Key result
In vitro incubation of bovine heart valves with 14C-glucose and 35S-sulfate revealed specific labelling and differing biosynthesis rates of hyaluronic acid, dermatan sulfate, chondroitin sulfate, and heparan sulfate.
This preclinical study characterizes the distinct metabolic profiles of glycosaminoglycans in bovine heart valves and identifies heparan sulfate in this tissue for the first time.
No immediate clinical implications; extends characterization of glycosaminoglycan metabolism in bovine heart valves.
Bovine heart valves metabolize up to 96% of exogenous 14C-glucose to lactate when incubated in vitro under appropriate conditions. Small proportions of the 14C-radioactivity are incorporated into glycogen, glycosaminoglycans and lipids and are oxydized to 14CO2. Difference between the valves of the left ventricle (aortic and mitral valve) and of the right ventricle (pulmonary and tricuspid valve) were found in the rate of glycolysis as well as in the collagen, glycogen and glycosaminoglycan content. The in vitro incorporation of [U-14C] glucose radioactivity into the total glycosaminoglycans resulted in a specific labelling of hyaluronic acid, dermatan sulfate and chondroitin sulfate, but the specific radioactivities of the individual glycosaminoglycans and their relative rates of biosynthesis differed markedly. The relative rates of biosynthesis were 2.9–7.6 for hyaluronate, 1.0 for dermatan sulfate and 0.26–0.59 for chondroitin sulfate. After labelling the sulfated glycosaminoglycans with 35S-sulfate, the metabolic heterogeneity of dermatan sulfate and chondroitin sulfate was confirmed, but, in addition, heparan sulfate – not previously detected in heart valves – was identified as a third sulfated glycosaminoglycan. Chemical analyses of heparan sulfate revealed a sulfate/uronic ratio of 0.5; its relative amount was found to be 2–4% of the total glycosaminoglycans. Analogous chemical and metabolic data were obtained with chordae tendineae, except that a higher relative percentage of dermatan sulfate was found than in the corresponding heart valves.
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Figura et al. (2008) studied this question. 14C-glucose and 35S-sulfate incubation was evaluated on Metabolism and biosynthesis rates of glycosaminoglycans. In vitro incubation of bovine heart valves with 14C-glucose and 35S-sulfate revealed specific labelling and differing biosynthesis rates of hyaluronic acid, dermatan sulfate, chondroitin sulfate, and heparan sulfate.
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