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Department of Physiology, Kanagawa Dental College, Yokosuka 238-8580, Japan
With conventional intracellular
recording methods, we investigated the mechanism of actions of reactive
oxygen species (ROS) derived from hypoxanthine and xanthine oxidase
(HX/XO) reactions on AH/type 2 myenteric neurons in the guinea pig
distal colon. Of the 54 neurons to which HX/XO was applied, 32 neurons
showed a transient membrane hyperpolarization(s) followed by a
long-lasting membrane depolarization. Two additional groups of 10 myenteric neurons exhibited only a membrane hyperpolarization(s) or a
late-onset membrane depolarization, respectively, and the remaining two
neurons did not show any response to HX/XO. Analysis of changes of the input resistance induced by HX/XO indicated that suppression and augmentation of the conductance of Ca2+-dependent
K+ channels are the ionic mechanisms underlying the
membrane hyperpolarization and depolarization, respectively. The
effects of HX/XO on myenteric neurons were mimicked by application of
caffeine or H2O2. The results suggest that
OH·, but neither H2O2 nor
O2·
, is responsible for HX/XO-induced
responses. The intracellular Ca2+ store may be the acting
site of ROS in colonic AH/type 2 neurons.
superoxide anion radical; hydrogen peroxide; hydroxyl radical; AH/type 2 neuron
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