Background/Aims: Gallbladder neurons are important governors of gallbl
adder function. In animal models, gallbladder ganglia can be regulated
both by neural and hormonal inputs. The purpose of this study was to
demonstrate the feasibility of obtaining recordings from human gallbla
dder neurons. Methods: Human gallbladders (n = 33) were bathed in oxyg
enated Krebs solution (37 degrees C) containing the vital fluorescent
stain 4-Di-2-ASP to localize the ganglia. Cells were characterized usi
ng conventional intracellular recording techniques, Results: The mean
resting membrane potential of human gallbladder neurons was -51.2 +/-
1.8 mV (n = 11), Depolarizing current pulses elicited only 1-4 spikes
regardless of the amplitude or duration of the stimulus. After-spike h
yperpolarizations had a mean duration of 144.5 +/- 19.2 ms (n = 10). A
nodal break excitation was not recorded with hyperpolarizing current p
ulses. Fiber tract stimulation elicited fast excitatory postsynaptic p
otentials in all neurons tested. Conclusion: Intracellular recordings
of human gallbladder neurons utilizing 4-Di-2-ASP are thus feasible, b
ut are very problematic due to the density of connective tissue overly
ing the ganglia, As human and guinea pig gallbladder neurons have simi
lar basic electrical properties, the guinea pig may be an appropriate
model for further electrophysiological studies into gallbladder diseas
e.