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Am J Physiol Endocrinol Metab ; 306(4): E414-23, 2014 Feb 15.
Article in English | MEDLINE | ID: mdl-24347057

ABSTRACT

Previously, we reported that low-dose leptin infusions into the fourth ventricle produced a small but significant increase in body fat. These data contrast with reports that injections of higher doses of leptin into the fourth ventricle inhibit food intake and weight gain. In this study, we tested whether exogenous leptin in the fourth ventricle opposed or contributed to weight loss caused by third ventricle leptin infusion by blocking diffusion of CSF from the third to the fourth ventricle. Male Sprague-Dawley rats received third ventricle infusions of PBS or 0.3 µg leptin/24 h from miniosmotic pumps. After 4 days, rats received a 3-µl cerebral aqueduct injection of saline or of thermogelling nanoparticles (hydrogel) that solidified at body temperature. Third ventricle leptin infusion inhibited food intake and caused weight loss. Blocking the aqueduct exaggerated the effect of leptin on food intake and weight loss but had no effect on the weight of PBS-infused rats. Leptin reduced both body fat and lean body mass but did not change energy expenditure. Blocking the aqueduct decreased expenditure of rats infused with PBS or leptin. Infusion of leptin into the third ventricle increased phosphorylated STAT3 in the VMHDM of the hypothalamus and the medial NTS in the hindbrain. Blocking the aqueduct did not change hypothalamic p-STAT3 but decreased p-STAT3 in the medial NTS. These results support previous observations that low-level activation of hindbrain leptin receptors has the potential to blunt the catabolic effects of leptin in the third ventricle.


Subject(s)
Body Weight/drug effects , Cerebral Aqueduct/drug effects , Eating/drug effects , Hypothalamus/drug effects , Leptin/pharmacology , Animals , Body Composition/drug effects , Cerebral Aqueduct/metabolism , Energy Metabolism/drug effects , Fourth Ventricle/drug effects , Fourth Ventricle/metabolism , Hydrogel, Polyethylene Glycol Dimethacrylate/pharmacology , Hypothalamus/metabolism , Male , Phosphorylation/drug effects , Rats , Rats, Sprague-Dawley , STAT3 Transcription Factor/metabolism , Third Ventricle/drug effects , Third Ventricle/metabolism
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