Ramipril pretreatment worsened renal injury and survival despite a reduction in renal inflammation in experimentally induced sepsis in mice

被引:3
作者
Bondeva, Tzvetanka [1 ]
Schindler, Katrin [1 ,2 ]
Schindler, Claudia [1 ,3 ]
Wolf, Gunter [1 ]
机构
[1] Jena Univ Hosp, Dept Internal Med III, Klinikum 1, D-07740 Jena, Germany
[2] Jena Univ Hosp, Inst Human Genet, Jena, Germany
[3] Jena Univ Hosp, Dept Expt Surg, Jena, Germany
关键词
Ramipril; sepsis; AKI; HIFs; apoptosis; ANGIOTENSIN-II; EXPRESSION; PERFUSION; SYSTEM;
D O I
10.1177/1470320320923977
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Introduction: The angiotensin converting enzyme inhibitor ramipril is a standard antihypertensive therapy for many patients. Because angiotensin II may promote inflammation, we were interested in whether basal pretreatment with ramipril may modify renal function and inflammation as well as systemic outcome in experimentally induced sepsis in mice. Material and methods: Ramipril (10 mg/kg/day) pretreatment or placebo (NaCl) was given intraperitoneally for 5 days to C57BL6/J mice, followed by either sham operation or cecal ligation and puncture sepsis induction. Real-time polymerase chain reaction and immunological stains were used to evaluate renal gene and protein expression, respectively. Plasma creatinine, neutrophil-gelatinase associated lipocalin, and blood urea nitrogen were used as markers for renal function. A clinical severity score was determined. Results: Administration of ramipril before cecal ligation and puncture surgery was associated with reduced renal inflammation but did not improved renal function and structure and even worsened the clinical status of septic mice. Conclusions: The data suggest that the effects of ramipril pretreatment are complex. Additional studies including monitoring of hemodynamic parameters are necessary to elucidate the exact mechanism(s) of this observation. In addition, the timing of the ramipril administration could be of importance.
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页数:8
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共 20 条
[1]   MORG1+/- mice are protected from histological renal damage and inflammation in a murine model of endotoxemia [J].
Bondeva, Tzvetanka ;
Schindler, Claudia ;
Schindler, Katrin ;
Wolf, Gunter .
BMC NEPHROLOGY, 2018, 19
[2]   Angiotensin II in Septic Shock: Effects on Tissue Perfusion, Organ Function, and Mitochondrial Respiration in a Porcine Model of Fecal Peritonitis [J].
Correa, Thiago D. ;
Jeger, Victor ;
Pereira, Adriano Jose ;
Takala, Jukka ;
Djafarzadeh, Siamak ;
Jakob, Stephan M. .
CRITICAL CARE MEDICINE, 2014, 42 (08) :E550-E559
[3]   Antihypertensive agents acting on the renin-angiotensin system and the risk of sepsis [J].
Dial, Sandra ;
Nessim, Sharon J. ;
Kezouh, Abbas ;
Benisty, Jacques ;
Suissa, Samy .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2014, 78 (05) :1151-1158
[4]   Characteristics of Clinical Sepsis Reflected in a Reliable and Reproducible Rodent Sepsis Model [J].
Gonnert, Falk A. ;
Recknagel, Peter ;
Seidel, Madlen ;
Jbeily, Nayla ;
Dahlke, Katja ;
Bockmeyer, Clemens L. ;
Winning, Johannes ;
Osche, Wolfgang L. ;
Claus, Ralf A. ;
Bauer, Michael .
JOURNAL OF SURGICAL RESEARCH, 2011, 170 (01) :E123-E134
[5]   Antagonist of the Type-1 ANG II receptor prevents against LPS-induced septic shock in rats [J].
Hagiwara, Satoshi ;
Iwasaka, Hideo ;
Hidaka, Seigo ;
Hasegawa, Akira ;
Koga, Hironori ;
Noguchi, Takayuki .
INTENSIVE CARE MEDICINE, 2009, 35 (08) :1471-1478
[6]   Preadmission Antihypertensive Drug Use and Sepsis Outcome: Impact of Angiotensin-Converting Enzyme Inhibitors (ACEIs) and Angiotensin Receptor Blockers (ARBs) [J].
Hsieh, Ming-Shun ;
How, Chorng-Kuang ;
Hsieh, Vivian Chia-Rong ;
Chen, Pau-Chung .
SHOCK, 2020, 53 (04) :407-415
[7]   Effect of Antihypertensive Medications on Sepsis-Related Outcomes: A Population-Based Cohort Study [J].
Kim, Joohae ;
Kim, Young Ae ;
Hwangbo, Bin ;
Kim, Min Jeong ;
Cho, Hyunsoon ;
Hwangbo, Yul ;
Lee, Eun Sook .
CRITICAL CARE MEDICINE, 2019, 47 (05) :E386-E393
[8]   The angiotensin II receptor blocker candesartan improves survival and mesenteric perfusion in an acute porcine endotoxin model [J].
Laesser, M ;
Oi, Y ;
Ewert, S ;
Fändriks, L ;
Åneman, A .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 2004, 48 (02) :198-204
[9]   MiR-130a-5p prevents angiotensin II-induced podocyte apoptosis by modulating M-type phospholipase A2 receptor [J].
Liu, Dongwei ;
Liu, Fengxun ;
Wang, Xutong ;
Qiao, Yingjin ;
Pan, Shaokang ;
Yang, Yang ;
Hu, Yifang ;
Zhang, Yilin ;
Tian, Fei ;
Liu, Zhangsuo .
CELL CYCLE, 2018, 17 (21-22) :2484-2495
[10]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408