| CPC A61M 25/10181 (2013.11) [A61M 25/10 (2013.01); A61M 25/1018 (2013.01); A61M 25/10184 (2013.11); A61M 29/00 (2013.01); A61N 1/36117 (2013.01); A61N 1/3627 (2013.01); A61N 1/368 (2013.01); A61N 1/37235 (2013.01); A61M 2025/102 (2013.01)] | 20 Claims |

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1. A programmable implantable pacemaker connectable to at least one electrically conductive lead for connecting to a heart of a patient suffering from a condition comprising at least one of hypertension, excessive fluid retention, or excessive sodium retention,
wherein the pacemaker is programmed to:
during a first pacing period, facilitate a synchronous pace of at least one atrium and at least one ventricle of the patient's heart;
during a second pacing period, asynchronously pace the at least one atrium of the patient's heart at an atrial pacing rate and synchronously pace the at least one ventricle of the patient's heart at a ventricular pacing rate, such that the atrial pacing rate exceeds the ventricular pacing rate,
wherein during the pacing of the second pacing period, a wall of the at least one atrium is stressed beyond a natural stress condition due to the atrial pacing rate,
wherein the stressed wall secretes a hormone at an elevated secretion level above a secretion level occurring while a natural atrial rate and a natural ventricular rate are equal,
wherein the elevated secretion level of the secreted hormone achieves a beneficial therapeutic effect in the patient, and
wherein the beneficial therapeutic effect includes at least one of: limiting a degree of vasoconstriction, limiting a degree of sodium retention, increasing urine output, inhibiting a renin-angiotensin system, inhibiting endothelin secretion, inhibiting systemic and renal sympathetic activity, or counteracting effects of at least one of norepinephrine, endothelin, or angiotensin II; and
repeatedly alternate the first pacing period and the second pacing period to pace the patient's heart, wherein each alternating second pacing period has a duration of at least ten minutes.
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