Sevoflurane alleviates lung injury and inflammatory response compared with propofol in a rat model of VV ECMO

医学 急性呼吸窘迫综合征 七氟醚 异丙酚 氧合指数 麻醉 体外膜肺氧合 充氧 内科学
作者
Rongzhi Zhang,Kerong Zhai,Jian Huang,Shilin Wei,Jianbao Yang,Yanchun Zhang,Xiangyang Wu,Yongnan Li,Bingren Gao
出处
期刊:Perfusion [SAGE Publishing]
卷期号:39 (1): 142-150 被引量:5
标识
DOI:10.1177/02676591221131217
摘要

Although venovenous extracorporeal membrane oxygenation (VV ECMO) is a reasonable salvage treatment for acute respiratory distress syndrome (ARDS), it requires sedating the patient. Sevoflurane and propofol have pulmonary protective and immunomodulatory properties. This study aimed to compare the effectiveness of sevoflurane and propofol on rats with induced ARDS undergoing VV ECMO.Fifteen sprague-dawley (SD) rats were randomly divided into three groups: Con group, sevoflurane (Sevo) group and propofol (Pro) group. Arterial blood gas tests were performed at time pointsT0 (baseline), T1 (the time to ARDS), and T2 (weaning from ECMO). Oxygenation index (PaO2/FiO2) was calculated, and lung edema assessed by determining the lung wet:dry ratio. The protein concentration in bronchial alveolar lavage fluid (BALF) was determined by using bicinchoninic acid assay. Haematoxylin and eosin staining was used to evaluate the lung pathological scores in each group. IL-1β and TNF-α were also measured in the BALF, serum and lung.Oxygenation index showed improvement in the Sevo group versus Pro group. The wet:dry ratio was reduced in the Sevo group compared with propofol-treated rats. Lung pathological scores were substantially lower in the Sevo group versus the Pro group. Protein concentrations in the BALF and levels of IL-1β and TNF-α in the Sevo group were substantially lower versus Pro group.This study demonstrates that compared with propofol, sevoflurane was more efficacious in improving oxygenation and decreasing inflammatory response in rat models with ARDS subject to VV ECMO treatment.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
zxzxzx完成签到,获得积分10
刚刚
哭泣青雪发布了新的文献求助10
刚刚
丘比特应助xxxx666g采纳,获得10
1秒前
watermelon发布了新的文献求助10
1秒前
xcchh完成签到,获得积分10
1秒前
沉舟完成签到 ,获得积分10
3秒前
千空应助七七采纳,获得10
3秒前
自然樱桃完成签到,获得积分10
3秒前
麦子完成签到,获得积分10
3秒前
lsy关注了科研通微信公众号
3秒前
4秒前
Axolotll发布了新的文献求助20
5秒前
5秒前
8秒前
虚心星星完成签到 ,获得积分20
8秒前
Ykn完成签到,获得积分10
8秒前
辛勤冰绿完成签到,获得积分10
9秒前
XZY完成签到,获得积分10
9秒前
李爱国应助小田儿采纳,获得10
9秒前
watermelon完成签到,获得积分10
10秒前
小李的李完成签到,获得积分10
11秒前
fangruofuyun完成签到,获得积分10
11秒前
科目三应助无奈的书琴采纳,获得10
11秒前
老唐老唐完成签到 ,获得积分10
13秒前
自觉的丹珍完成签到,获得积分10
13秒前
闪闪的金鱼完成签到 ,获得积分10
14秒前
14秒前
15秒前
大模型应助草莓大果汁采纳,获得10
16秒前
hjc完成签到 ,获得积分10
17秒前
科研通AI6.2应助Mortisssssssss采纳,获得10
17秒前
李明月完成签到,获得积分10
18秒前
123完成签到,获得积分10
18秒前
开朗的千雁完成签到 ,获得积分10
18秒前
19秒前
稳重墨镜发布了新的文献求助10
20秒前
21秒前
追寻澜完成签到 ,获得积分10
21秒前
Sxq完成签到,获得积分10
21秒前
22秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Modern Epidemiology, Fourth Edition 5000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Digital Twins of Advanced Materials Processing 2000
Propeller Design 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 化学工程 生物化学 物理 计算机科学 内科学 复合材料 催化作用 物理化学 光电子学 电极 冶金 细胞生物学 基因
热门帖子
关注 科研通微信公众号,转发送积分 6015269
求助须知:如何正确求助?哪些是违规求助? 7591856
关于积分的说明 16148330
捐赠科研通 5162928
什么是DOI,文献DOI怎么找? 2764236
邀请新用户注册赠送积分活动 1744789
关于科研通互助平台的介绍 1634673