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A treatment targeting shared reward circuitry may retain broader clinical utility

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Whilst, Ex-4 did not modify secretory currents evoked by the cholinergic agonist, carbachol ( n = 6, p = 0.0815, Figure 5B), currents evoked by the Na + channel agonist, veratridine were potentiated ( n = 8, p = 0.0085, Figure 5C)

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Anyone considering these therapies should undergo appropriate blood testing, cancer screening, and supervision by a health professional

95% CI, 0.87 to 0.06