Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/8759
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dc.contributor.authorVozzo, R.-
dc.contributor.authorWittert, G.-
dc.contributor.authorChapman, I.-
dc.contributor.authorFraser, R.-
dc.contributor.authorHope, P.-
dc.contributor.authorHorowitz, M.-
dc.contributor.authorAlshaher, M.-
dc.contributor.authorKumar, V.-
dc.contributor.authorMorley, J.-
dc.date.issued1999-
dc.identifier.citationComparative Biochemistry and Physiology C: Toxicology and Pharmacology, 1999; 123(2):145-151-
dc.identifier.issn1532-0456-
dc.identifier.urihttp://hdl.handle.net/2440/8759-
dc.description.abstractNitric oxide (NO) synthase inhibitors reduce food intake in rodents and chickens, suggesting that NO may stimulate feeding. We used two competitive, non-selective inhibitors of NO synthase (NOS), (NG-monomethyl-L-arginine ester [L-NMMA] and NG-nitro-L-arginine methyl ester [L-NAME]), to evaluate the role of NO mechanisms in the control of food intake in a marsupial model previously used in studies of appetite regulation. Adult male Sminthopsis crassicaudata (n = 11-16, 15 +/- 0.3 g, mean +/- S.E.M.) received L-NMMA (50, 100, 200 and 1000 mg/kg), L-NAME (50, 100 and 200 mg/kg), L-arginine (L-arg) the precursor of NO (1000 and 2000 mg/kg), L-NAME (200 mg/kg) in combination with L-arg (2000 mg/kg), or saline (0.9%). All drugs were administered intraperitoneally after 24 h of food deprivation, after which food was immediately made available ad libitum. Food intake was measured 0, 0.5, 1, 2, 4 and 24 h after treatments. In addition, we studied the effect of acute L-NAME administration on hypothalamic, cortical, hepatic and cardiac NOS activity by quantifying citrulline production. L-NMMA (1000 mg/kg) and L-NAME (100 and 200 mg/kg) suppressed food intake by 25%, 21%, and 30%, respectively, over 24 h after treatments (P < 0.05). L-arg (1000 and 2000 mg/kg) by itself had no significant effect on food intake when compared with saline (P > 0.05). When administered in combination with L-NAME (200 mg/kg), L-arg (2000 mg/kg) reversed L-NAME induced suppression of appetite (P> 0.05). Furthermore, L-NAME (200 mg/kg) significantly decreased hypothalamic (P < 0.01), cortical (P < 0.01) and hepatic (P < 0.03) NOS activity. L-NAME had no effect on cardiac NOS activity (P> 0.05). These data show that peripheral administration of L-NAME has a significant central effect, particularly in brain areas involved in appetite regulation, and suggest in marsupials, as in other mammals and birds, that NO plays a role in the regulation of food intake.-
dc.description.statementofresponsibilityRosalie Vozzo; Gary A Wittert; Ian M Chapman; Robert Fraser; Perdita J Hope; Michael Horowitz; Motaz M Alshaher; Vijaya B Kumar; John E Morley-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.source.urihttp://dx.doi.org/10.1016/s0742-8413(99)00022-5-
dc.subjectAnimals-
dc.subjectMarsupialia-
dc.subjectNitric Oxide-
dc.subjectNG-Nitroarginine Methyl Ester-
dc.subjectomega-N-Methylarginine-
dc.subjectFeeding Behavior-
dc.subjectMale-
dc.subjectNitric Oxide Synthase-
dc.titleEvidence that nitric oxide stimulates feeding in the marsupial Sminthopsis crassicaudata-
dc.typeJournal article-
dc.identifier.doi10.1016/S0742-8413(99)00022-5-
pubs.publication-statusPublished-
dc.identifier.orcidWittert, G. [0000-0001-6818-6065]-
dc.identifier.orcidHorowitz, M. [0000-0002-0942-0306]-
dc.identifier.orcidMorley, J. [0000-0001-6444-2965]-
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