Chronic serotonin infusion reduces mean arterial pressure in male Dahl-SS rats resistant to diuretics, suggesting a new therapeutic avenue.
Serotonin (5-hydroxytryptamine, 5-HT) causes a sustained reduction in mean arterial pressure (MAP) during chronic (one week) infusion in both normo- and hypertensive rats. We hypothesized that the hypotensive effect of 5-HT will remain intact in male Dahl-SS rats that are unresponsive to a diuretic. Male Dahl-SS rats on a normal or 4% NaCl diet were instrumented with radiotelemeters for blood pressure measurement. Following the collection of baseline MAP, Alzet mini-pumps containing 5-HT (25 ug/kg/min) were implanted. On the same day as pump implantation, rats were either: 1) switched to drinking water containing the diuretic trichlormethiazide (TCM- 250 mg/L) or 2) maintained on regular drinking water. Following a week of infusion, blood samples were collected, and standard blood chemistry panels were run to investigate any potential effects on liver, kidney, or cardiometabolic parameters as well as electrolyte balance. On normal salt after 1 week of infusion, rats receiving both 5-HT and TCM had a significantly lower MAP (122.0 ±3.3 mmHg; n=5) than rats receiving 5-HT alone (p=0.0030, 131±2.7 mmHg; n=5). After 1 week of infusion, high salt diet rats receiving both 5-HT and TCM had the greatest reduction in MAP (−20.7±1.7 mmHg; n=4). 5-HT administration did not modify kidney or liver function as assessed by measurements of plasma in rats on normal salt diet. Collectively, these data suggest 5-HT may be an effective additive to current front-line anti-hypertensive medications. Furthermore, 5-HT remains effective even when drug resistance develops to at least one of those standard monotherapies (thiazide diuretics).
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Kram et al. (2025) studied this question.
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