PMID- 21958002 OWN - NLM STAT- MEDLINE DCOM- 20120223 LR - 20111021 IS - 1557-8577 (Electronic) IS - 1549-1684 (Linking) VI - 14 IP - 5 DP - 2011 Oct TI - Effect of growth hormone treatment on pancreatic inflammation, oxidative stress, and apoptosis related to aging in SAMP8 mice. PG - 501-12 LID - 10.1089/rej.2011.1166 [doi] AB - Aging 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-alpha [TNF-alpha], interleukin-beta [IL-beta], 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-kappaB (NF-kappaB p65 and NF-kappaBp50-105. However, the protein expression of NF-kappaB p52-100 and inhibitor kappa B (IkappaB) alpha was increased with age in the pancreas of SAMP8 mice. On the other hand, the expression of IkappaB 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. FAU - Cuesta, Sara AU - Cuesta S AD - Department Physiology, Medical School, University Complutense of Madrid Medical School, University Complutense of Madrid, Madrid, Spain. FAU - Kireev, Roman AU - Kireev R FAU - Garcia, Cruz AU - Garcia C FAU - Forman, Katherine AU - Forman K FAU - Vara, Elena AU - Vara E FAU - Tresguerres, Jesus A F AU - Tresguerres JA LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110929 PL - United States TA - Rejuvenation Res JT - Rejuvenation research JID - 101213381 RN - 0 (I-kappa B Proteins) RN - 0 (Interleukin-1beta) RN - 0 (NF-kappa B) RN - 0 (RNA, Messenger) RN - 0 (X-Linked Inhibitor of Apoptosis Protein) RN - 0 (bcl-Associated Death Protein) RN - 0 (bcl-X Protein) RN - 12629-01-5 (Human Growth Hormone) RN - EC 1.14.13.39 (Nitric Oxide Synthase Type II) SB - IM MH - Aging/*drug effects/pathology MH - Animals MH - Apoptosis/*drug effects MH - Gene Expression Regulation/drug effects MH - Human Growth Hormone/administration & dosage/*pharmacology MH - I-kappa B Proteins/metabolism MH - Inflammation/genetics/*pathology MH - Interleukin-1beta/genetics/metabolism MH - Male MH - Mice MH - Mice, Mutant Strains MH - NF-kappa B/metabolism MH - Nitric Oxide Synthase Type II/genetics/metabolism MH - Oxidative Stress/*drug effects MH - Pancreas/drug effects/metabolism/*pathology MH - RNA, Messenger/genetics/metabolism MH - X-Linked Inhibitor of Apoptosis Protein/genetics/metabolism MH - bcl-Associated Death Protein/genetics/metabolism MH - bcl-X Protein/genetics/metabolism EDAT- 2011/10/01 06:00 MHDA- 2012/02/24 06:00 CRDT- 2011/10/01 06:00 PHST- 2011/10/01 06:00 [entrez] PHST- 2011/10/01 06:00 [pubmed] PHST- 2012/02/24 06:00 [medline] AID - 10.1089/rej.2011.1166 [doi] PST - ppublish SO - Rejuvenation Res. 2011 Oct;14(5):501-12. doi: 10.1089/rej.2011.1166. Epub 2011 Sep 29.