Nitrate and nitrite should be viewed as storage pools for NO rather than inert waste products, as nitrite can be recycled back to bioactive NO in blood and tissues.
NO generated from L-arginine by NO synthases (NOSs) in the endothelium and in other cells plays a central role in several aspects of vascular biology. The biological activity of NO is acutely terminated by oxidation to nitrite and nitrate, and these compounds have long been considered only as inert end-products of NO. However, this dogma is now being challenged because recent research convincingly has shown that the nitrite ion can be recycled back to bioactive NO again in blood and tissues. Nitrite reduction to NO can occur via several routes involving enzymes, proteins, vitamins, or even simple protons. This pathway may serve as a backup system for NO generation in conditions such as hypoxia, in which the NOS/L-arginine system is compromised, but detrimental effects can also be foreseen. With this new knowledge, nitrate and nitrite should probably be viewed as storage pools for NO rather than inert waste products. Here we discuss novel aspects of nitrite-dependent NO generation in vivo and its role in vascular control.
Lundberg et al. (Fri,) conducted a review in Vascular biology. Nitrate and nitrite should be viewed as storage pools for NO rather than inert waste products, as nitrite can be recycled back to bioactive NO in blood and tissues.