Subject(s)
Alanine Transaminase/cerebrospinal fluid , Aspartate Aminotransferases/cerebrospinal fluid , Brain Neoplasms/enzymology , Creatine Kinase/cerebrospinal fluid , Ischemic Attack, Transient/enzymology , Brain Neoplasms/cerebrospinal fluid , Humans , Ischemic Attack, Transient/cerebrospinal fluidABSTRACT
Phosphatidylethanolamine reacts with 1,4-benzoquinone with the formation of a red unstable intermediary product consisting of one phosphatidylethanolamine residue and one 1,4-benzoquinone residue. The secondary reaction products are purple, violet, and reddish brown. Consequently, the absorption maximum shifts from 430 nm to 490 nm during the reaction. Finally, brown macromolecular end-products are formed. Phospholipids derived from choline, such as phosphatidylcholine, lysophosphatidylcholine, sphingomyelin, contribute only a little to the browning reactions, in comparison with phospholipids containing a primary amino-group (phosphatidylethanolamine, lysophosphatidylethanolamine, phosphatidylserine). The browning of a natural mixture of egg phospholipids depends on the content of derivatives containing a primary amino-group.
