The proteasome inhibitor mg132 protects against acute pancreatitis

The cell-permeant MG132 tripeptide (Z-Leu-Leu-Leu-aldehyde) is a peptide aldehyde proteasome inhibitor that also inhibits other proteases, including calpains and cathepsins. By blocking the proteasome, this tripeptide has been shown to induce the expression of cell-protective heat shock proteins (HS...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Letoha Tamás
Somlai Csaba
Takács Tamás
Szabolcs Annamária
Rakonczay Zoltán
Pintér Olivérné Jármay Katalin
Szalontai Tamás
Varga Ilona
Kaszaki József
Boros Imre Miklós
Duda Ernő
Hackler László
Kurucz István
Penke Botond
Dokumentumtípus: Cikk
Megjelent: 2005
Sorozat:FREE RADICAL BIOLOGY AND MEDICINE 39 No. 9
Tárgyszavak:
doi:10.1016/j.freeradbiomed.2005.06.003

mtmt:1244808
Online Access:http://publicatio.bibl.u-szeged.hu/26329
Leíró adatok
Tartalmi kivonat:The cell-permeant MG132 tripeptide (Z-Leu-Leu-Leu-aldehyde) is a peptide aldehyde proteasome inhibitor that also inhibits other proteases, including calpains and cathepsins. By blocking the proteasome, this tripeptide has been shown to induce the expression of cell-protective heat shock proteins (HSPs) in vitro. Effects of MG132 were studied in an in vivo model of acute pancreatitis. Pancreatitis was induced in male Wistar rats by injecting 2 x 100 microug/kg cholecystokinin octapeptide intraperitoneally (ip) at an interval of 1 h. Pretreating the animals with 10 mg/kg MG132 ip before the induction of pancreatitis significantly inhibited IkappaB degradation and subsequent activation of nuclear factor-kappaB (NF-kappaB). MG132 also increased HSP72 expression. Induction of HSP72 and inhibition of NF-kappaB improved parameters of acute pancreatitis. Thus MG132 significantly decreased serum amylase, pancreatic weight/body weight ratio, pancreatic myeloperoxidase activity, proinflammatory cytokine concentrations, and the expression of pancreatitis-associated protein. Parameters of oxidative stress (GSH, MDA, SOD, etc.) were improved in both the serum and the pancreas. Histopathological examinations revealed that pancreatic specimens of animals pretreated with the peptide demonstrated milder edema, cellular damage, and inflammatory activity. Our findings show that simultaneous inhibition of calpains, cathepsins, and the proteasome with MG132 prevents the onset of acute pancreatitis.
Terjedelem/Fizikai jellemzők:1142-1151
ISSN:0891-5849