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1.
BMJ Open ; 14(6): e079212, 2024 Jun 10.
Article in English | MEDLINE | ID: mdl-38858161

ABSTRACT

INTRODUCTION: Severe septic cardiomyopathy (SCM) is one of the main causes of refractory septic shock (RSS), with a high mortality. The application of venoarterial extracorporeal membrane oxygenation (ECMO) to support the impaired cardiac function in patients with septic shock remains controversial. Moreover, no prospective studies have been taken to address whether venoarterial ECMO treatment could improve the outcome of patients with sepsis-induced cardiogenic shock. The objective of this study is to assess whether venoarterial ECMO treatment can improve the 30-day survival rate of patients with sepsis-induced refractory cardiogenic shock. METHODS AND ANALYSIS: ExtraCorporeal Membrane Oxygenation in the therapy for REfractory Septic shock with Cardiac function Under Estimated is a prospective, multicentre, non-randomised, cohort study on the application of ECMO in SCM. At least 64 patients with SCM and RSS will be enrolled in an estimated ratio of 1:1.5. Participants taking venoarterial ECMO during the period of study are referred to as cohort 1, and patients receiving only conventional therapy without ECMO belong to cohort 2. The primary outcome is survival in a 30-day follow-up period. Other end points include survival to intensive care unit (ICU) discharge, hospital survival, 6-month survival, quality of life for long-term survival (EQ-5D score), successful rate of ECMO weaning, long-term survivors' cardiac function, the number of days alive without continuous renal replacement therapy, mechanical ventilation and vasopressor, ICU and hospital length of stay, the rate of complications potentially related to ECMO treatment. ETHICS AND DISSEMINATION: The trial has been approved by the Clinical Research and Application Institutional Review Board of the Second Affiliated Hospital of Guangzhou Medical University (2020-hs-51). Participants will be screened and enrolled from ICU patients with septic shock by clinicians, with no public advertisement for recruitment. Results will be disseminated in research journals and through conference presentations. TRIAL REGISTRATION NUMBER: NCT05184296.


Subject(s)
Extracorporeal Membrane Oxygenation , Shock, Cardiogenic , Shock, Septic , Extracorporeal Membrane Oxygenation/methods , Humans , Shock, Septic/therapy , Shock, Septic/mortality , Shock, Septic/complications , Prospective Studies , Shock, Cardiogenic/therapy , Shock, Cardiogenic/mortality , Cardiomyopathies/therapy , Multicenter Studies as Topic , Male , Intensive Care Units , Female , Adult , Survival Rate
2.
Molecules ; 18(9): 10285-300, 2013 Aug 26.
Article in English | MEDLINE | ID: mdl-24064445

ABSTRACT

This study was conducted to investigate the effect of Nelumbinis Plumula total alkaloid (NPA) and its main alkaloid components on oxidative stress induced by tert-butyl hydroperoxide (t-BHP) in the human hepatocellular HepG2 cell line. According to HPLC analysis, several major alkaloid compounds such as liensinine, isoliensinine and neferine were present in NPA. The cytotoxic effects in 0.55 mM t-BHP-induced HepG2 cells were significantly inhibited by NPA and the major compound in NPA, neferine, showed the strongest activities. The protective effect of neferine against oxidative stress induced by t-BHP may be associated with decreased ROS formation, TBARS generation, LDH release and increased GSH levels, suggesting their involvement of the cytoprotective on oxidative stress. The effects were comparable with quercetin, which was used as positive control. Overall, total alkaloid and alkaloid compounds from Nelumbinis Plumula displayed a significant cytoprotective effect against oxidative stress. Further study is needed to elucidate the relationship between the chemical structures of the components in NPA and their protective effect on oxidative stress.


Subject(s)
Benzylisoquinolines/pharmacology , Free Radical Scavengers/pharmacology , Nelumbo/chemistry , Oxidative Stress , Plant Extracts/pharmacology , Alkaloids/chemistry , Alkaloids/pharmacology , Benzylisoquinolines/chemistry , Biphenyl Compounds/chemistry , Drug Evaluation, Preclinical , Free Radical Scavengers/chemistry , Free Radicals/chemistry , Glutathione , Hep G2 Cells , Humans , Isoquinolines/chemistry , Isoquinolines/pharmacology , L-Lactate Dehydrogenase/metabolism , Malondialdehyde/metabolism , Oxidants/toxicity , Phenols/chemistry , Phenols/pharmacology , Picrates/chemistry , Plant Extracts/chemistry , Reactive Oxygen Species/metabolism , Thiobarbituric Acid Reactive Substances/metabolism , tert-Butylhydroperoxide/toxicity
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