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Pregled bibliografske jedinice broj: 989774

Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis*


Yang, Shaolong; Lim, Yow-Pin; Zhou, Mian; Salvemini, Philomena; Schwinn, Horst; Josic, Djuro; Koo, Douglas J.; Chaudry, Irshad H.; Wang, Ping
Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis* // Critical Care Medicine, 30 (2002), 3; 617-622 doi:10.1097/00003246-200203000-00021 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 989774 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis*

Autori
Yang, Shaolong ; Lim, Yow-Pin ; Zhou, Mian ; Salvemini, Philomena ; Schwinn, Horst ; Josic, Djuro ; Koo, Douglas J. ; Chaudry, Irshad H. ; Wang, Ping

Izvornik
Critical Care Medicine (0090-3493) 30 (2002), 3; 617-622

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
inter-α-inhibitors ; hemodynamic stability ; sepsis

Sažetak
The major forms of human inter-alpha-inhibitor proteins circulating in the plasma are inter-alpha-inhibitor (IalphaI, containing one light peptide chain called bikunin and two heavy chains) and pre-alpha-inhibitor (PalphaI, containing one light and one heavy chain). Although it has been reported that a decrease in IalphaI/PalphaI is correlated with an increased mortality rate in septic patients, it remains unknown whether administration of IalphaI/PalphaI early after the onset of sepsis has any beneficial effects on the cardiovascular response and outcome of the septic animal. The aim of this study, therefore, was to determine whether IalphaI and PalphaI have any salutary effects on the depressed cardiovascular function, liver damage, and mortality rate after polymicrobial sepsis. Prospective, controlled, randomized animal study. A university research laboratory. Male adult rats were subjected to polymicrobial sepsis by cecal ligation and puncture or sham operation followed by the administration of normal saline (i.e., resuscitation). At 1 hr after cecal ligation and puncture, human IalphaI/PalphaI at a dose of 30 mg/kg body weight or vehicle (normal saline, 1 mL/rat) were infused intravenously over a period of 30 mins. At 20 hrs after cecal ligation and puncture (i.e., the late, hypodynamic stage of sepsis), cardiac output was measured by using a dye dilution technique, and blood samples were collected for assessing oxygen content. Oxygen delivery, consumption, and extraction ratio were determined. Plasma concentrations of liver enzymes alanine aminotransferase and aspartate aminotransferase as well as lactate and tumor necrosis factor-alpha also were measured. In additional animals, the necrotic cecum was excised at 20 hrs after cecal ligation and puncture with or without IalphaI/PalphaI treatment, and survival was monitored for 10 days thereafter. The results indicate that administration of human IalphaI/PalphaI early after the onset of sepsis maintained cardiac output and systemic oxygen delivery, whereas it increased oxygen consumption and extraction at 20 hrs after cecal ligation and puncture. The elevated concentrations of alanine aminotransferase, aspartate aminotransferase, tumor necrosis factor-alpha, and lactate were attenuated by IalphaI/PalphaI treatment. In addition, administration of human IalphaI/PalphaI improved the survival rate from 30% to 89% in septic animals at day 10 after cecal ligation and puncture and cecal excision. Human IalphaI/PalphaI appears to be a useful agent for maintaining hemodynamic stability and improving survival during the progression of polymicrobial sepsis.

Izvorni jezik
Engleski

Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)



POVEZANOST RADA


Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju

Profili:

Avatar Url Đuro Josić (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

Yang, Shaolong; Lim, Yow-Pin; Zhou, Mian; Salvemini, Philomena; Schwinn, Horst; Josic, Djuro; Koo, Douglas J.; Chaudry, Irshad H.; Wang, Ping
Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis* // Critical Care Medicine, 30 (2002), 3; 617-622 doi:10.1097/00003246-200203000-00021 (međunarodna recenzija, članak, znanstveni)
Yang, S., Lim, Y., Zhou, M., Salvemini, P., Schwinn, H., Josic, D., Koo, D., Chaudry, I. & Wang, P. (2002) Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis*. Critical Care Medicine, 30 (3), 617-622 doi:10.1097/00003246-200203000-00021.
@article{article, author = {Yang, Shaolong and Lim, Yow-Pin and Zhou, Mian and Salvemini, Philomena and Schwinn, Horst and Josic, Djuro and Koo, Douglas J. and Chaudry, Irshad H. and Wang, Ping}, year = {2002}, pages = {617-622}, DOI = {10.1097/00003246-200203000-00021}, keywords = {inter-α-inhibitors, hemodynamic stability, sepsis}, journal = {Critical Care Medicine}, doi = {10.1097/00003246-200203000-00021}, volume = {30}, number = {3}, issn = {0090-3493}, title = {Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis\ast}, keyword = {inter-α-inhibitors, hemodynamic stability, sepsis} }
@article{article, author = {Yang, Shaolong and Lim, Yow-Pin and Zhou, Mian and Salvemini, Philomena and Schwinn, Horst and Josic, Djuro and Koo, Douglas J. and Chaudry, Irshad H. and Wang, Ping}, year = {2002}, pages = {617-622}, DOI = {10.1097/00003246-200203000-00021}, keywords = {inter-α-inhibitors, hemodynamic stability, sepsis}, journal = {Critical Care Medicine}, doi = {10.1097/00003246-200203000-00021}, volume = {30}, number = {3}, issn = {0090-3493}, title = {Administration of human inter-α-inhibitors maintains hemodynamic stability and improves survival during sepsis\ast}, keyword = {inter-α-inhibitors, hemodynamic stability, sepsis} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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