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Prior to experimentation, the enzyme was thawed at room temperature and small amounts of precipitated enzyme were removed by centrifugation at 10,000 g for 10 min, and 30 kDa centrifugal filters were used to buffer exchange the supernatant enzyme into the desired reaction buffer (typically 50 mM KPi, pH 7.4)

Hyperaldosteronism is associated with impaired vascular reactivity, and it has been shown that aldosterone induces a G6PD-deficient phenotype to impair endothelial function, and aldosterone antagonism or gene transfer of G6PD improves vascular reactivity [9]

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