Melatonin pretreatment improves liver function and hepatic perfusion after hemorrhagic shock
| Autor: | Julia Weiler, Darius Kubulus, Alexander Mathes, Inge Bauer, Stephan Ziegeler, Hauke Rensing, Sascha Pradarutti, Alexander Bentley, Beate Wolf |
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| Rok vydání: | 2007 |
| Předmět: |
Indocyanine Green
Male medicine.medical_specialty Resuscitation Shock Hemorrhagic Critical Care and Intensive Care Medicine Melatonin receptor Melatonin Rats Sprague-Dawley chemistry.chemical_compound hemic and lymphatic diseases Internal medicine medicine Animals Rats Disease Models Animal Endocrinology chemistry Liver Shock (circulatory) Emergency Medicine Liver function medicine.symptom Luzindole Perfusion Nicotinamide adenine dinucleotide phosphate Intravital microscopy NADP medicine.drug Liver Circulation |
| Zdroj: | Shock (Augusta, Ga.). 29(1) |
| ISSN: | 1073-2322 |
| Popis: | Exogenous administration of pineal hormone melatonin (MEL) has been demonstrated to attenuate organ damage in models of I/R and inflammation by antioxidative effects. However, specific organ-protective effects of MEL with respect to hemorrhagic shock have not been investigated yet. In the present study, we evaluated the role of MEL pretreatment for hepatic perfusion, redox state, and function after hemorrhage and resuscitation, with emphasis on MEL receptor activation. In a model of hemorrhagic shock (MAP 35 +/- 5 mmHg for 90 min) and reperfusion (2 h), we measured nicotinamide adenine dinucleotide phosphate (reduced form; NADPH) autofluorescence, hepatic microcirculation, and hepatocellular injury by intravital microscopy, as well as plasma disappearance rate of indocyanine green (PDRICG) as a sensitive maker of liver function in rat. Pretreatment with 10 mg kg(-1) MEL (i.v.) 15 min before induction of hemorrhage resulted in a significantly improved PDR(ICG) compared with controls (MEL/shock, 15.02% min(-1) +/- 2.9 SD vs. vehicle/shock, 6.18 +/- 4.6 SD; P = 0.001). Intravital microscopy after reperfusion revealed an improved hepatic perfusion index, redox state, and reduced hepatocellular injury in pretreated animals compared with the vehicle group. Melatonin receptor antagonist luzindole (LZN; 2.5 mg kg(-1)) almost completely abolished the protective effects of MEL pretreatment with respect to liver function (MEL + LZN/shock PDR(ICG), 7.31% min(-1) +/- 3.4 SD). Beneficial effects regarding hepatic perfusion, redox state, and cellular injury were not influenced by LZN, indicating that they may depend on antioxidative effects of MEL. However, liver function after hemorrhage is effectively maintained by MEL pretreatment via receptor-dependent pathways. |
| Databáze: | OpenAIRE |
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