Induction of heat shock protein 70 (HSP70) by zinc bis (DL-hydrogen aspartate) reduces ischemic small-bowel tissue damage in rats

Langenbecks Arch Chir. 1997;382(1):43-8. doi: 10.1007/BF02539308.

Abstract

The aim of the study was to determine whether the induction of HSP70 by Zn2+ is able to protect the small bowel of rats against ischemia. Twenty-four male Wistar rats (weight 200-300 g) were divided into four groups: (1) saline treatment for 24 h (n = 4); (2) Zn2+ treatment for 24 h (n = 4); (3) Saline pretreatment for 24 h and ischemia (n = 8); (4) Zn2+ pretreatment for 24 h and ischemia (n = 8). Pretreatment with Zn2+ was carried out by intraperitoneal administration of 50 mg/kg zinc bis (DL-hydrogen aspartate) = 10 mg/kg Zn2+. Ischemia in a defined segment of the small bowel was produced by ligation of the mesenteric vein and artery and ligation of both ends of the segment. Tissue samples were collected before and 2, 4 and 6 h after ligation and investigated by histology, immunohistochemistry and Western blotting. Twenty-four h after i.p. Zn2+ injection, the small bowel expressed increased HSP70 tissue levels. Histology with subsequent grading of ischemic tissue injury showed significantly decreased tissue necrosis after Zn2+ pretreatment and HSP70 induction compared with saline pretreated controls. In conclusion, this study proves that Zn2+ is inducing HSP70 in the small bowel in vivo and hereby able to protect the small bowel against ischemia.

MeSH terms

  • Animals
  • Aspartic Acid / pharmacology*
  • HSP70 Heat-Shock Proteins / metabolism*
  • Injections, Intraperitoneal
  • Intestinal Mucosa / blood supply
  • Intestinal Mucosa / pathology
  • Intestine, Small / blood supply*
  • Intestine, Small / pathology
  • Ischemia / pathology*
  • Male
  • Mesenteric Vascular Occlusion / pathology
  • Premedication
  • Rats
  • Zinc / pharmacology*

Substances

  • HSP70 Heat-Shock Proteins
  • Aspartic Acid
  • Zinc