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Liposomal ATP protects the liver from injury during shock.

AbstractLiposomes are useful drug carriers. In this study, adenosine triphosphate (ATP) was entrapped in liposomes (Lip-ATP). Anesthetized rats were given Lip-ATP (5 mg/kg as ATP), free ATP (5 mg/kg) or saline (control group) during stabilization. Then, the rats were exposed to 30 min of hypovolemic shock and 30 min of reperfusion. Administration of Lip-ATP significantly improved hepatic blood flow during shock (13.2 +/- 1.7 ml/min/100 g tissue in the Lip-ATP group vs. 9.4 +/- 2.2, in the control group, and 8.9 +/- 2.9 in the free ATP group) and during reperfusion (20.9 +/- 2.3, 16.3 +/- 2.2, and 16.2 +/- 1.8 ml/min/100 g tissue, respectively). The serum levels of hepatic enzymes (ALT, AST and LDH) were significantly lower in the Lip-ATP group after reperfusion when compared with the control and free ATP groups. Administration of Lip-ATP also produced the best recovery of hepatic ATP level. These findings indicate that Lip-ATP increased hepatic blood flow during shock and reperfusion, presumably by improving the energy charge and metabolism of the hepatocytes. Thus, Lip-ATP appears to be a useful agent for liver injury induced by hypovolemic shock.
AuthorsH Konno, A F Matin, Y Maruo, S Nakamura, S Baba (Affiliation: Second Department of Surgery, Hamamatsu University School of Medicine, Japan.)
JournalEuropean surgical research. Europäische chirurgische Forschung. Recherches chirurgicales européennes (Eur Surg Res) Vol. 28 Issue 2 Pg. 140-5 ( 1996) ISSN: 0014-312X SWITZERLAND
PMID8834372 (Publication Type: Journal Article)
Chemical References
  • Liposomes
  • Adenosine Triphosphate
  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Alanine Transaminase
Topics
  • Adenosine Triphosphate (administration & dosage)
  • Alanine Transaminase (metabolism)
  • Animals
  • Aspartate Aminotransferases (metabolism)
  • Blood Flow Velocity
  • Infusions, Intravenous
  • L-Lactate Dehydrogenase (metabolism)
  • Liposomes (metabolism)
  • Liver (metabolism, pathology, physiopathology)
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion
  • Shock (drug therapy, metabolism, pathology)