Abstract
Diabetes is the third leading cause of death in the US1. Prior to the discovery of insulin by Banting and Best in 1921, most diabetic mortality resulted from hyperglycemic ketoacidosis. Since that time, cardiovascular disease secondary to the diabetic state has become the leading cause of death in the diabetic population. While insulin replacement therapy appears sufficient to prevent severe hyperglycemic episodes, control is not sufficient to avert cardiovascular complications. Indeed, there is considerable evidence that insulin, itself, may play a deleterious role in the adverse cardiovascular sequelae associated with diabetes. Under normal conditions, the body releases only that amount of insulin required for control of blood glucose. In contrast, replacement therapy for the diabetic individual involves a bolus of insulin, resulting in early excessive levels followed by declining levels with time.
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Tenner, T.E., Zhang, X.J., Lombardini, J.B. (2003). Hypoglycemic Effects of Taurine in the Alloxan-Treated Rabbit, a Model for Type 1 Diabetes. In: Lombardini, J.B., Schaffer, S.W., Azuma, J. (eds) Taurine 5. Advances in Experimental Medicine and Biology, vol 526. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-0077-3_13
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DOI: https://doi.org/10.1007/978-1-4615-0077-3_13
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