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老年小鼠在改良的外科脓毒症模型中表现出器官功能障碍以及长期炎症、免疫抑制和体重减轻。

Old Mice Demonstrate Organ Dysfunction as well as Prolonged Inflammation, Immunosuppression, and Weight Loss in a Modified Surgical Sepsis Model.

机构信息

Department of Surgery, University of Florida College of Medicine, Gainesville, FL.

Department of Biostatistics, University of Florida College of Medicine, Gainesville, FL.

出版信息

Crit Care Med. 2019 Nov;47(11):e919-e929. doi: 10.1097/CCM.0000000000003926.

Abstract

OBJECTIVES

Our goal was to "reverse translate" the human response to surgical sepsis into the mouse by modifying a widely adopted murine intra-abdominal sepsis model to engender a phenotype that conforms to current sepsis definitions and follows the most recent expert recommendations for animal preclinical sepsis research. Furthermore, we aimed to create a model that allows the study of aging on the long-term host response to sepsis.

DESIGN

Experimental study.

SETTING

Research laboratory.

SUBJECTS

Young (3-5 mo) and old (18-22 mo) C57BL/6j mice.

INTERVENTIONS

Mice received no intervention or were subjected to polymicrobial sepsis with cecal ligation and puncture followed by fluid resuscitation, analgesia, and antibiotics. Subsets of mice received daily chronic stress after cecal ligation and puncture for 14 days. Additionally, modifications were made to ensure that "Minimum Quality Threshold in Pre-Clinical Sepsis Studies" recommendations were followed.

MEASUREMENTS AND MAIN RESULTS

Old mice exhibited increased mortality following both cecal ligation and puncture and cecal ligation and puncture + daily chronic stress when compared with young mice. Old mice developed marked hepatic and/or renal dysfunction, supported by elevations in plasma aspartate aminotransferase, blood urea nitrogen, and creatinine, 8 and 24 hours following cecal ligation and puncture. Similar to human sepsis, old mice demonstrated low-grade systemic inflammation 14 days after cecal ligation and puncture + daily chronic stress and evidence of immunosuppression, as determined by increased serum concentrations of multiple pro- and anti-inflammatory cytokines and chemokines when compared with young septic mice. In addition, old mice demonstrated expansion of myeloid-derived suppressor cell populations and sustained weight loss following cecal ligation and puncture + daily chronic stress, again similar to the human condition.

CONCLUSIONS

The results indicate that this murine cecal ligation and puncture + daily chronic stress model of surgical sepsis in old mice adhered to current Minimum Quality Threshold in Pre-Clinical Sepsis Studies guidelines and met Sepsis-3 criteria. In addition, it effectively created a state of persistent inflammation, immunosuppression, and weight loss, thought to be a key aspect of chronic sepsis pathobiology and increasingly more prevalent after human sepsis.

摘要

目的

通过修改一种广泛应用的腹腔内脓毒症小鼠模型,将人类对手术性脓毒症的反应“反向翻译”为小鼠,使其表现型符合当前脓毒症定义,并遵循最近有关动物临床前脓毒症研究的专家建议。此外,我们旨在创建一种模型,以研究衰老对脓毒症宿主长期反应的影响。

设计

实验研究。

设置

研究实验室。

对象

年轻(3-5 个月)和年老(18-22 个月)C57BL/6j 小鼠。

干预措施

小鼠未接受干预,或接受盲肠结扎和穿刺引起的多微生物脓毒症,随后进行液体复苏、镇痛和抗生素治疗。盲肠结扎和穿刺后,亚组小鼠接受每日慢性应激 14 天。此外,对模型进行了修改,以确保遵循“临床前脓毒症研究的最低质量阈值”建议。

测量和主要结果

与年轻小鼠相比,年老小鼠在盲肠结扎和穿刺以及盲肠结扎和穿刺+每日慢性应激后死亡率增加。年老小鼠在盲肠结扎和穿刺后 8 小时和 24 小时出现明显的肝肾功能障碍,血浆天冬氨酸转氨酶、血尿素氮和肌酐升高支持这一结果。与人类脓毒症类似,年老小鼠在盲肠结扎和穿刺+每日慢性应激后 14 天出现低水平全身性炎症,并出现免疫抑制,表现为与年轻脓毒症小鼠相比,多种促炎和抗炎细胞因子和趋化因子的血清浓度升高。此外,年老小鼠在盲肠结扎和穿刺+每日慢性应激后表现出髓系来源抑制细胞群体的扩张和持续体重减轻,这与人类情况相似。

结论

结果表明,这种老年小鼠盲肠结扎和穿刺+每日慢性应激手术性脓毒症模型符合当前临床前脓毒症研究最低质量阈值指南,并符合 Sepsis-3 标准。此外,它有效地创建了一种持续炎症、免疫抑制和体重减轻的状态,这被认为是慢性脓毒症病理生物学的一个关键方面,并且在人类脓毒症后越来越普遍。

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