Hepatocellular Leakage Enzymes|
The hepatocellular leakage enzymes are useful in detecting injury to liver parenchymal cells.
Generally, increased serum activity represents enzyme leakage from cells through damaged cell membranes.
- ALT: Used in small animals only. Largely liver-specific,
but can also increase in severe myopathies (release of muscle enzyme)
- AST: Used in small and large animals. Present liver as well
as skeletal muscle and erythrocytes.
- SDH: Liver specific in nearly all species. Used in large
animals in place of ALT (which is not a good marker of liver disease
in large animals).
- GLDH: Liver specific
in all species. Used in large animal panels concurrently with SDH
(due to superior storage stability) and on exotic (non-mammalian)
panels as a marker of liver injury.
- LDH: Lactic dehydrogenase is seen in both liver and muscle, so like AST it is not liver specific. LDH is discussed further under muscle enzymes.
Serum activity of the leakage enzymes increases when a sufficient number of hepatocytes
experience increased membrane permeability. Serum levels depend on both the number of
cells affected and the severity of injury to individual cells. Serum levels do not
correlate with reversibility. Diffuse hypoxia (reversible injury) may result in greater
serum activity than end-stage cirrhosis (irreversible injury). Increases are not specific with
regard to the nature of the injury.
- "Primary" hepatic disorders
- inflammation: Viral, bacterial, fungal, immune-mediated, idiopathic. Inflammation can be suppurative or non-suppurative. Note
that primary bile duct obstruction may result in secondary hepatocellular
injury as accumulated bile acids are toxic to cells. Leakage enzyme levels in end-stage liver disease or portosystemic shunts may be normal or
only mildly increased due to reduced number of cells and minimal active
- intoxications: Drugs, chemicals, plants. These can cause very high enzyme activity if
associated with diffuse necrosis.
- neoplasms: Hepatocellular and bile duct carcinomas, metastatic neoplasia.
Variable increases are possible depending on the extent of active hepatocellular injury.
- Disorders with secondary hepatic effects
- circulatory: Heart failure, shock,
severe anemia, portosystemic shunts, septicemia, gastrointestinal
disease in horses (displaced colon, acute colitis).
- metabolic: Endocrine disease (producing fatty liver, e.g. diabetes mellitus,
Cushing's disease, and idiopathic lipidosis), hyperthyroidism (? toxic effect of thyroid hormone on liver cells), acute pancreatitis.
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