Trioses and related substances: tools for the study of pancreatic beta-cell function

Abstract

Trioses, such as D-glyceraldehyde, have been used extensively for the study of stimulus-secretion coupling mechanisms in pancreatic beta-cells. It is generally assumed that trioses enter the glycolytic pathway at the triose phosphate level, and stimulate insulin release in a manner analogous to glucose. This review focuses on a number of triose effects that are not entirely consistent with this model. These effects are likely to result, at least in part, from the actions of alpha-ketoaldehydes. One such compound, methylglyoxal, appears to be a major contaminant of triose preparations, and exerts effects on the beta-cell identical to some of those evoked by glyceraldehyde. A related substance, hydroxypyruvaldehyde, is a product of triose autoxidation, which could exert similar effects. Study of the actions of trioses and alpha-ketoaldehydes could assist our understanding of cellular physiology, in general, and beta-cell function, in particular. These substances are also likely to be of pathophysiological importance, especially in the context of sugar toxicity and autoxidative cell damage.