败血症
医学
病理生理学
代谢综合征
生理盐水
一氧化氮
全身炎症反应综合征
结扎
内科学
免疫学
药理学
肥胖
胃肠病学
作者
Raquel Pires Nakama,Aparecida Donizette Malvezi,Maria Isabel Lovo‐Martins,Lucas Felipe dos Santos,Ana Paula Canizares Cardoso,Gustavo Scacco,Andressa Mendes Dionísio de Freitas,Marli Cardoso Martins‐Pinge,Phileno Pinge‐Filho
出处
期刊:Life Sciences
[Elsevier]
日期:2021-10-08
卷期号:286: 120033-120033
被引量:7
标识
DOI:10.1016/j.lfs.2021.120033
摘要
Sepsis is a potentially fatal systemic inflammatory response and its underlying pathophysiology is still poorly understood. Studies suggest that obesity, a component of metabolic syndrome (MS), is associated with sepsis survival. Therefore, this study focused on investigating the influence of MS on mortality and cardiovascular dysfunction induced by sublethal cecal ligation and puncture (SL-CLP).Newborn Swiss mice received monosodium glutamate (MSG) (4 mg kg-1 day-1, s.c.) during the first 5 d of life for MS induction, while the control pups received equimolar saline solution. On the 75th day, SL-CLP was used to induce mild sepsis (M-CLP) in the MS (MS-M-CLP) and control (SAL-M-CLP) mice. The effect of MS on sepsis in mice was assessed by determining the survival rate and quantification of nitric oxide (NO) in the plasma, and associating this data with hematological and cardiovascular parameters.MS improved the survival of septic mice, preventing impairment to hematological and cardiovascular parameters. In addition, MS attenuated plasmatic NO increase, which is a typical feature of sepsis.These findings provide new insights into the relationship between obesity and mild sepsis in mice, thus revealing an approach in favor of the "obesity paradox."
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