Prenatal diagnostics: an offer you can't refuse?
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Biomedical subjects
Publications and source records attributed to B Petersson.
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Aryl hydrocarbon hydroxylase (AHH) inducibility, carbon monoxide in expired air (CO), serum gammaglutamyl-transferase (GGT), and total cholesterol were compared in equal-sized, age-matched samples of healthy middle-aged males born in 1921, 1934-1936, and 1946 attending the ongoing preventive medical population program in Malmö. AHH did not differ in various age - and smoking or non-smoking groups, and there were no correlations between AHH, GGT, and cholesterol. The findings provide evidence against the recent hypothesis that low cholesterol may mediate or reflect a carcinogenic mechanism through a state of general enzyme induction in the body.
Although transplantations of vascularized pancreas in diabetic patients show steadily improving results, the immediate operative risks and life-long immunosuppressive medication involved represent considerable disadvantages. Efforts are being made to develop simpler and safer methods of transplantation with isolated pancreatic islet grafts, e.g., isolated islets, fetal pancreas, or dispersed adult pancreas. Iso-, allo-, and xenografts of such preparations have been shown to reverse diabetes in animals. However, attempts to apply these techniques in clinical practice have remained largely unsuccessful, and major technical advances are needed before success is achieved. Attempts to use whole, segmented, or isolated islets from pancreatic grafts as a cure for diabetes in animals and in diabetic patients are reviewed. The importance to the graft's permanent function, of adequate preparation and storage of the graft, and of beta-cell growth and vascularization are reviewed. Various forms of immunomodulation by pretreatment of grafts in vitro have been employed in animal models of diabetes, but none of these have yet been employed with long-term success in humans. Recurrence of a specific autoimmune response toward the beta-cell in a spontaneously diabetic recipient is a potential mechanism for destruction of transplanted islet tissue.
Glucose exerts different effects on the hormone secretion from pancreatic B- and A-cells. In order to assess whether this can be linked to a difference in the effects of glucose on the phospholipid metabolism of these two cell types, islets were isolated from streptozotocin-treated (A-cell enriched islets) or normal guinea-pigs (B-cell rich islets). A-cell enriched islets contained more phospholipids when correction was made for the difference in size. Glucose-stimulated (16.7 mM) phospholipid and diacylglycerol biosynthesis, as estimated from 14C-glucose incorporation, was somewhat more stimulated in normal islets as compared with that of A-cell enriched islets. Triacylglycerol biosynthesis was, however, stimulated to the same extent. The pattern of 14C-glucose incorporation into the different phospholipid classes was very similar in both kinds of islets. Despite their smaller size, A-cell enriched islets incorporated, however, as much 14C-glucose as normal islets into most phospholipid classes. The present results are in line with previous findings of differences in glucose handling between the two cell types.
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