Why the study?
Does exogenously applied fructose 1,6-bisphosphate enter cells and act as a glycolytic intermediate to improve isometric force in hypoxic vascular smooth muscle?
Does exogenously applied fructose 1,6-bisphosphate enter cells and act as a glycolytic intermediate to improve isometric force in hypoxic vascular smooth muscle?
Exogenously added fructose 1,6-bisphosphate can enter vascular smooth muscle cells and serve as a glycolytic intermediate, modestly improving isometric force during hypoxia at high concentrations.
No immediate clinical role; leaves open translation of glycolytic rescue to human vascular ischemia.
Exogenously administered fructose 1,6-bisphosphate reportedly protects ischemic or hypoxic tissue and facilitates metabolic recovery. The mechanism of action of exogenous fructose 1,6-bisphosphate has been an issue of considerable debate, since there is a lack of direct evidence that fructose 1,6-bisphosphate can cross the cell membrane and act as an intermediate in glycolysis. We synthesized [1,6-13C]fructose 1,6-bisphosphate and directly examined its cellular metabolism in hog carotid artery segments using 13C-nuclear magnetic resonance (NMR) spectroscopy. [1,6-13C]fructose 1,6-bisphosphate (2.1 mM) was metabolized by hog carotid artery during normoxia and hypoxia with a major metabolic product being [3-13C]lactate. The production of [3-13C]lactate was greater during hypoxia than during normoxia, indicating that fructose 1,6-bisphosphate metabolism responded to the energetic state of the tissue. We found that exogenously added fructose 1,6-bisphosphate at 2.1 mM did not significantly improve the ability of hypoxic hog carotid artery to maintain isometric force, whereas 20 mM fructose 1,6-bisphosphate did significantly, although modestly, improve isometric force maintenance. These results indicate that exogenously added fructose 1,6-bisphosphate is capable of entering cells and serving as a glycolytic intermediate.
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Hardin et al. (1994) studied this question.
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