Literature DB >> 21909000

Prompt myocardial damage contributes to hepatic, renal, and intestinal injuries soon after a severe burn in rats.

Rong Xiao1, Ze-Yuan Lei, Yong-Ming Dang, Yue-Sheng Huang.   

Abstract

BACKGROUND: Ischemic/hypoxic myocardial damage and functional impairment of the myocardium occurs immediately after major burns. This experimental study investigated whether the prompt cardiac dysfunction initiates hepatic, renal, and intestinal injuries soon after a severe burn.
METHODS: Wistar rats were randomized to a sham burn group, a burn group (subjected to 30% total body surface area third-degree burn) that was subdivided into two groups: a simple burn group, observed at 0.5 hour, 1 hour, 3 hours, 6 hours, 12 hours, 24 hours postburn and a group medicated with propranolol (a cardiac inhibitor), cedilanid (a cardiotonic agent), enalaprilat (an angiotensin converting enzyme inhibitor), and cedilanid plus enalaprilat injected at 0.5 hour postburn and observed at 6 hours later. Serum cardiac troponin I, total bile acid, beta2-microglobulin concentrations, and diamine oxidase activity were measured to reflect the severity of cardiac, hepatic, renal, and intestinal injuries that were confirmed by histopathologic observations. Cardiac function and organs' blood flow were also recorded.
RESULTS: Histopathologic changes and serum cardiac troponin I increase occurred significantly earlier than the other organs, and the organ damage developments followed a similar pattern. Myocardial injury was significantly aggravated in rats treated with propranolol, with further decreases in myocardial function, blood flow to the liver, kidneys, and intestines significantly decreased, and injuries were aggravated. In contrast, these conditions were greatly improved in the rats treated with enalaprilat, cedilanid, or with both.
CONCLUSION: The prompt cardiac dysfunction has some initiating effects on ischemic/hypoxic injury to organs such as the liver, kidneys, and intestines soon after a severe burn.

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Year:  2011        PMID: 21909000     DOI: 10.1097/TA.0b013e31822175f6

Source DB:  PubMed          Journal:  J Trauma        ISSN: 0022-5282


  6 in total

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Review 2.  Alcohol Modulation of the Postburn Hepatic Response.

Authors:  Michael M Chen; Stewart R Carter; Brenda J Curtis; Eileen B O'Halloran; Richard L Gamelli; Elizabeth J Kovacs
Journal:  J Burn Care Res       Date:  2017 Jan/Feb       Impact factor: 1.845

3.  Myocardial autophagy after severe burn in rats.

Authors:  Rong Xiao; Miao Teng; Qiong Zhang; Xiao-hua Shi; Yue-sheng Huang
Journal:  PLoS One       Date:  2012-06-29       Impact factor: 3.240

Review 4.  Cardiovascular Dysfunction Following Burn Injury: What We Have Learned from Rat and Mouse Models.

Authors:  Ashley N Guillory; Robert P Clayton; David N Herndon; Celeste C Finnerty
Journal:  Int J Mol Sci       Date:  2016-01-02       Impact factor: 5.923

5.  Impairment of μ-calpain activation by rhTNFR:Fc reduces severe burn-induced membrane disruption in the heart.

Authors:  Meng-Shu Cao; Ting-Yan Zhao; Zhi-Long Song; Hong-Ting Lu; Yun Zheng; Xiao-Ming Gu; Tao Lu; Qiong Wang; Jing-Jun Zhou
Journal:  Cell Death Discov       Date:  2022-01-10

6.  A brief history of treatment of burn injury in China.

Authors:  Zhiyong Sheng
Journal:  Burns Trauma       Date:  2013-09-18
  6 in total

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