Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol

59Fe was incorporated in vivo into intestinal sacs prepared in control rats as well as in animals with turpentine sterile abscesses and 59Fe counts were detected in the intestinal wall, in blood, in liver, in spleen and in femur of animals, at different time intervals (20, 40 and 120 min) following...

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Publicado: 1987
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rat
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03790355_v9_n1_p23_Gutnisky
http://hdl.handle.net/20.500.12110/paper_03790355_v9_n1_p23_Gutnisky
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spelling paper:paper_03790355_v9_n1_p23_Gutnisky2023-06-08T15:40:34Z Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol beta adrenergic receptor iron iron 59 isoprenaline propranolol radioisotope turpentine animal experiment bone digestive system drug absorption drug toxicity inflammation intoxication liver nonhuman oral drug administration pharmacokinetics rat spleen Animal Female Inflammation Intestinal Absorption Iron Isoproterenol Liver Propranolol Rats Rats, Inbred Strains Turpentine 59Fe was incorporated in vivo into intestinal sacs prepared in control rats as well as in animals with turpentine sterile abscesses and 59Fe counts were detected in the intestinal wall, in blood, in liver, in spleen and in femur of animals, at different time intervals (20, 40 and 120 min) following i.v. injection of isoproterenol (10 μg/kg, body weight) or of (-)-propranolol (2 mg/kg, body weight). In rats without inflammation isoproterenol alone enhanced significantly iron counts in blood, spleen, liver and femur, but not in intestinal cells, whereas propranolol evoked opposite actions, the influence being more marked after 40 min, reaching maximal values at 120 min. In animals with sterile turpentine abscesses explored 40 min after injections, iron intestinal counts in turpentine, in turpentine plus isoproterenol and in turpentine plus propranolol groups were significantly lower than in normal saline injected controls (p < 0.001) and the opposite was the case at 120 min. In blood, iron counts at 20 and 40 min were higher in saline controls (p < 0.05) than in the turpentine group, whereas at 120 min, values in the turpentine plus isoproterenol group were higher than (p < 0.01) in saline injected controls with turpentine alone. Also, at all time intervals explored, iron counts in blood in the propranolol plus turpentine group were smaller (p < 0.01) than in saline injected controls or in the group with turpentine alone. At 120 min the % of 59Fe uptake in liver from turpentine plus isoproterenol animals was greater than in saline injected controls, than in turpentine alone, or than in turpentine plus propranolol rats. No differences among groups were detected in spleen or in femur. Results in rats with turpentine abscesses suggest that isoproterenol acts favoring iron transport from intestinal cells enhancing its movement into blood, whereas propranolol appears associated to the opposite action. Moreover, beta adrenoceptors appear to be involved not only during early stages of intestinal absorption but also during further distribution and final uptake by storage organs, such as the liver. 1987 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03790355_v9_n1_p23_Gutnisky http://hdl.handle.net/20.500.12110/paper_03790355_v9_n1_p23_Gutnisky
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic beta adrenergic receptor
iron
iron 59
isoprenaline
propranolol
radioisotope
turpentine
animal experiment
bone
digestive system
drug absorption
drug toxicity
inflammation
intoxication
liver
nonhuman
oral drug administration
pharmacokinetics
rat
spleen
Animal
Female
Inflammation
Intestinal Absorption
Iron
Isoproterenol
Liver
Propranolol
Rats
Rats, Inbred Strains
Turpentine
spellingShingle beta adrenergic receptor
iron
iron 59
isoprenaline
propranolol
radioisotope
turpentine
animal experiment
bone
digestive system
drug absorption
drug toxicity
inflammation
intoxication
liver
nonhuman
oral drug administration
pharmacokinetics
rat
spleen
Animal
Female
Inflammation
Intestinal Absorption
Iron
Isoproterenol
Liver
Propranolol
Rats
Rats, Inbred Strains
Turpentine
Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol
topic_facet beta adrenergic receptor
iron
iron 59
isoprenaline
propranolol
radioisotope
turpentine
animal experiment
bone
digestive system
drug absorption
drug toxicity
inflammation
intoxication
liver
nonhuman
oral drug administration
pharmacokinetics
rat
spleen
Animal
Female
Inflammation
Intestinal Absorption
Iron
Isoproterenol
Liver
Propranolol
Rats
Rats, Inbred Strains
Turpentine
description 59Fe was incorporated in vivo into intestinal sacs prepared in control rats as well as in animals with turpentine sterile abscesses and 59Fe counts were detected in the intestinal wall, in blood, in liver, in spleen and in femur of animals, at different time intervals (20, 40 and 120 min) following i.v. injection of isoproterenol (10 μg/kg, body weight) or of (-)-propranolol (2 mg/kg, body weight). In rats without inflammation isoproterenol alone enhanced significantly iron counts in blood, spleen, liver and femur, but not in intestinal cells, whereas propranolol evoked opposite actions, the influence being more marked after 40 min, reaching maximal values at 120 min. In animals with sterile turpentine abscesses explored 40 min after injections, iron intestinal counts in turpentine, in turpentine plus isoproterenol and in turpentine plus propranolol groups were significantly lower than in normal saline injected controls (p < 0.001) and the opposite was the case at 120 min. In blood, iron counts at 20 and 40 min were higher in saline controls (p < 0.05) than in the turpentine group, whereas at 120 min, values in the turpentine plus isoproterenol group were higher than (p < 0.01) in saline injected controls with turpentine alone. Also, at all time intervals explored, iron counts in blood in the propranolol plus turpentine group were smaller (p < 0.01) than in saline injected controls or in the group with turpentine alone. At 120 min the % of 59Fe uptake in liver from turpentine plus isoproterenol animals was greater than in saline injected controls, than in turpentine alone, or than in turpentine plus propranolol rats. No differences among groups were detected in spleen or in femur. Results in rats with turpentine abscesses suggest that isoproterenol acts favoring iron transport from intestinal cells enhancing its movement into blood, whereas propranolol appears associated to the opposite action. Moreover, beta adrenoceptors appear to be involved not only during early stages of intestinal absorption but also during further distribution and final uptake by storage organs, such as the liver.
title Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol
title_short Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol
title_full Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol
title_fullStr Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol
title_full_unstemmed Intestinal iron absorption during turpentine sterile inflammation in the rat. Influences of isoproterenol and propranolol
title_sort intestinal iron absorption during turpentine sterile inflammation in the rat. influences of isoproterenol and propranolol
publishDate 1987
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03790355_v9_n1_p23_Gutnisky
http://hdl.handle.net/20.500.12110/paper_03790355_v9_n1_p23_Gutnisky
_version_ 1768542843744288768