Effect of vasoactive intestinal peptide and naloxone combination on urinary N-acetyl-ß-D-glucosaminidase level and kidney histology of rats exposed to severe hemorrhage

Akin M. Z., Tunçel N. S. E., Giirer F., Kural N., Uslu S.

Pharmacology, vol.47, no.3, pp.194-199, 1993 (Scopus) identifier identifier

  • Publication Type: Article / Article
  • Volume: 47 Issue: 3
  • Publication Date: 1993
  • Doi Number: 10.1159/000139097
  • Journal Name: Pharmacology
  • Journal Indexes: Scopus
  • Page Numbers: pp.194-199
  • Keywords: Blood reperfusion, Hemorrhage, Kidney, N-acetyl-ß-D- glucosaminidase, Naloxone, Vasocative intestinal peptide
  • Anadolu University Affiliated: Yes

Abstract

Renal hypoperfusion which occurs in hemorrhagic shock creates an environment in which cellular injury and organ dysfunction can occur during the episode of shock as well as reoxygenation and reperfusion. At the same time, mast cell degranulation which is observed during hemorrhage may have an additinal deleterious effect on the kidney. Twenty-two (Mus norvégiens albinos) rats (200-250 g) of either sex were used. The animals were divided into three groups. Group 1, the control group, was exposed to a 40% hemorrhage. Group 2 was exposed to 40% hemorrhage and then shed blood reperfused. Group 3 was exposed to 40% hemorrhage, and in addition to shed blood reperfusion 25 ng kg-1 vasoactive intestinal peptide (VIP) + 5 mg kg-1 naloxone (NLX) were given. At the end of the experiment the kidneys were evaluated either histologically or by measurement of the urinary N-acetyl-ß-Z)-glu- cosaminidase (NAG) activity. Shed blood reperfusion caused continuation of ischemic tissue damage and elevation of uri- nay NAG activity. Addition of VIP and NLX to the blood reperfusion caused a decrease in urinary NAG excretion, and the histology of renal tissue was almost normal. © 1993 S. Karger AG, Basel.