Literature DB >> 29661284

Pyruvate in reduced osmolarity oral rehydration salt corrected lactic acidosis in sever scald rats.

Rui Liu1, Shu-Ming Wang2, Zong-Yu Li3, Wen Yu4, Hui-Ping Zhang5, Fang-Qiang Zhou6.   

Abstract

BACKGROUND: A novel pyruvate-based oral rehydration salt (Pyr-ORS) was demonstrated of superiority over bicarbonate- or citrate-based one to preserve organ function and correct lactic acidosis in rehydration of lethal shock in animals. This study further compared these effects between low-osmolar Pyr-ORS and equimolar citrate-based counterpart.
METHODS: Eighty rats, using a fatal burn shock model, were randomized into four groups (two subgroups per group: n = 10): the sham group (group SR), Pyr-ORS group (group PR), WHO-ORS III group (group CR), and no rehydration group. ORS was delivered by manual gavage during 24 h following burns. Oral administration consisted of half of counted volume in the initial 8 h plus the rest in the later 16 h. Systemic hemodynamics, visceral organ surface blood flow, organ function, and metabolic acidosis were determined at 8 h and 24 h after burn. Another set of rats with identical surgical procedures without tests was observed for survival.
RESULTS: Survival was markedly improved in the groups PR and CR; the former showed a higher survival rate than the latter at 24 h (40% versus 20%, P < 0.05). Systemic hemodynamics, visceral blood flow, and function of heart, liver, and kidney were greatly restored in group PR, compared with group CR (all P < 0.05). Hypoxic lactic acidosis was efficiently reversed in group PR, instead of group CR, (pH 7.36 versus 7.11, base excess 2.1 versus -9.1 mmol/L, lactate 4.28 versus 8.18 mmol/L; all P < 0.05) at 24 h after injury.
CONCLUSIONS: Pyruvate was advantageous over citrate in low-osmolar ORS for protection of organs and survival; pyruvate, but not citrate, in the ORS corrected hypoxic lactic acidosis in rats subjected to lethal burn shock in 24 h.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Burn; Lactic acidosis; Oral rehydration salt; Pyruvate; Shock

Mesh:

Substances:

Year:  2018        PMID: 29661284     DOI: 10.1016/j.jss.2018.01.018

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  4 in total

1.  Histone deacetylase inhibitor attenuates intestinal mucosal injury in fatally scalded rats.

Authors:  Rui Liu; Shu-Ming Wang; Si-Jia Guo; Ming-Ming Ma; Yi-Li Fu
Journal:  Ann Transl Med       Date:  2022-01

2.  Pyruvate as a Potential Beneficial Anion in Resuscitation Fluids.

Authors:  Fang-Qiang Zhou
Journal:  Front Med (Lausanne)       Date:  2022-07-12

3.  Pyruvate alleviates high glucose-induced endoplasmic reticulum stress and apoptosis in HK-2 cells.

Authors:  Xiao Meng Zhang; Yi Zhen Wang; Jin Dong Tong; Xu Chao Ning; Fang Qiang Zhou; Xiu Hong Yang; Hui Min Jin
Journal:  FEBS Open Bio       Date:  2020-04-10       Impact factor: 2.693

4.  Downregulation of miR-27b promotes skin wound healing in a rat model of scald burn by promoting fibroblast proliferation.

Authors:  Qingxia Bi; Jingyan Liu; Xueming Wang; Furong Sun
Journal:  Exp Ther Med       Date:  2020-09-04       Impact factor: 2.447

  4 in total

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