Changes of salivary amylase in serum and parotid gland during pharmacological and physiological stimulation

J Physiol Paris. 2001 Jan-Dec;95(1-6):141-5. doi: 10.1016/s0928-4257(01)00018-3.

Abstract

Although serum amylase level is an important diagnostic factor in certain salivary and pancreatic diseases, little information is available regarding the mechanism by which parotid amylase reaches the circulatory system. The present study was carried out to investigate the relationship between parotid isoamylase concentrations in blood serum and in parotid tissue in response to various stimuli. Wistar rats were fed with standard laboratory rodent chow; water was supplied ad libitum. In the first experiment, after a 16-h fasting, rats received either 5 mg/kg pilocarpine or saline (control). In the second study, after fasting, half of the rats were fed for 1 h, the other half received no food. In the third experiment, the changes in serum and tissue enzyme levels were monitored in freely fed animals during the peak-food intake phase, the first 2 h of the dark period. Amylase concentration was determined by using starch as a substrate. Pancreatic and parotid isoamylase levels in serum were separated by gel-electrophoresis utilizing differences in ionic properties of the isoenzymes. As expected, pilocarpine strongly stimulated tissue amylase discharge and serum amylase elevation. Similar, but less pronounced changes were observed not only during refeeding of fasted animals, but also in nonfasted rats during their peak-feeding period. Our data suggest that pharmacological stimulation, such as with pilocarpine or feeding in fasted state, as well as a mild stimulation of parotid function by spontaneous food intake during nonfasted state results in a decrease in parotid tissue amylase activity and a proportional increase in serum levels of parotid isoamylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amylases / blood*
  • Animal Feed
  • Animals
  • Eating / physiology*
  • Fasting / physiology
  • Female
  • Muscarinic Agonists / pharmacology*
  • Parotid Gland / enzymology*
  • Pilocarpine / pharmacology*
  • Rats
  • Rats, Wistar
  • Saliva / enzymology*

Substances

  • Muscarinic Agonists
  • Pilocarpine
  • Amylases