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Peptide YY regulates bone turnover in rodents.

Peptide YY regulates bone turnover in rodents. Research Abstract Details 

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  • Peptide YY regulates bone turnover in rodents. Abstract Text:

    katherine e wortleyKatherine E Wortley,karen garciaKaren Garcia,haruka okamotoHaruka Okamoto,karen thabetKaren Thabet,keith d andersonKeith D Anderson,victor shenVictor Shen,jim p hermanJim P Herman,david valenzuelaDavid Valenzuela,george d yancopoulosGeorge D Yancopoulos,matthias h Matthias H ,andrew murphyAndrew Murphy,mark w sleemanMark W Sleeman,katherine e wortleyKatherine E Wortley,karen garciaKaren Garcia,haruka okamotoHaruka Okamoto,karen thabetKaren Thabet,keith d andersonKeith D Anderson,victor shenVictor Shen,jim p hermanJim P Herman,david valenzuelaDavid Valenzuela,george d yancopoulosGeorge D Yancopoulos,matthias h Matthias H ,andrew murphyAndrew Murphy,mark w sleemanMark W Sleeman,

    BACKGROUND & AIMS: Peptide YY (PYY) and pancreatic polypeptide (PPY) are members of the neuropeptide Y peptide family. The neuropeptide Y receptor signaling pathway has been implicated in a number of physiologic processes, including the regulation of energy balance and bone mass. To investigate the contribution of endogenous PYY and PPY to these processes, we generated both Pyy- and Ppy-deficient mice. METHODS: Pyy(-/-) and Ppy(-/-) mice and their respective wild-type littermates were studied from 8 weeks to 9 months of age. Food intake, metabolic parameters, and locomotor activity were monitored using indirect calorimetry. Body composition and bone parameters were analyzed using dual energy x-ray absorptiometry, histomorphometry, and vertebral compression testing. RESULTS: Studies in these mice showed an osteopenic phenotype specific to the Pyy-deficient line, which included a reduction in trabecular bone mass and a functional deficit in bone strength. Furthermore, female Pyy(-/-) mice showed a greater sensitivity to ovariectomy-induced bone loss compared with wild-type littermates. No food intake or metabolic phenotype was apparent in male or female Pyy(-/-) mice on standard chow. However, female Pyy(-/-) mice on a high-fat diet showed a greater propensity to gain body weight and adiposity. No metabolic or osteopenic phenotype was observed in Ppy-deficient mice. CONCLUSIONS: These results indicate that endogenous PYY plays a critical role in regulating bone mass. In comparison, its role in regulating body weight is minor and is confined to situations of high-fat feeding.

    Peptide YY regulates bone turnover in rodents. Publishing Authors By Initials

    ke wortleyKE Wortley,k garciaK Garcia,h okamotoH Okamoto,k thabetK Thabet,kd andersonKD Anderson,v shenV Shen,jp hermanJP Herman,d valenzuelaD Valenzuela,gd yancopoulosGD Yancopoulos,mh MH ,a murphyA Murphy,mw sleemanMW Sleeman,ke wortleyKE Wortley,k garciaK Garcia,h okamotoH Okamoto,k thabetK Thabet,kd andersonKD Anderson,v shenV Shen,jp hermanJP Herman,d valenzuelaD Valenzuela,gd yancopoulosGD Yancopoulos,mh MH ,a murphyA Murphy,mw sleemanMW Sleeman,

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    Peptide YY regulates bone turnover in rodents. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Gastroenterology

    VOLUME: 133

    Page Numbers: 1534-43

    Journal Abbreviation: Gastroenterology

    ISSN: 1528-0012

    DAY: 15

    MONTH: 08

    YEAR: 2007

    Peptide YY regulates bone turnover in rodents. Information

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    LANGUAGE: eng

    NlmUniqueID: 374630

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    Grant and Affiliation Information for Peptide YY regulates bone turnover in rodents.

    AFFILIATION: Regeneron Pharmaceuticals Inc, Tarrytown, New York, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Gastroenterology

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