Metallothionein protects against cerulein-induced acute pancreatitis: Analysis using transgenic mice

Kai Fu, Tatsuo Tomita, Michael P. Sarras, Robert C. De Lisle, Glen K. Andrews

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Oxidative stress has been proposed to play a role in the early events of acute pancreatitis, and metallothionein (MT) can provide protection against oxidative stress. Using transgenic mice, we characterized the effects of depletion of MT-I and -II, or overexpression of MT-I, on pancreatic responses during cerulein-induced acute pancreatitis. In MT-I/-II knockout mice, repeated rejections of cerulein caused (a) higher serum amylase levels at 3 and 7 h after the initiation of acute pancreatitis; (b) earlier and stronger upregulation of oxidative stress-responsive genes, including heme oxygenase (HO)-1 and c-fos; and (c) exacerbated tissue damage (edema and polymorphonuclear neutrophil infiltration) compared with nontransgenic 129/SvCPJ mice. Total pancreatic glutathione (GSH + GSSG) content was similar between the knockout and nontransgenic 129/SvCPJ mice. Interestingly, during acute pancreatitis, CD-1 mice pretreated with L-buthionine-[S,R]sulfoximine (BSO), which dramatically depleted pancreatic GSH, also had more severe pancreatitis, based on the same three criteria listed above, relative to untreated controls. No effects were observed with BSO treatment alone. Finally, during cerulein-induced acute pancreatitis, MT-I overexpressing transgenic mice (>20-fold increase in pancreatic MT-I content) had lower serum α-amylase levels between 7 and 24 h and delayed upregulation of HO-1 mRNA levels, but no difference in c-fos mRNA induction relative to the appropriate strata of nontransgenic mice. Diminished tissue damage (particularly cellular necrosis) was noted in these MT-I overexpressing transgenic mice. Total pancreatic GSH content was similar in these transgenic and nontransgenic mice during cerulein-induced acute pancreatitis. These studies suggest that pancreatic MT can function as an intracellular antioxidant as does GSH and that these intracellular antioxidants play a protective role during cerulein-induced acute pancreatitis.

Original languageEnglish (US)
Pages (from-to)238-246
Number of pages9
JournalPancreas
Volume17
Issue number3
DOIs
StatePublished - Oct 1998

Fingerprint

Ceruletide
Metallothionein
Pancreatitis
Transgenic Mice
129 Strain Mouse
Heme Oxygenase-1
Oxidative Stress
Amylases
Up-Regulation
Antioxidants
Messenger RNA
Glutathione Disulfide
Neutrophil Infiltration
Serum
Knockout Mice
Glutathione
Edema
Necrosis

Keywords

  • Acute pancreatitis
  • Glutathione
  • Metallothionein
  • Mouse
  • Oxidative stress
  • Transgenic mice

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Hepatology
  • Endocrinology

Cite this

Metallothionein protects against cerulein-induced acute pancreatitis : Analysis using transgenic mice. / Fu, Kai; Tomita, Tatsuo; Sarras, Michael P.; De Lisle, Robert C.; Andrews, Glen K.

In: Pancreas, Vol. 17, No. 3, 10.1998, p. 238-246.

Research output: Contribution to journalArticle

Fu, Kai ; Tomita, Tatsuo ; Sarras, Michael P. ; De Lisle, Robert C. ; Andrews, Glen K. / Metallothionein protects against cerulein-induced acute pancreatitis : Analysis using transgenic mice. In: Pancreas. 1998 ; Vol. 17, No. 3. pp. 238-246.
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