Literature DB >> 1179150

Sources of the serum isoamylases and their normal range of variation with age.

G Skude.   

Abstract

The isoamylases in various human tissue homogenates and body fluids were separated by agarose gel electrophoresis. Nothing suggested any significant production of amylase in the liver. Minute amounts of amylase belonging to the pancreatic group of isoamylases might be produced by the glands of the proximal duodenum. The specific group of isoamylases produced in the female genital tract could not be demonstrated in serum or urine. The activity of amylase in serum was derived from two groups of isoenzymes, one group originating from the salivary glands, the other from the pancreatic gland. The contribution of each of these two sources to the total serum amylase was determined from early foetal life to adult age. A very low activity of the salivary isoamylases was regularly found in serum from 14-week-old foetuses. The activity increased steadily with age and reached the normal adult level, about 80 U/l, at the age of 5 years. The pancreatic group of isoamylases in serum developed later; the majority of children below 3 months had no demonstrable pancreatic isoamylase activity. The activity rose slowly to reach adult level, about 80 U/l, at the age of 10 to 15 years. The activity did not vary with sex, and the diurnal variation of the isoamylase was negligible. In children with cystic fibrosis of the pancreas the activity of pancreatic isoamylases in serum was low.

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Year:  1975        PMID: 1179150

Source DB:  PubMed          Journal:  Scand J Gastroenterol        ISSN: 0036-5521            Impact factor:   2.423


  12 in total

1.  Hyperamylasemia and S-type isozyme dominance in liver cirrhosis.

Authors:  Y Hatta; N Yoshikawa; H Funatomi; S Taguchi
Journal:  Int J Pancreatol       Date:  1987 Oct-Dec

2.  Severe acute pancreatitis and normal serum amylase activity due to pancreatic isoamylase deficiency.

Authors:  A Borgström; M Bohe
Journal:  Dig Dis Sci       Date:  1989-04       Impact factor: 3.199

3.  Amylase activity in human bile.

Authors:  L A Donaldson; S N Joffe; W McIntosh; M J Brodie
Journal:  Gut       Date:  1979-03       Impact factor: 23.059

4.  Frusemide-induced increases in serum isoamylases.

Authors:  B O Kristensen; J Skov; N A Peterslund
Journal:  Br Med J       Date:  1980-10-11

5.  A normal paediatric amylase range.

Authors:  P J Aggett; F Taylor
Journal:  Arch Dis Child       Date:  1980-03       Impact factor: 3.791

6.  Management of Acute Pancreatitis in the Pediatric Population: A Clinical Report From the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition Pancreas Committee.

Authors:  Maisam Abu-El-Haija; Soma Kumar; Jose Antonio Quiros; Keshawadhana Balakrishnan; Bradley Barth; Samuel Bitton; John F Eisses; Elsie Jazmin Foglio; Victor Fox; Denease Francis; Alvin Jay Freeman; Tanja Gonska; Amit S Grover; Sohail Z Husain; Rakesh Kumar; Sameer Lapsia; Tom Lin; Quin Y Liu; Asim Maqbool; Zachary M Sellers; Flora Szabo; Aliye Uc; Steven L Werlin; Veronique D Morinville
Journal:  J Pediatr Gastroenterol Nutr       Date:  2018-01       Impact factor: 2.839

7.  Selective deficiency of pancreatic amylase.

Authors:  K Sjölund; A Häggmark; I Ihse; G Skude; U Kärnström; M Wikander
Journal:  Gut       Date:  1991-05       Impact factor: 23.059

8.  Hyperamylasaemia after duodenoscopy and retrograde cholangiopancreatography.

Authors:  G Skude; L Wehlin; T Maruyama; J Ariyama
Journal:  Gut       Date:  1976-02       Impact factor: 23.059

9.  Clinical evaluation of the pancreatitis-like isoamylase pattern in normal persons.

Authors:  M Otsuki; M Maeda; H Yuu; T Yamasaki; K Okano; S Baba
Journal:  Gastroenterol Jpn       Date:  1978

10.  Elevated serum levels of pancreatic secretory proteins in cigarette smokers after secretin stimulation.

Authors:  G Balldin; A Borgström; A Eddeland; S Genell; L Hagberg; K Ohlsson
Journal:  J Clin Invest       Date:  1980-07       Impact factor: 14.808

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