Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Human responses to bacterial endotoxin

R Burrell1

  • 1Department of Microbiology and Immunology, West Virginia University Health Sciences Center, Morgantown 26506-9177.

Circulatory Shock
|July 1, 1994
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Molecular typing of enteroviruses: comparing 5'UTR, VP1 and whole genome sequencing methods.

Pathology·2022
Same author

Studies to further investigate the inhibition of human liver microsomal CYP2C8 by the acyl-β-glucuronide of gemfibrozil.

Drug metabolism and disposition: the biological fate of chemicals·2011
Same author

Use of effluent water in sewage treatment plants.

Sewage works journal·2010
Same author

A matched-pair, randomized study evaluating the efficacy and safety of Acticoat silver-coated dressing for the treatment of burn wounds.

The Journal of burn care & rehabilitation·1998
Same author

Pre-emptive epidural analgesia may prevent phantom limb pain.

Regional anesthesia·1995
Same author

Human immune toxicity.

Molecular aspects of medicine·1993
Same journal

Study of septic shock in the non-human primate: relationship of pathophysiological response to therapy with anti-TNF antibody.

Circulatory shock·1994
Same journal

Pentoxifylline inhibits mediator synthesis in an equine in vitro whole blood model of endotoxemia.

Circulatory shock·1994
Same journal

Endocrine and carbohydrate responses to interleukin-6 in vivo.

Circulatory shock·1994
Same journal

Endothelin-1 causes accumulation of leukocytes in the pulmonary circulation.

Circulatory shock·1994
Same journal

Functional requirement of the two TNF receptors for induction of apoptosis in PC60 cells and the role of mitochondria in TNF-induced cytotoxicity.

Circulatory shock·1994
Same journal

Beneficial effects of the phosphodiesterase inhibitors BRL 61063, pentoxifylline, and rolipram in a murine model of endotoxin shock.

Circulatory shock·1994
See all related articles

This review summarizes human responses to bacterial endotoxin (lipopolysaccharide). It details cardiovascular, pulmonary, metabolic, and inflammatory effects, aiding understanding of endotoxin-induced diseases.

Area of Science:

  • Microbiology
  • Immunology
  • Toxicology

Background:

  • Bacterial endotoxins, specifically lipopolysaccharides (LPS), are potent inflammatory substances found in Gram-negative bacteria.
  • Exposure to LPS can occur through various routes, leading to significant physiological responses in humans.
  • Understanding these responses is crucial for managing infections and inflammatory conditions.

Purpose of the Study:

  • To critically review and summarize existing literature on human responses to bacterial endotoxin (LPS).
  • To consolidate information on the physiological effects of defined LPS doses administered to healthy human subjects.
  • To provide a basis for understanding the pathophysiology of diseases caused by LPS.

Main Methods:

  • Systematic literature review focusing on studies involving human subjects.

Related Experiment Videos

  • Inclusion criteria: studies administering defined doses of intravenous or aerosolized LPS to healthy individuals.
  • Emphasis on analyzing cardiovascular, pulmonary, metabolic, and inflammatory parameters.
  • Main Results:

    • Summarizes documented human physiological responses to controlled LPS exposure.
    • Highlights effects on cardiovascular (e.g., blood pressure, heart rate), pulmonary (e.g., lung function), metabolic (e.g., glucose metabolism), and inflammatory markers (e.g., cytokine levels).
    • Identifies dose-dependent and route-dependent variations in responses.

    Conclusions:

    • Human exposure to bacterial endotoxin elicits complex and measurable physiological responses.
    • The reviewed data enhances understanding of LPS-mediated pathophysiology in clinical settings.
    • This summary serves as a valuable resource for researchers and clinicians dealing with endotoxin-related conditions.