HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Hydroxyethyl starch 130/0.4 prevents the early pulmonary inflammatory response and oxidative stress after hemorrhagic shock and resuscitation in rats.

AbstractBACKGROUND:
This study was designed to determine the effects of various resuscitation fluids on pulmonary capillary leakage and pulmonary edema after HS and fluid resuscitation (HS/R) and to determine whether an antiinflammatory or antioxidative mechanism was involved.
METHODS:
We induced HS by bleeding male Sprague-Dawley rats to a blood pressure of 30 to 40 mm Hg for 60 min. 60 min later, the rats were killed (HS group) or immediately resuscitated with L-isomer lactated Ringer's solution (HS+LR group), shed blood (HS+BL group), or hydroxyethyl starch (HS+HES group) to maintain the blood pressure to the original value during the 60-min resuscitation period. 3 h after resuscitation, pulmonary capillary leakage and wet/dry weight ratio, levels of tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, malondialdehyde (MDA), oxidized and reduced glutathione (GSH and GSSG), myeloperoxidase (MPO) activity, nuclear factor (NF)-kappaB, activator protein (AP)-1 activation, and lung microscopic and ultrastructural histological changes were measured.
RESULTS:
HES and BL treatment significantly improved pulmonary capillary leakage, wet/dry weight ratio and lung injuries after HS/R. In addition, both HES and BL could attenuate the increase in TNF-alpha, IL-6, MPO levels and NF-kappaB activation. However, HES but not BL could attenuate the increase in MDA level and GSSH/GSH ratio and AP-1 activation.
CONCLUSIONS:
HES might attenuate pulmonary injuries by modulating pulmonary inflammatory response and oxidative stress, whereas BL attenuates pulmonary injuries by modulating pulmonary inflammatory response but not oxidative stress.
AuthorsPengfei Wang, Yousheng Li, Jieshou Li
JournalInternational immunopharmacology (Int Immunopharmacol) Vol. 9 Issue 3 Pg. 347-53 (Mar 2009) ISSN: 1878-1705 [Electronic] Netherlands
PMID19166983 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Hydroxyethyl Starch Derivatives
  • Interleukin-6
  • NF-kappa B
  • Plasma Substitutes
  • Transcription Factor AP-1
  • Tumor Necrosis Factor-alpha
  • Malondialdehyde
  • Peroxidase
  • Glutathione
  • Glutathione Disulfide
Topics
  • Animals
  • Blood Pressure (drug effects, physiology)
  • Capillary Permeability (drug effects)
  • Disease Models, Animal
  • Glutathione (metabolism)
  • Glutathione Disulfide (metabolism)
  • Hydroxyethyl Starch Derivatives (therapeutic use)
  • Interleukin-6 (metabolism)
  • Male
  • Malondialdehyde (metabolism)
  • NF-kappa B (metabolism)
  • Oxidative Stress (drug effects)
  • Peroxidase (metabolism)
  • Plasma Substitutes (pharmacology)
  • Pneumonia (etiology, prevention & control)
  • Pulmonary Circulation (drug effects)
  • Rats
  • Rats, Sprague-Dawley
  • Resuscitation
  • Shock, Hemorrhagic (complications)
  • Transcription Factor AP-1 (metabolism)
  • Tumor Necrosis Factor-alpha (metabolism)

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: