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Advanced Age Impairs Intestinal Antimicrobial Peptide Response and Worsens Fecal Microbiome Dysbiosis Following Burn Injury in Mice.高龄损伤肠道抗菌肽反应并加重烧伤小鼠粪便微生物失调
Shock. 2020 Jan;53(1):71-77. doi: 10.1097/SHK.0000000000001321.
2
Atg9a deficiency causes axon-specific lesions including neuronal circuit dysgenesis.Atg9a 缺乏导致轴突特异性病变,包括神经元回路发育不良。
Autophagy. 2018;14(5):764-777. doi: 10.1080/15548627.2017.1314897. Epub 2018 Mar 6.
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The past and present of serum aminotransferases and the future of liver injury biomarkers.血清转氨酶的过去与现在以及肝损伤生物标志物的未来
EXCLI J. 2016 Dec 15;15:817-828. doi: 10.17179/excli2016-800. eCollection 2016.
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Happily (n)ever after: Aging in the context of oxidative stress, proteostasis loss and cellular senescence.从此不再幸福:在氧化应激、蛋白质稳态丧失和细胞衰老背景下的衰老
Redox Biol. 2017 Apr;11:482-501. doi: 10.1016/j.redox.2016.12.001. Epub 2016 Dec 7.
5
Alcohol potentiates postburn remote organ damage through shifts in fluid compartments mediated by bradykinin.酒精通过缓激肽介导的体液分布变化增强烧伤后远隔器官损伤。
Shock. 2015 Jan;43(1):80-4. doi: 10.1097/SHK.0000000000000265.
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An alteration of the gut-liver axis drives pulmonary inflammation after intoxication and burn injury in mice.肠道-肝脏轴的改变可导致中毒和烧伤后小鼠肺部炎症。
Am J Physiol Gastrointest Liver Physiol. 2014 Oct 1;307(7):G711-8. doi: 10.1152/ajpgi.00185.2014. Epub 2014 Aug 7.
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Predicting mortality from burns: the need for age-group specific models.预测烧伤死亡率:对特定年龄组模型的需求。
Burns. 2014 Sep;40(6):1106-15. doi: 10.1016/j.burns.2014.03.010. Epub 2014 May 17.
8
Survival and cell mediated immunity after burn injury in aged mice.老年小鼠烧伤后的存活情况及细胞介导免疫
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Simvastatin protects hepatocytes from apoptosis by suppressing the TNF-α/caspase-3 signaling pathway in mice with burn injury.辛伐他汀通过抑制 TNF-α/caspase-3 信号通路保护烧伤小鼠肝细胞免于凋亡。
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高龄加剧烫伤烧伤小鼠模型的肝损伤。

Advanced age heightens hepatic damage in a murine model of scald burn injury.

机构信息

From the Division of G.I., Trauma, and Endocrine Surgery, (J.-P.I., D.M.B. S.K., T.W., R.H.M., E.J.K.), Division of Burn Research, Department of Surgery (D.M.B., T.W., R.H.M., E.J.K.), Department of Immunology and Microbiology (D.M.B., T.W., E.J.K.), Division of Alcohol Research, Department of Surgery (R.H.M., E.J.K.), University of Colorado, Aurora, Colorado.

出版信息

J Trauma Acute Care Surg. 2021 Apr 1;90(4):731-737. doi: 10.1097/TA.0000000000003048.

DOI:10.1097/TA.0000000000003048
PMID:33306599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7979479/
Abstract

BACKGROUND

Elderly burn patients exhibit a lower survival rate compared with younger counterparts. The liver is susceptible to damage after burn injury, which predisposes to poor outcomes. Lipid homeostasis and the antioxidant glutathione system play fundamental roles in preserving liver integrity. Herein, we explored changes in these major pathways associated with liver damage in the aging animals after burn injury.

METHODS

We compared liver enzymes, histology, lipid-peroxidation, and glutathione-metabolism profiles from young and aged female mice after a 15% total body surface area burn. Mice were euthanized at 24 hours after injury, and livers and serum were collected.

RESULTS

Aged burn animals exhibited elevated (p < 0.05) aspartate aminotransferase and alanine aminotransferase levels and increased inflammatory cell infiltration, edema, and necrosis compared with their younger counterparts. The percentage of adipophilin-stained area in livers from young sham, young burn, aged sham, and aged burn groups was 10%, 44%, 16%, and 78% (p < 0.05), respectively. Liver malondialdehyde levels were 1.4 ± 0.5 nmol/mg, 2.06 ± 0.2 nmol/mg, 1.81 ± 0.12 nmol/mg, and 3.45 ± 0.2 nmol/mg (p < 0.05) in young sham, young burn, aged sham, and aged burn mice, respectively. Oxidized glutathione (GSSG) content increased 50% in the young burn, and 88% in aged burn animals compared with the young sham group (p < 0.05). The reduced glutathione GSH/GSSG ratio was significantly reduced by 54% in aged burn mice compared with young sham animals (p < 0.05). Furthermore, glutathione peroxidase gene expression showed a 96% decrease in the aged burn group compared with young sham mice (p < 0.05).

CONCLUSION

Aged burn animals exhibit severe liver damage from heightened lipid peroxidation and inadequate antioxidative response. The increased peroxidation is associated with abundant lipid deposits in hepatic tissue postburn and a weak antioxidative response due to hepatic glutathione peroxidase downregulation. Further studies will focus on the functional significance of these findings concerning hepatic homeostasis.

摘要

背景

与年轻患者相比,老年烧伤患者的存活率较低。烧伤后肝脏容易受损,导致预后不良。脂质稳态和抗氧化谷胱甘肽系统在维持肝脏完整性方面发挥着重要作用。在此,我们探讨了这些与烧伤后老年动物肝脏损伤相关的主要途径的变化。

方法

我们比较了年轻和老年雌性小鼠在体表面积 15%烧伤后 24 小时的肝脏酶、组织学、脂质过氧化和谷胱甘肽代谢谱。在受伤后 24 小时处死小鼠,采集肝脏和血清。

结果

与年轻烧伤动物相比,老年烧伤动物的天门冬氨酸转氨酶和丙氨酸转氨酶水平升高(p < 0.05),炎症细胞浸润、水肿和坏死增加。年轻假手术、年轻烧伤、老年假手术和老年烧伤组肝脏中脂联素染色面积百分比分别为 10%、44%、16%和 78%(p < 0.05)。年轻假手术、年轻烧伤、老年假手术和老年烧伤组肝脏丙二醛水平分别为 1.4 ± 0.5 nmol/mg、2.06 ± 0.2 nmol/mg、1.81 ± 0.12 nmol/mg 和 3.45 ± 0.2 nmol/mg(p < 0.05)。与年轻假手术组相比,年轻烧伤组和老年烧伤组的氧化型谷胱甘肽(GSSG)含量分别增加了 50%和 88%(p < 0.05)。与年轻假手术动物相比,老年烧伤组的还原型谷胱甘肽 GSH/GSSG 比值降低了 54%(p < 0.05)。此外,与年轻假手术组相比,老年烧伤组的谷胱甘肽过氧化物酶基因表达降低了 96%(p < 0.05)。

结论

老年烧伤动物的肝脏损伤严重,脂质过氧化增加,抗氧化反应不足。增加的过氧化与肝组织中大量的脂质沉积以及肝谷胱甘肽过氧化物酶下调导致的抗氧化反应减弱有关。进一步的研究将集中于这些发现对肝脏稳态的功能意义。