Abstract
Over the past 20 years, we have collaborated with several laboratories in using mathematical modeling to describe and quantitate whole-body Vitamin A Metabolism in the rat. Steady state models have been developed for animals at different levels of vitamin A status (Green et al., 1985; Lewis et al., 1990; Green and Green, 1994a; Kelley and Green, 1998) and in response to other variables (Kelley et al., 1998; Jang et al., 2000; Kelley et al., 2000). Limited experimental and mathematical evidence (Green and Green, 1994b; Novotny et al., 1995; v Reinersdorff et al., 1998) suggests that there are many similarities in Vitamin A Metabolism between rats and humans. As discussed at the 5th Conference on Mathematical Modeling in Experimental Nutrition in 1994 (Green and Green, 1996), modeling studies have uniquely contributed to current understanding of whole-body Vitamin A Metabolism. In particular, interpretation of kinetic data has revealed previously unrecognized complexities in vitamin A dynamics that facilitate homeostatic control of plasma (and probably tissue) vitamin A levels.
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Green, M.H., Green, J.B. (2003). The Use of Model-Based Compartmental Analysis to Study Vitamin A Metabolism in a Non-Steady State. In: Novotny, J.A., Green, M.H., Boston, R.C. (eds) Mathematical Modeling in Nutrition and the Health Sciences. Advances in Experimental Medicine and Biology, vol 537. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-9019-8_11
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DOI: https://doi.org/10.1007/978-1-4419-9019-8_11
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