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3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss

Aging is associated with accumulation of various tryptophan degradation products that may having either bone anabolic or catabolic effects. In epidemiologic studies, elevated levels of 3-hydroxyanthranilic acid (3-HAA) are associated with a higher bone mineral density (BMD). We have previously shown...

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Autores principales: Isales, Carlos, Ding, Ke-Hong, Bollag, Wendy, McGee-Lawrence, Meghan, Hill, William, Shi, Xing-ming, Fulzele, Sadanand, Hamrick, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680843/
http://dx.doi.org/10.1093/geroni/igab046.2547
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author Isales, Carlos
Ding, Ke-Hong
Bollag, Wendy
McGee-Lawrence, Meghan
Hill, William
Shi, Xing-ming
Fulzele, Sadanand
Hamrick, Mark
author_facet Isales, Carlos
Ding, Ke-Hong
Bollag, Wendy
McGee-Lawrence, Meghan
Hill, William
Shi, Xing-ming
Fulzele, Sadanand
Hamrick, Mark
author_sort Isales, Carlos
collection PubMed
description Aging is associated with accumulation of various tryptophan degradation products that may having either bone anabolic or catabolic effects. In epidemiologic studies, elevated levels of 3-hydroxyanthranilic acid (3-HAA) are associated with a higher bone mineral density (BMD). We have previously shown that the C57BL/6 mouse loses bone mass with age. Thus, we hypothesized that administering 3-HAA via a daily intraperitoneal (IP) injection would result in preserved or increased BMD. In an IACUC-approved protocol, we injected 26-month-old C57BL/6 mice with either a low dose (0.5 mg) or high dose (5 mg) of 3-HAA IP five days a week for eight weeks. At the end of this time mice were sacrificed and body composition and bone mineral density measured by DigiMus. BMD was significantly lower in the high dose 3-HAA group: 0.0570 + 0.004 vs 0.0473 + 0.006 vs 0.0432 + 0.0075 gm/cm2, (means+SD, Control vs 0.5 mg 3HAA vs 5 mg 3HAA, p=0.004, 0 vs 5.0 mg, n=6-9/group). 3-HAA had no significant impact on body composition (lean body mass: 86.7 + 1.7% vs 86.2 + 2.7% vs 86.1 + 2.0%, Control vs 0.5 mg vs 5.0 mg 3-HAA, p=ns; and fat mass 12.6 + 2.0% vs 13.8 + 2.7% vs 13.9 + 2.0% vs 0.2%, Control vs 0.5 vs 5 mg 3-HAA, p=ns). Thus, 3-HAA did not prevent bone loss in older mice but instead significantly worsened bone loss. 3-HAA is known to have both pro- and anti- oxidant effects depending on the environment. These data would suggest that at the higher concentrations 3-HAA is acting predominantly as a pro-oxidant molecule accelerating age-related bone loss.
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spelling pubmed-86808432021-12-17 3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss Isales, Carlos Ding, Ke-Hong Bollag, Wendy McGee-Lawrence, Meghan Hill, William Shi, Xing-ming Fulzele, Sadanand Hamrick, Mark Innov Aging Abstracts Aging is associated with accumulation of various tryptophan degradation products that may having either bone anabolic or catabolic effects. In epidemiologic studies, elevated levels of 3-hydroxyanthranilic acid (3-HAA) are associated with a higher bone mineral density (BMD). We have previously shown that the C57BL/6 mouse loses bone mass with age. Thus, we hypothesized that administering 3-HAA via a daily intraperitoneal (IP) injection would result in preserved or increased BMD. In an IACUC-approved protocol, we injected 26-month-old C57BL/6 mice with either a low dose (0.5 mg) or high dose (5 mg) of 3-HAA IP five days a week for eight weeks. At the end of this time mice were sacrificed and body composition and bone mineral density measured by DigiMus. BMD was significantly lower in the high dose 3-HAA group: 0.0570 + 0.004 vs 0.0473 + 0.006 vs 0.0432 + 0.0075 gm/cm2, (means+SD, Control vs 0.5 mg 3HAA vs 5 mg 3HAA, p=0.004, 0 vs 5.0 mg, n=6-9/group). 3-HAA had no significant impact on body composition (lean body mass: 86.7 + 1.7% vs 86.2 + 2.7% vs 86.1 + 2.0%, Control vs 0.5 mg vs 5.0 mg 3-HAA, p=ns; and fat mass 12.6 + 2.0% vs 13.8 + 2.7% vs 13.9 + 2.0% vs 0.2%, Control vs 0.5 vs 5 mg 3-HAA, p=ns). Thus, 3-HAA did not prevent bone loss in older mice but instead significantly worsened bone loss. 3-HAA is known to have both pro- and anti- oxidant effects depending on the environment. These data would suggest that at the higher concentrations 3-HAA is acting predominantly as a pro-oxidant molecule accelerating age-related bone loss. Oxford University Press 2021-12-17 /pmc/articles/PMC8680843/ http://dx.doi.org/10.1093/geroni/igab046.2547 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Isales, Carlos
Ding, Ke-Hong
Bollag, Wendy
McGee-Lawrence, Meghan
Hill, William
Shi, Xing-ming
Fulzele, Sadanand
Hamrick, Mark
3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss
title 3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss
title_full 3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss
title_fullStr 3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss
title_full_unstemmed 3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss
title_short 3-Hydroxyanthranilic acid Administration Did Not Prevent Age Related Bone Loss
title_sort 3-hydroxyanthranilic acid administration did not prevent age related bone loss
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680843/
http://dx.doi.org/10.1093/geroni/igab046.2547
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