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Hybridoma ; 14(4): 369-76, 1995 Aug.
Article in English | MEDLINE | ID: mdl-8522349

ABSTRACT

To test the effect of endogenous pancreatic polypeptide (PP) on rat hepatic glucose homeostasis by immunoneutralization, a rat PP-specific monoclonal antibody (MAb) was produced. Binding of this IgG1 monoclonal antibody was inhibited 50% by 350 pM rat PP. Immunohistochemistry showed that the antibody produced the expected pattern of endocrine cell staining in rat pancreas. Groups of six adult male Sprague-Dawley rats were given 5 mg of Protein-A-purified anti-PP MAb or anti-KLH MAb (control) ip every 48 hr for 5 dosing intervals. The rate of hepatic glucose output during isolated liver perfusion was 0.25 +/- 0.03 mg/g/min for the PP MAb-treated rats and 0.17 +/- 0.02 mg/g/min for the control group (p < 0.05). Liver glycogen content was 21.8 +/- 2.9 mg/g for the PP MAb-treated rats and 14.7 +/- 2.4 mg/g for the control group (N = 5). Chronic in vivo immunoneutralization of PP with this new monoclonal antibody suggests that PP influences glucose homeostasis in the rat by affecting hepatic glucose output.


Subject(s)
Antibodies, Monoclonal/biosynthesis , Antibodies, Monoclonal/physiology , Glucose/physiology , Homeostasis/immunology , Pancreatic Polypeptide/immunology , Animals , Antibodies, Monoclonal/pharmacology , Antibody Specificity/physiology , Cell Fusion/immunology , Glucose/immunology , Hybridomas , Liver/immunology , Liver/physiology , Male , Mice , Mice, Inbred Strains , Pancreatic Polypeptide/physiology , Rats , Rats, Sprague-Dawley
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