Department of Physiology, Medical School, University Complutense of Madrid, Avda. Complutense s/n, Madrid, Spain.
J Gerontol A Biol Sci Med Sci. 2011 Aug;66(8):823-34. doi: 10.1093/gerona/glr083. Epub 2011 Jun 10.
The effect of a chronic combined treatment with growth hormone (GH) plus melatonin (Mel) on different age-related processes in cytosolic and nuclear fractions of hearts from SAMP8 mice (2 and 10 months) has been investigated. The parameters studied have been messenger RNA expressions of IL-1, IL-10, NFkBp50, NFkBp52, TNFα, eNOS, iNOS, HO-1, HO-2, BAD, BAX, and Bcl2 and protein expressions of iNOS, eNOS, TNFα, IL-1, IL-10, NFkBp50, NFKbp52, and caspase activity (3 and 9). Our results supported the existence of a proapoptotic and oxidative status together with inflammatory processes in the heart of old mice, with increases of inflammatory cytokines, caspase activity, HO-1, BAX, NFkBp50, and NFkBp52 and decreases of eNOS and Bcl2. Also, we were able to observe the translocation of NFkB to nuclei. The combined treatment was able to partially reduce the incidence of these deleterious changes, showing differences with the separated treatments with GH and Mel as were investigated in previous articles from our group.
我们研究了生长激素(GH)和褪黑素(Mel)联合治疗对 SAMP8 小鼠(2 个月和 10 个月)心肌胞质和核部分不同年龄相关过程的影响。研究的参数包括白细胞介素-1(IL-1)、白细胞介素-10(IL-10)、核因子 kappa B 抑制蛋白 p50(NFkBp50)、核因子 kappa B 抑制蛋白 p52(NFkBp52)、肿瘤坏死因子-α(TNFα)、内皮型一氧化氮合酶(eNOS)、诱导型一氧化氮合酶(iNOS)、血红素加氧酶-1(HO-1)、血红素加氧酶-2(HO-2)、BAD、BAX 和 Bcl2 的信使 RNA 表达以及 iNOS、eNOS、TNFα、IL-1、IL-10、NFkBp50、NFKbp52 和 caspase 活性(3 和 9)的蛋白表达。我们的结果支持在老年小鼠心脏中存在促凋亡和氧化状态以及炎症过程,炎症细胞因子、caspase 活性、HO-1、BAX、NFkBp50 和 NFkBp52 增加,eNOS 和 Bcl2 减少。此外,我们还观察到 NFkB 向核内的易位。联合治疗能够部分减轻这些有害变化的发生,与我们之前小组研究的单独使用 GH 和 Mel 治疗的差异。