der Mg-Konzentration der Badelösung.
5. Nach Reizung blieb das PNAP zunächst klein und kehrte dann innerhalb 30–60 msec nach Einzelreiz bis zu einigen hundert msec nach langer tetanischer Reizung zur ursprünglichen Amplitude zurück. Das verkleinerte PNAP war nicht von einem anschließenden vergrößerten PNAP gefolgt.
6. Wurden aktive synaptische Stellen durch die Mikroelektrode gereizt, so konnte bei 30% aller Stellen ein antidromes Aktionspotential ausgelöst werden. Der Verlauf der Erregbarkeit nach einem Vorreiz wurde untersucht.
7. Aus diesen Versuchen wurde geschlossen: a) das PNAP wird aktiv in die marklosen Nervenfasern der Endplatte hinein- und mindestens über weite Strecken auch aktiv weitergeleitet; b) während und nach tetanischer Reizung wird die Amplitude des PNAP durch negative Nachpotentiale (Nachdepolarisationen), die sich bei repetitiver Reizung addieren, reduziert; c) die Größe des PNAP scheint keinen entscheidenden Einfluß auf die Menge des ACh zu haben, das durch einen präsynaptischen Impuls freigesetzt wird.
Summary
1. Active synaptic regions were identified in Mg-blocked nerve-muscle preparations (mainly M. cutaneous pectoris) of the frog by the recording of extracellular min.e.p.p.s. The search for these regions was helped by the use of high power dissecting microscopes and transmitted illumination.
2. E.p.p.s evoked by orthodromic stimulation and recorded at active synaptic regions were preceded by small all-or-nothing potential changes, the presynaptic nerve action potential (PNAP). Near the myelinated portion of the motor axon the PNAP had a triphasic positive-negative-positive shape with a predominantly negative deflection, whereas towards the ultimate end of the terminal the PNAP became more and more monophasic positive.
3. The conduction velocity of the PNAP was minimal near the transition from the myelinated axon to the non-myelinated nerve twigs and increased towards the end of the motor nerve terminal. The overall conduction velocity was around 30 cm/sec.
4. During repetitive stimulation at frequencies above 5/sec the PNAP was almost always smaller than its control value at 1/sec, whereas the e.p.p. showed the expected increase in amplitude. The actual size of the PNAP depended on the frequency of stimulation, on the number of preceding volleys, and on the Mg-concentration of the bathing solution.
5. After stimulation the PNAP remained depressed for periods from 30–60 msec after a single stimulus to some hundreds of msec after prolonged stimulation. There was no period of an increased PNAP following the period of the reduced PNAP.
6. Stimulating active synaptic regions through the recording microelectrode resulted in 30% of the trials in the appearance of antidromic spike potentials. The excitability cycle was investigated following single conditioning pulses.
7. It was concluded that: a) the PNAP actively invaded nerve terminals and was actively conducted over most of the length of the non-myelinated nerve twigs; b) negative afterpotentials (afterdepolarizations) which built up considerably during repetitive stimulation, reduced the size of the PNAP during and after tetanic trains; c) the size of the PNAP did not play a significant role in determining the amount of transmitter released by a presynaptic impulse.
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This work was supported by the Deutsche Forschungsgemeinschaft.
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Braun, M., Schmidt, R.F. Potential changes recorded from the frog motor nerve terminal during its activation. Pflügers Archiv 287, 56–80 (1966). https://doi.org/10.1007/BF00362454
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DOI: https://doi.org/10.1007/BF00362454