ArticleShock (Augusta, Ga.)2015
Caffeine Improves Heart Rate Without Improving Sepsis Survival.
Article in Shock (Augusta, Ga.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed, 10 citations in OpenAlex.
- Caffeine and preterm infants: multiorgan effects and therapeutic creep: scope to optimise dose and timing.Pediatric research · 2026Review
- Caffeine-Induced Sleep Restriction Alters the Gut Microbiome and Fecal Metabolic Profiles in Mice.International journal of molecular sciences · 2022Article
- Hydrocortisone, Ascorbic Acid, and Thiamine (HAT) Therapy Decreases Oxidative Stress, Improves Cardiovascular Function, and Improves Survival in Murine Sepsis.Shock (Augusta, Ga.) · 2020Article
- Neurokinin-1 Receptor Deficiency Improves Survival in Murine Polymicrobial Sepsis Through Multiple Mechanisms in Aged Mice.Shock (Augusta, Ga.) · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
introductionCaffeine is consumed on a daily basis for its nervous system stimulant properties and is a global adenosine receptor antagonist. Because adenosine receptors have been found to play a major role in regulating the immune response to a septic insult, we investigated if caffeine consumption prior to a septic insult would alter immunological and physiological responses, as well as survival.
methodsTwo separate experimental designs were used, both using outbred female ICR mice. In the first experiment, mice were administered 20 mg/kg of caffeine (equal to 2-3 cups of coffee for a human) or normal saline intraperitoneally at the time of cecal ligation and puncture (CLP). Immunological parameters including cytokines and local cell recruitment were measured. In the second experiment, caffeine (10 mg/kg per hour) was delivered continuously for 24 h via a subcutaneous infusion pump placed the day prior to CLP, and hemodynamic parameters were examined. In both experiments, survival was followed for 5 days.
resultsA single dose of caffeine at the initiation of sepsis did not alter survival. This single dose of caffeine did significantly increase in plasma levels of the chemokine KC 6 h after the onset of sepsis compared with septic mice given normal saline. There were no changes in interleukin 6 (IL-6) or IL-10 levels in the caffeine groups. Peritoneal lavages performed 24 h after CLP showed no difference in the levels of IL-6, tumor necrosis factor, KC, macrophage inflammatory protein 1, IL-10, or the IL-1 receptor antagonist between caffeine- and normal saline-treated mice. In addition, the lavages yielded similar numbers of cells (4.1 × 10 vehicle vs. 6.9 × 10 caffeine) and bacterial colony-forming units (CFUs, 4.1 million CFUs vehicle vs. 2.8 million CFUs caffeine). In the infusion group, caffeine also did not alter survival. However, caffeine infusion did increase the heart rate prior to CLP and prevented the decline in heart rate after CLP.
conclusionCaffeine increased the heart rate in mice but does not impact cytokine responses or survival during the acute phase of a polymicrobial sepsis challenge. These data indicate that patients consuming caffeine will not be at risk for increased sepsis mortality.
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