Selective KCa3.1 Channel Activators as Novel Antihypertensives
40-80 fold selectivity for KCa3.1 over KCa2 Lowers blood pressure without affecting heart rate
Treatment for hypertension Protection of organ function for transplantation Diabetic ischemia Neuropathic pain
Calcium-activated potassium channels (KCa) regulate endothelium-derived hyperpolarization (EDH) vasodilator responses. Localization and differential expression of KCa3.1 and KCa2 channels presents a challenge for selective stimulation of either channel. Therefore, adverse effects are observed when dual KCa activator compounds are used as anti-hypertensive therapeutics. The current market is in need of drugs that selectively activate these channels, which will eliminate adverse effects caused by dual KCa activator compounds. Current anti-hypertensive drugs activate both KCa3.1 and KCa2. This adversely results in sedation and reduced heart rate. This is likely due to activation of KCa2 channels in neuronal and cardiac tissue. Studies show that in mice treated with dual KCa activator compounds, blood pressure was significantly lowered, but heart rate was also reduced. UC Davis researchers have identified novel compounds that are highly selective for KCa3.1 activation versus KCa2.In vivo studies demonstrate that in mice treated with this novel KCa3.1 activator, blood pressure was lowered without exerting KCa2-mediated effects on heart rate. The chemical compositions differ from current anti-hypertensive drugs and provides a new approach for lowering blood pressure without affecting heart rate.
20170056376
Additional Technologies by these Inventors Tech ID/UC Case 24214/2014-540-0 Related Cases 2014-540-0
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