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1.
Neuroscience ; 104(2): 397-405, 2001.
Article in English | MEDLINE | ID: mdl-11377843

ABSTRACT

Embryonic neurons transplanted to the adult CNS extend axons only for a developmentally defined period. There are certain intercellular factors that control the axonal extension, one of which may be the expression of the bcl-2 protein. In this study, rats with complete striatal dopamine fiber denervation received embryonic day 14 mouse ventral mesencephalon cells overexpressing human bcl-2 or control wild-type ventral mesencephalon cells. All rats were treated with cyclosporine to prevent rejection and the surviving grafts were analyzed for cell survival and outgrowth of dopaminergic fibers. The results demonstrate that bcl-2 overexpression does not enhance neuronal graft survival. However, the bcl-2 overexpressing neurons had a higher number of dopaminergic fibers that grew longer distances. These results show that overexpression of bcl-2 can result in longer distance axonal growth of transplanted fetal dopaminergic neurons and that genetic modification of embryonic donor cells may enhance their ability to reinnervate a neuronal target territory.


Subject(s)
Brain Tissue Transplantation/methods , Dopamine/metabolism , Graft Survival/genetics , Growth Cones/transplantation , Neostriatum/surgery , Proto-Oncogene Proteins c-bcl-2/metabolism , Substantia Nigra/transplantation , Animals , Cells, Cultured , Denervation , Female , Fetus , Growth Cones/metabolism , Growth Cones/ultrastructure , Humans , Male , Mice , Mice, Transgenic , Neostriatum/pathology , Neostriatum/physiopathology , Oxidopamine , Parkinson Disease/metabolism , Parkinson Disease/physiopathology , Parkinson Disease/surgery , Phenotype , Proto-Oncogene Proteins c-bcl-2/genetics , Rats , Rats, Sprague-Dawley , Substantia Nigra/cytology , Substantia Nigra/metabolism
2.
Gut ; 46(3): 327-31, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10673292

ABSTRACT

OBJECTIVE: Recent research suggests that oats do not harm intestinal villi in adults with coeliac disease. As the immunological effects of oats have not been examined in detail, it was decided to compare the immunological responses of a gluten free diet including oats with those of a conventional gluten free diet. DESIGN: A randomised controlled intervention study over 6-12 months. SUBJECTS: Forty adults with newly diagnosed coeliac disease and 52 with coeliac disease in remission were examined. INTERVENTION: The effects of a gluten free diet including oats and a conventional gluten free diet were compared. MAIN OUTCOME MEASURES: Serum levels of gliadin and reticulin antibodies as well as numbers of intraepithelial lymphocytes (IELs) in intestinal mucosa were examined before and after the intervention. RESULTS: The rate of disappearance of gliadin and reticulin antibodies did not differ between the diet groups in patients with newly diagnosed coeliac disease. Oats also had no effect on gliadin or reticulin antibody levels in the patients with remission. The number of IELs decreased similarly regardless of the diet of newly diagnosed patients, and no increase in the number of IELs was found in the patients in remission with or without oats. CONCLUSIONS: These results strengthen the view that adult patients with coeliac disease can consume moderate amounts of oats without adverse immunological effects.


Subject(s)
Avena/immunology , Celiac Disease/immunology , Glutens/immunology , Adult , Antibody Formation , Celiac Disease/diet therapy , Humans , Lymphocyte Count
3.
Lipids ; 32(7): 707-14, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9252958

ABSTRACT

6,9,12,15,18-Heneicosapentaenoic acid (21:5n-3) (HPA), present in small amounts in fish oils, has been prepared by chemical elongation of eicosapentaenoic acid (EPA) and its biological properties compared with EPA and docosahexaenoic acid (DHA). All the double bonds of HPA are displaced one carbon away from the carboxyl group when compared to EPA. HPA is incorporated into phospholipids and into triacylglycerol in cell culture to a similar extent as EPA and DHA. HPA is a stronger inhibitor of the conversion of alpha-linoleic acid and dihomo-gamma-linolenic acid to arachidonic acid (AA) in hepatoma cells than are EPA, DHA, and AA. HPA is a poor substrate for prostaglandin H synthase and for 5-lipoxygenase, but it inactivates prostaglandin H synthase as rapidly as do AA, EPA, and DHA. HPA inhibits thromboxane synthesis in isolated platelets as efficiently as EPA. EPA, HPA, and DHA are all weak inducers of acyl-CoA oxidase in hepatoma cells. Therefore, since fish oils contain only small amounts of HPA, it is unlikely that this fatty acid is of particular significance for the biological effects of these oils, possibly with the exception that it is a strong inhibitor of AA synthesis.


Subject(s)
Arachidonic Acid/biosynthesis , Eicosanoids/biosynthesis , Fatty Acids, Omega-3/metabolism , Lipid Metabolism , Animals , Arachidonate 5-Lipoxygenase/metabolism , Delta-5 Fatty Acid Desaturase , Docosahexaenoic Acids/metabolism , Eicosapentaenoic Acid/metabolism , Fatty Acid Desaturases/antagonists & inhibitors , Fatty Acid Desaturases/metabolism , Linoleoyl-CoA Desaturase , Liver/cytology , Liver/metabolism , Liver Neoplasms, Experimental/metabolism , Macrophages, Peritoneal/cytology , Macrophages, Peritoneal/metabolism , Male , Mice , Phospholipids/metabolism , Prostaglandin-Endoperoxide Synthases/metabolism , Rats , Substrate Specificity , Triglycerides/metabolism
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