HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

In vivo stress preconditioning.

Abstract
The heat shock or stress protein response is a highly conserved defense mechanism. Activation of the stress protein response by mild hyperthermia or by pharmacological agents allows cells to withstand a subsequent metabolic insult that would otherwise be lethal, a phenomenon referred as "thermotolerance" or "preconditioning." Heat shock response is characterized by increased expression of stress proteins that provide cellular protection, e.g., via increased chaperoning activity in all organisms, from bacteria to animals and humans. Indeed, there is experimental evidence that overexpression of specific heat shock proteins or heat shock factors produce protective effects similar to those observed after stress preconditioning. The purpose of this review is first to discuss the methods used to induce in vivo thermotolerance with mild hyperthermia or pharmacological agents. Then, as an example of the organ protection provided by in vivo stress preconditioning, the second part of this paper will examine how the induction of thermotolerance modulates the lung inflammatory response associated with acute lung injury, thus providing broad organ and tissue protection against oxidative stress associated this syndrome.
AuthorsMelissa Pespeni, Maki Hodnett, Jean-Francois Pittet
JournalMethods (San Diego, Calif.) (Methods) Vol. 35 Issue 2 Pg. 158-64 (Feb 2005) ISSN: 1046-2023 [Print] United States
PMID15649842 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S., Review)
Chemical References
  • Antioxidants
  • HSP72 Heat-Shock Proteins
  • Heat-Shock Proteins
  • Molecular Chaperones
  • Pyrrolidines
  • Thiocarbamates
  • pyrrolidine dithiocarbamic acid
  • Nitric Oxide
Topics
  • Animal Experimentation
  • Animals
  • Animals, Laboratory
  • Antioxidants (pharmacology)
  • Blotting, Western
  • Electrophoresis, Polyacrylamide Gel
  • Fever
  • HSP72 Heat-Shock Proteins
  • Heat-Shock Proteins (biosynthesis, metabolism)
  • Hot Temperature
  • Humans
  • Inflammation
  • Lung (pathology)
  • Lung Injury
  • Mice
  • Molecular Chaperones (metabolism)
  • Nitric Oxide (metabolism)
  • Oxidative Stress
  • Pyrrolidines (chemistry)
  • Rats
  • Research Design
  • Stress, Physiological
  • Thiocarbamates (chemistry)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: