Hypoglycin A is a water-soluble liver toxin, that upon ingestion, leads to
hypoglycemia through the inhibition of gluconeogenesis, a metabolic pathway that leads to the generation of glucose from non-carbohydrate carbon sources (i.e.
glucogenic amino acids,
lactate, and
glycerol). In addition, it also limits Acyl and carnitine cofactors, which are instrumental in the oxidation of large fatty acids. Hypoglycin A undergoes
deamination, forming α-ketomethylene-cyclopropylpropionic acid (KMCPP), which then forms MCPA through
oxidative decarboxylation. Hypoglycin A (and
hypoglycin B) is found in the
ackee fruit, the national fruit of Jamaica, and, like
Litchi chinensis, is a member of the family
Sapindaceae. The fruit is rich in fatty acids, zinc, protein, and vitamin A. In the fully ripened
arils of the fruit, Hypoglycin A is present at only 0.1ppm, but in the unripened fruit it can exceed a concentration of 1000ppm. ==Toxicity==