Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.2.1.108 (lactase)
2,133 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A method for the histochemical demonstration of "hetero-beta-galactosidase" was elaborated. The enzyme is demonstrated in cryostat sections by the semipermeable membrane technique. Pairs of membranes--one pre-washed in saline--are used. The most sensitive method is post-coupling demonstration with 6-Br-2-naphthyl-beta-D-glucoside. The incubation time must be short, to avoid diffusion. The method allows cellular localization. The method with alpha-naphthyl-beta-D-glucoside and hexazonium-p-rosaniline is less sensitive, but localization is better. Indigogenic methods are the least sensitive. The enzyme is localized in the supranuclear zone of differentiated enterocytes of the human, monkey and rabbit small intestine, with maximum activity in the jejunum. The activity of the enzyme is low in patients with coeliac sprue, in the active phase of the disease. In isolated lactase deficiency it is normal. In the kidney, the enzyme is localized chiefly in the cytoplasm of the proximal tubule cells.
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PMID:Demonstration of "hetero-beta-galactosidase" "in situ". 9 37

A broad overview of the modalities available for the medical treatment of malabsorptions is presented with emphasis on practical applications. The more common disorders, such as sprue, lactase deficiency, and pancreatic insufficiency, are generally managed successfully with specific dietary and drug regimens. Nonspecific dietary therapy is available for patients to whom specific therapy cannot be offered.
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PMID:[The medical management of malabsorption (author's transl)]. 40 72

Thirty-eight specimens obtained by jejunal biopsy from 22 children suffering from mucoviscidosis were examined by histochemical techniques. In 27% of the patients the findings were within normal limits. In 18% of cases, associated coeliacal sprue was disclosed. The remaining cases displayed slight morphological abnormalities associated with trehalase and/or lactase deficiency, and in 41% there was hypersecretion of viscous mucus filling up dilated crypts and adhering to the surface of villi. The findings as observed in enterobiopsis are not pathognostic of mucoviscidosis. They however, should make one to think of it, particularly if trehalase and/or lactase deficiency is found associated with hypersecretion of viscous mucus and an almost normal morphological appearance. Neither normal findings nor that of coeliacal sprue exclude the diagnosis of mucoviscidosis. It appears that malabsorption in mucoviscidosis is not only pancreatogenic; the intestinal mucosa may be contributory to a various degree as well.
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PMID:[Jejunal mucosa in children with mucoviscidosis]. 120 86

In a retrospective study, jejunal mucosal disaccharidase and alkaline phosphatase activities have been investigated in 40 controls and patients with proven celiac sprue (n = 26), lactase deficiency (n = 26), osteoporosis or osteomalacia (n = 16), chronic pancreatitis (n = 12), giardiasis (n = 7), or Crohn's disease (n = 7). Apart from a nonselective reduction of mucosal enzyme activities in the sprue syndrome and a selective reduction of lactase activity in the patients with primary lactase deficiency, assays of mucosal disaccharidases revealed only inconstant or slight deviations from the control group and were not of diagnostic significance for any of the above-mentioned disorders. Isolated forms of enzyme deficiencies other than lactase deficiency, such as sucrase-isomaltase or trehalase deficiency were not present among 168 investigations carried out from 1972-1982. It is concluded that assay of small intestinal disaccharidase or alkaline phosphatase activities does not expand the diagnostic impact of morphological examination of small bowel biopsy specimens and modern noninvasive methods for the detection of carbohydrate malabsorption. Thus, the method does not appear a necessary or relevant investigation in routine clinical practice.
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PMID:Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists? 274 34