Journal
JOURNAL OF NEUROPHYSIOLOGY
Volume 84, Issue 6, Pages 2777-2785Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.2000.84.6.2777
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- NIDDK NIH HHS [P01 DK-41315] Funding Source: Medline
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Myenteric afterhyperpolarizing (AH) neurons are primary afferent neurons within the gastrointestinal tract. Stimulation of the intestinal mucosa evokes action potentials (AP) that are followed by a slow afterhyperpolarization (AHP(slow)) in the soma. The role of intracellular Ca2+ ([Ca2+](i)) and ryanodine-sensitive Ca2+ stores in modulating the electrical activity of myenteric AH neurons was investigated by recording membrane potential and bis-fura-2 fluorescence from 34 AH neurons. Mean resting [Ca2+](i) was similar to 200 nM. Depolarizing current pulses that elicited APs evoked AHP(slow) and an increase in [Ca2+](i), with similar time courses. The amplitudes and durations of AHP(slow) and the Ca2+ transient were proportional to the number of evoked APs, with each AP increasing [Ca2+](i) by similar to 50 nM. Ryanodine (10 muM) significantly reduced both the amplitude and duration (by 60%) of the evoked Ca2+ transient and AHP(slow) over the range of APs tested (1-15). Calcium-induced calcium release (CICR) was graded and proportional to the number of APs, with each AP triggering a rise in [Ca2+](i) of similar to 30 nM Ca2+ via CICR. This indicates that CICR amplifies Ca2+ influx. Similar changes in [Ca2+](i) and AHP(slow) were evoked by two APs in control and six APs in ryanodine. Thus, the magnitude of the change in bulk [Ca2+](i) and not the source of the Ca2+ is the determinant of the magnitude of AHP(slow). Furthermore, lowering of free [Ca2+](i), either by reducing extracellular Ca2+ or injecting high concentrations of Ca2+ buffer, induced depolarization, increased excitability, and abolition of AHP(slow). In addition, activation of synaptic input to AH neurons elicited a slow excitatory postsynaptic potential (sEPSP) that was completely blocked in ryanodine. These results demonstrate the importance of [Ca2+](i) and CICR in sensory processing in AH neurons. Activity-dependent CICR may be a mechanism to grade the output of AH neurons according to the intensity of sensory input.
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