Nicotine-induced depolarization lowers intracellular pH in rat superior cervical ganglia, likely due to metabolic stimulation following Na+ entry.
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No immediate clinical implications; leaves open nicotine effects on ganglionic pH in intact cardiovascular systems.
The intracellular pH (pH(i)) of rat isolated superior cervical ganglia incubated in normal Krebs solution (pH(o)=7.37) was estimated to be 7.33 from the uptake of a weak acid, (14)C-5,5-dimethyloxazolidine-2,4-dione (DMO). Addition of 30 muM nicotine for 30 min reduced the DMO-estimated pH(i) by 0.15 units to 7.18. This effect was prevented by hexamethonium (2.5 mM) or by depolarizing the ganglion with K(+) (124 mM).2. (3)H-Nicotine (30 muM) was concentrated within the ganglia to an intracellular/extracellular concentration ratio (C(i)/C(o)) of 5.54 in normal Krebs solution and 4.61 in 2.5 mM hexamethonium. This would suggest an intracellular pH of 6.54 and 6.63 respectively. In ganglia previously depolarized by K(+) the corresponding values for C(i)/C(o) were 4.02 (minus hexamethonium, estimated pH(i) 6.95) and 4.17 (plus hexamethonium, estimated pH(i) 6.94).3. A multicompartment cell interior comprising an acid cytoplasm (pH approximately 6.6) and more alkaline nucleus and mitochondria is proposed to explain the difference between the values of pH(i) estimated from the uptake of DMO and nicotine. It is suggested that the fall in pH(i) during nicotine-depolarization results from metabolic stimulation following Na(+) entry.
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Brown et al. (1972) studied this question.
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