Abstract
Sodium bicarbonate (NaHCO(3)) has been recognized as a possible therapy to target chronic kidney disease (CKD) progression. Several small clinical trials have demonstrated that supplementation with NaHCO(3) or other alkalizing agents slows renal functional decline in patients with CKD. While the benefits of NaHCO(3) treatment have been thought to result from restoring pH homeostasis, a number of studies have now indicated that NaHCO(3) or other alkalis may provide benefit regardless of the presence of metabolic acidosis. These data have raised questions as to how NaHCO(3) protects the kidneys. To date, the physiological mechanism(s) that mediates the reported protective effect of NaHCO(3) in CKD remain unclear. In this review, we first examine the evidence from clinical trials in support of a beneficial effect of NaHCO(3) and other alkali in slowing kidney disease progression and their relationship to acid-base status. Then, we discuss the physiological pathways that have been proposed to underlie these renoprotective effects and highlight strengths and weaknesses in the data supporting each pathway. Finally, we discuss how answering key questions regarding the physiological mechanism(s) mediating the beneficial actions of NaHCO(3) therapy in CKD is likely to be important in the design of future clinical trials. We conclude that basic research in animal models is likely to be critical in identifying the physiological mechanisms underlying the benefits of NaHCO(3) treatment in CKD. Gaining an understanding of these pathways may lead to the improved implementation of NaHCO(3) as a therapy in CKD and perhaps other disease states.