The action of human saliva on starch was first reported by Leuchs in 1831, long before enzymes were recognized as such. Subsequently, experiments were carried out to estimate the amount of this enzyme in saliva, and it became apparent that the amylase content varied under different conditions. Two possible sources of this variation are the type of stimulation and the secretary rate of flow. Several investigators1-4 have studied the amylolytic power of saliva following stimulation by a particular food or beverage, and others5-10 that following the ingestion of a particular type of diet. Unfortunately, many of the studies employed methods of amylase estimation that were only qualitative or, at best, semiquantitative. Frequently the taste stimulus was hardly specific. There have been several reports4' 11, 12 comparing the amylase content of resting and stimulated saliva.The following experiments were carried out to determine whether the concentration of parotid salivary amylase is in any way related to the type of taste stimulation or to the flow rate. The effect of four gustatory modalities (sour, salt, sweet, bitter) was tested by a procedure which eliminated or reduced other forms of reflex stimulationfor example, olfactory, visual, auditory, and mechanical.
EXPERIMENTAL METHODS
MaterialsParotid saliva.-The orifice of Stenson's duct and surrounding oral mucosa were carefully wiped with a sterile dry swab to reduce the possibility of microbial contamination of the saliva.13 A suction cup'4 was placed over the orifice of the duct and the saliva was led into a graduated tube by a length of polyethylene tubing. Samples were collected I-11 hours after the midday meal from 17 adult subjects (9 females, 8 males) on at last three separate occasions for each type of stimulation. Routine sterility tests were made on the parotid saliva samples by plating on blood agar.The effects of four different types of gustatory stimuli (sour, sweet, salty, and bitter) were studied. Solutions of citric acid (3 per cent), sucrose (40 per cent), sodium chloride (30 per cent), or quinine sulfate (0.15 per cent) were applied to the dorsum and lateral edges of the tongue every 20 seconds for 5-10 minutes with a cotton swabstick.