6533b831fe1ef96bd129854f
RESEARCH PRODUCT
The variation of acetylcholine release from myenteric neurones with stimulation frequency and train length. Role of presynaptic muscarine receptors.
Ignaz WesslerHeinz Kilbingersubject
PharmacologyMuscarinePulse (signal processing)Guinea PigsScopolamineMyenteric PlexusStimulationGeneral MedicineInhibitory postsynaptic potentialReceptors MuscarinicAcetylcholineElectric StimulationFeedbackchemistry.chemical_compoundchemistryNegative feedbackMuscarinic acetylcholine receptormedicineAnimalsNeuroscienceAcetylcholineMyenteric plexusmedicine.drugdescription
1. The effects of scopolamine on the release of 3H-acetylcholine (ACh) from the guinea-pig myenteric plexus were studied at different stimulation frequencies (0.03–10 Hz) and train lengths (1–180 pulses). Release of 3H-ACh was measured in the absence of cholinesterase inhibitors as the outflow of tritium from myenteric plexus-longitudinal muscle preparations preloaded with 3H-choline. 2. In control experiments the volley output of 3H-ACh declined with increasing train length and increasing stimulation frequency. Stimulation by one pulse produced the highest volley output. 3. Scopolamine facilitated the evoked output of 3H-ACh via blockade of presynaptic muscarine receptors. A significant increase was already observed when the preparation was stimulated with 3 pulses at 10 Hz which indicates that the inhibitory muscarinic mechanism becomes operational within 200 ms. The facilitatory effects of scopolamine depended on both train length and frequency of stimulation. Maximal increases in 3H-ACh output were seen with brief trains (3 and 6 pulses) at a high frequency (10 Hz), or with longer trains (20 and 180 pulses) at lower frequencies (0.3 and 1 Hz). 4. Scopolamine compensated for the frequencydependent decline of 3H-ACh volley output only during brief periods of stimulation (3 and 6 pulses). It is therefore concluded that the decline in volley output during the first few pulses of a train is due to the negative feedback mechanism which is activated by the transmitter released by the preceding impulses. With longer trains of stimulation the negative feedback mechanism plays only a minor role in regulating the output per pulse.
year | journal | country | edition | language |
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1983-09-01 | Naunyn-Schmiedeberg's archives of pharmacology |