Population
Isolated rabbit superior mesenteric artery (RMA) precontracted with norepinephrine (5 microM)
Comparison
Glyburide and potassium channel openers vs Charybdotoxin, glipizide, or varying pH conditions
Design
Preclinical
Authors
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Glyburide's vascular KATP blockade in animal models should not alter clinical practice; leaves open translation of pH-dependent mechanisms to human vessels.
Glyburide effectively blocks the vascular relaxation induced by diverse potassium channel openers, suggesting a shared mechanism of KATP channel activation that is highly pH-dependent.
Meisheri et al. (2008) studied this question.
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