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Two molecules of Keap1 form a homodimer through the N-terminal BTB domain, and the C-terminal globular domains, called the DC domains, are positioned apart from each other (Ogura et al., 2010

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KPV increases blood flow by activating endothelial nitric oxide synthase (eNOS), which increases the generation of nitric oxide, a potent vasodilator that relaxes blood vessels and reduces blood pressure

It may enhance lipid metabolism by reducing the buildup of lipids such as TGs, FFAs, and CHOL (in particular, the production and secretion of CHOL and Bas)

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