Advertisement

A Heat-Shock Protein Co-Inducer Treatment Improves Behavioral Performance in Rats Exposed to Hypoxia

Conference paper
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 701)

Abstract

We investigated the effect of a heat-shock protein co-inducer, arimoclomol (CytRx, LA, CA), on hypoxia-adaptive responses using a ratmodel of simulated altitude exposure (hypobaric hypoxia).Cognitive functionwasmeasured using a T-maze and an object recognition test.Motor functionwasmeasured using an inclined-screen test and an adhesion removal test. Immunohistochemical analyses were assessed in brain for heat-shock protein 70 (HSP 70), intercellular adhesion molecule 1 (ICAM- 1) and apoptosis (TUNEL staining). Results show that both cognitive and motor performanceswere improved in rats treated with arimoclomol during hypoxic exposure; the hypoxia-induced expression of HSP70 and ICAM-1, and TUNEL-positive cells were reduced in brainwith the treatment.Our data suggest that the arimoclomol treatment reduces the hypoxia-induced stress in brain tissue, and also improves the behavioral performance in rats during hypoxic adaptation.

Keywords

TUNEL Staining Hypobaric Hypoxia Hypoxic Exposure Object Recognition Test Sticky Tape 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Sorensen JG, Norry FM, Scannapieco AC, and Loeschcke V (2005) Altitudinal variation for stress resistance traits and thermal adaptation in adult Drosophila buzzatii from the NewWorld.J Evol Biol 18(4): 829-837Google Scholar
  2. 2.
    Zhong N, Zhang Y, Fang QZ, and Zhou ZN (2000) Intermittent hypoxia exposure-induced heatshock protein 70 expression increases resistance of rat heart to ischemic injury. Acta Pharmacol Sin 21(5), 467-472PubMedGoogle Scholar
  3. 3.
    Murphy J, Song D,Welsh FA, Wilson DF, and Pastuszko A (1999) Regional expression of heat shock protein 72 mRNA following mild and severe hypoxia in neonatal piglet brain. Adv Exp Med Biol 471: 155-163PubMedCrossRefGoogle Scholar
  4. 4.
    Soti C, Nagy E, Giricz Z, Vigh L, Csermely P, and Ferdinandy P (2005) Heat shock proteins as emerging therapeutic targets. Br J Pharmacol 146(6):769-780.PubMedCrossRefGoogle Scholar
  5. 5.
    Snoeckx H, Cornelussen RN, van Nieuwenhoven FA, Reneman RS, and Van Der Vusse GJ (2001) Heat shock proteins and cardiovascular pathophysiology. Physiol Rev 81(4), 1461-1497PubMedGoogle Scholar
  6. 6.
    Xu K, Puchowicz MA, and LaManna JC (2004) Renormalization of regional brain blood flow during prolonged mild hypoxic exposure in rats. Brain Res 1027 (1-2):188-191PubMedCrossRefGoogle Scholar
  7. 7.
    Pichiule P and LaManna JC (2002) Angiopoietin-2 and rat brain capillary remodeling during adaptation and deadaptation to prolonged mild hypoxia. J Appl Physiol 93 (3):1131-1139PubMedGoogle Scholar
  8. 8.
    Puchowicz MA, Xu K, Sun X, Ivy A, Emancipator D, and LaManna JC (2007) Diet-induced ketosis increases capillary density without altered blood flow in rat brain. AmJ Physiol Endocrinol Metab 292 (6):E1607-E1615CrossRefGoogle Scholar
  9. 9.
    Dore-Duffy P, Balabanov R, Beaumont T, Hritz MA, Harik SI, and LaManna JC (1988) Endothelial activation following prolonged hypobaric hypoxia. Microvasc Res 57 (2):75-85CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  1. 1.Departments of Physiology and BiophysicsCase Western Reserve UniversityClevelandUSA
  2. 2.Department of AnatomyCase Western Reserve UniversityClevelandUSA
  3. 3.Johns Hopkins University Applied Physics LaboratoryLaurelUSA

Personalised recommendations