-transparent.png){kind=logo}
1. During pretreatment with isoproterenol (ISP) for 2 min the accumulation of cyclic AMP increased in a dose-dependent manner but amylase release did not increase even in the highest dose of ISP used. 2. After a brief pretreatment with ISP, the following 10-min incubations with fresh medium without ISP caused increase in amylase secretion (residual secretion). However, cyclic AMP accumulation returned to the non-treated level during the residual secretion of amylase. 3. Both residual amylase release and cyclic AMP accumulation after pretreatment with ISP were enhanced in the presence of isobutyl-methylxanthine. Residual amylase release was not affected in the absence of extracellular calcium ion. 4. We suggest that there may be another pathway than cyclic AMP to cause residual amylase secretion induced by brief pretreatment with ISP in rat parotid acinar cells.
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
January 1982,
Archives internationales de pharmacodynamie et de therapie,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
April 1980,
Pflugers Archiv : European journal of physiology,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
April 1970,
Biochimica et biophysica acta,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
October 1968,
Biochimica et biophysica acta,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
January 1982,
Quarterly journal of experimental physiology (Cambridge, England),
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
January 1964,
Archives of biochemistry and biophysics,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
May 2006,
Regulatory peptides,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
February 1988,
Biochemical and biophysical research communications,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
September 1993,
Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology,
Y Suzuki-Hatta, and
H Takemura, and
Y Koike-Nakaya, and
H Ohshika
May 1968,
European journal of pharmacology,
