Abstract:Stroke is a severe neurological disorder in humans that results from an interruption of the blood supply to the brain. Worldwide, stoke affects over 100 million people each year and is the second largest contributor to disability. Dyslipidemia is a modifiable risk factor for stroke that is associated with an increased risk of the disease. Traditional and non-traditional lipid measures are proposed as biomarkers for the better detection of subclinical disease. In the central nervous system, lipids and lipid med… Show more
“…Between the two subtypes of ischemic ABI models, PM and TM, these ischemic injuries harbored few differences in their transcriptomic signatures. However, we found that lipidomics of PM and TM revealed variations between them during the first 72H after injury, showing that lipid metabolism is sensitive to ischemia, which is consistent with the previous investigation 48 .…”
In response to acute brain injury (ABI) threats, neuroimmune cells rapidly transition from a quiescent into an activated state, but the dynamic molecular alterations are partially understood. Here, we integrated the dynamics of multi-omics datasets in four ABI mice models. Transcriptomics revealed diversification of thermogenesis, synaptic, and neuroinflammatory genes for ABI at the early phase (12H). Transcriptomics and proteomics combined analysis singled out 15 co-variation risk genes for ABIs. Besides, lipid metabolite alteration reflected a discrepancy between permanent ischemic brain injuries and transient ischemic brain injuries at the middle phase (24H). Together, our data elucidate a potential therapeutic resource for ABIs.
“…Between the two subtypes of ischemic ABI models, PM and TM, these ischemic injuries harbored few differences in their transcriptomic signatures. However, we found that lipidomics of PM and TM revealed variations between them during the first 72H after injury, showing that lipid metabolism is sensitive to ischemia, which is consistent with the previous investigation 48 .…”
In response to acute brain injury (ABI) threats, neuroimmune cells rapidly transition from a quiescent into an activated state, but the dynamic molecular alterations are partially understood. Here, we integrated the dynamics of multi-omics datasets in four ABI mice models. Transcriptomics revealed diversification of thermogenesis, synaptic, and neuroinflammatory genes for ABI at the early phase (12H). Transcriptomics and proteomics combined analysis singled out 15 co-variation risk genes for ABIs. Besides, lipid metabolite alteration reflected a discrepancy between permanent ischemic brain injuries and transient ischemic brain injuries at the middle phase (24H). Together, our data elucidate a potential therapeutic resource for ABIs.
“…As already mentioned above, lipids not only serve as structural components, but also exert crucial biological roles as signaling molecules. This aspect is extensively discussed in the review article proposed by Kloska and collaborators, who focused their attention on the role of lipid mediators in the risk and pathology of ischemic stroke [18]. Notably, a lively metabolism of polyunsaturated fatty acid has been documented in ischemic brain, and different lipid mediators are implicated in the neuroprotective or neurodegenerative effects occurring in the post-stroke brain tissue.…”
Although initially regarded as a passive system to store energy, lipids are now considered to play crucial, structural and functional roles in almost all the biological processes involved in the regulation of physiological and pathological conditions [...]
“…Mechanisms underlying neuroprotection and lung protection reported include interfering with vascular resistance, vasopermeability change, anti-oxidation, and anti-inflammation. 55,56 However, we consider that improvement of hemodynamics plays the major role in reservation of neurological and pulmonary function due to their consistency of trends.…”
The goal of the study was to investigate the efficacy of lipid supplement to epinephrine-based therapy in resuscitation of asphyxia-induced cardiac arrest in aged rats. Methods: The study included two parts: in experiment A, rats underwent asphyxial cardiac arrest and cardiopulmonary resuscitation, randomized to receive epinephrine and normal saline (control group, n=22), epinephrine and intralipid 20% (long-chain triglycerides (LCT) group, n=22) or epinephrine and lipovenoes 20% (LCT/medium-chain triglcerides (MCT) group, n=22). Return of spontaneous circulation, recurrence of asystole after resuscitation, hemodynamic metrics, arterial blood gas values, neurological assessment score and indexes of pulmonary transudation were recorded. In experiment B, rats using the same model and resuscitation protocol were randomly divided into 21 groups: Control 0 , Control 20 ,
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