Literature DB >> 27190249

Gradually increased oxygen administration promoted survival after hemorrhagic shock.

Xin Luo1, Gan Chen1, Guoxing You1, Bo Wang1, Mingzi Lu1, Jingxiang Zhao1, Ying Wang1, Yujing Yin2, Lian Zhao1, Hong Zhou1.   

Abstract

Gradually increased oxygen administration (GIOA) seems promising in hemorrhagic shock. However, the effects of GIOA on survival remain unclear, and details of GIOA are to be identified. After the induction of hemorrhagic shock, the rats were randomized into five groups (n = 9): normoxic group (Normo), hyperoxic group (Hypero), normoxic to hyperoxic group (GIOA1), long-time hypoxemic to hyperoxic group (GIOA2), and short-time hypoxemic to hyperoxic group (GIOA3). Survival was recorded for 96 h, plasma alanine transaminase, oxidative stress, hemodynamics, and blood gas were measured. The mean survival time of the GIOA3 was significantly longer than that of the Normo, Hypero, and GIOA2. Plasma alanine transaminase levels were significantly lower in the Normo, GIOA1, and GIOA3 compared to the Hypero and GIOA2 at 2 h post-resuscitation (PR). Plasma 3-nitrotyrosine levels at 2 h PR were significantly lower in the GIOA2 and GIOA3 compared to the Normo and Hypero. Central venous oxygen saturation at 2 h PR in the GIOA3 was significantly higher than the Normo; however, no significant difference was observed between GIOA1 and Normo. Besides, at 2 h PR, mean arterial pressure in the GIOA3 was significantly higher than the GIOA2; however, no significant difference was observed between GIOA1 and GIOA2. (1) GIOA could significantly prolong survival time compared to normoxemic resuscitation and hyperoxic resuscitation; (2) early moments of GIOA are critical to the benefits; and (3) hypoxemia at onset of resuscitation may be imperative, more works are needed to determine the optimal initial oxygen concentration of GIOA.
© 2016 by the Society for Experimental Biology and Medicine.

Entities:  

Keywords:  Hemorrhagic shock; gradual treatment; hyperoxic; hypoxemic; normoxic; resuscitation

Mesh:

Substances:

Year:  2016        PMID: 27190249      PMCID: PMC4994905          DOI: 10.1177/1535370216644996

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


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