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Effect of growth hormone treatment on pancreatic inflammation, oxidative stress, and apoptosis related to aging in SAMP8 mice

dc.contributor.authorCuesta Sancho, Sara
dc.contributor.authorKireev, Roman
dc.contributor.authorGarcía Martín, M. Cruz
dc.contributor.authorForman, Katherine
dc.contributor.authorVara Ameigeiras, Elena María
dc.contributor.authorFernández-Tresguerres Hernández, Jesús Ángel
dc.date.accessioned2024-02-07T11:39:16Z
dc.date.available2024-02-07T11:39:16Z
dc.date.issued2011-10-20
dc.description.abstractAging is associated with an increase in inflammation, oxidative stress, and apoptosis. Furthermore, aging is accompanied by an alteration of the growth hormone (GH) -insulin-like growth factor-1 (IGF-1) axis. The aim of this study was to examine the regulation of these parameters in the pancreas of old mice and how GH treatment could affect this process. Male senescence-accelerated prone mice (SAMP8) and male senescence-accelerated resistant mice (SAMR1) 2 (young) and 10 months old were used (n = 40). Animals were divided into five experimental groups: 1 and 2, SAMP8/R1 young control; 3 and 4, SAMP8/R1 old control (untreated); and 5, SAMP8 old treated with GH. Physiologically equivalent doses of GH were administered for 1 month (2 mg subcutaneously [s.c.]/kg/day) and several parameters were analyzed. Aging was associated with increased inflammation, oxidative stress, and apoptosis (increased tumor necrosis factor-α [TNF-α], interleukin-β [IL-β], IL-6, monocyte chemoattractant protein-1 [MCP1], IL-2, heme oxygenase [HO-1], inducible nitric oxide synthase [iNOS], and nitric oxide metabolites [NOx]). The ratio of anti/pro apoptotic mRNA expression-B cell lymphoma 2 (Bcl-2) Bcl-2-associated X protein (BAX) + Bcl-xL/Bcl-2-associated death promoter (BAD)-was decreased during aging in SAMP8 mice. X-inhibitor of apoptosis (XIAP) was decreased during the aging process. Furthermore, no changes were observed in protein expression of nuclear factor-κB (NF-κB p65 and NF-κBp50-105. However, the protein expression of NF-κB p52-100 and inhibitor kappa B (IκB) alpha was increased with age in the pancreas of SAMP8 mice. On the other hand, the expression of IκB beta was decreased with aging. These results indicate that aging is associated with significant alterations in the relative expression of pancreatic genes involved in inflammation, oxidative stress, and apoptosis. According to our results, GH administration to old SAMP8 mice was able to improve pancreas from this parameters.
dc.description.departmentDepto. de Fisiología
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipJunta de Andalucía
dc.description.statuspub
dc.identifier.citationSara Cuesta, Roman Kireev, Cruz García, Katherine Forman, Elena Vara, and Jesús A.F. Tresguerres. Effect of Growth Hormone Treatment on Pancreatic Inflammation, Oxidative Stress, and Apoptosis Related to Aging in SAMP8 Mice. Rejuvenation Research.Oct 2011.501-512.http://doi.org/10.1089/rej.2011.1166
dc.identifier.doi10.1089/rej.2011.1166
dc.identifier.issn1557-8577
dc.identifier.officialurlhttps://www.liebertpub.com/doi/10.1089/rej.2011.1166?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/21958002/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/99912
dc.issue.number5
dc.journal.titleRejuvenation Research
dc.language.isoeng
dc.page.final512
dc.page.initial501
dc.publisherMary Ann Liebert
dc.relation.projectIDRETICEF RD06/0013
dc.relation.projectIDRD06/0013/0008
dc.relation.projectIDP07-CTS-03135
dc.relation.projectIDPI081644
dc.relation.projectIDAF 2007 66878-C02-01
dc.rights.accessRightsrestricted access
dc.subject.cdu577.334
dc.subject.cdu612
dc.subject.cdu616.37-002
dc.subject.keywordoxidative stress
dc.subject.ucmFisiología
dc.subject.unesco2401.13 Fisiología Animal
dc.titleEffect of growth hormone treatment on pancreatic inflammation, oxidative stress, and apoptosis related to aging in SAMP8 mice
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number14
dspace.entity.typePublication
relation.isAuthorOfPublication0d603462-8bef-4318-8649-c22d87d22059
relation.isAuthorOfPublication930cde02-596a-4969-9a07-ea88da7c5aa0
relation.isAuthorOfPublication9a0743f9-114a-4742-97ef-87ebacb5d9c4
relation.isAuthorOfPublication.latestForDiscovery0d603462-8bef-4318-8649-c22d87d22059

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